200 results about "Plant development" patented technology

New ACC synthase genes from pineapple are disclosed which have utility as targets for the generation of transgenic plants in which the expression of ACC synthase is substantially controlled to effect the regulation of plant development, and, in particular, initiation of natural flowering.

The present invention provides compositions and methods for modulating plant development by modulating the expression or activity of plant polycomb genes including FIE and MEA.

A method for treating a seedling by dipping the roots of the seedling into a composition containing a slow release, particulate urea-formaldehyde polymer, which is useful as a fertilizer for enhancing the extended delivery of nitrogen needed for plant development and growth and to the composition useful as the root dip, or as a soil drench.

A slow release, particulate urea-formaldehyde polymer useful as a fertilizer for enhancing the extended delivery of nitrogen needed for plant development and growth and a granular fertilizer made with the particulate urea-formaldehyde polymer.

Methods and compositions for modulating plant development are provided. Nucleotide sequences and amino acid sequences encoding Ovule Development Protein 2 (ODP2) proteins are provided. The sequences can be used in a variety of methods including modulating development, developmental pathways, altering oil content in a plant, increasing transformation efficiencies, modulating stress tolerance, and modulating the regenerative capacity of a plant. Transformed plants, plant cells, tissues, and seed are also provided.

The present invention is directed to methods for delaying a plant development process comprising exposing a plant or plant part to one or more bacteria or enzymes. In specific embodiments, the one or more bacteria are selected from the group consisting of Rhodococcus spp., Pseudomonas chloroaphis, Brevibacterium ketoglutamicum, and a mixture comprising any combination of these bacteria. Apparatuses for delaying a plant development process comprising a catalyst that comprises one or more of the above bacteria.

Agent for the agronomic treatment of a living plant supported by a moist substrate, for example a soil, wherein said agent is in the solid and divided state, and comprises solid particles containing at least one active entity for the agronomic treatment, characterized in that each particle comprises: —a nucleus consisting of a grain of a solid material which is inert with respect to the substrate, comprising an inner developed surface area which is greater than its apparent surface area and, as a result, suitable for adsorption and / or absorption, —the active entity for agronomic treatment, absorbed into the grain and / or adsorbed at the surface of said grain, —a membrane encapsulating the nucleus comprising the active entity, consisting of at least one hydrophilic polymer which is permeable to the outside with respect to the active entity, when it is in direct or indirect contact with the moist substrate.

Expressed Sequence Tags (ESTs) isolated from maize are disclosed. The ESTs provide a unique molecular tool for the targeting and isolation of novel genes for plant protection and improvement. The disclosed ESTs have utility in the development of new strategies for understanding critical plant developmental and metabolic pathways. The disclosed ESTs have particular utility in isolating genes and promoters, identifying and mapping the genes involved in developmental and metabolic pathways, and determining gene function. Sequence homology analyses using the ESTs provided in the present invention, will result in more efficient gene screening for desirable agronomic traits. An expanding database of these select pieces of the plant genomics puzzle will quickly expand the knowledge necessary for subsequent functional validation, a key limitation in current plant biotechnology efforts.

Expressed Sequence Tags (ESTs) isolated from soybean are disclosed. The ESTs provide a unique molecular tool for the targeting and isolation of novel genes for plant protection and improvement. The disclosed ESTs have utility in the development of new strategies for understanding critical plant developmental and metabolic pathways. The disclosed ESTs have particular utility in isolating genes and promoters, identifying and mapping the genes involved in developmental and metabolic pathways, and determining gene function. Sequence homology analyses using the ESTs provided in the present invention, will result in more efficient gene screening for desirable agronomic traits. An expanding database of these select pieces of the plant genomics puzzle will quickly expand the knowledge necessary for subsequent functional validation, a key limitation in current plant biotechnology efforts.

An intelligent plant development library environment is presented. Contemplated environments comprise an EPC knowledge system capable of incorporating know-how of one or more construction firms in the form of assembly objects. Assembly objects represent construction components (e.g., bolts, cable trays, pipes, processing units, deliverables, etc.) that can be incorporated into a plant design. Assembly objects are stored in an assembly database and include available contexts considered relevant to the assembly objects. An inference engine is utilized to derive a specified context related to a plant design from one or more design tools. The inference engine applies rule sets to infer which assembly objects to instantiate as construction objects. The inference engine can further configure the design tools to incorporate the instantiated construction objects into a plant construction project model. Example rule sets include forward chaining rules, backward chaining rules, case-based reasoning rules, inductive reasoning rules, or abductive reasoning rules.

