97 results about "Microbial Genetic" patented technology

The invention discloses genetically engineered bacteria capable of increasing the yield of lactoyl-N-trisaccharide II and a production method, and belongs to the field of microbial genetic engineering. According to the invention, the expression of glmM, glmU, glmS and lgtA in a lactoyl-N-trisaccharide II synthetic pathway is regulated and controlled in a combined manner, so the carbon flux of a metabolic pathway is accurately regulated and controlled, and the metabolic pressure is relieved; the expression of wecB, nagB and lacZ in an escherichia coli host, namely the lactoyl-N-trisaccharide IIsynthetic pathway is knocked out, so the yield of the lactoyl-N-trisaccharide II is further increased; in a flask shaking experiment, the capacity of escherichia coli for producing the lactoyl-N-trisaccharide II is increased to 4.82 g/L from 0.53 g/L; in a fermentation tank with a volume of 3 L, the yield of the lactoyl-N-trisaccharide II reaches 46.2 g/L; and thus, thegenetically engineered bacteria have industrial application prospect.

The invention belongs to the technical field of microbial genetic engineering, specifically relates to a recombinant bovine tuberculosis specific antigen protein with three fused genes and a preparation method thereof. The gene of the bovine tuberculosis specific fusion antigen protein has a nucleotide sequence and an amino acid sequence shown as in a sequence list SEQ ID NO:1. The invention discloses a recombinant Escherichia coli BL21/pET28a-RCE capable of expressing the bovine tuberculosis specific fusion antigen protein. The Escherichia coli is conserved in China Center for Type Culture Collection (CCTCC) with a conservation number CCTCC NO:M208244. The invention further discloses a preparation method of the three gene fused antigen protein.

Biofungicidal composition from a biologically pure culture of a Chilean bacterial isolate obtained from soils of the seventh region of Maule, Chile, corresponding to Paenibacillus polymyxa SCHC33, strain with the deposit number RGM2141 granted by the depository authority of the Chilean Collection of Microbial Genetic Resources (CChRGM) to be used as an environmentally friendly, biological control agent against fungal plant diseases, particularly fruits susceptible to infection by Botrytis cinerea, efficiently inhibiting conidial germination and mycelium proliferation of said phytopathogenic fungus, furthermore protects plant leaves and fruits from infection by the same fungus, and has the potential to be used in biological control of other fungi and in general of phytopathogenic microorganisms.

The invention discloses a high efficient expression method for an actinomyces-based nitrile hydratase gene in escherichia coli, and belongs to the field of microbial genetic engineering technology. The method processes high efficiency and safety. It is benefit for large scaled nitrile hydratase extraction and purification, and further theoretical research about nitrile hydratase that a large amount of soluble nitrile hydratase can be obtained in a short expression period by applications of the method.

The invention aims to provide an inducible promoter, a gene induced expression control system based on the inducible promoter, and an improved microbial genetic operation tool developed based on the expression control system. L-Arabinose is used as an inducing agent. Arabinose is a carbon source common in the nature and free of inhibitory action on cell growth. The induced expression system enables gene expression level to be up-regulated up to 800 times, is better in preciseness and can be used in controlled expression of target genes in Fusiformis or other microbial cells and to optimize existing genetic modification technology and develop new tools.

The invention discloses a novel promoter and application thereof, and belongs to the field of microbial genetic engineering. According to a method disclosed by the invention, the related promoter Pd(-35 to -10) HpaII gene is formed by series connection modification on the core area based on the promoter PHpaII; under control and transcription of the novel promoter Pd(-35 to -10) HpaII, the fibrinolytic activity of the recombinant nattokinase is up to 200.8 FU/ml. The method is efficient, safe and capable of effectively improving the expression quantity of nattokinase, and provides a theoretical basis for further study on influence of the promoter on heterologous gene expression.

The invention relates to a low-frequency ultrasonic-mediated method for transforming microbial, which comprises the following steps: (1) culturing bacteria to a logarithmic phase in a liquid culture medium; (2) adding a substrate to be transformed into a glass bottle containing the liquid culture medium in the step 1; (3) putting the glass bottle in the step 2 into the cavity of an ultrasonic instrument; (4) starting the ultrasonic instrument, wherein the frequency is 0.1-1000KHz, the power is 0.01-1000 Watts, non-probe type contact is adopted, the whole transformation process is carried out in the solution of a bioreactor, and ultrasonic waves are continuously adjustable or intermittent; and (5) recovering cells, transferring, and coating a panel. The invention can be used for operating a single cell and a single reactor, can realize high flux, has the advantages of simple operation and voluntary control, and can realize remote control.

The invention belongs to the field of microbial genetic engineering, and discloses a GTP cyclohydrolase I gene folE and application. A nucleotide sequence of the GTP cyclohydrolase I gene folE is shown as SEQ ID NO:1. The gene is derived from food-borne lactobacillus plantarum, is safe and can be used in the field of later-stage food fermentation. A gene knockout strain screening method can be used for improving the screening efficiency of knockout strains. The key role of gene folE gene in folic acid synthesis is proved, and a certain theoretical basis is provided for the research and development of folic acid synthesis functional food. The GTP cyclohydrolase I gene folE and application analyze that the gene is derived from food-grade microorganisms and is safe; and the GTP cyclohydrolaseI gene folE and application analyze that the gene folE gene has nothing to do with cell morphology and strain growth except playing an important role in folic acid synthesis.

