49results about How to "Strain stability" patented technology

The invention relates to a microbial inoculum for fermenting and producing organic fertilizers, comprising cellulomonas, bacillus, lactobacillus, methagen, thiobacillus, streptomyces, thermoactinomyces, thermomonospora, azotobacter, nitrosomonas, nitrobacter, rhizobium, aspergillus, yeast, penicillium, humicola, rhizopus and mycorrhizal fungi. In addition, the invention also relates to organic fertilizers fermented and produced by using the microbial inoculum and a method for fermentation and production.

The invention relates to a microbial agent used for producing a soil modifying agent by fermentation, consisting of fiber monad, bacillus, lactobacillus, methanobacteria, thiobacillus, streptomycete, high-temperature actinomyces, high-temperature monad, azotobacteria, nitration monad, nitration bacilus, rhizobium, koji mold, leaven, blue mold, detritus mold, rhizopus as well as mycorrhizal fungi and substrate. In addition, the invention also relates to a soil modifying agent produced by the fermentation of the microbial agent, application thereof and the like.

The present disclosure relates to the use of a switch for the production of heterologous non-catabolic compounds in microbial host cells. In one aspect, provided herein are genetically modified microorganisms that produce non-catabolic compounds more stably when serially cultured under aerobic conditions followed by microaerobic conditions, and methods of producing non-catabolic compounds by culturing the genetically modified microbes under such culture conditions. In another aspect, provided herein are genetically modified microorganisms that produce non-catabolic compounds more stably when serially cultured in the presence of maltose followed by the reduction or absence of maltose, and methods of producing non-catabolic compounds by culturing the genetically modified microbes under such culture conditions.

The present invention presents a high tensile strength cold rolled steel sheet having excellent formability, impact resistance and strain age hardening characteristics, and the production thereof. As a specific means, a slab having a composition which contains, by mass %, 0.15% or less of C, 0.02% or less of Al, and 0.0050 to 0.0250% of N at N/Al of 0.3 or higher, and has N in a solid solution state at 0.0010% or more, is first hot rolled at the finish rolling delivery-side temperature of 800° C. or above, and is subsequently coiled at the coiling temperature of 750° C. or below to prepare a hot rolled plate. Then, after cold rolling, the hot rolled plate is continuously cooled at a temperature from the recrystallization temperature to 900° C. at a holding time of 10 to 120 seconds, and is cooled by primary cooling in which the hot rolled plate is cooled to 500° C. or below at a cooling rate of 10 to 300° C./s, and furthermore if necessary, by secondary cooling in which a residence time is 300 seconds or less in a temperature range of the primary cooling stopping temperature or higher and 350° C. or higher. Provided is a steel sheet containing a ferritic phase having an average crystal grain size of 10 mum or less at an area ratio of 50% or more, and if necessary, a martensitic phase at an area ratio of 3% or more as a second phase.

A physical quantity sensor includes a deformable body in which strain occurs in response to a stress applied thereto, a vibrator vibrating with a frequency according to the strain or with an amplitude according to the strain, and a processor processing a signal output from the vibrator. The vibrator is mounted to the deformable body such that the strain transmits to the vibrator. The processor is bonded to the deformable body such that the strain does not substantially transmit to the processor. This physical quantity sensor can stably detects strain and tension acting on an object.

The invention relates to a method for producing, purifying and appraising protein, in particular to a method for expression of recombinant human her2/neu ICD in Pasteur yeast as well as optimized large scale industrialized fermentation production and purification of the recombinant human her2/neu ICD.

The invention discloses Pseudomonas fluorescens RQ3-01 with an accession number of CGMCC No. 14471. In addition, the invention also discloses the application of the Pseudomonas fluorescens to degradation of poorly-soluble inorganic phosphorus. The Pseudomonas fluorescens of the invention is a dominant strain selected with the poorly-soluble inorganic phosphorus as a phosphorus source, and the strain converts the poorly-soluble inorganic phosphorus into bioavailable soluble phosphate during the growth and reproduction. Moreover, the Pseudomonas fluorescens of the invention also has the functions of degrading organic phosphorus and degrading potassium, can effectively increase the contents of available phosphorus and available potassium in soil, and has the functions of promoting plant growth and increasing yield.