The present invention is related to a family of novel spatiotemporally active Rubisco promoters (SEQ ID NO: 1, 2, 3) obtainable from light grown Brassica seedlings. Furthermore the invention is related to transgene expression in specific plant organs or at specific stages of plant development. DNA constructs and expression cassettes comprising at least one of the promoter sequences functionally fused in frame with genes encoding desired gene products are disclosed. Seeds from transformed homologous and herterologous plants and from subsequent generation of the transformed plants are collected and used for efficient production of desired gene products, especially in contained conditions.

This invention relates to constructs for the conditional or regulated expression of transgenes in plants using site-specific recombinase systems. The constructs comprise a variety of constitutive, inducible, tissue specific or developmental stage-specific promoters operably linked to either a transgene or the elements of one or more site-specific recombinase system. By matching promoters, responsive to various inducers, plant tissues or plant developmental states with the recombinase systems, stop fragments and transgenes, virtually any trait may be expressed at any plant development stage or in any plant generation.

A method of modifying morphology in a plant by introducing into a plant at least one chimaeric gene having a promoter sequence operably associated with a nucleic acid sequence, the promoter sequence being operable to direct expression in specific cells of the plant and the nucleic acid sequence encoding at least one gene product capable of altering the metabolism of or causing death of the specific cells and / or nearby cells. In particular, the promoter sequence is operable to direct expression in lateral bud or lateral shoot and the nucleic acid encoding at least one gene product capable of disrupting the metabolism of or causing the death of the lateral bud or lateral shoot or nearby cells. Preferably the promoter sequence has the sequence shown as SEQ ID No. 1 or SEQ ID No. 7 or SEQ ID No. 4, or a part thereof capable of regulating expression of a gene, or a sequence having at least 60%, preferably at least 75%, homology to SEQ ID No. 1 or SEQ ID No. 7 and being capable of regulating expression of a gene.

The present invention relates to methods for stimulating root growth and / or enhancing the formation of lateral or adventitious roots and / or altering root geotropism comprising expression of a plant cytokinin oxidase or comprising expression of another protein that reduces the level of active cytokinins in plants or plant parts. The invention also relates to novel plant cytokinin oxidase proteins, nucleic acid sequences encoding cytokinin oxidase proteins as well as to vectors, host cells, transgenic cells and plants comprising said sequences. The invention also relates to the use of said sequences for improving root-related characteristics including increasing yield and / or enhancing early vigor and / or modifying root / shoot ratio and / or improving resistance to lodging and / or increasing drought tolerance and / or promoting in vitro propagation of explants and / or modifying cell fate and / or plant development and / or plant morphology and / or plant biochemistry and / or plant physiology. The invention also relates to the use of said sequences in the above-mentioned methods. The invention also relates to methods for identifying and obtaining proteins and compounds interacting with cytokinin oxidase proteins. The invention also relates to the use of said compounds as a plant growth regulator or herbicide.

The present invention is directed to methods for delaying a plant development process comprising exposing a plant or plant part to one or more bacteria or enzymes. In specific embodiments, the one or more bacteria are selected from the group consisting of Rhodococcus spp., Pseudomonas chloroaphis, Brevibacterium ketoglutamicum, and a mixture comprising any combination of these bacteria. Apparatuses for delaying a plant development process comprising a catalyst that comprises one or more of the above bacteria.

Expressed Sequence Tags (ESTs) isolated from maize are disclosed. The ESTs provide a unique molecular tool for the targeting and isolation of novel genes for plant protection and improvement. The disclosed ESTs have utility in the development of new strategies for understanding critical plant developmental and metabolic pathways. The disclosed ESTs have particular utility in isolating genes and promoters, identifying and mapping the genes involved in developmental and metabolic pathways, and determining gene function. Sequence homology analyses using the ESTs provided in the present invention, will result in more efficient gene screening for desirable agronomic traits. An expanding database of these select pieces of the plant genomics puzzle will quickly expand the knowledge necessary for subsequent functional validation, a key limitation in current plant biotechnology efforts.

