COMPOSITIONS AND METHODS TO IMPROVE TOMATO PRODUCTION

Abstract

The present invention provides compositions comprising both Methylobacterium and compositions comprising Methylobacterium with depletion of substances that promote the growth of microorganisms residing in a tomato plant or seed; methods for improving tomato production, methods for preparing the compositions, and methods for treating a tomato plant, part of the plant, or seed with the compositions comprising Methylobacterium are also provided.

Description

INTERNATIONAL PATENT APPLICATIONFORCOMPOSITIONS AND METHODS FOR IMPROVING TOMATO PRODUCTIONCROSS REFERENCE TO RELATED APPLICATIONS

[0001] This International patent application claims the benefit of U.S Provisional Patent Application No. 61 / 954,390, filed March 17, 2014, which is incorporated herein by reference in its entirety.SEQUENCE LISTING STATEMENT

[0002] A sequence listing containing the file named 53907-138691_SL.txt which is14,824,679 bytes (measured in MS-Windows®) and created on December 3, 2014, comprises 9,188 sequences, is provided herewith via the USPTO's EFS system, and is incorporated herein by reference in its entirety.BACKGROUND

[0003] One-carbon organic compounds such as methane and methanol are found extensively in nature, and are utilized as carbon sources by bacteria classified as methanotrophs and methylotrophs. Methanotrophic bacteria include species in the genera Methylobacter, Methylomonas, Methylomicrobium, Methylococcus, Methylosinus, Methylocystis,Methylosphaera, Methylocaldum, and Methylocella (Lidstrom, 2006). Methanotrophs possess the enzyme methane monooxygenase, that incorporates an atom of oxygen from 02into methane, forming methanol. All methanotrophs are obligate one-carbon utilizers that are unable to use compounds containing carbon-carbon bonds. Methylotrophs, on the other hand, can also utilize more complex organic compounds, such as organic acids, higher alcohols, sugars, and the like. Thus, methylotrophic bacteria are facultative methylotrophs. Methylotrophic bacteria include species in the genera Methylobacterium, Hyphomicrobium, Methylophilus, Methylobacillus, Methylophaga, Aminobacter, Methylorhabdus, Methylopila, Methylosulfonomonas, Marino sulfonomonas, Paracoccus, Xanthobacter, Ancylobacter (also known as Microcyclus), Thiobacillus, Rhodopseudomonas, Rhodobacter, Acetobacter, Bacillus, Mycobacterium, Arthobacter, and Nocardia (Lidstrom, 2006).

[0004] Most methylotrophic bacteria of the genus Methylobacterium are pink-pigmented. They are conventionally referred to as PPFM bacteria, being pink-pigmented facultative methylotrophs. Green (2005, 2006) identified twelve validated species in the genusMethylobacterium, specifically M. aminovorans, M. chloromethanicum, M.dichloromethanicum, M. extorquens, M. fujisawaense, M. mesophilicum, M. organophilum, M. radiotolerans, M. rhodesianum, M. rhodinum, M. thiocyanatum, and M. zatmanii.However, M. nidulans is a nitrogen- fixing Methylobacterium that is not a PPFM (Sy et al, 2001). Methylobacterium are ubiquitous in nature, being found in soil, dust, fresh water, sediments, and leaf surfaces, as well as in industrial and clinical environments (Green, 2006).SUMMARY

[0005] Provided herein are compositions comprising Methylobacterium that are depleted of substances that promote growth of resident bacteria on the plant or seed, compositions comprising a solid substance with adherent Methylobacterium grown thereon or an emulsion having Methylobacterium grown therein, compositions comprising certain Methylobacterium isolates and derivatives thereof, methods of using the compositions to improve tomato production, and methods of making the compositions. Such compositions are in certain instances referred to herein as simply "Methylobacterium-contaimng compositions". In certain embodiments, the Methylobacterium in the composition or that is used is strain NLS0037, a variant thereof, or a strain having polymorphic DNA markers present inNLS0037 that are absent from a strain that does not increase tomato seedling growth in comparison to an untreated control. In certain embodiments, the Methylobacterium in the composition or that is used is strain NLS0037 and the composition is used to treat a tomato seed. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1- 4594. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1- 4594 with the proviso that the gene is not found in M. extorquens AMI, M. extorquens PA1, or M. extorquens ME4. In certain embodiments, the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4. In certainembodiments, the Methylobacterium in the composition or that is used is a Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0020 (NRRL B- 50930), NLS0021 (NRRL B-50939), NLS0037 (NRRL B-50941), NLS0038 (NRRL B- 50942), NLS0042 (NRRL B-50932), NLS0046 (NRRL B-50929), NLS0062 (NRRL B- 50937), NLS0064 (NRRL B-50938), NLS0065 (NRRL B-50935), NLS0066 (NRRL B- 50940), NLS0068 (NRRL B-50934), NLS0069 (NRRL B-50936), NLS0089 (NRRL B- 50933), and derivatives thereof. In certain embodiments, the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941),NLS0066 (NRRL B-50940), and derivatives thereof. In certain embodiments, any of the aforementioned compositions can further comprise an agriculturally acceptable excipient, an agriculturally acceptable adjuvant, or combination thereof.

[0006] Methods for improving tomato production comprising applying a coating or partial coating of a composition comprising Methylobacterium to a tomato plant, a part thereof, or to a tomato seed, wherein said composition comprises a solid substance with adherentMethylobacterium grown thereon, an emulsion having Methylobacterium grown therein, or compositions comprising certain Methylobacterium isolates and derivatives thereof, and wherein said tomato plant or tomato plant grown from said seed exhibits a trait improvement selected from the group consisting of an increased rate of root growth, leaf growth, seedling growth, seed production, fruit production, scion production, rootstock production, and / or increased total biomass decreased cycle time, and combinations thereof when compared to an untreated control tomato plant or a control tomato plant grown from an untreated seed are provided herein. Methods comprising applying a composition comprising Methylobacterium to a tomato plant, a part thereof, or to a tomato seed, wherein said composition comprises: (i) a solid substance with adherent Methylobacterium grown thereon; (ii) an emulsion having Methylobacterium grown therein; (iii) a Methylobacterium that has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594; or (iv) a Methylobacterium selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B-50940), and derivatives thereof, and wherein said tomato plant or tomato plant grown from said seed exhibits a trait improvement selected from the group consisting of an increased rate of root growth, leaf growth, seedling growth, seed production, fruit production, scion production, rootstock production, and / or increased total biomass when compared to an untreated control tomato plant or a control tomato plant grown from an untreated seed, thereby obtaining improved tomato production, are also provided. In certain embodiments, the composition comprises Methylobacterium at a titer of about 1 x 106CFU / gm to about 1 x 1014CFU / gm for a solid composition or at a titer of about 1 x 106CFU / mL to about 1 x 1011CFU / mL for a liquid composition containing the solid substance or for the emulsion. In certain embodiments, the Methylobacterium has at least one polymorphic DNA element that is present inMethylobacterium strain NLS0037 but that is absent from a strain that does not increase tomato seedling growth. In certain embodiments, the applied composition coats or partially coats said plant or a part thereof, or said seed. In certain embodiments, the composition is applied in a hydroponic solution. In certain embodiments, the methods further comprise: (i)growing said tomato plant or tomato plant grown from said seed; and / or (ii) harvesting seedlings, rootstock, scions, fruit, or seed from said tomato plant or tomato plant grown from said seed. In certain embodiments, the solid substance with adherent Methylobacterium is not a substance that promotes growth of resident microorganisms on the tomato plant, the part thereof, or the tomato seed. In certain embodiments, the composition comprises an agriculturally acceptable adjuvant and / or excipient. In certain embodiments of any of the aforementioned methods, the composition is depleted of substances that promote growth of resident microorganisms on said plant or seed. In certain embodiments, theMethylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 with the proviso that the gene is not found in extorquens AMI, M. extorquens PA1, or extorquens ME4. In certain embodiments, the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4. In certain embodiments, the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B- 50941), NLS0066 (NRRL B-50940), and derivatives thereof. Also provided are tomato plant parts or tomato seeds obtained by any of the aforementioned methods and that are coated or partially coated with a composition comprising Methylobacterium.

[0007] Methods for improving tomato plant production comprising applying a composition comprising Methylobacterium to a tomato plant, a part thereof, or tomato seed, wherein said composition is depleted of substances that promote growth of resident microorganisms on said plant or seed and wherein said plant or plant grown from said seed exhibits a trait improvement selected from the group consisting of an increased rate of leaf growth, an increased rate of root growth, increased total biomass production, increased seed yield, decreased cycle time, and combinations thereof when compared to an untreated control tomato plant or a control tomato plant grown from an untreated seed. In certainembodiments, the composition comprises a solid substance with adherent Methylobacterium grown thereon. In certain embodiments, the solid substance is not a substance that promotes growth of resident microorganisms on the tomato plant, the part thereof, or the tomato seed. In certain embodiments, the composition comprises Methylobacterium at a titer of about 1 x 106CFU / gm to about 1 x 1014CFU / gm. In certain embodiments, the composition comprises a liquid, a solid substance with Methylobacterium adhered thereto in a liquid, a solid substance with Methylobacterium adhered thereto in an emulsion, or an emulsion. In certainembodiments, the composition comprises Methylobacterium at a titer of about 1 x 106CFU / mL to about 1 x 1011CFU / mL. In certain embodiments, the methods further comprise: (i) growing said tomato plant or tomato plant grown from said seed; and / or (ii) harvesting seedlings, rootstock, scions, fruit, or seed from said tomato plant or tomato plant grown from said seed. In certain embodiments, the Methylobacterium has at least one polymorphic DNA element that is present in at least one Methylobacterium strain selected from the group consisting of NLS0037 but that is absent from a strain that does not increase tomato seedling growth. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 with the proviso that the gene is not found in extorquens AMI, M. extorquens PA1, or M. extorquens ME4. In certain embodiments, the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4. In certain embodiments, the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0020 (NRRL B-50930), NLS0021 (NRRL B-50939), NLS0037 (NRRL B-50941), NLS0038 (NRRL B-50942), NLS0042 (NRRL B-50932), NLS0046 (NRRL B-50929), NLS0062 (NRRL B-50937), NLS0064 (NRRL B-50938), NLS0065 (NRRL B-50935), NLS0066 (NRRL B-50940), NLS0068 (NRRL B-50934), NLS0069 (NRRL B-50936), NLS0089 (NRRL B-50933), and derivatives thereof. In certain embodiments, the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B-50940), and derivatives thereof. In certain embodiments of any of the aforementioned methods, the composition coats or partially coats said plant or a part thereof, or said seed. In certain embodiments the tomato plant part or tomato seed is immersed or partially immersed in the composition. In certain embodiments of any of the aforementioned methods, the composition is applied in a hydroponic solution. Also provided are tomato plants, plant parts or tomato seeds obtained by any of the aforementioned methods and that are coated or partially coated with a composition comprising Methylobacterium.

[0008] Compositions comprising: (a) (i) a solid substance with adherent Methylobacterium grown thereon; (ii) an emulsion comprising Methylobacterium; or (iii) certainMethylobacterium sp. are provided. In certain embodiments, compositions comprising: (i) a solid substance with adherent Methylobacterium grown thereon; (ii) an emulsion with Methylobacterium grown therein or contained therein; or (iii) a Methylobacterium; whereinsaid Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 or wherein theMethylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4, and wherein said composition further comprises an agriculturally acceptable adjuvant and / or excipient or wherein the composition comprises a hydroponic solution of man-made origin are provided. In certain embodiments, the compositions can comprise: (i) a solid substance with adherent Methylobacterium grown thereon or (ii) an emulsion with Methylobacterium grown therein or contained therein, wherein saidMethylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 or wherein theMethylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4, and wherein said composition further comprises an agriculturally acceptable adjuvant and / or excipient or wherein the composition comprises a hydroponic solution of man-made origin. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 with the proviso that the gene is not found in extorquens AMI, M. extorquens PA1, ox M. extorquens ME4. In certain embodiments, theMethylobacterium has at least one polymorphic DNA element that is present inMethylobacterium isolate NLS0037. In certain embodiments, the Methylobacterium is NLS0037 a variant thereof, or a strain having polymorphic DNA markers present inNLS0037 that are absent from a strain that does not increase tomato seedling growth in comparison to an untreated control. In certain embodiments, the Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594. In certain embodiments the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4. In certain embodiments, the Methylobacterium is selected from the group consisting of NLS0017 (NRRL B-50931), NLS0020 (NRRL B-50930), NLS0021 (NRRL B-50939), NLS0037 (NRRL B-50941), NLS0038 (NRRL B-50942), NLS0042 (NRRL B-50932), NLS0046 (NRRL B-50929), NLS0062 (NRRL B-50937), NLS0064 (NRRL B-50938), NLS0065 (NRRL B-50935), NLS0066 (NRRL B-50940), NLS0068 (NRRL B-50934), NLS0069 (NRRL B-50936), NLS0089 (NRRL B-50933), and derivatives thereof. In certain embodiments, the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B-50940), and derivatives thereof. In certain embodiments, the composition is depleted of substances that promotegrowth of resident microorganisms on a plant or seed. In certain embodiments, the substance that promotes growth of resident microorganisms on a plant or seed is selected from the group consisting of a carbon source, a nitrogen source, a phosphorous source, a sulfur source, a magnesium source, and combinations thereof. In certain embodiments, the compositions further comprise an agriculturally acceptable adjuvant and / or excipient. In certainembodiments, the solid substance with adherent Methylobacterium grown thereon has a Methylobacterium titer of at least about 5 x 108CFU / gm to at least about 1 x 1014CFU / gm. In certain embodiments, the aforementioned compositions are adapted for use in treating a tomato plant or seed or is used to treat a tomato plant or seed. Also provided herein is a tomato plant part or tomato seed that is coated or partially coated with any of theaforementioned compositions. Also provided herein is a tomato plant part or tomato seed that is immersed or partially immersed in any of the aforementioned compositions.

[0009] Also provided herein are methods of identifying compositions, plant parts, plant seeds, or processed plant products comprising Methylobacterium sp. NLS017 or NLS066 by assaying for the presence of nucleic acid sequences contained in SEQ ID NO: 4595-9188 in those materials. In certain embodiments, such methods can comprise subjecting a sample suspected of containing Methylobacterium sp. NLS017 or NLS066 to a nucleic acid analysis technique and determining that the sample contains one or more nucleic acid containing a sequence of at least about 20, 50, 100, 200, 500, or a 1000 nucleotides that is identical to at least one of SEQ ID NO: 4595-9188, wherein the presence of a sequence that is identical to at least one of SEQ ID NO: 4595-7278 is indicative of the presence of NLS017 and wherein the presence of a sequence that is identical to at least one of SEQ ID NO: 7279-9188 is indicative of the presence of NLS066. Such nucleic acid analyses include, but are not limited to, techniques based on nucleic acid hybridization, polymerase chain reactions, massspectroscopy, nanopore based detection, branched DNA analyses, combinations thereof, and the like.

[0010] Also provided herein are methods of identifying Methylobacterium sp. that can confer useful traits to plants by assaying for the presence of nucleic acid sequences contained in SEQ ID NO: 4595-9188 in the Methylobacterium sp. In certain embodiments, such methods can comprise subjecting a candidate Methylobacterium sp. to a nucleic acid analysis technique and determining that the sample contains one or more nucleic acid containing a sequence of at least about 20, 50, 100, 200, 500, or a 1000 nucleotides that is identical to at least one of SEQ ID NO: 4595-9188 indicates that the candidate Methylobacterium sp. that can confer a useful traits to a plant. Such nucleic acid analyses include, but are not limitedto, techniques based on nucleic acid hybridization, polymerase chain reactions, mass spectroscopy, nanopore based detection, branched DNA analyses, combinations thereof, and the like.DESCRIPTIONDefinitions

[0011] As used herein, the phrases "adhered thereto" and "adherent" refer toMethylobacterium that are associated with a solid substance by growing, or having been grown, on a solid substance.

[0012] As used herein, the phrase "agriculturally acceptable adjuvant" refers to a substance that enhances the performance of an active agent in a composition for treatment of plants and / or plant parts. In certain compositions, an active agent can comprise a mono-culture or co-culture of Methylobacterium.

[0013] As used herein, the phrase "agriculturally acceptable excipient" refers to an essentially inert substance that can be used as a diluent and / or carrier for an active agent in a composition for treatment of plants and / or plant parts. In certain compositions, an active agent can comprise a mono-culture or co-culture of Methylobacterium.

[0014] As used herein, the term "Methylobacterium" refers to bacteria that are facultative methylotrophs of the genus Methylobacterium. The term Methylobacterium, as used herein, thus does not encompass includes species in the genera Methylobacter, Methylomonas, Methylomicrobium, Methylococcus, Methylosinus, Methylocystis, Methylosphaera,Methylocaldum, and Methylocella, which are obligate methanotrophs.

[0015] As used herein, the phrase "co-culture of Methylobacterium" refers to aMethylobacterium culture comprising at least two strains of Methylobacterium or at least two species of Methylobacterium.

[0016] As used herein, the phrase "contaminating microorganism" refers to microorganisms in a culture, fermentation broth, fermentation broth product, or composition that were not identified prior to introduction into the culture, fermentation broth, fermentation broth product, or composition.

[0017] As used herein, the phrase "derivatives thereof, when used in the context of a Methylobacterium strain, refers to any strain that is obtained from the Methylobacterium strain. Derivatives of a Methylobacterium strain include, but are not limited to, variants of the strain obtained by selection, variants of the strain selected by mutagenesis and selection, and genetically transformed isolates obtained from the Methylobacterium strain.