The invention discloses a bio-type drip irrigation saline-alkaline soil improver and a preparation method thereof. According to the present invention, the bio-type drip irrigation saline-alkaline soil improver is prepared from amino acids, potassium fulvate, urea, monoammonium phosphate, potassium nitrate and dry powder fungicide, has good water solubility, can be used through the drip tube system, can rapidly reduce the salt content and the pH value of soil, further has effects of saline-alkaline land improving, biological activity, crop growth promoting, crop yield increasing and crop quality improving, and can effectively improve the soil fertility and increase the crop yield after the long-term use of the bio-type drip irrigation saline-alkaline soil improver, wherein the strain of the used dry powder fungicide is stable, and the spore has strong tolerance and strong adaptability.

The present invention relates to a composition which comprises: an oligosaccharide which is free of sialyloligosaccharide, and free sialic acid.

The invention discloses a low-salt culture medium of Lactobacillus rhamnosus comprising a basic culture medium and an optimized culture medium, wherein that basic culture medium comprises yeast peptone, yeast powder, glucose, lactose, isomaltooligosaccharide, L-Malic acid, manganese sulfate, the balance of sterile water, pH 6.50-7.00. The optimized medium consistes of yeast peptone, yeast powder,glucose, lactose, isomaltooligosaccharide, L-Malic acid, citric acid, manganese sulfate, the balance of sterile water, pH 6.50-7.00. The culture medium is suitable for the propagation of Lactobacillusrhamnosus, and the number of viable bacteria in fermentation broth could reach more than 109 CFU/ml.

The invention provides a preparation method of a transistor with a stressed channel and the transistor with the stressed channel. The method comprises the following steps: providing a substrate which comprises a device layer; forming a transistor, including a source electrode and a drain electrode formed in the device layer and a grid electrode formed on the surface of the device layer; forming an insulation protective layer on the surface of the device layer; forming a stress layer on the surface of the insulation protective layer; suspending the device layer where there is a conducting channel of the grid electrode of the transistor such that the device layer is curled under the action of the stress layer, thus leading to tensile strain of the conducting channel of the grid electrode of the transistor. The invention has advantages as follows: the device layer where there is the grid electrode is curled freely and the device layer undergoes strain under the action of the tensile strain; and as the strain is introduced by physical deformation, strain is stable and is not easy to disappear.

The invention relates to the technical field of bioscience and detection reagents. The invention specifically discloses a preparation method and application of a polyclonal antibody for specifically recognizing protein USP42. The method comprises the following steps: (1), protein USP42 antigenic epitope analysis: selecting a target fragment as recombinant expression of protein USP42 through the antigenic epitope analysis, wherein the gene sequence of the target fragment is shown as SEQ ID N0.1 in a sequence table; and respectively introducing BamH1 and Not I restriction enzyme cutting sites into an upstream primer and a downstream primer. According to the invention, the preparation of the polyclonal antibody of USP42 is realized.

The invention relates to a recombinant protein and a production, purification and identification method thereof, in particular to a recombinant human apolipoprotein A-II (rhApoA-II) expressed in saccharomyces pastorianus, and the optimized method for high-density fermentation, production and purification of the recombinant human apolipoprotein A-II.

The invention provides a carbon fiber-based intelligent fabric. The carbon fiber-based intelligent fabric comprises a fabric layer and a strain functional layer, the strain functional layer is prepared from functional slurry with conductivity, and the functional slurry comprises a resin-coated carbon fiber material and an interface bonding material. According to the carbon fiber-based intelligent fabric, the resin-coated carbon fiber is adopted as a conductive material, the compatibility between the resin-coated carbon fiber and the interface bonding material is enhanced, so that the interface bonding force between the prepared strain functional layer and the fabric is remarkably improved, then the sensitivity of a strain sensor prepared on the basis of the carbon fiber-based intelligent fabric is greatly improved, and the requirements of practical application are met.