The invention belongs to the biology and biological technical field, and discloses a plant in-situ regeneration and agrobacterium transformation method. Agrobacterium is coated on a wound of a plant root stock, a callus which is generated by inducing a plant in-vitro tissue on a culture medium is used as a scion, and the scion is grafted onto the root stock through a cleft graft method. Root stock wound cells can realize in-situ organ regeneration under the induction of an exogenous callus, so that a transgenic regeneration bud can be obtained. Compared with the traditional plant genetic transformation method combining the tissue culture, a one-by-one genotype fumbling tissue culture condition can be avoided, a novel technological platform can be provided to the genetic transformation of plants, meanwhile, a novel plant regeneration system is established, and a research system is provided to the study of plant development biology.

Expressed Sequence Tags (ESTs) isolated from cotton are disclosed. The ESTs provide a unique molecular tool for the targeting and isolation of novel genes for plant protection and improvement. The disclosed ESTs have utility in the development of new strategies for understanding critical plant developmental and metabolic pathways. The disclosed ESTs have particular utility in isolating genes and promoters, identifying and mapping the genes involved in developmental and metabolic pathways, and determining gene function. Sequence homology analyses using the ESTs provided in the present invention, will result in more efficient gene screening for desirable agronomic traits. An expanding database of these select pieces of the plant genomics puzzle will quickly expand the knowledge necessary for subsequent functional validation, a key limitation in current plant biotechnology efforts.

A composition to stimulate the development and growth of plants that comprises at least a Tsukamurella paurometabola strain, biofertilizing agent that optimize the assimilation of the organic matter by plants, favoring the intake of nitrogen and phosphorus by the plant. Said agent is able of increasing the growth and development of the plants after the application of this biofertilizer directly to the soil or in a natural or artificial substrate, with organic matter, or after its application in any type of soil or substrate with an organic complement

Expressed Sequence Tags (ESTs) isolated from cotton are disclosed. The ESTs provide a unique molecular tool for the targeting and isolation of novel genes for plant protection and improvement. The disclosed ESTs have utility in the development of new strategies for understanding critical plant developmental and metabolic pathways. The disclosed ESTs have particular utility in isolating genes and promoters, identifying and mapping the genes involved in developmental and metabolic pathways, and determining gene function. Sequence homology analyses using the ESTs provided in the present invention, will result in more efficient gene screening for desirable agronomic traits. An expanding database of these select pieces of the plant genomics puzzle will quickly expand the knowledge necessary for subsequent functional validation, a key limitation in current plant biotechnology efforts.

A light harvester or collector collects solar radiation from an unshaded location adjacent a growing plant. The light harvester can be either imaging (e.g., parabolic reflectors) or non-imaging (e.g., compound parabolic concentrator). The concentrated solar radiation is projected into a light transmitter that conducts the light through the plant's outer canopy and into the inner canopy to a diffuser which disperses and reradiates the light into the inner canopy. The diffused light transforms a non-productive, potentially leafless zone of the plant into a productive zone so that more fruit can be produced per volume of land surface. The system can prevent transmission of infrared into the inner canopy so that the inner canopy zone is not heated and the amount of water lost to transpiration is reduced. The system can also modify other spectral components to affect plant development and to control pests and diseases.

Alfin1 cDNA encodes a putative transcription factor associated with salt tolerance in alfalfa (Medicago sativa L). The recombinant protein binds DNA in a sequence specific manner, including promoter fragments of the salt inducible gene MsPRP2. Alfin1 function was tested in transgenic alfalfa under the control of the 35S promoter in the sense and antisense orientations with the endogenous MsPRP2 as a reporter gene. Calli overexpressing Alfin1 were more resistant to growth inhibition by 171 mM NaCl than vector transformed controls, while calli expressing Alfin1 antisense were more sensitive to salt inhibition. Transgenic plants overexpressing Alfin1 in the sense orientation grew well. In contrast, the antisense transgenic plants grew poorly in soil, demonstrating that Alfin1 expression is essential for normal plant development. Transgenic calli and plant roots overexpressing Alfin1 showed enhanced levels of endogenous MsPRP2 mRNA accumalution. However, MsPRP2 mRNA accumulation was also regulated in a tissue specific manner as shown in leaves of transgenics overexpressing Alfin1. These results suggest that Alfin1 acts as a transcriptional regulator in plants and MsPRP2 expression in alfalfa. Alfin1 overexpressing transgenics showed salinity tolerance comparable to one of our salt-tolerant plants, indicating that Alfin1 also functions in gene regulation in salt tolerance.