[0018] As used herein, the term "emulsion" refers to a colloidal mixture of two immiscible liquids wherein one liquid is the continuous phase and the other liquid is the dispersed phase. In certain embodiments, the continuous phase is an aqueous liquid and the dispersed phase is liquid that is not miscible, or partially miscible, in the aqueous liquid.

[0019] As used herein, the phrase "essentially free of contaminating microorganisms" refers to a culture, fermentation broth, fermentation product, or composition where at least about 95% of the microorganisms present by amount or type in the culture, fermentation broth, fermentation product, or composition are the desired Methylobacterium or other desired microorganisms of pre-determined identity.

[0020] As used herein, the phrase "inanimate solid substance" refers to a substance which is insoluble or partially soluble in water or aqueous solutions and which is either non-living or which is not a part of a still-living organism from which it was derived.

[0021] As used herein, the phrase "mono-culture of Methylobacterium" refers to aMethylobacterium culture consisting of a single strain of Methylobacterium.

[0022] As used herein, the term "peptide" refers to any polypeptide of 50 amino acid residues or less.

[0023] As used herein, the term "tomato" refers to any Solarium lycopersicon hybrid or variety having either a determinant or indeterminant growth habit.

[0024] As used herein, the phrase "tomato seedlings" includes tomato plants from the germination stage through all vegetative stages.

[0025] As used herein, the phrase "tomato plants" includes tomato seedlings from the germination stage through all vegetative stages and tomato plants in all reproductive stages.

[0026] As used herein, the phrase "tomato plant" is inclusive of both tomato seedlings and tomato plants in all reproductive stages.

[0027] As used herein, the term "protein" refers to any polypeptide having 51 or more amino acid residues.

[0028] As used herein, a "pesticide" refers to an agent that is insecticidal, fungicidal, nematocidal, bacteriocidal, or any combination thereof.

[0029] As used herein, the phrase "bacteriostatic agent" refers to agents that inhibit growth of bacteria but do not kill the bacteria.

[0030] As used herein, the phrase "pesticide does not substantially inhibit growth of said Methylobacterium " refers to any pesticide that when provided in a composition comprising a fermentation product comprising a solid substance wherein a mono-culture or co-culture of Methylobacterium is adhered thereto, results in no more than a 50% inhibition ofMethylobacterium growth when the composition is applied to a plant or plant part in comparison to a composition lacking the pesticide. In certain embodiments, the pesticide results in no more than a 40%, 20%>, 10%>, 5%, or 1% inhibition of Methylobacterium growth when the composition is applied to a plant or plant part in comparison to a composition lacking the pesticide.

[0031] As used herein, the term "PPFM bacteria" refers without limitation to bacterial species in the genus Methylobacterium other than M. nodularis.

[0032] As used herein, the phrase "solid substance" refers to a substance which is insoluble or partially soluble in water or aqueous solutions.

[0033] As used herein, the phrase "solid phase that can be suspended therein" refers to a solid substance that can be distributed throughout a liquid by agitation.

[0034] As used herein, the term "non-regenerable" refers to either a plant part or processed plant product that cannot be regenerated into a whole plant.

[0035] As used herein, the phrase "substantially all of the solid phase is suspended in the liquid phase" refers to media wherein at least 95%, 98%, or 99% of solid substance(s) comprising the solid phase are distributed throughout the liquid by agitation.

[0036] As used herein, the phrase "substantially all of the solid phase is not suspended in the liquid phase" refers to media where less than 5%, 2%, or 1% of the solid is in a particulate form that is distributed throughout the media by agitation.

[0037] As used herein, the phrase "resident microorganism" refers to resident bacteria, fungi or yeast.

[0038] As used herein, the phrase "substance that promotes growth of residentmicroorganisms on a plant or seed" refers to a carbon source, a nitrogen source, aphosphorous source, and combinations thereof.

[0039] To the extent to which any of the preceding definitions is inconsistent with definitions provided in any patent or non-patent reference incorporated herein by reference, any patent or non-patent reference cited herein, or in any patent or non-patent reference found elsewhere, it is understood that the preceding definition will be used herein.Methylob cterium-containing compositions depleted of substances that promote growth of resident bacteria on a plant or seed, methods of their use, and methods of making

[0040] Compositions comprising Methylobacterium that are depleted of substances that promote growth of resident bacteria on a plant or seed, methods of using the compositions to improve tomato production, and methods of making the compositions are provided herein. Incertain embodiments of any of the aforementioned compositions, the composition comprises a solid substance wherein a mono-culture or co-culture of Methylobacterium is adhered thereto. In certain embodiments where the Methylobacterium is adhered to a solid substance, the composition comprises a colloid formed by the solid substance wherein a mono-culture or co-culture of Methylobacterium is adhered thereto and a liquid. In certain embodiments, the colloid is a gel. In certain embodiments of certain aforementioned compositions,composition is an emulsion that does not contain a solid substance.

[0041] Compositions that comprise a solid substance with adherent Methylobacterium grown thereon is provided. In certain embodiments, the adherent Methylobacterium can be at a titer of at least about 5 x 108CFU / gm to at least about 5 x 1013CFU / gm or about 1 x 1014CFU / gm and the composition is depleted of substances that promote growth of residentmicroorganisms on a plant or seed.

[0042] In certain embodiments, the compositions containing Methylobacterium provided or used herein are depleted of substances that promote growth of the resident microorganisms when one or more of those substances are absent or are essentially absent. In certain embodiments, the composition is depleted of substances that promote growth of the resident microorganisms when those substances are present at a percentage of no more than about 5%, 2%, 1%, 0.5%, 0.2%, or 0.1%> of the total mass, mass / total volume, or total volume of the composition. In certain embodiments, substance that promotes growth of residentmicroorganisms on a plant or seed is selected from the group consisting of a carbon source, a nitrogen source, a phosphorous source, a sulfur source, a magnesium source, andcombinations thereof. Carbon sources include, but are not limited to, alcohols,monosaccharides, disaccharides, polysaccharides, lipids, fatty acids, and the like. Alcohols that are depleted include, but are not limited to, methanol, ethanol, glycerol, and the like. Nitrogen sources include, but are not limited to, ammonia and various compounds containing amino groups that can be metabolized by microorganisms. In certain embodiments, the substance that is depleted is a source of two or more of a carbon source, a nitrogen source, a phosphorous source, a sulfur source, and a magnesium source. For example, the composition that is depleted of amino acids or peptides and lacks other carbon or nitrogen sources is depleted for both a carbon and a nitrogen source. In certain embodiments, the composition comprises an agriculturally acceptable adjuvant and / or excipient.

[0043] Resident microorganisms on the plant or seed include, but are not limited to bacteria, fungi, and yeast. Substances that promote the growth of such microorganisms can be identified by methods including, but not limited to, assaying the plant or seed surface for theamount or number of microorganisms present prior to exposure of the plant or seed to the substance (or to a composition containing the substance), exposing the assayed plant or seed to the substance or composition in parallel with a control composition lacking the substance, and then re-assaying the plant or seed surface for the amount or number of microorganisms present after a suitable time interval and under suitable conditions of temperature to allow growth of the resident microorganisms. Assays for numbers of microorganisms include, but are not limited to, determinations of colony forming units per an amount of plant or seed exposed to the substance and the control.

[0044] Without seeking to be limited by theory, it is believed that the compositions containing Methylobacterium provided or used herein that are depleted of substances that promote growth of the resident microorganisms can result in superior results in comparison to other compositions containing such substances when applied to plants, plant parts, or seeds. Such superior results are believed to include, but are not limited to, improved plant yield, pathogen resistance, insect resistance, fruit ripening and the like. While not seeking to be limited by theory, it is believed that the compositions containing Methylobacterium that are depleted of substances that promote growth of the resident microorganisms allow for more efficient and or extensive colonization of the plant, part thereof, or seed as competition for one or more of space or nutrients by the resident microorganisms is reduced.

[0045] Also provided herein are methods for improving tomato production that comprise applying any of the aforementioned compositions ox Methylobacterium provided herein to a tomato plant, tomato plant part, or tomato seed, and, optionally, growing the plant and / or harvesting seedlings, rootstock, scions, fruit, or seed from the plant or a plant grown from the seed. In certain embodiments, the composition coats or partially coats the tomato plant, plant part, or seed. The treated tomato plant or plant grown from the seed exhibits an increased rate of seedling growth, increased rate of root growth, an increased rate of leaf growth, increased seed production, a decreased cycle time (from seed planting to seed, rootstock, scion, or fruit production) and / or increased total biomass compared to an untreated control tomato plant or control tomato plant grown from untreated seed, thereby obtaining improved tomato production. In certain embodiments, application of the composition provides for at least about a 5%, 10%, 15%, 20%>, 30%> or 40%> increase in root growth rate, leaf growth rate, seed, rootstock, scion, or fruit production rate, and / or increased total biomass in the tomato plant, tomato plant part, or a tomato plant derived therefrom in comparison to an untreated control tomato plant or control tomato plant grown from an untreated seed. In certain embodiments, application of the composition provides for about a 5% or 10% to about a15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 60%, or 70% increase in root growth rate, leaf growth rate, seedling growth rate, seed production, fruit production, and / or increased total biomass in the plant, plant part, or a plant derived therefrom in comparison to an untreated control tomato plant or control tomato plant grown from an untreated seed. In certain embodiments, application of the composition provides for at least about a 5%, 10%>, 15%, 20%), 30%) or 40%) decrease in cycle time (i.e. time from seed to progeny seed, to usable rootstock, to usable scion, graft, or fruit) in the treated tomato plant or a tomato plant grown from a treated seed in comparison to the untreated control tomato plant or control tomato plant grown from an un-treated seed. In certain embodiments, application of the composition provides for about a 5% or 10% to about a 15%, 20%, 25%, 30%, 35%, 40%, 45%, or 50% decrease in cycle time in the treated tomato plant or a tomato plant grown from a treated seed in comparison to an untreated control tomato plant or control tomato plant grown from an untreated seed. In certain embodiments, the tomato plant part is a leaf, a stem, a flower, a root, a tuber, or a seed. In certain embodiments, the method further comprises the steps of growing the plant and / or the step of harvesting at least one plant part selected from the group consisting of a leaf, a stem, a flower, a root, a fruit, or a seed from the tomato plant or plant part. In certain embodiments of any of the aforementioned methods, the methods further comprise obtaining a processed food or feed composition from the plant or plant part. In certain embodiments, the processed food composition comprises chopped or cut tomato fruit.

[0046] Also provided are methods of making a tomato plant or tomato plant seed treatment composition that comprises Methylobacterium and is depleted of substances that promote growth of resident bacteria on a plant or seed is provided herein. Such method comprises (i) growing a mono-culture or co-culture of Methylobacterium in media that comprises an aqueous phase, a liquid phase and a solid phase, or an emulsion, thereby obtaining aMethylobacterium-contaimng media; (ii) separating the Methylobacterium from at least one other portion of the Methylobacterium-contaimng media; and (iii) reconstituting theMethylobacterium in a matrix lacking substances that promote growth of resident bacteria on a plant or seed. In certain embodiments, the separation step is effected by centrifugation, filtration, or settling of the Methylobacterium-contaimng media and removal of excess liquid or emulsion therefrom. In certain embodiments, the substance that promotes growth of resident bacteria on a plant or seed is selected from the group consisting of a carbon source, a nitrogen source, a phosphorous source, and combinations thereof. In certain embodiments, the matrix is a liquid, an emulsion, or one or more solids, and comprises an agriculturally acceptable adjuvant and / or excipient. Still in certain embodiments; the Methylobacterium aregrown in media comprising a liquid phase and a solid substance with adherent Methylobacterium grown thereon. The solid substance is separated from the liquid phase of the Methylobacterium-contaimng media, and the solid substance with adherentMethylobacterium grown thereon is reconstituted in the aforementioned matrix. In certain embodiments of the methods, the Methylobacterium sp., is selected from the group consisting of aminovorans, M. extorquens, M. fujisawaense, M. mesophilicum, M. radiotolerans, M. rhodesianum, M. nodularis, M. phyllosphaerae, M thiocyanatum, and oryzae. In certain embodiments of the methods, the Methylobacterium is not M. radiotolerans or M. oryzae. In certain embodiments of the methods, the Methylobacterium is adhered to a solid substance. In certain embodiments of the methods, the Methylobacterium is adhered to the solid substance is combined with a liquid to form a composition that is a colloid. In certain embodiments of the methods, the colloid is a gel. In certain embodiments of the methods, the Methylobacterium adhered to the solid substance is provided by culturing theMethylobacterium in the presence of the solid substance. In certain embodiments of the methods, the composition comprises an emulsion. In certain embodiments of the methods, the Methylobacterium is provided by culturing the Methylobacterium in an emulsion.

[0047] Methods where Methylobacterium are cultured in biphasic media comprising a liquid phase and a solid substance have been found to significantly increase the resultant yield of Methylobacterium relative to methods where the Methylobacterium are cultured in liquid media alone. In certain embodiments, the methods can comprise growing theMethylobacterium in liquid media with a particulate solid substance that can be suspended in the liquid by agitation under conditions that provide for Methylobacterium growth. In certain embodiments where particulate solid substances are used, at least substantially all of the solid phase can thus be suspended in the liquid phase upon agitation. Such particulate solid substances can comprise materials that are about 1 millimeter or less in length or diameter. In certain embodiments, the degree of agitation is sufficient to provide for uniformdistribution of the particulate solid substance in the liquid phase and / or optimal levels of culture aeration. However, in other embodiments provided herein, at least substantially all of the solid phase is not suspended in the liquid phase, or portions of the solid phase are suspended in the liquid phase and portions of the solid phase are not suspended in the liquid phase. Non-particulate solid substances can be used in certain biphasic media where the solid phase is not suspended in the liquid phase. Such non-particulate solid substances include, but are not limited to, materials that are greater than about 1 millimeter in length or diameter. Such particulate and non-particulate solid substances also include, but are not limited to,materials that are porous, fibrous, or otherwise configured to provide for increased surface areas for adherent growth of the Methylobacterium. Biphasic media where portions of the solid phase are suspended in the liquid phase and portions of the solid phase are not suspended in the liquid phase can comprise a mixture of particulate and non-particulate solid substances. Such particulate and non-particulate solid substances used in any of the aforementioned biphasic media also include, but are not limited to, materials that are porous, fibrous, or otherwise configured to provide for increased surface areas for adherent growth of the Methylobacterium. In certain embodiments, the media comprises a colloid formed by a solid and a liquid phase. A colloid comprising a solid and a liquid can be pre-formed and added to liquid media or can be formed in media containing a solid and a liquid. Colloids comprising a solid and a liquid can be formed by subjecting certain solid substances to a chemical and / or thermal change. In certain embodiments, the colloid is a gel. In certain embodiments, the liquid phase of the media is an emulsion. In certain embodiments, the emulsion comprises an aqueous liquid and a liquid that is not miscible, or only partially miscible, in the aqueous liquid. Liquids that are not miscible, or only partially miscible, in water include, but are not limited to, any of the following: (1) liquids having a miscibility in water that is equal to or less than that of pentanol, hexanol, or heptanol at 25 degrees C; (2) liquids comprising an alcohol, an aldehyde, a ketone, a fatty acid, a phospholipid, or any combination thereof; (3) alcohols selected from the group consisting of aliphatic alcohols containing at least 5 carbons and sterols; (4) an animal oil, microbial oil, synthetic oil, plant oil, or combination thereof; and / or, (5) a plant oil is selected from the group consisting of corn, soybean, cotton, peanut, sunflower, olive, flax, coconut, palm, rapeseed, sesame seed, safflower, and combinations thereof. In certain embodiments, the immiscible or partially immiscible liquid can comprises at least about 0.02% to about 20% of the liquid phase by mass. In certain embodiments, the methods can comprise obtaining a biphasic culture media comprising the liquid, the solid, and Methylobacterium and incubating the culture under conditions that provide for growth of the Methylobacterium. Biphasic culture medias comprising the liquid, the solid, and Methylobacterium can be obtained by a variety of methods that include, but are not limited to, any of: (a) inoculating a biphasic media comprising the liquid and the solid substance with Methylobacterium; (b) inoculating the solid substance with Methylobacterium and then introducing the solid substance comprising the Methylobacterium into the liquid media; (c) inoculating the solid substance withMethylobacterium, incubating the Methylobacterium on the solid substance, and then introducing the solid substance comprising the Methylobacterium into the liquid media; or (d)any combination of (a), (b), or (c). Methods and compositions for growing Methylobacterium in biphasic media comprising a liquid and a solid are disclosed in co-assigned U.S. Patent Application No . 13 / 907, 161, filed May 31, 2013, which is incorporated herein by reference in its entirety, and in co-assigned International Patent Application PCT / US 13 / 43722, filed May 31, 2013, which is incorporated herein by reference in its entirety.