The invention discloses plant development associated protein, an encoding gene and application thereof. The protein provided by the invention is the protein of (a) or (b): (a) the protein formed by amino acid sequences shown as a third sequence in a sequence table; or (b) plant development associated derived protein formed through the substitution and / or lack and / or addition of one or a plurality of amino acid residue radicals on the protein of the third sequence in the sequence table. The plant development is embodied by the properties of the strain height of developed strains and / or the size of leaf angles and / or the fertility of the developed strains and / or the size of specific organs. The invention also obtains a reccanbinant vector containing the encoding gene OsIBP1, and when the reccanbinant vector is used for converting target plants, transgenic plants with shortened strain height of the developed strains and / or reduced leaf angles and / or reduced fertility of the developed strains and / or reduced size of the specific organs can be obtained. Thereby, OsIBP1 can be used as a potential molecular breeding tool for improving the plant strain types and improving the plant yield.

A method of improving the growth of plants belonging to the family Cannabaceae sensu stricto by providing a plant nutrient solution about the plant roots and a gas mixture circulating about the plant shoot; by selecting the gas mixture and plant nutrient solution temperature independently of the other; and providing a plant nutrient solution to gas mixture temperature differential of approximately 0° F. or of at least approximately 15° F. during different phases of plant development, in order to change the plant development to improve a desired plant organ for industrial, scientific, and medical purposes. Infection of plants by Pythium, Fusarium, Verticillium, and Rizoctonia are treated or prevented by selecting a gas mixture temperature that is approximately 65 to 85° F. and a plant nutrient solution temperature that is approximately 35 to 65° F.

Expressed Sequence Tags (ESTs) isolated from soybean are disclosed. The ESTs provide a unique molecular tool for the targeting and isolation of novel genes for plant protection and improvement. The disclosed ESTs have utility in the development of new strategies for understanding critical plant developmental and metabolic pathways. The disclosed ESTs have particular utility in isolating genes and promoters, identifying and mapping the genes involved in developmental and metabolic pathways, and determining gene function. Sequence homology analyses using the ESTs provided in the present invention, will result in more efficient gene screening for desirable agronomic traits. An expanding database of these select pieces of the plant genomics puzzle will quickly expand the knowledge necessary for subsequent functional validation, a key limitation in current plant biotechnology efforts.

A method of modifying morphology in a plant by introducing into a plant at least one chimaeric gene having a promoter sequence operably associated with a nucleic acid sequence, the promoter sequence being operable to direct expression in specific cells of the plant and the nucleic acid sequence encoding at least one gene product capable of altering the metabolism of or causing death of the specific cells and / or nearby cells. In particular, the promoter sequence is operable to direct expression in lateral bud or lateral shoot and the nucleic acid encoding at least one gene product capable of disrupting the metabolism of or causing the death of the lateral bud or lateral shoot or nearby cells. Preferably the promoter sequence has the sequence shown as SEQ ID No. 1 or SEQ ID No. 7 or SEQ ID No. 4, or a part thereof capable of regulating expression of a gene, or a sequence having at least 60%, preferably at least 75%, homology to SEQ ID No. 1 or SEQ ID No. 7 and being capable of regulating expression of a gene.

The element is intended to be placed in a receptacle for the cultivation of at least one plant, and includes:a substantially solid body including a substrate adapted to enable said plant to develop;at least one seed of said plant disposed on the body in at least one seed receiving area;a layer for holding the seed(s) in said receiving area, comprising a dried mineral powder.The holding layer results from drying a deposition of a holding composition including a mineral powder suspended in water.