[0048] Methods where Methylobacterium are cultured in media comprising an emulsion have also been found to significantly increase the resultant yield of Methylobacterium relative to methods where the Methylobacterium are cultured in liquid media alone. In certain embodiments, the methods for making the compositions provided herein can comprise growing the Methylobacterium agent in an emulsion under conditions that provide for Methylobacterium growth. Medias comprising the emulsion and Methylobacterium can be obtained by a variety of methods that include, but are not limited to, any of: (a) inoculating a media comprising the emulsion with Methylobacterium; (b) inoculating the aqueous liquid with the Methylobacterium, introducing the non-aqueous liquid, and mixing to form an emulsion; (c) inoculating the aqueous liquid with the Methylobacterium, introducing the nonaqueous liquid, and mixing to form an emulsion; or (d) any combination of (a), (b), or (c). In certain embodiments, the emulsion comprises an aqueous liquid and a liquid that is not miscible, or only partially miscible, in the aqueous liquid. Non-aqueous liquids that are not miscible, or only partially miscible, in water include, but are not limited to, any of the following: (1) liquids having a miscibility in water that is equal to or less than that of n- pentanol, n-hexanol, or n-heptanol at 25 degrees C; (2) liquids comprising an alcohol, an aldehyde, a ketone, a fatty acid, a phospholipid, or any combination thereof; (3) alcohols is selected from the group consisting of aliphatic alcohols containing at least 5, 6, or 7 carbons and sterols; (4) an animal oil, microbial oil, synthetic oil, plant oil, or combination thereof; and / or, (5) a plant oil is selected from the group consisting of corn, soybean, cotton, peanut, sunflower, olive, flax, coconut, palm, rapeseed, sesame seed, safflower, and combinations thereof. In certain embodiments, the immiscible or partially immiscible non-aqueous liquid can comprise at least about 0.02% to about 20% of the emulsion by mass. In certain embodiments, the immiscible or partially immiscible non-aqueous liquid can comprise at least about any of about 0.05%, 0.1%, 0.5%, or 1% to about 3%, 5%, 10%, or 20% of the emulsion by mass. Methods and compositions for growing Methylobacterium in media comprising an emulsion are disclosed in co-assigned US Provisional Patent Application No. 61 / 829,987, filed May 31, 2013, which is incorporated herein by reference in its entirety.

[0049] In certain embodiments, the fermentation broth, fermentation broth product, or compositions that comprise Methylobacterium sp. can further comprise one or more introduced microorganisms of pre-determined identity other than Methylobacterium. Other microorganisms that can be added include, but are not limited to, microorganisms that are biopesticidal or provide some other benefit when applied to a plant or plant part.Biopesticidal or otherwise beneficial microorganisms thus include, but are not limited to, various Bacillus sp., Pseudomonas sp., Coniothyrium sp., Pantoea sp., Streptomyces sp., and Trichoderma sp. Microbial biopesticides can be a bacterium, fungus, virus, or protozoan. Particularly useful biopesticidal microorganisms include various Bacillus subtilis, Bacillus thuringiensis, Bacillus pumilis, Pseudomonas syringae, Trichoderma harzianum,Trichoderma virens, and Streptomyces lydicus strains. Other microorganisms that are added can be genetically engineered or naturally occurring isolates that are available as pure cultures. In certain embodiments, it is anticipated that the bacterial or fungal microorganism can be provided in the fermentation broth, fermentation broth product, or composition in the form of a spore.

[0050] In certain embodiments, the liquid culture medium is prepared from inexpensive and readily available components, including, but not limited to, inorganic salts such as potassium phosphate, magnesium sulfate and the like, carbon sources such as glycerol, methanol, glutamic acid, aspartic acid, succinic acid and the like, and amino acid blends such as peptone, tryptone, and the like. Exemplary liquid media that can be used include, but are not limited to, ammonium mineral salts (AMS) medium (Whittenbury et al, 1970), Vogel- Bonner (VB) minimal culture medium (Vogel and Bonner, 1956), and LB broth ("Luria - Bertani Broth").

[0051] In general, the solid substance used in the methods and compositions that provide for the efficient growth of Methylobacterium can be any suitable solid substance which is insoluble or only partially soluble in water or aqueous solutions. Such suitable solid substances are also non-bacteriocidal or non-bacterio static with respect to Methylobacterium when the solid substances are provided in the liquid culture media. In certain embodiments, such suitable solid substances are also solid substances that are readily obtained in sterile form or rendered sterile. Solid substances used herein can be sterilized by any method that provides for removal of contaminating microorganisms and thus include, but are not limited to, methods such as autoclaving, irradiation, chemical treatment, and any combination thereof. These solid substances include natural substances of animal, plant, microbial, fungal, or mineral origin, manmade substances, or combinations of natural and manmadesubstances. In certain embodiments, the solid substances are inanimate solid substances. Inanimate solid substances of animal, plant, microbial, or fungal origin can be obtained from animals, plants, microbes, or fungi that are unviable (i.e. no longer living) or that have been rendered unviable. Diatom shells are thus inanimate solid substances when previously associated diatom algae have been removed or otherwise rendered inviable. Since diatom shells are inanimate solid substances, they are not considered to be photo synthetic organisms or photo synthetic microorganisms. In certain embodiments, solid substances include, but are not limited to, sand, silt, soil, clay, ash, charcoal, diatomaceous earth and other similar minerals, ground glass or glass beads, ground ceramic materials, ceramic beads, bentonite, kaolin, talc, perlite, mica, vermiculite, silicas, quartz powder, montmorillonite, and combinations thereof. In certain embodiments, the solid substance can be a polymer or polymeric beads. Polymers that can be used as a solid substance include, but are not limited to, various polysaccharides such as cellulosic polymers and chitinous polymers which are insoluble or only partially soluble in water or aqueous solutions, agar (i.e. galactans), and combinations thereof. In certain embodiments, the solid substance can be an insoluble or only partially soluble salt crystal. Salt crystals that can be used include, but are not limited to, insoluble or only partially soluble carbonates, chromates, sulfites, phosphates, hydroxides, oxides, and sulfides. In certain embodiments, the solid substance can be a microbial cell, fungal cell, microbial spore, or fungal spore. In certain embodiments, the solid substance can be a microbial cell or microbial spore wherein the microbial cell or microbial spore is not a photo synthetic microorganism. In certain embodiments, the microbial cell or microbial spore is not a photo synthetic microorganism, where the photo synthetic microorganism is selected from the group consisting of algae, cyanobacteria, diatoms, Botryococcus braunii, Chlorella, Dunaliella tertiolecta, Gracilaria, Pleurochrysis carterae, Sargassum, and Ulva. In still other embodiments, the solid substance can be an inactivated (i.e. unviable) microbial cell, fungal cell, microbial spore, or fungal spore. In still other embodiments, the solid substance can be a quiescent (i.e. viable but not actively dividing) microbial cell, fungal cell, microbial spore, or fungal spore. In still other embodiments, the solid substance can be cellular debris of microbial origin. In still other embodiments, the solid substance can be particulate matter from any part of a plant. Plant parts that can be used to obtain the solid substance include, but are not limited to, cobs, husks, hulls, leaves, roots, flowers, stems, barks, seeds, and combinations thereof. Products obtained from processed plant parts including, but not limited to, bagasse, wheat bran, soy grits, crushed seed cake, stover, and the like can also be used. Such plant parts, processed plants, and / or processed plant parts can be milled to obtainthe solid material in a particulate form that can be used. In certain embodiments, wood or a wood product including, but not limited to, wood pulp, sawdust, shavings, and the like can be used. In certain embodiments, the solid substance can be a particulate matter from an animal(s), including, but not limited to, bone meal, gelatin, ground or powdered shells, hair, macerated hide, and the like.

[0052] In certain embodiments, the solid substance is provided in a particulate form that provides for distribution of the solid substance in the culture media. In certain embodiments, the solid substance is comprised of particle of about 2 microns to about 1000 microns in average length or average diameter. In certain embodiments, the solid substance is comprised of particle of about 1 microns to about 1000 microns in average length or average diameter. In certain embodiments, the solid substance is a particle of about 1, 2, 4, 10, 20, or 40 microns to any of about 100, 200, 500, 750, or 1000 microns in average length or average diameter. Desirable characteristics of particles used in the methods and compositions provided herein include suitable wettability such that the particles can be suspended throughout the media upon agitation.

[0053] In certain embodiments, the solid substance is provided in the media as a colloid wherein the continuous phase is a liquid and the dispersed phase is the solid. Suitable solids that can be used to form colloids in liquid media used to grow Methylobacterium include, but are not limited to, various solids that are referred to as hydro colloids. Such hydrocolloids used in the media, methods and compositions provided herein can be hydrophilic polymers, of plant, animal, microbial, or synthetic origin. Hydrocolloid polymers used in the methods can contain many hydroxyl groups and / or can be polyelectrolytes. Hydrocolloid polymers used in the compositions and methods provided herein include, but are not limited to, agar, alginate, arabinoxylan, carrageenan, carboxymethylcellulose, cellulose, curdlan, gelatin, gellan, β-glucan, guar gum, gum arabic, locust bean gum, pectin, starch, xanthan gum, and mixtures thereof. In certain embodiments, the colloid used in the media, methods, and compositions provided herein can comprise a hydrocolloid polymer and one or more proteins.

[0054] In certain embodiments, the solid substance can be a solid substance that provides for adherent growth of Methylobacterium on the solid substance. Methylobacterium that are adhered to a solid substance are Methylobacterium that cannot be substantially removed by simply washing the solid substance with the adherent Methylobacterium with growth media whereas non-adherent Methylobacterium can be substantially removed by washing the solid substance with liquid growth media. In this context, "substantially removed" means that at least about 30%, 40%, 50%>, 60%>, 70%>, or 80%> the Methylobacterium present are removedwhen the solid substance is washed with three volumes of liquid growth media. Such washing can be effected by a variety of methods including, but not limited to, decanting liquid from a washed solid phase or passing liquid through a solid phase on a filter that permits flow through of bacteria in the liquid. In certain embodiments, the adherentMethylobacterium that are associated with the solid can include both Methylobacterium that are directly attached to the solid and / or Methylobacterium that are indirectly attached to the solid substance. Methylobacterium that are indirectly attached to the solid substance include, but are not limited to, Methylobacterium that are attached to another Methylobacterium or to another microorganism that is attached to the solid substance, Methylobacterium that are attached to the solid substance by being attached to another substance that is attached to the solid substance, and the like. In certain embodiments, at least 10%, 20%, 30%>, 40%>, 50%>, 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5% or 99.9% of the Methylobacterium in the fermentation broth, fermentation broth product, or compositions are Methylobacterium that are adhered to the solid substance. In certain embodiments, adherent Methylobacterium can be present on the surface of the solid substance in the fermentation broth, fermentation broth product, or composition at a density of at least about 1 Methylobacterium / 20 square micrometers, of at least about 1 Methylobacterium! '10 square micrometers, of at least about 1 Methylobacterium / '10 square micrometers, of at least about 1 Methylobacterium! 5 square micrometers, of at least about 1 Methylobacterium / 2 square micrometers, or of at least about 1 Methylobacterium / 'square micrometer. In certain embodiments, adherent Methylobacterium can be present on the surface of the solid substance in the fermentation broth, fermentation broth product, or composition at a density of at least about 1 Methylobacterium / 20 square micrometers to about 1 Methylobacterium / 'square micrometer, of at least about 1Methylobacterium! '10 square micrometers to about 1 Methylobacterium! 'square micrometer, of at least about 1 Methylobacterium / '10 square micrometers to about 1Methylobacterium! 'square micrometer, of at least about 1 Methylobacterium! 5 square micrometers to about 1 Methylobacterium / 'square micrometer, or of at least about 1Methylobacterium / 2 square micrometers to about 1 Methylobacterium / 'square micrometer. In certain embodiments, adherent Methylobacterium can be present on the surface of the solid substance in the fermentation broth, fermentation broth product, or composition at a density of at least about 1 Methylobacterium / 20 square micrometers to about 1 Methylobacterium / 2 square micrometers, of at least about 1 Methylobacterium! 10 square micrometers to about 1 Methylobacterium / 2 square micrometers, of at least about 1 Methylobacterium! '10 square micrometers to about 1 Methylobacterium / 2 square micrometers, or of at least about 1Methylobacterium! 5 square micrometers to about 1 Methylobacterium / 2 square micrometers. Biphasic fermentation broths provided herein can comprise a liquid phase that contains nonadherent Methylobacterium. In certain embodiments, titers of non-adherentMethylobacterium in the liquid phase can be less than about 100,000, 10,000, or 1,000 CFU / ml.

[0055] Biphasic culture methods provided can yield fermentation broths withMethylobacterium at a titer of greater than about 5 x 108colony- forming units per milliliter, at a titer of greater than about 1 x 109colony- forming units per milliliter, at a titer of greater than about 1 x 1010colony- forming units per milliliter, at a titer of at least about 3 x 1010colony- forming units per milliliter. In certain embodiments, fermentation broths provided herein can comprise Methylobacterium at a titer of at least about 5 x 108colony- forming units per milliliter to at least about 3 x 1010colony- forming units per milliliter, at least about 5 x108colony- forming units per milliliter to at least about 4 x 1010colony- forming units per milliliter, or at least about 5 x 108colony- forming units per milliliter to at least about 6 x 1010colony- forming units per milliliter. In certain embodiments, fermentation broths provided herein can comprise Methylobacterium at a titer of at least about 1 x 109colony- forming units per milliliter to at least about 3 x 1010colony- forming units per milliliter, at least about 1 x109colony- forming units per milliliter to at least about 4 x 1010colony- forming units per milliliter, or at least about 1 x 109colony- forming units per milliliter to at least about 6 x 1010colony- forming units per milliliter. In certain embodiments, fermentation broths provided herein will comprise Methylobacterium at a titer of at least about 1 x 1010colony- forming units per milliliter to at least about 3 x 1010colony- forming units per milliliter, at least about1 x 1010colony- forming units per milliliter to at least about 4 x 1010colony- forming units per milliliter, or at least about 1 x 1010colony- forming units per milliliter to at least about 6 x 1010colony- forming units per milliliter. In certain embodiments, fermentation broths provided herein will comprise Methylobacterium at a titer of, at least about 3 x 1010colony- forming units per milliliter to at least about 4 x 1010colony- forming units per milliliter, or at least about 3 x 1010colony- forming units per milliliter to at least about 6 x 1010colony- forming units per milliliter.

[0056] Solid substances with adherent Methylobacterium can be obtained as fermentation products can be used to make various compositions useful for treating plants or plant parts to improve plant yield, plant insect resistance, plant fungal disease resistance, and / or to improve tomato production. In certain embodiments, the composition comprises Methylobacterium and is depleted of substances that promote growth of resident bacteria. Compositionsprovided herein comprising Methylobacterium, solid substances with Methylobacterium grown thereon, or comprising emulsions with Methylobacterium grown therein can be used to treat plants or plant parts. Plants, plant parts, and, in particular, plant seeds that have been at least partially coated or coated with the fermentation broth products or compositions comprising Methylobacterium are thus provided. Also provided are processed plant products that contain the fermentation broth products or compositions with Methylobacterium or adherent Methylobacterium. Solid substances with adherent Methylobacterium can be used to make various compositions that are particularly useful for treating plant seeds. Seeds that have been at least partially coated with the fermentation broth products or compositions are thus provided. Also provided are processed seed products, including, but not limited to, meal, flour, feed, and flakes that contain the fermentation broth products or compositions provided herein. In certain embodiments, the processed plant product will be non- regenerable (i.e. will be incapable of developing into a plant). In certain embodiments, the solid substance used in the fermentation product or composition that at least partially coats the plant, plant part, or plant seed or that is contained in the processed plant, plant part, or seed product comprises a solid substance and associated or adherent Methylobacterium that can be readily identified by comparing a treated and an untreated plant, plant part, plant seed, or processed product thereof. Partial coating of a plant, a plant part, or a seed includes, but is not limited to coating at least about 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 98%o, 99%), or about 99.5% of the surface area of the plant, plant part, or plant seed.

[0057] Methods of preparing a plant or plant seed treatment composition that comprises Methylobacterium and is depleted of substances that promote growth of resident bacteria on a plant or seed are also provided herein. Such methods can comprise (i) growing a monoculture or co-culture of Methylobacterium in media that comprises: (a) an aqueous phase; (b) a liquid phase and a solid phase; or (c) an emulsion, thereby obtaining a Methylobacterium- containing media; (ii) separating the Methylobacterium from at least one other portion of the Methylobacterium-contaimng media; and (iii) reconstituting the Methylobacterium in a matrix lacking substances that promote growth of resident bacteria on a plant or seed. In certain embodiments, the separation step is effected by centriiugation, filtration, or settling of the Methylobacterium-contaimng media and removal of excess liquid or emulsion therefrom. In certain embodiments where the Methylobacterium are grown in the presence of a solid substance, the separation will provide a fraction containing Methylobacterium with adherent growth to the solid substance and some non-adherent Methylobacterium that can be reconstituted in the matrix. In certain embodiments, the substance that promotes growth ofresident bacteria on a plant or seed is selected from the group consisting of a carbon source, a nitrogen source, a phosphorous source, a sulfur source, a magnesium source, andcombinations thereof. In certain embodiments, the matrix is a liquid, an emulsion, or one or more solids, and comprises an agriculturally acceptable adjuvant and / or excipient. In certain embodiments; the Methylobacterium are grown in media comprising a liquid phase and a solid substance with adherent Methylobacterium grown thereon. The solid substance is separated from the liquid phase of the Methylobacterium-contaimng media, and the solid substance with adherent Methylobacterium grown thereon is reconstituted in theaforementioned matrix. In certain embodiments, the matrix can be a liquid including, but not limited to, water, and aqueous buffer depleted of substances that promote growth of resident bacteria on a plant or seed, or an aqueous solution depleted of substances that promote growth of resident bacteria on a plant or seed.

[0058] In certain embodiments, the Methylobacterium sp. that improve tomato production can be identified by testing newly isolated candidate Methylobacterium sp. for the presence of polymorphic nucleic acid sequences that are present in exemplary Methylobacterium sp. provided herein that improve tomato seedling growth rates and that are absent fromMethylobacterium sp. that do not improve tomato seedling growth rates. In certain embodiments, the polymorphic nucleic acid sequences that are present in the identified Methylobacterium sp. that improves tomato production are also present in one or more of the exemplary Methylobacterium sp. isolates NLS0037 provided herein that improves tomato seedling growth rate but are absent from one or more of the Methylobacterium sp. isolates that do not improve tomato seedling growth rates. Such nucleic acid polymorphisms that occur in the Methylobacterium sp. that improve tomato production can include, but are not limited to, single nucleotide polymorphisms, RFLP, AFLP and / or other DNA variations such as repetitive sequences, insertion sequences, transposons, and genomic islands occurring as a result of insertions, deletions, and substitutions (Indels) in the bacterial genome which includes both the chromosomal DNA as well as any extrachromosomal nucleic acid elements that can be present in the Methylobacterium sp. that improve tomato production. Such extrachromosomal nucleic acid elements include, but are not limited to, plasmids,bacteriophage DNA or RNA, and the like. Methods used to identify such nucleotide polymorphisms include, but are not limited to, single base extension (SBE) techniques, allele specific hybridization (ASH), real-time PCR detection {e.g. TaqMan™; U.S. Pat. Nos.5,804,375; 5,538,848; 5,487,972; and 5,210,015, which are each incorporated herein by reference in their entireties), combinations of ASH and RT-PCR (KASP™ detection systems,LGC Genomics, Middlesex, UK) and deep sequencing techniques (U.S. Patent Appl. No. 20120264632, incorporated herein by reference in its entirety).

[0059] Also provided herein are compositions, methods of making the compositions, and methods of using the compositions to improve tomato production. Such improved tomato production includes, but is not limited to, increased root growth rate, leaf growth rate, seedling growth rate, seed production, fruit production, scion production, rootstock production, and / or increased total biomass in comparison to an untreated control tomato plant. In certain embodiments, the compositions or methods comprise or use any of the following Methylobacterium sp. isolates provided in the following Table 1 or derivatives of the isolates. In certain embodiments, such derivatives can include variants but are not limited to, variants of the isolates obtained by selection, variants of the isolates selected by mutagenesis and selection, and genetically transformed isolates obtained from the isolates.

[0060] Table 1. Methylobacterium sp. isolates

[0061] 1Deposit number for strain to be deposited with the AGRICULTURAL RESEARCH SERVICE CULTURE COLLECTION (NRRL) of the National Center for AgriculturalUtilization Research, Agricultural Research Service, U.S. Department of Agriculture, 1815 North University Street, Peoria, Illinois 61604 U.S.A. under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure. Subject to 37 CFR § 1.808(b), all restrictions imposed by the depositor on the availability to the public of the deposited material will be irrevocably removed upon the granting of any patent from this patent application.

[0062] Co-assigned patent applications that disclose additional specific uses of theMethylobacterium strains of Table 1 such as: (1) increasing corn yield (US 61 / 911780, filed 12 / 4 / 2013; and International Application claiming benefit of the same filed on 12 / 4 / 2014); (2) increasing soybean yield (US 61 / 911698, filed 12 / 4 / 2013; and International Application claiming benefit of the same filed on 12 / 4 / 2014); (3) improving lettuce cultivation(International Patent Application PCT / US 14 / 68558 filed on 12 / 4 / 2014); (4) providing fungal disease resistance (US 62 / 045950, filed 9 / 4 / 2014; US 62 / 013,464 , filed 6 / 17 / 2014) and are each incorporated herein by reference in their entireties. Specifically incorporated herein by reference in their entireties are the genomic nucleic acid sequences of NLS017, NLS020, NLS037, NLS042, NLS065, and NLS066 that are disclosed in International Application filed on 12 / 4 / 2014 and claiming benefit of US 61 / 954840, filed 3 / 18 / 2014, and US 61 / 911516, filed 12 / 4 / 2013. Such genomic nucleic acid sequences can be used to identify compositions, plant parts, plant seeds, or processed plant products comprising NLS017, NLS020, NLS037, NLS042, NLS065, and NLS066.

[0063] Also provided herein are Methylobacterium sp. that provide for improved tomato production where the Methylobacterium sp. have any of: (i) at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594; or (ii) at least one gene encoding at least one protein that is orthologous to a reference protein of Table 4. A Methylobacterium sp. has at least one gene that isorthologous to a protein having an amino acid sequence of at least one of SEQ ID NO: 1- 4594, or to the corresponding SEQ ID NO of a reference protein of Table 4, when a chromosome and / or any extrachromosomal DNA in that Methylobacterium sp. contains a gene encoding a protein that has at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100% sequence identity across the entire length of the amino acid sequence of at least one of SEQ ID NO: 1-4594. The Methylobacterium sp. can also have at least two, three, four, six, eight, 10, 15, or 20 genes encoding proteins that are orthologous to proteins having an amino acid sequence of SEQ ID NO: 1-4594 or encoding proteins that are orthologous to the corresponding SEQ ID NO of areference protein of Table 4. In certain embodiments, the Methylobacterium sp. can contain at least one gene encoding a protein that is orthologous to a reference protein having the amino acid sequence of SEQ ID NO: 1- 2684 of Table 4. In certain embodiments, theMethylobacterium sp. can contain at least one gene encoding a protein that is orthologous to reference protein having the amino acid sequence of SEQ ID NO: 2585-4594 of Table 4. In certain embodiments, the Methylobacterium sp. can contain at least one gene encoding a protein that is orthologous to reference protein having the amino acid sequence of SEQ ID NO: 2969 or 212 of Table 4. Examples of proteins that are orthologous to SEQ ID NO: 2969 include, but are not limited to, the orthologous proteins identified as transcriptional regulator XRE family proteins of SEQ ID NO: 2969 and 399 that are provided in Table 4. Examples of proteins that are orthologous to SEQ ID NO: 212 include, but are not limited to, proteins having the amino acid sequence of SEQ ID NO: 212 and 2828 that are similar to proteins identified as members of the LysR family transcriptional regulators. Compositions comprising any of the aforementioned Methylobacterium sp. and an agriculturally acceptable excipient, adjuvant, or combination thereof are also provided along with tomato seeds or leaves that are at least partially coated with such compositions and methods of using such compositions as seed or foliar treatments to improve tomato production.

[0064] A Methylobacterium sp. can be determined to contain a gene encoding a protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 by a variety of different techniques. In certain embodiments, a Methylobacterium sp. can be determined to contain a gene encoding a protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 by assembling a complete electronic genomic sequence comprising chromosomal and extrachromosomal DNA sequences present in that Methylobacterium sp. with a computer and associated software, and determining if any of the open reading frames (ORF) present in that DNA sequence encode a protein having the aforementioned percent sequence identity. In such embodiments, the ORF can be identified by performing a six-way translation of the electronically assembled sequence and querying the translated with an amino acid sequence of SEQ ID NO: 1-4594 or the corresponding SEQ ID NO: of a reference protein of Table 4. In other embodiments, the present or absence of a given sequence within a Methylobacterium sp. an amino acid sequence of SEQ ID NO: 1- 4594 or the corresponding SEQ ID NO: of a reference protein of Table 4 can be determined by a nucleic acid analysis or protein analysis technique. Examples of nucleic acid sequences that encode the proteins of SEQ ID NO: l-4594 include, but are not limited to, SEQ ID NO: 4595-9188, respectively. Such nucleic acid analyses include, but are not limited to,techniques based on nucleic acid hybridization, polymerase chain reactions, mass spectroscopy, nanopore based detection, branched DNA analyses, combinations thereof, and the like. Protein analysis techniques include, but are not limited to, immuno-detection, mass spectroscopy, combinations thereof, and the like.

[0065] Compositions provided herein that are useful for treating tomato plants or plant parts that comprise Methylobacterium, and / or are depleted of substances that promote growth of resident bacteria on a plant or seed, contain a solid substance with adherentMethylobacterium grown thereon, or that comprise emulsions with Methylobacterium grown therein can also further comprise an agriculturally acceptable adjuvant or an agriculturally acceptable excipient. An agriculturally acceptable adjuvant or an agriculturally acceptable excipient is typically an ingredient that does not cause undue phytotoxicity or other adverse effects when exposed to a plant or plant part. In certain embodiments, the solid substance can itself be an agriculturally acceptable adjuvant or an agriculturally acceptable excipient so long as it is not bacteriocidal or bacteriostatic to the Methylobacterium. In otherembodiments, the composition further comprises at least one of an agriculturally acceptable adjuvant or an agriculturally acceptable excipient. Any of the aforementioned compositions can also further comprise a pesticide. Pesticides used in the composition include, but are not limited to, an insecticide, a fungicide, a nematocide, and a bacteriocide. In certain embodiments, the pesticide used in the composition is a pesticide that does not substantially inhibit growth of the Methylobacterium. As Methylobacterium are gram negative bacteria, suitable bacteriocides used in the compositions can include, but are not limited to, bacteriocides that exhibit activity against gram positive bacteria but not gram negative bacteria. Compositions provided herein can also comprise a bacteriostatic agent that does not substantially inhibit growth of the Methylobacterium. Bacteriostatic agents suitable for use in compositions provided herein include, but are not limited to, those that exhibit activity against gram positive bacteria but not gram negative bacteria. Any of the aforementioned compositions can also be an essentially dry product {i.e. having about 5% or less water content), a mixture of the composition with an emulsion, or a suspension. Any of the compositions provided herein can be used to coat or partially coat a plant, plant, part, or plant seed. Partial coating of a plant, a plant part, or a seed includes, but is not limited to coating at least about 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or about 99.5% of the surface area of the plant, plant part, or plant seed.

[0066] Agriculturally acceptable adjuvants used in the compositions that compriseMethylobacterium include, but are not limited to, components that enhance product efficacyand / or products that enhance ease of product application. Adjuvants that enhance product efficacy can include various wetters / spreaders that promote adhesion to and spreading of the composition on plant parts, stickers that promote adhesion to the plant part, penetrants that can promote contact of the active agent with interior tissues, extenders that increase the half- life of the active agent by inhibiting environmental degradation, and humectants that increase the density or drying time of sprayed compositions. Wetters / spreaders used in the compositions can include, but are not limited to, non-ionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, organo-silicate surfactants, and / or acidified surfactants. Stickers used in the compositions can include, but are not limited to, latex-based substances, terpene / pinolene, and pyrrolidone-based substances. Penetrants can include mineral oil, vegetable oil, esterified vegetable oil, organo-silicate surfactants, and acidified surfactants. Extenders used in the compositions can include, but are not limited to, ammonium sulphate, or menthene-based substances. Humectants used in the compositions can include, but are not limited to, glycerol, propylene glycol, and diethyl glycol. Adjuvants that improve ease of product application include, but are not limited to, acidifying / buffering agents, anti-foaming / de- foaming agents, compatibility agents, drift-reducing agents, dyes, and water conditioners. Anti-foaming / de- foaming agents used in the compositions can include, but are not limited to, dimethopolysiloxane. Compatibility agents used in the compositions can include, but are not limited to, ammonium sulphate. Drift-reducing agents used in the compositions can include, but are not limited to, polyacrylamides, and polysaccharides. Water conditioners used in the compositions can include, but are not limited to, ammonium sulphate.

[0067] Methods of treating plants and / or plant parts with the fermentation broths, fermentation broth products, and compositions comprising Methylobacterium are also provided herein. Treated plants, and treated plant parts obtained therefrom, include, but are not limited to, a tomato, plant. Plant parts that are treated include, but are not limited to, leaves, stems, flowers, roots, seeds, fruit, tubers, coleoptiles, and the like. Seeds or other propagules of any of the aforementioned plants can be treated with the fermentation broths, fermentation broth products, fermentation products, and / or compositions provided herein.

[0068] In certain embodiments, plants and / or plant parts are treated by applying the fermentation broths, fermentation broth products, fermentation products, and compositions that comprise Methylobacterium as a spray. Such spray applications include, but are not limited to, treatments of a single plant part or any combination of plant parts. Spraying can be achieved with any device that will distribute the fermentation broths, fermentation brothproducts, fermentation products, and compositions to the plant and / or plant part(s). Useful spray devices include a boom sprayer, a hand or backpack sprayer, crop dusters (e.g. aerial spraying), and the like. Spraying devices and or methods providing for application of the fermentation broths, fermentation broth products, fermentation products, and compositions to either one or both of the adaxial surface and / or abaxial surface can also be used. Plants and / or plant parts that are at least partially coated with any of a biphasic fermentation broth, a fermentation broth product, fermentation product, or compositions that comprise a solid substance with Methylobacterium adhered thereto are also provided herein. Also provided herein are processed plant products that comprise a solid substance with Methylobacterium adhered thereto. Any of the compositions provided herein can be used to coat or partially coat a plant, plant, part, or plant seed. Partial coating of a plant, a plant part, or a seed includes, but is not limited to coating at least about 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or about 99.5% of the surface area of the plant, plant part, or plant seed.

[0069] In certain embodiments, tomato seeds are treated by exposing the seeds to the fermentation broths, fermentation broth products, fermentation products, and compositions that comprise Methylobacterium. Seeds can be treated with the fermentation broths, fermentation broth products, and compositions provided herein by methods including, but not limited to, imbibition, coating, spraying, and the like. In certain embodiments, surface sterilized seeds are treated with a composition comprising Methylobacterium. In certain embodiments, non-sterilized seeds (i.e. seeds that have not been subjected to surface sterilization) are treated with a composition comprising Methylobacterium that has been depleted of substances that promote growth of resident microorganisms on the seed. Seed treatments can be effected with both continuous and / or a batch seed treaters. In certain embodiments, the coated seeds may be prepared by slurrying seeds with a coatingcomposition containing a fermentation broth, fermentation broth product, or compositions that comprise the solid substance with Methylobacterium and air drying the resulting product. Air drying can be accomplished at any temperature that is not deleterious to the seed or the Methylobacterium, but will typically not be greater than 30 degrees Centigrade. The proportion of coating that comprises a solid substance and Methylobacterium includes, but is not limited to, a range of 0.1 to 25% by weight of the seed, 0.5 to 5% by weight of the seed, and 0.5 to 2.5% by weight of seed. Partial coating of a seed can includes, but is not limited to coating at least about 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%), or about 99.5% of the surface area of the seed. In certain embodiments, a solidsubstance used in the seed coating or treatment will have Methylobacterium adhered thereon. In certain embodiments, a solid substance used in the seed coating or treatment will be associated with Methylobacterium and will be a fermentation broth, fermentation broth product, or composition obtained by the methods provided herein. Various seed treatment compositions and methods for seed treatment disclosed in U.S. Patent Nos. 5,106,648, 5,512,069, and 8, 181 ,388 are incorporated herein by reference in their entireties and can be adapted for use with an active agent comprising the fermentation broths, fermentation broth products, or compositions provided herein. In certain embodiments, the composition used to treat the seed can contain agriculturally acceptable excipients that include, but are not limited to, woodflours, clays, activated carbon, diatomaceous earth, fine-grain inorganic solids, calcium carbonate and the like. Clays and inorganic solids that can be used with the fermentation broths, fermentation broth products, or compositions provided herein include, but are not limited to, calcium bentonite, kaolin, china clay, talc, perlite, mica, vermiculite, silicas, quartz powder, montmorillonite and mixtures thereof. Agriculturally acceptable adjuvants that promote sticking to the seed that can be used include, but are not limited to, polyvinyl acetates, polyvinyl acetate copolymers, hydro lyzed polyvinyl acetates,polyvinylpyrrolidone- vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers, polyvinyl methyl ether, polyvinyl methyl ether-maleic anhydride copolymer, waxes, latex polymers, celluloses including ethylcelluloses and methylcelluloses, hydroxy methylcelluloses, hydro xypropylcellulose, hydroxymethylpropylcelluloses, polyvinyl pyrrolidones, alginates, dextrins, malto-dextrins, polysaccharides, fats, oils, proteins, karaya gum, jaguar gum, tragacanth gum, polysaccharide gums, mucilage, gum arables, shellacs, vinylidene chloride polymers and copolymers, soybean-based protein polymers and copolymers, lignosulfonates, acrylic copolymers, starches, polyvinylacrylates, zeins, gelatin, carboxymethylcellulose, chitosan, polyethylene oxide, acrylamide polymers and copolymers, polyhydroxyethyl acrylate, methylacrylamide monomers, alginate, ethylcellulose, polychloroprene and syrups or mixtures thereof. Other useful agriculturally acceptable adjuvants that can promote coating include, but are not limited to, polymers and copolymers of vinyl acetate, polyvinylpyrrolidone- vinyl acetate copolymer and water-soluble waxes. Various surfactants, dispersants, anticaking-agents, foam-control agents, and dyes disclosed herein and in U.S. Patent No. 8,181,388 can be adapted for use with an active agent comprising the fermentation broths, fermentation broth products, or compositions provided herein.

[0070] In certain embodiments, PPFMs that are used to increase tomato production could also be applied in a hydroponic solution as an addition to the hydroponic pool. Such hydroponic solutions are solutions comprising at least minerals necessary for tomato plant growth. Hydroponic solutions suitable for growth of tomato plants and seedlings include, but are not limited, to those described in U.S. Patent Nos. 8,091,275 and U.S. 7,818,916, which are each incorporated herein by reference in their entireties with respect to the hydroponic solutions disclosed therein.

[0071] Provided herein are compositions that comprise Methylobacterium that provide increased tomato fruit, scion, or rootstock production and increased tomato seedling growth relative to untreated plants that have not been exposed to the compositions. In certain embodiments, plant parts, including, but not limited to, a seed, a leaf, a fruit, a stem, a root, a tuber, or a coleoptile can be treated with the compositions provided herein to increase tomato production. Treatments or applications can include, but are not limited to, spraying, coating, partially coating, immersing, and / or imbibing the plant or plant parts with the compositions provided herein. In certain embodiments, a seed, a leaf, a fruit, a stem, a root, a tuber, or a coleoptile can be immersed and / or imbibed with a liquid, semi-liquid, emulsion, or slurry of a composition provided herein. Such seed immersion or imbibition can be sufficient to provide for improved tomato production in a treated plant or plant part in comparison to an untreated plant or plant part. Improved tomato production includes, but is not limited, to increased seedling growth, root growth, increased leaf growth, increased seed, scion, or rootstock production, and / or increased total biomass in comparison to untreated control plants. In certain embodiments, plant seeds can be immersed and / or imbibed for at least 1, 2, 3, 4, 5, or 6 hours. Such immersion and / or imbibition can, in certain embodiments, be conducted at temperatures that are not deleterious to the plant seed or the Methylobacterium. In certain embodiments, the seeds can be treated at about 15 to about 30 degrees Centigrade or at about 20 to about 25 degrees Centigrade. In certain embodiments, seed imbibition and / or immersion can be performed with gentle agitation.

[0072] Compositions provided herein comprising Methylobacterium are therefore expected to be useful in improving tomato production.In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a composition with Methylobacterium at a titer of at least about 1 x 106colony- forming units per milliliter, at least about 5 x 106colony- forming units per milliliter, at least about 1 x 107colony- forming units per milliliter, at least about 5 x 108colony- forming units per milliliter, at least about 1 x 109colony- forming unitsper milliliter, at least about 1 x 1010colony- forming units per milliliter, or at least about 3 x 1010colony- forming units per milliliter. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improving tomato production can be a composition with Methylobacterium at a titer of about least about 1 x 106colony- forming units per milliliter, at least about 5 x 106colony- forming units per milliliter, at least about 1 x 107colony- forming units per milliliter, or at least about 5 x 108colony- forming units per milliliter to at least about 6 x 1010colony- forming units per milliliter of a liquid or an emulsion. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improving tomato production can be a fermentation broth product with a Methylobacterium titer of a solid phase of that product is at least about 5 x 108colony- forming units per milliliter to at least about 5 x 1013colony- forming units ofMethylobacterium per gram of the solid phase. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improving tomato production can be a composition with a Methylobacterium titer of at least about 1 x 106colony- forming units per gram, at least about 5 x 106colony- forming units per gram, at least about 1 x 107colony- forming units per gram, or at least about 5 x 108colony- forming units per gram to at least about 6 x 1010colony- forming units of Methylobacterium per gram of particles in the composition containing the particles that comprise a solid substance wherein a mono-culture or co-culture of Methylobacterium is adhered thereto. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improving tomato production can be a composition with a Methylobacterium titer of at least about 1 x 106colony- forming units per mL, at least about 5 x 106colony- forming units per mL, at least about 1 x 107colony- forming units per mL, or at least about 5 x 108colony- forming units per mL to at least about 6 x 1010colony- forming units of Methylobacterium per mL in a composition comprising an emulsion wherein a mono-culture or co-culture of a Methylobacterium adhered to a solid substance is provided therein or grown therein. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improving tomato production can be a composition with a Methylobacterium titer of at least about 1 x 106colony- forming units per mL, at least about 5 x 106colony- forming units per mL, at least about 1 x 107colony- forming units per mL, or at least about 5 x 108colony- forming units per mL to at least about 6 x 1010colony- forming units of Methylobacterium per mL of in a composition comprising an emulsion wherein a mono-culture or co-culture of aMethylobacterium is provided therein or grown therein.

[0073] In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a composition with a Methylobacterium sp. at a titer of at least about 1 xlO4colony- forming units per milliliter, at least about 1 xlO5colony- forming units per milliliter, at least about 1 xlO6colony- forming units per milliliter, at least about 5x106colony- forming units per milliliter, at least about 1 xlO7colony- forming units per milliliter, at least about 5 x 108colony- forming units per milliliter, at least about 1 x 109colony- forming units per milliliter, at least about 1 x 1010colony- forming units per milliliter, or at least about 3 x 1010colony- forming units per milliliter. In certainembodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a composition with Methylobacterium sp. at a titer of at least about 1 xlO4colony- forming units per milliliter, at least about 1 xlO5colony- forming units per milliliter, about least about 1 xlO6colony- forming units per milliliter, at least about 5x106colony- forming units per milliliter, at least about 1 xlO7colony- forming units per milliliter, or at least about 5 x 108colony- forming units per milliliter to at least about 6 x 1010colony- forming units per milliliter of a liquid or an emulsion. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a fermentation broth product with a Methylobacterium sp. titer of a solid phase of that product is at least about 1 xlO4colony- forming units per gram, at least about 1 xlO5colony- forming units per gram, at least about 1 xlO6colony- forming units per gram, at least about 5x106colony- forming units per gram, at least about 1 xlO7colony- forming units per gram, at least about 5 x 108colony- forming units per gram, at least about lxlO9colony- forming units per gram, or at least about 5x109colony- forming units per gram to at least about 6 x 1010colony- forming units of Methylobacterium per gram, at least about 1 x 1011colony- forming units of Methylobacterium per gram, at least about 1 x 1012colony- forming units of Methylobacterium per gram, at least about 1 x 1013colony- forming units ofMethylobacterium per gram, or at least about 5 x 1013colony- forming units ofMethylobacterium per gram of the solid phase. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a composition with a Methylobacterium titer of at least about 1 xlO6colony- forming units per gram, at least about 5x106colony- forming units per gram, at least about 1 xlO7colony- forming units per gram, at least about 5 x 108colony- forming units per gram, at least about lxlO9colony- forming units per gram, or at least about 5xl09colony- forming units per gram to at least about 6x1010colony- forming units of Methylobacterium per gram, at least about lxlO11colony- forming units of Methylobacterium per gram, at least about lxlO12colony-forming units of Methylobacterium per gram, at least about lxlO13colony- forming units of Methylobacterium per gram, or at least about 5x1013colony- forming units ofMethylobacterium per gram of particles in the composition containing the particles that comprise a solid substance wherein a mono-culture or co-culture of Methylobacterium sp. is adhered thereto. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a composition with aMethylobacterium titer of at least about 1 xlO6colony- forming units per mL, at least about 5x106colony- forming units per mL, at least about 1 xlO7colony- forming units per mL, or at least about 5 x 108colony- forming units per mL to at least about 6 x 1010colony- forming units of Methylobacterium per mL in a composition comprising an emulsion wherein a monoculture or co-culture of a Methylobacterium sp. adhered to a solid substance is provided therein or grown therein. In certain embodiments, an amount of a composition provided herein that is sufficient to provide for improved tomato production can be a composition with a Methylobacterium titer of at least about 1 xlO6colony- forming units per mL, at least about 5x106colony- forming units per mL, at least about 1 xlO7colony- forming units per mL, or at least about 5x108colony- forming units per mL to at least about 6 x 1010colony- forming units of Methylobacterium per mL of in a composition comprising an emulsion wherein a monoculture or co-culture of a Methylobacterium sp. is provided therein or grown therein.EXAMPLES

[0074] The following examples are included to demonstrate preferred embodiments of the invention. It will be appreciated by those of skill in the art that the techniques disclosed in the following examples represent techniques discovered by the Applicants to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the instant disclosure, appreciate that many changes can be made in the specific embodiments that are disclosed, while still obtaining like or similar results, without departing from the scope of the invention**.Example 1. Culturing of PPFM strains in a liquid growth media supplemented with a solid substance

[0075] The liquid growth medium used to culture the PPFM cultures was a base salts medium supplemented with glycerol, peptone, and diatomaceous earth. The base salts medium used was ammonium mineral salts (AMS) medium. AMS medium contains, perliter, 700 milligrams of dibasic potassium phosphate anhydrous, 540 milligrams of monobasic potassium phosphate anhydrous, one gram of magnesium sulfate heptahydrate, 500 milligrams of ammonium chloride anhydrous, and 200 milligrams of calcium chloride dihydrate.

[0076] AMS base medium was prepared from three stock solutions, listed below:Stock solution I: for one liter at 50X concentrationdibasic potassium phosphate, anhydrous 35 gramsmonobasic potassium phosphate, anhydrous 27 gramsStock solution II: for one liter at 50X concentrationmagnesium sulfate heptahydrate 50 gramsammonium chloride, anhydrous 25 gramsStock solution III: for one liter at 50X concentrationcalcium chloride dihydrate 10 grams

[0077] Stock solutions I, II, and III were autoclaved separately.

[0078] To prepare one liter of liquid AMS medium with glycerol, peptone, anddiatomaceous earth, the following were added to 920 ml of distilled water:20 ml of stock solution I20 ml of stock solution II20 ml of stock solution III20 ml of a 50% glycerol stock solution10 grams of peptone2 grams of diatomaceous earth

[0079] The resulting solution with suspended diatomaceous earth was sterilized by autoclaving.

[0080] Two liters of the above AMS medium were placed into a four-liter flask. Two milliliters of liquid culture PPFMs were added to the media to inoculate. The flask was then placed in an incubated shaker set to 240 RPM and 30 degrees Celsius. The cultures were grown for six days and then stored at 4 degrees Celsius for future use.Example 2. Seed inoculation of Tomatoes

[0081] Commercial Sweet Olive™ tomato seeds were treated with the PPFM strainNLS0037, and then grown over a time period of about 12-14 days. The titer of strain NLS0037 was 2.0 X 107CFU / mL. Two liters of the culture were initially grown in liquid AMS-GP media plus diatomaceous earth at 2 grams / liter (see Example 1). A 100 ml of the culture media was spun down in a centrifuge to form a pellet. The supernatant was then drained and room temperature tap water was added to bring the solution back to its initialvolume of 100 ml. Seeds were planted in 100 cell Horticube sheets (an artificial growth media) and treated with 1 ml of solution applied directly to the seed by pipette at the time of planting. The growth media and watering practices simulate a hydroponic treatment. Each experimental unit (control and treated) contained 100 tomato seedlings. The wet weight of each seedling was measured, with the means being reported in Table 2.

[0082] Table 2. Control and PPFM Treated Tomato Seedling Wet WeightsExample 3. Identification of nucleic acid polymorphisms present in Methylo bacterium that improve tomato production

[0083] Whole genome sequencing libraries for the Illumina™ high-throughput sequencing platform are generated for Methylobacterium sp. isolates provided in Table 1 using Illumina TRUSEQ™ or NEXTERA™ DNA sample preparation kits (described on the internet sites res.illumina.com / documents / products / datasheets / datasheet_truseq_dna_sample_prep_kits.pdf andres. illumina. co m / documents / products / datasheets / datashee t_nextera_dna_sample_prep .pdf) using the methods described by the manufacturer. The resultant libraries are then subjected to pyro sequencing (Siqueira JF et al. J Oral Microbiol. 2012; 4: 10.3402 / jom.v4i0.10743). Raw pyro sequencing -generated genomic sequence data are subjected to adaptor- and quality- based trimming for quality control. Whole-genome Shotgun Sequence Assembly (1) is achieved by assembling quality-passed data using the de novo assembler Velvet (2). For gene finding and annotation, reference training data is leveraged from TIGRFAM (9), Pfam, COG (10), and UniReflOO (11). The rRNAs are identified with RNAmmer (5), protein- coding genes are identified with Glimmer (3) or Maker (6), and tRNAs are identified with tRNAscan-SE (4). Gene functions are assigned with blastx (7), blastp (7), HMMER (8), and InterProScan against comprehensive protein databases described above (Reference Data).

[0084] Detection of polymorphisms (SNP or other DNA variations occurring as a result of insertions, deletions, and substitutions (Indels)) in the Methylobacterium sp. isolates of Table 1 is performed with BWA (12) and the Samtools suite (on the internet atsamtools.sourceforge.net / ), structural variation is identified with BreakDancer (on the internet at breakdancer.sourceforge.net / ) and CoGE (on the internet at genomevolution.org / CoGe / ). Polymorphisms diagnostic for Methylobacterium that secrete anti- fungal agents are identified by comparisons of the sequences of exemplary Methylobacterium isolate NLS0037 that improve tomato seedling growth but that are absent from one or more Methylobacterium isolates that do not improve tomato. Polymorphisms present in exemplary Methylobacterium isolate NLS0037 that improve tomato production but that are absent in exemplaryMethylobacterium isolates that do not improve tomato production are then used to identify other Methylobacterium isolates that improve tomato production.References for Example 41. Miller JR, Koren S, Sutton G (2010) Assembly algorithms for next-generation sequencing data. Genomics 95: 315-327.2. Zerbino DR, Birney E (2008) Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18: 821-829.3. Delcher AL, Bratke KA, Powers EC, Salzberg SL (2007) Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 23: 673-679.4. Lowe TM, Eddy SR (1997) tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 25: 955-964.5. Lagesen K, Hallin P, Rodland EA, Staerfeldt HH, Rognes T, et al. (2007) RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res 35: 3100-3108.6. Cantarel B, Korf I, Robb S, et al. (2008) MAKER: An easy-to-use annotation pipeline designed for emerging model organism genomes. Genome Research 18: 188-196.7. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, et al. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25: 3389-3402.8. Eddy SR (2009) A new generation of homology search tools based on probabilistic inference. Genome Inform 23: 205-211.9. Haft DH, Selengut JD, White O (2003) The TIGRFAMs database of protein families. Nucleic Acids Res 31 : 371-373.10. Tatusov RL, Fedorova ND, Jackson JD, Jacobs AR, Kiryutin B, et al. (2003) The COG database: an updated version includes eukaryotes. BMC Bioinformatics 4: 41.11. Suzek BE, Huang H, McGarvey P, Mazumder R, Wu CH (2007) UniRef: comprehensive and non-redundant UniProt reference clusters. Bioinformatics 23: 1282-1288.12. Li H. and Durbin R. (2009) Fast and accurate short read alignment with Burrows- Wheeler Transform. Bioinformatics, 25: 1754-60.Example 5. Testing of Additional Methylobacterium isolates for stimulation of tomato seedling growth

[0085] Methylobacterium isolates NLS0017, NLS0037, NLS0038, and NLS0066 were tested for stimulation of tomato seedling growth essentially as described in Example 2 with the exceptions that dry rather than wet weight of the seedlings was determined and that the amount applied to each seed was 0.25 mL rather than 1 mL. The results of such analyses are shown in Table 3.

[0086] Table 3. Percent Increase in Seedling Dry Weight relative to control forNLS0017, NLS0037, NLS0038, and NLS0066 treatments

[0087] The NLS0017 and NLS0066 strains were identified as isolates capable of providing improved tomato seedling growth while NLS0038 was identified as an isolate that did not improve tomato seedling growth in these experiments.Example 6. Identification of Orthologous Genes present in Methylobacterium sp. that can improve tomato production

[0088] The PPFM strains listed in Table 1 were grown on solid agar media comprising Ammonium Mineral Salts (AMS) plus glycerol and peptone at 30° C for 5 days, essentiallyas described in co-assigned U.S. Patent Application Publication No. US20130324407 and incorporated herein by reference in its entirety. Genomic DNA was extracted using MO-BIO (Carlsbad, CA) Ultra Clean Microbial DNA Isolation kit, and 1 μg of high quality DNA was used for Illumina Nextera XT library preparation followed by Illumina 2x100 paired-end sequencing on a HiSeq2000 system. Raw Illumina genomic sequence data were subjected to adaptor- and quality-based trimming for quality control. Whole-genome Shotgun Sequence Assembly was achieved by assembling quality-passed data using the de novo assembler SPADES (33). For gene finding and annotation, reference training data was leveraged from TIGRFAM (9), Pfam, COG (10), and UniReflOO (11). The rRNAs were identified with RNAmmer (5), protein-coding genes were identified with Glimmer (3) and Maker (6), and tRNAs were identified with tRNAscan-SE (4). Gene functions were assigned with blastx (7), blastp (7), HMMER (8), and InterProScan against comprehensive protein databases described above (Reference Data). Detection of polymorphisms (SNP or other DNA variations occurring as a result of insertions, deletions, and substitutions (Indels)) in theMethylobacterium sp. isolates was performed with BWA (12) and the Samtools suite (on the internet at samtools.sourceforge.net / ) and the Genome Analysis Toolkit (GATK, on the world wide web internet site "broadinstitute.org / gatk / "), structural variation was identified with BreakDancer (on the internet at breakdancer.sourceforge.net / ) and CoGE (on the internet at genome vo lution. org / Co Ge / ) .

[0089] Genes that encoded open reading frames were predicted from the assembled whole genomic sequences of NLS0017, NLS0038, and NLS066 essentially as described above. Within and between genome orthologous genes were clustered using OrthoMCL (available on the world wide web internet site "orthomcl.org / orthomcl / "). Putative functional annotations were assigned to gene products using BLASTP (available on the internet site "blast.ncbi.nlm.nih.gov / Blast.cgi") against the UniProt database (available on the world wide web internet site " uniprot.org / "). Genes present in individual genomes of NLS0017 and NLS0066 that could improve tomato production (as shown in Example 5) but absent in the genome of NLS0038 that did not improve tomato production (as shown in Example 5) were identified in OrthoMCL clusters using custom software. The encoded proteins found in the Methylobacterium NLS0017 and NLS0066 that could improve tomato production are provided in the sequencing listing as SEQ ID NO: 1-4594. The nucleic acid sequences that encode the proteins of SEQ ID NO: 1-4594 are SEQ ID NO: 4595-9188, respectively. The proteins encoded by genes present in NLS0017 but absent from NLS0038 are provided as SEQ ID NO: 1-2684. The proteins encoded by genes present in NLS0066 but absent fromNLS0038 are provided as SEQ ID NO: 2685-4594. Orthologous gene groups representing genes encoding proteins found in the genomes of at least two individual genomes ofNLS0017 and NLS0066 that could improve tomato production (as shown in Example 5) but that are absent in the genome of NLS0038 that did not improve tomato production are provided in Table 4. In Table 4, groups of orthologous genes are provided in each row, where the longest sequence and associated unique Seq ID Number are designated as a reference sequence to represent the ortholog cluster (Column 3 of Table 4). The ortholog group identification number is provided in column 1 of Table 4, the closest gene identity based on database comparisons is provided in column 2 of Table 4, and the reference sequence for each ortholog cluster is provided in column 3 of Table 4. Examples of ortholog sequences found in NLS0017 and NLS0066 are provided as SEQ ID NO in Table 4, columns 4, and 5, respectively.

[0090] Table 4. Orthologous Genes found in NLS0017 and NLS0066 that are absent in NLS0038Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:3930v20141116 hypothetical protein 2703 34 2703 sulfitexytochrome C oxidoreductase subunit3960v20141116 A 2704 36 27043964v20141116 transposase 2705 37 2705 putative sulfite ytochrome c oxidoreductase3974v20141116 subunit B 38 38 27064022v20141116 hypothetical protein 42 42 2707 hypothetical protein4025v20141116 MexAMl_METAlpl708 43 43 27084057v20141116 major facilitator superfamily protein 49 49 27094058v20141116 hypothetical protein 50 50 27104061v20141116 hypothetical protein 51 51 27114068v20141116 pyruvate kinase 52 52 27124075v20141116 hypothetical protein 2713 53 27134082v20141116 FAD-dependent oxidoreductase 55 55 27144084v20141116 hypothetical protein 2715 57 2715ECF subfamily RNA polymerase sigma-244106v20141116 factor 2716 58 27164113v20141116 short-chain dehydrogenase / reductase SDR 59 59 27174124v20141116 MarR family transcriptional regulator 2718 60 27184146v20141116 two component transcriptional regulator 2721 61 27214147v20141116 hypothetical protein 62 62 27224155v20141116 hypothetical protein Mrad2831 1363 64 64 2723 cobalt-containing nitrile hydratase subunit4162v20141116 alpha 65 65 27264163v20141116 regulatory protein 67 67 27274165v20141116 formyl transferase 2728 69 27284192v20141116 aldo / keto reductase 72 72 27294214v20141116 aliphatic nitrilase 74 74 2730Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:4228v20141116 hypothetical protein 75 75 27314269v20141116 TonB-dependent siderophore receptor 2732 77 27324288v20141116 ABC transporter-like protein 84 84 27344325v20141116 FAD-dependent oxidoreductase 91 91 27364327v20141116 hypothetical protein 92 92 27374335v20141116 hypothetical protein Mrad2831 6489 2738 93 27384353v20141116 transposase partial 95 95 27394354v20141116 magnesium transporter 96 96 2740 spermidine / putrescine ABC transporter4356v20141116 ATP-binding protein 2741 97 27414376v20141116 hypothetical protein 2743 103 27434407v20141116 hypothetical protein 107 107 27444409v20141116 Asp / Glu racemase 2745 109 2745 binding-protein-dependent transport system4410v20141116 inner membrane protein 110 110 27464412v20141116 MFS transporter 2748 111 27484421v20141116 hypothetical protein 112 112 27514424v20141116 hypothetical protein 2752 113 2752 sulfonate ABC transporter ATP-binding4442v20141116 lipoprotein 117 117 27534460v20141116 partition protein 121 121 27554464v20141116 extracellular ligand-binding receptor 2756 123 27564466v20141116 hypothetical protein 2757 124 27574482v20141116 hypothetical protein 2758 126 27584499v20141116 sulfo lactate dehydrogenase 127 127 27604505v20141116 hypothetical protein 2761 130 27614506v20141116 ABC transporter-like protein 131 131 27624507v20141116 hypothetical protein 2763 132 27634508v20141116 inner-membrane translocator 133 133 2764Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:branched-chain amino acid transporter4509v20141116 permease subunit LivH 134 134 27654518v20141116 hypothetical protein 135 135 27664519v20141116 Hypothetical protein 2767 136 27674520v20141116 MFS transporter 137 137 27704522v20141116 D-amino acid dehydrogenase small subunit 2771 138 27714525v20141116 allantoate amidohydrolase 141 141 27724534v20141116 ABC transporter ATP-binding protein 143 143 27754537v20141116 beta- lactamase 2776 144 27764542v20141116 4-phosphopantetheinyl transferase 2777 146 27774546v20141116 hypothetical protein 147 147 27784562v20141116 hypothetical protein 2779 151 27794563v20141116 urea ABC transporter permease 2780 153 27804564v20141116 amino acid ABC transporter permease 154 154 2782 branched-chain amino acid ABC transporter4566v20141116 substrate-binding protein 155 155 27844574v20141116 hypothetical protein 157 157 27874579v20141116 ABC transporter substrate-binding protein 2788 160 2788UDP-3-0-acyl N-acetylglucosamine4582v20141116 deacetylase 2789 162 27894584v20141116 MFS transporter 164 164 27904586v20141116 hypothetical protein 165 165 27914588v20141116 3 OS ribosomal protein S13 2792 166 2792 nitrate ABC transporter substrate-binding4601v20141116 protein 2794 167 27944607v20141116 glutaminase 2795 170 27954610v20141116 hypothetical protein 171 171 2796 glyoxalase / bleomycin resistance4612v20141116 protein / dioxygenase 2797 172 2797Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:4613v20141116 shikimate kinase 173 173 27984614v20141116 hypothetical protein 174 174 27994615v20141116 putative sulfite oxidase subunit YedY 175 175 28004616v20141116 R A polymerase sigma factor 176 176 28014619v20141116 hypothetical protein Mrad2831 0815 177 177 28024624v20141116 hypothetical protein Mnod 0273 179 179 28034627v20141116 ferric reductase 180 180 28054628v20141116 hypothetical protein 181 181 28064634v20141116 hypothetical protein Mrad2831 4175 2807 185 28074642v20141116 hypothetical protein 187 187 28084644v20141116 hypothetical protein 2809 188 28094646v20141116 hypothetical protein 189 189 28104648v20141116 hypothetical protein 2811 190 28114652v20141116 response regulator receiver protein 192 192 2812 hypothetical protein4654v20141116 MexAMl_METAlp3794 193 193 28134656v20141116 HupE / UreJ protein 195 195 28144657v20141116 hypothetical protein 2815 196 28154659v20141116 hypothetical protein 198 198 28164661v20141116 cupin 2817 200 28174663v20141116 hypothetical protein 2818 201 28184665v20141116 hypothetical protein 2819 202 2819 response regulator receiver sensor hybrid4676v20141116 histidine kinase 204 204 28204681v20141116 hypothetical protein 205 205 28214683v20141116 hypothetical protein 2822 206 28224684v20141116 hypothetical protein M446 2722 2823 207 28234686v20141116 hypothetical protein 208 208 28244687v20141116 peptidase S14 ClpP 209 209 2825Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ IDIdentifier Annotation NO: NO: NO:4688v20141116 hypothetical protein 210 210 28264689v20141116 hypothetical protein 2827 211 28274690v20141116 LysR family transcriptional regulator 212 212 28284691v20141116 hypothetical protein 213 213 28294692v20141116 hypothetical protein 2830 214 28304694v20141116 hypothetical protein 2831 215 28314695v20141116 hypothetical protein M446 0699 217 217 28324696v20141116 MazF family transcriptional regulator 218 218 28334697v20141116 hypothetical protein Mnod 6017 219 219 2834Fmn-binding pyridoxamine 5 -phosphate4699v20141116 oxidase 2835 220 28354704v20141116 siderophore biosynthesis protein 2836 222 28364705v20141116 hypothetical protein 2837 223 28374706v20141116 sorbosone dehydrogenase 2838 224 28384710v20141116 sensor histidine kinase 225 225 28394715v20141116 peptidase 2840 226 28404716v20141116 metallophosphoesterase 227 227 28414720v20141116 nitrile hydratase subunit beta 2842 228 28424721v20141116 hypothetical protein 229 229 28434723v20141116 hypothetical protein 230 230 28444725v20141116 NAD-dependent epimerase / dehydratase 2845 231 28454743v20141116 AsnC family transcriptional regulator 233 233 28484750v20141116 hypothetical protein 2849 234 28494751v20141116 hypothetical protein 2850 235 28504752v20141116 hypothetical protein 2851 236 28514756v20141116 hypothetical protein 2852 237 28524757v20141116 hypothetical protein 2853 238 28534759v20141116 peptidase M20 2854 239 28544766v20141116 iron reductase 2855 242 2855Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:4767v20141116 hypothetical protein 243 243 28564771v20141116 AsnC family transcriptional regulator 244 244 28574772v20141116 transcriptional regulator 245 245 28584774v20141116 hypothetical protein 2859 246 28594789v20141116 fusaric acid resistance protein 247 247 28614796v20141116 pyruvate dehydrogenase 249 249 28624800v20141116 GntR family transcriptional regulator 2863 250 28634801v20141116 hypothetical protein 251 251 28644802v20141116 hypothetical protein 252 252 28654806v20141116 Protein of unknown function DUF2474 2866 255 28662 4-dihydroxyhept-2-ene-l 7-dioic acid4811v20141116 aldolase 258 258 28684814v20141116 hypothetical protein 259 259 28694834v20141116 DltE 263 263 2873 methyl- accepting chemotaxis4838v20141116 receptor / sensory transducer 264 264 28754842v20141116 hypothetical protein 2876 266 28764843v20141116 ABC transporter substrate-binding protein 267 267 28774844v20141116 ABC transporter permease 268 268 28784847v20141116 hypothetical protein 270 270 2879 two component LuxR family transcriptional4849v20141116 regulator 272 272 28804850v20141116 Peptidase family M20 / M25 / M40 protein 273 273 28814851v20141116 peptide ABC transporter permease 2882 274 28824877v20141116 DoxX family protein 2886 278 2886 binding-protein-dependent transport system4883v20141116 inner membrane protein 280 280 2887 methionine ABC transporter ATP-binding4884v20141116 protein 281 281 2888Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ IDIdentifier Annotation NO: NO: NO:4885v20141116 hypothetical protein 282 282 2889Glucose-methanol-choline (GMC)4907v20141116 oxidoreductase:NAD binding site 286 286 28924910v20141116 LysR family transcriptional regulator 289 289 28934911v20141116 orotate pho sphoribo sy ltransferase 291 291 28944912v20141116 hypothetical protein 2895 292 28954917v20141116 membrane protein 295 295 28964918v20141116 RND family efflux transporter MFP subunit 2897 296 28974920v20141116 hypothetical protein 2899 298 28994921v20141116 hypothetical protein 299 299 29004923v20141116 NLPA lipoprotein 301 301 29014947v20141116 hypothetical protein 303 303 29064954v20141116 LuxR family transcriptional regulator 2907 308 29074958v20141116 cupin 2908 311 29084961v20141116 amino acid ABC transporter 312 312 29104963v20141116 response regulator receiver protein 314 314 29114983v20141116 Hypothetical protein 2914 316 29144986v20141116 hypothetical protein 317 317 29164989v20141116 peptidase S9 319 319 29174992v20141116 N-acetyltransferase GCN5 320 320 29184993v20141116 glutamate carboxypeptidase 2919 321 29194995v20141116 hypothetical protein Mchl 4780 322 322 29205001v20141116 nitrate reductase 2921 325 29215016v20141116 hypothetical protein 327 327 29235017v20141116 diguanylate cyclase 2924 328 29245018v20141116 hypothetical protein 329 329 29255019v20141116 hypothetical protein 330 330 29265028v20141116 hypothetical protein 2928 335 29285030v20141116 ABC transporter permease 337 337 2929Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:5034v20141116 carbohydrate-selective porin OprB 339 339 29305036v20141116 hypothetical protein 340 340 29315039v20141116 hypothetical protein 342 342 29325070v20141116 amidase 347 347 2939 type I protein secretion ATP-binding protein5071v20141116 HlyB 348 348 29405073v20141116 hypothetical protein 349 349 2941 gamma carboxymucono lactone5075v20141116 decarboxylase 352 352 29425076v20141116 D-serine dehydratase 2943 353 29435085v20141116 hypothetical protein Mchl 4781 2944 359 29445092v20141116 ABC transporter substrate-binding protein 365 365 29455099v20141116 MarR family transcriptional regulator 368 368 29475121v20141116 histidine kinase 371 371 29495124v20141116 DSBA oxidoreductase 373 373 2950 methyl- accepting chemotaxis sensory5125v20141116 transducer 2951 374 29515129v20141116 crotonase 376 376 2952 amino acid ABC transporter substrate-5133v20141116 binding protein 379 379 2953 ferredoxin subunit of nitrite reductase and5137v20141116 ring-hydroxylating dioxygenase 380 380 29545138v20141116 ABC transporter 2955 381 29555139v20141116 peptide ABC transporter 382 382 29565182v20141116 hypothetical protein 2962 386 29625190v20141116 chromosome partitioning protein ParA 391 391 29655196v20141116 secretion protein HlyD family protein 397 397 29665197v20141116 hypothetical protein 398 398 29675199v20141116 XRE family transcriptional regulator 2969 399 2969Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:COG0346: Lactoylglutathione lyase and5203v20141116 related lyases 2970 402 29705204v20141116 COG3386: Gluconolactonase partial 403 403 29715207v20141116 ABC transporter permease 2972 405 29725208v20141116 ABC transporter permease 406 406 29735209v20141116 dihydroorotase 2974 407 29745236v20141116 epoxide hydrolase 2977 408 29775238v20141116 OmpA / MotB domain-containing protein 2978 410 29785242v20141116 hypothetical protein 411 411 29795243v20141116 hypothetical protein 412 412 29805244v20141116 endoribonuclease L-PSP 413 413 29825245v20141116 molybdenum cofactor biosysynthesis protein 414 414 29835255v20141116 peptide ABC transporter permease 416 416 2984 sugar ABC transporter substrate-binding5256v20141116 protein 417 417 29855257v20141116 hypothetical protein 2986 418 29865333v20141116 xanthine dehydrogenase 2991 421 29915352v20141116 hypothetical protein 430 430 29935357v20141116 ferredoxin 433 433 29945365v20141116 3-isopropylmalate dehydrogenase 439 439 2995 methyl- accepting chemotaxis sensory5371v20141116 transducer 442 442 29965372v20141116 group 1 glycosyl transferase 2997 444 29975373v20141116 chemotaxis protein CheW 2998 445 29985422v20141116 alanine racemase domain-containing protein 451 451 30095423v20141116 ArsR family transcriptional regulator 452 452 30105426v20141116 hypothetical protein 453 453 30115428v20141116 hypothetical protein 455 455 30125430v20141116 HxlR family transcriptional regulator 3013 457 3013Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ IDIdentifier Annotation NO: NO: NO:5433v20141116 peptidase C14 3014 460 30145434v20141116 hypothetical protein 461 461 30155436v20141116 LysR family transcriptional regulator 3016 463 30165442v20141116 hypothetical protein 3017 466 30175443v20141116 hypothetical protein 467 467 30185444v20141116 hypothetical protein Mext 0240 468 468 30195445v20141116 type 11 methyltransferase 469 469 30205446v20141116 phosphoglycerate mutase 470 470 30215447v20141116 myo-inositol-1 -phosphate synthase 3022 471 30225448v20141116 chemotaxis protein CheA 3023 472 30235450v20141116 NAD-dependent epimerase / dehydratase 3024 474 30245451v20141116 radical SAM protein 475 475 30255452v20141116 Hypothetical protein 3026 476 30265453v20141116 hypothetical protein Mrad2831 1317 3027 477 3027 response regulator receiver modulated CheB5454v20141116 methylesterase 3028 478 30285500v20141116 porin 484 484 30385506v20141116 hypothetical protein 3040 486 30405507v20141116 hypothetical protein 487 487 30415508v20141116 hypothetical protein Mpop 0725 3042 488 30425509v20141116 hypothetical protein 3043 489 30435510v20141116 hypothetical protein 3044 490 30445516v20141116 hypothetical protein Mpop 1265 491 491 30465517v20141116 chromosome partitioning protein 492 492 30475569v20141116 metal dependent phosphohydrolase 495 495 30535573v20141116 hypothetical protein Mext 1867 497 497 30545580v20141116 hypothetical protein Mpop 2258 3056 500 30565583v20141116 hypothetical protein Mpop 3020 3057 502 30575585v20141116 hypothetical protein Mpop 0722 503 503 3058Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:5586v20141116 hypothetical protein Mpop 0723 504 504 30595589v20141116 XRE family transcriptional regulator 505 505 30605598v20141116 PBS lyase 3061 510 30615599v20141116 chemotaxis protein CheY 511 511 30625647v20141116 GDP-mannose 4 6-dehydratase 3071 516 30715658v20141116 hypothetical protein Mrad2831 3432 517 517 30725662v20141116 hypothetical protein 520 520 30745665v20141116 Hypothetical protein 3075 522 30755668v20141116 cytochrome B561 523 523 3076Pho sphoribo sylamino imidazo le-5670v20141116 succinocarboxamide synthase 3077 525 30775673v20141116 chemotaxis sensory transducer protein 527 527 30785778v20141116 hypothetical protein 3089 548 30895784v20141116 hypothetical protein 3090 552 30905785v20141116 hypothetical protein 3091 554 30915786v20141116 Sulfur oxidation protein SoxZ 557 557 30925787v20141116 sulfur oxidation cytochrome c protein SoxA 558 558 30935788v20141116 MFS transporter 560 560 3094 mandelate racemase / muconate lactonizing5789v20141116 protein 3095 561 30955792v20141116 PAS domain-containing protein 563 563 30965793v20141116 sugar transporter 3097 564 30975843v20141116 Hypothetical protein 569 569 31065849v20141116 hypothetical protein Mrad2831 5253 3107 575 31075851v20141116 chemotaxis protein 576 576 31085852v20141116 AsnC family transcriptional regulator 3109 577 31095854v20141116 hypothetical protein 3110 578 31105855v20141116 hypothetical protein 3111 579 31115856v20141116 NAD-glutamate dehydrogenase 3112 580 3112Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:5857v20141116 hypothetical protein 581 581 31135860v20141116 transcriptional regulator XRE family 3114 584 31145862v20141116 2-nitropropane dioxygenase 3116 585 31165926v20141116 dioxygenase 3126 588 31265929v20141116 gamma-glutamyltransferase 589 589 3128R D efflux system outer membrane5930v20141116 lipoprotein NodT family 3129 590 31295936v20141116 Hypothetical protein 592 592 31305938v20141116 Cytochrome c class I 593 593 31315939v20141116 hypothetical protein 3132 594 31325988v20141116 extracellular ligand-binding receptor 600 600 31445993v20141116 hypothetical protein Mrad2831 6386 604 604 31456001v20141116 transporter 606 606 31476006v20141116 Leu / I le / V al-binding family protein 3148 608 31486007v20141116 hypothetical protein 609 609 31496010v20141116 hypothetical protein Mrad2831 1535 610 610 31506012v20141116 hypothetical protein 3151 613 31516014v20141116 hypothetical protein 614 614 31526016v20141116 family 5 extracellular solute-binding protein 616 616 31536017v20141116 acyl-CoA dehydrogenase 3154 617 31546021v20141116 diguanylate cyclase 618 618 31576023v20141116 hydroxymethylglutaryl-CoA lyase 3158 619 31586024v20141116 hypothetical protein 3159 620 3159NAD-binding 3-hydroxyacyl-CoA6026v20141116 dehydrogenase 3160 621 3160L-carnitine dehydratase / bile acid-inducible6027v20141116 protein F 622 622 3161Fe-S type tartrate / iumarate subfamily6093v20141116 hydro-lyase subunit alpha 625 625 3166Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:6095v20141116 hypothetical protein 3167 626 31676101v20141116 glutathione S-transferase 627 627 31686115v20141116 NAD-dependent epimerase / dehydratase 629 629 31716116v20141116 sorbosone dehydrogenase 630 630 31726117v20141116 cytochrome C 3173 631 31736118v20141116 hypothetical protein Mrad2831 0725 632 632 31746119v20141116 serine / threonine protein phosphatase 3175 633 31756124v20141116 hypothetical protein 636 636 31766125v20141116 malate synthase G 3177 637 31776126v20141116 LysR family transcriptional regulator 3178 638 31786130v20141116 alanine racemase 641 641 31796131v20141116 3-hydroxyisobutyrate dehydrogenase 3180 642 31806133v20141116 acyl carrier protein 644 644 31816134v20141116 hypothetical protein 645 645 31826135v20141116 hypothetical protein 3183 646 31836137v20141116 hypothetical protein 3184 648 3184L-carnitine dehydratase / bile acid-inducible6142v20141116 protein F 649 649 31856143v20141116 acetolactate synthase 3186 650 31866188v20141116 GntR family transcriptional regulator 656 656 31946193v20141116 hypothetical protein 657 657 3195FAD linked oxidase domain-containing6194v20141116 protein 658 658 3196TRAP transporter solute receptor TAXI6200v20141116 family protein 3197 662 31976201v20141116 hypothetical protein Mext 2439 3198 663 31986202v20141116 alpha / beta hydrolase 664 664 31996203v20141116 electron transporter 3200 665 32006204v20141116 hypothetical protein 666 666 3201Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:6205v20141116 hypothetical protein 667 667 32026206v20141116 amine oxidase 3203 668 32036207v20141116 2-hydroxyacid dehydrogenase 669 669 32046209v20141116 hypothetical protein 3205 670 3205Bcr / CflA subfamily drug resistance6210v20141116 transporter 3206 671 3206 acyl-CoA dehydrogenase domain-containing6214v20141116 protein 3207 672 32076219v20141116 acyl-CoA dehydrogenase 674 674 32086220v20141116 succinate-semialdehyde dehydrogenase 675 675 32096221v20141116 dihydrodipicolinate synthetase 676 676 32106225v20141116 hypothetical protein 680 680 32116226v20141116 potassium-transporting ATPase subunit B 3212 681 32126229v20141116 type III effector Hrp-dependent protein 3213 682 32136230v20141116 Lacl family transcriptional regulator 3214 683 32146231v20141116 putative aldolase 684 684 32156233v20141116 glycosyl transferase family 1 685 685 32166235v20141116 hypothetical protein 687 687 32176236v20141116 serine / threonine dehydratase 688 688 32186238v20141116 hypothetical protein 689 689 32196239v20141116 oxidase 690 690 32206241v20141116 SPW repeat-containing protein 3221 693 32216243v20141116 tartronate semialdehyde reductase 694 694 32226245v20141116 ABC transporter permease 695 695 3223 binding-protein-dependent transport system6246v20141116 inner membrane protein 3224 696 32246247v20141116 ABC transporter substrate-binding protein 3225 697 3225 spermidine / putrescine ABC transporter6248v20141116 ATPase 698 698 3226Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:6249v20141116 dihydropyrimidinase 699 699 32276250v20141116 po ly-beta-hydroxybutyrate po lymerase 700 700 32286253v20141116 aldo / keto reductase 3229 702 32296254v20141116 circadian phase modifier CpmA 703 703 32306325v20141116 hypothetical protein 709 709 32316328v20141116 GCN5 family acetyltransferase 712 712 32326329v20141116 MFS transporter 713 713 32336331v20141116 major facilitator superfamily protein 715 715 3234L-carnitine dehydratase / bile acid-inducible6332v20141116 protein F 3235 716 32356333v20141116 hypothetical protein 3236 717 32366334v20141116 dihydroxy-acid dehydratase 3237 718 32376337v20141116 3-hydroxyisobutyrate dehydrogenase 3238 721 32386340v20141116 2-dehydropantoate 2-reductase 724 724 32396343v20141116 cytochrome C 726 726 32406346v20141116 hypothetical protein 3241 729 32416347v20141116 alanine racemase 730 730 32426348v20141116 hypothetical protein 3243 731 32436351v20141116 D-galactarate dehydratase 733 733 32446353v20141116 LysR family transcriptional regulator 734 734 32453-hydroxy-2-methylbutyryl-CoA6358v20141116 dehydrogenase 3246 735 32466413v20141116 flagellar protein FlgA 736 736 32546414v20141116 altronate dehydratase 737 737 3255D-isomer specific 2-hydroxyacid6415v20141116 dehydrogenase NAD-binding subunit 738 738 32566423v20141116 flp fap pilin component 739 739 32576430v20141116 inner-membrane translocator 744 744 32586431v20141116 sn-glycerol-3-phosphate ABC transporter 745 745 3259Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:substrate-binding protein6432v20141116 hypothetical protein 746 746 32606435v20141116 family 5 extracellular solute-binding protein 3261 748 32616438v20141116 hypothetical protein 3262 749 32626440v20141116 gamma-glutamyltransferase 751 751 32636441v20141116 prolyl-tR A synthetase 752 752 3264HAD-superfamily phosphatase subfamily6444v20141116 IIIC domain protein 3265 753 32656445v20141116 4-methylmuconolactone transporter 3266 754 32666446v20141116 GCN5 family acetyltransferase 755 755 32676449v20141116 hypothetical protein 757 757 32686452v20141116 diguanylate cyclase / phosphodiesterase 759 759 32696453v20141116 putative alkaline phosphatase 760 760 3270 binding-protein-dependent transport system6454v20141116 inner membrane protein 761 761 32716456v20141116 hypothetical protein 3272 763 32726457v20141116 amidase 3273 764 32736460v20141116 iron-containing alcohol dehydrogenase 3274 765 32746461v20141116 acetyl-CoA acetyltransferase 766 766 32756462v20141116 pimeloyl-CoA dehydrogenase large subunit 767 767 32766463v20141116 acyl-CoA dehydrogenase 768 768 32776465v20141116 Icl family transcriptional regulator 769 769 32786466v20141116 hypothetical protein Mnod 2193 770 770 32796469v20141116 acetylornithine deacetylase 3280 772 32806578v20141116 hypothetical protein 775 775 32896580v20141116 ABC transporter substrate-binding protein 776 776 32906581v20141116 hypothetical protein 777 777 32916586v20141116 dimethylmenaquinone methyltransferase 3292 779 32926589v20141116 hypothetical protein 3293 781 3293Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:6594v20141116 GntR family transcriptional regulator 3295 785 32956595v20141116 LysR family transcriptional regulator 786 786 32966600v20141116 methylase 789 789 32976605v20141116 4-phytase 792 792 3298 amino acid ABC transporter substrate-6609v20141116 binding protein 3299 796 32996610v20141116 ABC transporter permease 797 797 33006611v20141116 hypothetical protein 798 798 3301 peptide ABC transporter substrate-binding6673v20141116 protein 800 800 33166674v20141116 ABC transporter ATP-binding protein 3317 801 33176679v20141116 MucR family transcriptional regulator 802 802 33186681v20141116 XRE family transcriptional regulator 804 804 33196682v20141116 hypothetical protein 805 805 33206685v20141116 hypothetical protein 808 808 33216688v20141116 hypothetical protein 3322 811 33226689v20141116 catalase 3323 812 33236690v20141116 hypothetical protein 3324 813 33246699v20141116 hypothetical protein Mrad2831 3163 3325 822 33256700v20141116 hypothetical protein 823 823 33266702v20141116 hypothetical protein 825 825 33276703v20141116 fatty acid metabolism AMP-binding protein 3328 826 33286704v20141116 hypothetical protein 3329 827 33296706v20141116 DeoR family transcriptional regulator 829 829 33306707v20141116 glucarate dehydratase 3331 830 33316708v20141116 PAS / PAC sensor protein 831 831 33326709v20141116 hypothetical protein 832 832 33336710v20141116 hypothetical protein 3334 833 33346711v20141116 hypothetical protein 3335 834 3335Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:6712v20141116 hypothetical protein Mrad2831 5112 835 835 33366714v20141116 alcohol dehydrogenase 836 836 33386715v20141116 hypothetical protein 3339 837 33396716v20141116 hypothetical protein 838 838 33406718v20141116 hypothetical protein 3341 840 33416719v20141116 hypothetical protein 841 841 33426721v20141116 hypothetical protein Mrad2831 3655 3343 843 33436722v20141116 hypothetical protein Mrad2831_0445 844 844 33446724v20141116 hypothetical protein 3345 845 33456729v20141116 hypothetical protein 850 850 33466731v20141116 photo system reaction center subunit H 3347 853 33476732v20141116 hypothetical protein Mrad2831_3817 854 854 33486736v20141116 hypothetical protein Mrad2831 2399 856 856 33496737v20141116 hypothetical protein 3350 857 33506738v20141116 hypothetical protein 3351 858 33516742v20141116 epimerase 3352 861 33526743v20141116 hypothetical protein 3353 862 3353NAD-binding D-isomer specific 2-6800v20141116 hydroxyacid dehydrogenase 3363 867 33636806v20141116 ArsR family transcriptional regulator 3364 872 33646807v20141116 cysteine dioxygenase 3365 873 33656808v20141116 hypothetical protein 874 874 33666809v20141116 (2Fe-2S)-binding domain-containing protein 875 875 33676810v20141116 aldehyde dehydrogenase 876 876 33686811v20141116 hypothetical protein Mnod 6032 3369 877 33696812v20141116 histone deacetylase 878 878 33706818v20141116 hypothetical protein 882 882 33716896v20141116 hypothetical protein Mrad2831 5186 3379 894 33796903v20141116 diguanylate cyclase 897 897 3380Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:6907v20141116 translation initiation factor IF-2 3381 899 33816909v20141116 hypothetical protein 3382 902 33826921v20141116 acetyl-CoA carboxylase 913 913 3383 binding-protein-dependent transport system6927v20141116 inner membrane protein 917 917 33846936v20141116 hypothetical protein 924 924 33856938v20141116 hypothetical protein 926 926 33866940v20141116 domain of unknown function family protein 3387 928 33876943v20141116 transposase IS4 family protein 930 930 3388 binding-protein-dependent transport system7006v20141116 inner membrane protein 3396 932 33967015v20141116 hypothetical protein 940 940 33977017v20141116 hypothetical protein 942 942 33987023v20141116 type III restriction endonuclease subunit R 3399 947 33997027v20141116 LysR family transcriptional regulator 3400 950 34007029v20141116 hypothetical protein 951 951 34027040v20141116 hypothetical protein 963 963 3403 arginine ABC transporter ATP-binding7042v20141116 protein 965 965 34047048v20141116 glyoxalase 969 969 3405 urea ABC transporter ATP-binding protein7050v20141116 UrtD 3406 971 3406 urea ABC transporter ATP-binding protein7051v20141116 UrtE 972 972 34077053v20141116 hypothetical protein 973 973 34087054v20141116 GntR family transcriptional regulator 3409 974 34097127v20141116 hypothetical protein Mnod 6985 3416 983 34167152v20141116 hydratase / decarboxylase 3418 1001 34187153v20141116 putative membrane protein 1002 1002 3419Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:Lipopolysaccharide biosynthesis protein-like7155v20141116 protein 3420 1004 34207156v20141116 aldolase 1005 1005 34217163v20141116 glycerophosphoryl diester phosphodiesterase 1011 1011 34227180v20141116 adenylate cyclase 1027 1027 3423 hypothetical protein7189v20141116 VOLCADRAFT l 19358 1034 1034 3425Glyoxalase / Bleomycin resistance7190v20141116 protein / Dioxygenase superfamily 3426 1035 34267200v20141116 competence protein ComEA 1046 1046 34277201v20141116 serine / threonine dehydratase 1047 1047 34287202v20141116 serine—glyoxylate aminotransferase 1048 1048 34297211v20141116 cytochrome C oxidase subunit III 1057 1057 3430 succinate dehydrogenase and fumarate7290v20141116 reductase iron-sulfur protein 3435 1064 34357291v20141116 succinate dehydrogenase membrane anchor 1065 1065 3436 succinate dehydrogenase cytochrome b7292v20141116 subunit 1066 1066 3437L(+)-tartrate or fumarate dehydratase7293v20141116 subunit beta 1067 1067 34387294v20141116 fumarate reductase 1068 1068 34397295v20141116 YCII-like protein 1069 1069 34407299v20141116 glycosyltransferase family 2 3441 1071 34417310v20141116 ABC transporter substrate-binding protein 3442 1074 34427311v20141116 glutathione ABC transporter permease GsiD 1075 1075 3443 oligopeptide / dipeptide ABC transporter7312v20141116 ATPase 1076 1076 34447313v20141116 ABC transporter-like protein 1077 1077 34457314v20141116 sodiumxalcium antiporter 3446 1078 3446Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:7315v20141116 methionyl-tR A formyltransferase 1079 1079 34477317v20141116 hypothetical protein 1080 1080 34497326v20141116 glycosyl transferase family protein 1088 1088 34507331v20141116 hypothetical protein Mrad2831 4126 3452 1090 34527332v20141116 4-oxalomesaconate hydratase 1091 1091 34537340v20141116 hypothetical protein FAES 2018 1098 1098 34547341v20141116 hypothetical protein M446 1279 3455 1099 34557343v20141116 hypothetical protein 3456 1101 34567349v20141116 diguanylate cyclase 3457 1107 34577350v20141116 hypothetical protein 1108 1108 34587354v20141116 acetyl-CoA synthetase 1111 1111 34597355v20141116 phenylacetic acid degradation protein 1112 1112 34607356v20141116 alcohol dehydrogenase 3461 1113 3461 nitrate / sulfonate / bicarbonate ABCtransporter periplasmic ligand-binding7357v20141116 protein 3462 1114 34627358v20141116 nitrate ABC transporter permease 3463 1115 34637360v20141116 hypothetical protein 1117 1117 34647363v20141116 hypothetical protein Mrad2831 1876 1120 1120 34657365v20141116 hypothetical protein Mrad2831 6026 3467 1121 34677368v20141116 enoyl-CoA hydratase / isomerase 3468 1124 34687370v20141116 nitrate ABC transporter ATPase 1126 1126 34697372v20141116 hypothetical protein 3470 1128 34707472v20141116 hypothetical protein Mext 2440 1131 1131 34827478v20141116 porin 3483 1132 3483 branched-chain amino acid ABC transporter7485v20141116 permease 1138 1138 34847538v20141116 RND family efflux transporter MFP subunit 3488 1185 34887554v20141116 phosphoheptose isomerase 3490 1198 3490Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:7555v20141116 GHMP kinase 3491 1199 34917570v20141116 IclR family transcriptional regulator 1215 1215 34927695v20141116 extracellular ligand-binding receptor 1233 1233 35067707v20141116 metal-dependent phosphohydrolase 1243 1243 35087711v20141116 2-hydroxyacid dehydrogenase 3509 1247 35097729v20141116 amino acid ABC transporter 3510 1264 35107730v20141116 GntR family transcriptional regulator 1265 1265 35117750v20141116 alpha-amylase 1283 1283 35127856v20141116 hypothetical protein 3528 1303 35287868v20141116 hypothetical protein 1313 1313 35297877v20141116 hypothetical protein Mchl 0532 3530 1319 35307879v20141116 glycosyl transferase 3531 1321 3531 binding-protein-dependent transport system7885v20141116 inner membrane protein 1327 1327 35327888v20141116 hypothetical protein Mrad2831 1281 3533 1330 35337890v20141116 taurine ABC transporter permease 1332 1332 35347913v20141116 D-lactate dehydrogenase 1351 1351 35368053v20141116 acetyltransferase 1371 1371 35588080v20141116 hypothetical protein 1397 1397 35608092v20141116 ABC transporter inner membrane protein 3561 1406 35618093v20141116 ABC transporter 1407 1407 3562 nitrate / sulfonate / bicarbonate ABC8094v20141116 transporter 3563 1408 35638109v20141116 Hypothetical protein 1423 1423 35648113v20141116 adenylate / guanylate cyclase 3565 1427 35658114v20141116 polysaccharide deacetylase 1428 1428 35668300v20141116 Ho lliday junction DNA helicase RuvB 1471 1471 35888301v20141116 None 3589 1472 35898310v20141116 monooxygenase 1480 1480 3590Reference. NLS0017 NLS0066Unique Ortholog Ortholog OrthologOrtholog Group SEQ ID SEQ ID SEQ ID Identifier Annotation NO: NO: NO:8313v20141116 GDP-L-fucose synthase 1483 1483 35918314v20141116 NAD-dependent epimerase / dehydratase 1484 1484 35928315v20141116 NAD-dependent epimerase / dehydratase 1485 1485 35938318v20141116 hypothetical protein 1488 1488 35948331v20141116 hypothetical protein 1498 1498 35958335v20141116 hypothetical protein 3596 1502 35968473v20141116 ABC transporter-like protein 1521 1521 36168485v20141116 hypothetical protein 1532 1532 36188524v20141116 oxidoreductase 1570 1570 36198573v20141116 alkanal monooxygenase 1614 1614 36208579v20141116 hypothetical protein 1620 1620 36218922v20141116 response regulator receiver protein 3641 1749 36419277v20141116 transposase 1821 1821 36849290v20141116 diguanylate cyclase 1834 1834 36859309v20141116 XRE family transcriptional regulator 3687 1847 36879777v20141116 hypothetical protein 1934 1934 3729RTX toxins and related Ca2+-binding10194v20141116 protein 1954 1954 378310335v20141116 hypothetical protein Mnod 7733 2033 2033 379410354v20141116 Hypothetical protein 3795 2048 379510358v20141116 hypothetical protein 2050 2050 379712071v20141116 None 2288 2288 4101 hypothetical protein12161v20141116 MexAMl_METAlp3214 4103 2360 410314172v20141116 Fis family transcriptional regulator 2469 2469 4343References for Example 61. Miller JR, Koren S, Sutton G (2010) Assembly algorithms for next-generation sequencing data. Genomics 95: 315-327.2. Zerbino DR, Birney E (2008) Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18: 821-829.3. Delcher AL, Bratke KA, Powers EC, Salzberg SL (2007) Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 23: 673-679.4. Lowe TM, Eddy SR (1997) tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 25: 955-964.5. Lagesen K, Hallin P, Rodland EA, Staerfeldt HH, Rognes T, et al. (2007) RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res 35: 3100-3108.6. Cantarel B, Korf I, Robb S, et al. (2008) MAKER: An easy-to-use annotation pipeline designed for emerging model organism genomes. Genome Research 18: 188-196.7. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, et al. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25: 3389-3402.8. Eddy SR (2009) A new generation of homology search tools based on probabilistic inference. Genome Inform 23: 205-211.9. Haft DH, Selengut JD, White O (2003) The TIGRFAMs database of protein families. Nucleic Acids Res 31 : 371-373.10. Tatusov RL, Fedorova ND, Jackson JD, Jacobs AR, Kiryutin B, et al. (2003) The COG database: an updated version includes eukaryotes. BMC Bioinformatics 4: 41.11. Suzek BE, Huang H, McGarvey P, Mazumder R, Wu CH (2007) UniRef: comprehensive and non-redundant UniProt reference clusters. Bioinformatics 23: 1282-1288.12. Li H. and Durbin R. (2009) Fast and accurate short read alignment with Burrows- Wheeler Transform. Bioinformatics, 25: 1754-60Other References1. Abanda-Nkpwatt, D., M. Musch, J. Tschiersch, M. Boettner, and W. Schwab. 2006.Molecular interaction between Methylobacterium extorquens and seedlings: growth promotion, methanol consumption, and localization of the methanol emission site. J. Exp. Bot. 57: 4025-4032.2. Broekaert WF, Terras FR, Cammue BP, Vanderleyden J (1990) An automated quantitative assay for fungal growth inhibition. FEMS Microbiology Letters 69: 55-60.3. Cao, Y-R, Wang, Q., Jin, R-X., Tang, S-K., He, W-X., Lai, H-X, Xu, L-H., and C-L Jiang. 2011. Methylobacterium soli sp. nov. a methanol-utilizing bacterium isolated from the forest soil. Antonie van Leeuwenhoek (2011) 99:629-634.4. Corpe, W.A., and D.V. Basile. 1982. Methanol-utilizing bacteria associated with green plants. Devel. Industr. Microbiol. 23: 483-493.5. Corpe, W.A., and S. Rheem. 1989. Ecology of the methylotrophic bacteria on living leaf surfaces. FEMS Microbiol. Ecol. 62: 243-250.176. Green, P.N. 2005. Methylobacterium. In Brenner, D.J., N.R. Krieg, and J.T. Staley (eds.). "Bergey's Manual of Systematic Bacteriology. Volume two, The Proteobacteria. Part C, The alpha-, beta-, delta-, and epsilonproteobacteria." Second edition. Springer, New York. Pages 567-571.7. Green, P.N. 2006. Methylobacterium. In Dworkin, M., S. Falkow, E. Rosenberg, K.-H. Schleifer, and E. Stackebrandt (eds.). "The Prokaryotes. A Handbook on the Biology of Bacteria. Volume 5. Proteobacteria: Alpha and Beta Subclasses." Third edition. Springer, New York. Pages 257-265.8. Holland, M.A. 1997. Methylobacterium and plants. Recent. Res. Devel. in Plant Physiol. 1 : 207-213.9. Holland, M.A., and J.C. Polacco. 1994. PPFMs and other covert contaminants: Is there more to plant physiology than just plant? Annu. Rev. Plant Physiol. Plant Mol. Biol. 45: 197- 209.10. Kutschera, U. 2007. Plant-associated methylobacteria as co-evolved phytosymbionts. A hypothesis. Plant Signal Behav. 2: 74-78.11. Lidstrom, M.E. 2006. Aerobic methylotrophic prokaryotes. In Dworkin, M., S. Falkow, E. Rosenberg, K.-H. Schleifer, and E. Stackebrandt (eds.). "The Prokaryotes. A Handbook on the Biology of Bacteria. Volume 2. Ecophysiology and biochemistry." Thirdedition. Springer, New York. Pages 618-634.12. Madhaiyan, M., S. Poonguzhali, H.S. Lee, K. Hari, S.P. Sundaram, and T.M. Sa. 2005. Pink-pigmented facultative methylotrophic bacteria accelerate germination, growth and yield of sugarcane clone Co86032 (Saccharum officinarum L.) Biol. Fertil. Soils 41 : 350-358.13. Madhaiyan, M., S. Poonguzhali, M. Senthilkumar, S. Seshadri, H. Chung, J. Yang, S. Sundaram, and T. Sa. 2004. Growth promotion and induction of systemic resistance in rice cultivar CO-47 (Oryza sativa L.) by Methylobacterium spp. Bot. Bull. Acad. Sin. 45: 315- 324.14. Madhaiyan, M., S. Poonguzhali, and T. Sa. 2007. Influence of plant species and environmental conditions on epiphytic and endophytic pink-pigmented facultativemethylotrophic bacterial populations associated with field-grown rice cultivars. J Microbiol Biotechnol. 2007 Oct; 17(10): 1645-54.15. Stanier, R.Y., N.J. Palleroni, and M. Doudoroff. 1966. The aerobic pseudomonads: A taxonomic study. J. Gen. Microbiol. 43: 159-271.16. Sy, A., Giraud, E., Jourand, P., Garcia, N., Willems, A., De Lajudie,P., Prin, Y., Neyra, M., Gillis, M., Boivin-Masson,C, and Dreyfus, B. 2001. Methylotrophic Methylobacterium Bacteria Nodulate and Fix Nitrogen in Symbiosis with Legumes. Jour. Bacteriol. 183(1):214- 220,17. Sy, A., A.C.J. Timmers, C. Knief, and J.A. Vorholt. 2005. Methylotrophic metabolism is advantageous for Methylobacterium extorquens during colonization of Medicago truncatula under competitive conditions. Appl. Environ. Microbiol. 71 : 7245-7252.18. Vogel, H.J., and D.M. Bonner. 1956. Acetylornithinase of Escherichia coli: Partial purification and some properties. J. Biol. Chem. 218: 97-106.19. Vogel, H. J. 1956. A convenient growth medium for N'eurospora (Medium N). Microbial Genet Bull 13: 42-4320. Whittenbury, R., S.L. Davies, and J.F. Wilkinson. 1970. Enrichment, isolation and some properties of methane-utilizing bacteria. J. Gen. Microbiol. 61 : 205-218.21. Vuilleumier S, Chistoserdova L, Lee MC, Bringel F, Lajus A, Zhou Y, Gourion B, Barbe V, Chang J, Cruveiller S, Dossat C, Gillett W, Gruffaz C, Haugen E,Hourcade E, Levy R, Mangenot S, Muller E, Nadalig T, Pagni M, Penny C, Peyraud R, Robinson DG, Roche D, Rouy Z, Saenampechek C, Salvignol G, Vallenet D, Wu Z, Marx CJ, Vorholt JA, Olson MV, Kaul R, Weissenbach J, Medigue C, Lidstrom ME.Methylobacterium genome sequences: a reference blueprint to investigate microbial metabolism of CI compounds from natural and industrial sources. PLoS One.2009;4(5):e5584. doi: 10.1371 / journal.pone.0005584. Epub 2009 May 18. PubMedPMID: 19440302; PubMed Central PMCID: PMC2680597.22. Marx CJ, Bringel F, Chistoserdova L, Moulin L, Farhan Ul Haque M, Fleischman DE, Gruffaz C, Jourand P, Knief C, Lee MC, Muller EE, Nadalig T, Peyraud R,Roselli S, Russ L, Goodwin LA, Ivanova N, Kyrpides N, Lajus A, Land ML, Medigue C, Mikhailova N, Nolan M, Woyke T, Stolyar S, Vorholt JA, Vuilleumier S. Complete genome sequences of six strains of the genus Methylobacterium. J Bacteriol. 2012Sep;194(17):4746-8. doi: 10.1128 / JB.01009-12. PubMed PMID: 22887658; PubMed Central PMCID: PMC3415506.23. Knief C, Frances L, Vorholt JA. Competitiveness of diverse Methylobacteriumstrains in the phyllosphere of Arabidopsis thaliana and identification ofrepresentative models, including M. extorquens PA1. Microb Ecol. 2010Aug;60(2):440-52. doi: 10.1007 / s00248-010-9725-3. Epub 2010 Aug 11. PubMed PMID: 20700590.

[0091] The inclusion of various references herein is not to be construed as any admission by the Applicants that the references constitute prior art. Applicants expressly reserve their right to challenge any allegations of unpatentability of inventions disclosed herein over the references included herein.

[0092] Having illustrated and described the principles of the present invention, it should be apparent to persons skilled in the art that the invention can be modified in arrangement and detail without departing from such principles.

[0093] Although the materials and methods of this invention have been described in terms of various embodiments and illustrative examples, it will be apparent to those of skill in the art that variations can be applied to the materials and methods described herein without departing from the concept, spirit and scope of the invention. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.

Claims

What is claimed is:

1. A method for improving tomato production, said method comprising applying a composition comprising Methylobacterium to a tomato plant, a part thereof, or to a tomato seed, wherein said composition comprises: (i) a solid substance with adherentMethylobacterium grown thereon; (ii) an emulsion having Methylobacterium grown therein; (iii) a Methylobacterium that has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594; or (iv) a Methylobacterium selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B-50940), and derivatives thereof; and wherein said tomato plant or tomato plant grown from said seed exhibits a trait improvement selected from the group consisting of an increased rate of root growth, leaf growth, seedling growth, seed production, fruit production, scion production, rootstock production, and / or increased total biomass when compared to an untreated control tomato plant or a control tomato plant grown from an untreated seed, thereby obtaining improved tomato production.

2. The method of claim 1, wherein said composition comprises Methylobacterium at a titer of about lxlO6 CFU / gm to about lxlO14 CFU / gm for a solid composition or at a titer of about lxlO6 CFU / mL to about lxlO11 CFU / mL for a liquid composition containing the solid substance or for the emulsion.

3. The method of claim 1, wherein said Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594.

4. The method of claim 3, wherein the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4.

5. The method of claim 1, wherein the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B- 50940), and derivatives thereof.

6. The method of claim 1, wherein said applied composition coats or partially coats said tomato plant or a part thereof, or said seed.

7. The method of claim 1, wherein the method further comprises: (i) growing said tomato plant or tomato plant grown from said seed; and / or (ii) harvesting seedlings, rootstock, scions, fruit, or seed from said tomato plant or tomato plant grown from said seed.

8. The method of claim 1, wherein the solid substance with adherent Methylobacterium is not a substance that promotes growth of resident microorganisms on the tomato plant, the part thereof, or the tomato seed.

9. The method of claim 1, wherein the composition comprises an agriculturally acceptable adjuvant and / or excipient.

10. The method of claim 1, wherein said composition is applied to said tomato plant, part thereof, or seed in a hydroponic solution.

11. The method of any one of claims 1-10, wherein said composition is depleted of substances that promote growth of resident microorganisms on said plant or seed.

12. A method for improving tomato plant production, said method comprising applying a composition comprising Methylobacterium to a tomato plant, a part thereof, or tomato seed, wherein said composition is depleted of substances that promote growth of resident microorganisms on said plant or seed and wherein said plant or plant grown from said seed exhibits a trait improvement selected from the group consisting of an increased rate of root growth, leaf growth, seedling growth, seed production, fruit production, scion production, rootstock production, and / or increased total biomass when compared to an untreated control tomato plant or a control tomato plant grown from an untreated seed, thereby obtaining improved tomato plant production.

13. The method of claim 12, wherein said composition comprises a solid substance with adherent Methylobacterium grown thereon.

14. The method of claim 12, wherein the solid substance is not a substance that promotes growth of resident microorganisms on the tomato plant, the part thereof, or the tomato seed.

15. The method of claim 14, wherein the composition comprises Methylobacterium at a titer of about lxlO6 CFU / gm to about lxlO14 CFU / gm.

16. The method of claim 12, wherein said composition comprises a liquid, a solid substance with Methylobacterium adhered thereto in a liquid, a solid substance withMethylobacterium adhered thereto in an emulsion, or an emulsion.

17. The method of claim 16, wherein said composition comprises Methylobacterium at a titer of about lxlO6 CFU / mL to about lxlO11 CFU / mL.

18. The method of claim 12, wherein the method further comprises: (i) growing said tomato plant or tomato plant grown from said seed; and / or (ii) harvesting rootstock, scions, fruit, or seed from said tomato plant or tomato plant grown from said seed.

19. The method of claim 12, wherein said Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594.

20. The method of claim 19, wherein the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4.

21. The method of claim 12, wherein the Methylobacterium strain is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B-50940), and derivatives thereof.

22. The method of any one of claims 12 to 21, wherein said composition coats or partially coats said plant or a part thereof, or said seed.

23. The method of anyone of claims 12 to 21, wherein said composition is applied in a hydroponic solution.

24. A composition comprising: (i) a solid substance with adherent Methylobacterium grown thereon; (ii) an emulsion with Methylobacterium grown therein or contained therein; or (iii) a Methylobacterium; wherein said Methylobacterium has at least one gene encoding at least one protein that is orthologous to a protein having an amino acid sequence of SEQ ID NO: 1-4594 or wherein the Methylobacterium has at least one gene encoding a protein that is orthologous to a reference protein of Table 4, and wherein said composition further comprises an agriculturally acceptable adjuvant and / or excipient or wherein the composition comprises a hydroponic solution of man-made origin.

25. The composition of claim 24, wherein the composition is depleted of substances that promotes growth of resident microorganisms on a plant or seed.

26. The composition of claim 24, wherein said substance that promotes growth of resident microorganisms on a plant or seed is selected from the group consisting of a carbon source, a nitrogen source, a phosphorous source, a sulfur source, a magnesium source, andcombinations thereof.

27. The composition of claim 24, wherein the solid substance with adherentMethylobacterium grown thereon has a Methylobacterium titer of at least about 5 x 108 CFU / gm to at least about 1 x 1014 CFU / gm.

28. The composition of claim 24, wherein the Methylobacterium is selected from the group consisting ofNLS0017 (NRRL B-50931), NLS0037 (NRRL B-50941), NLS0066 (NRRL B-50940), and derivatives thereof.

29. The composition of any one of claims 24-28, wherein the composition is adapted for use in treating a plant or seed.

30. A tomato plant part or tomato seed that is coated or partially coated with the composition of any one of claims 24 to 28.

31. A tomato plant part or tomato seed that is immersed or partially immersed in the composition of any one of claims 24 to 28.

32. A tomato plant part or tomato seed that is coated or partially coated with acomposition comprising Methylobacterium, or that is immersed or partially immersed in a composition comprising Methylobacterium, wherein the tomato plant part or tomato seed is obtained by the method described in any one of claims 1-10 or 12-21.