The present invention relates to the fields of microbiology and microbial genetics. More specifically, the invention relates to novel bacterial strains and processes employing these strains for the fermentative production of amino acids such as threonine.

The invention relates to a travel route planning method and system based on a microbial genetic algorithm. The method comprises the steps of constructing a scenic spot database; the user defines a playing area and an interested theme; searching scenic spot data from a scenic spot database according to the requirements of the user; defining population size, chromosome length, iteration times, crossover probability and mutation probability; encoding the scenic spot data and randomly initializing a first-generation population; calculating the fitness of each individual in the population accordingto the fitness function; screening out individuals with the best fitness; if the number of iterations is reached, decoding is carried out to generate an optimal path, planning is ended, otherwise, individuals in the current generation population are paired randomly, and individuals needing to be crossed and mutated are screened; and then a crossover event occurs at a certain probability, a mutation event occurs at a certain probability, and the step of fitness calculation is executed circularly. While reasonable route recommendation is provided, consumption of computing resources is reduced,and the response speed of recommendation results is increased.

The invention discloses an oryza sativa autophagy-related protein OsATG8b (oryza sativa autophagy-related gene 8b) and application of a coding gene of the oryza sativa autophagy-related protein OsATG8b to improvement of heavy metal tolerability or accumulation of plants. Expression of the gene in engineered saccharomyces cerevisiae can improve cadmium tolerability of yeasts and reduce the content of cadmium in the yeasts, so that the protein OsATG8b shows a heavy metal cadmium detoxication capability. If the gene is expressed in engineering bacteria in a transgenic manner, on the one hand, heavy metal cadmium tolerability of the engineering bacteria can be improved, on the other hand, heavy metal cadmium accumulation in transgenic saccharomyces cerevisiae can be reduced, and accordingly the engineering bacteria can be applied to microorganism genetic modification engineering aiming at heavy metal cadmium pollution. The gene has a potential to be applied to cadmium-resistant genetic engineering breeding of plants, and by regulation of expression of the gene in the plants, heavy metal cadmium tolerability of transgenic plants can be changed, heavy metal cadmium accumulation in the transgenic plants can be changed as well, so that the problem of quality decline caused by cadmium enrichment of agricultural products acquired from heavy metal cadmium polluted soil is solved. The gene has a potential to be applied to low-cadmium or cadmium-resistant genetic engineering breeding of crops.

The invention discloses a method for preparing microorganism competent cells by using constant-pressure room-temperature plasmas, and belongs to the application of a plasma technology in a biological technical field. According to the basic principle provided by the invention, energetic ions and charged particles in the plasmas are used for interacting with proteins and genetic materials in the microorganism cells, so as to finally cause the property change of the cells. Therefore, the cells are at a physiological status which is the most suitable for capturing and containing external DNA. The method provided by the invention uses the constant-pressure room-temperature plasmas with a liquid circulation system, and uses helium as a plasma discharging gas to take effect on the microorganism cells, so that the competent cells can be efficiently and conveniently prepared. The method is efficient, fast, safe and convenient, and can be widely used for as a novel experimental technique in fields including microbial genetics, molecular genetics and genetic engineering,.

The invention relates to the technical fields of microbial genetic breeding and biological active substance production, and discloses a method for enhancing worm grass fermentation biomass. The method comprises the following steps: (1) preparing a worm grass protoplast; (2) carrying out mutagenesis on the worm grass protoplast, and regenerating the protoplast; (3) selecting the bacterial colony, and inoculating a PDA (potato dextrose agar) culture medium; (4) inoculating a liquid fermentation culture medium; and (5) obtaining the active product containing worm grass biomass, polysaccharide, cordycepin and the like. The worm grass strain with high hypha growth speed and high biomass is obtained by mutagenesis for the first time; by using white jade snail viscera and shells as the main raw material and adding proper glucose, K2HPO4, MgSO4 and other nutrient substances, the mutagenesis worm grass strain is inoculated and subjected to submerged fermentation to produce the worm grass mycelia. The method is simple to operate, sufficiently utilizes the waste resources and enhances the worm grass fermentation biomass. The fermentation product can be used in an animal feed additive to become a green food, thereby avoiding adding antibiotics in the animal feed.

The invention discloses a method for transforming Bacillus siamensis by electric shock, belonging to the technical field of microbial genetic engineering. The invention comprehensively optimizes factors such as preparation of competent cell, concentration of plasmid, electric shock parameter and the like during electric shock transformation of Bacillus siamensis JFL15, and establishes a simple andeffective genetic transformation method of Bacillus siamensis for the first time. The genetic transformation method of Bacillus siamensis of the invention is simple in operation, high in conversion rate, stable in effect, and can be used for the knockout of CRISPR -cas9 gene and the large plasmid () 11kbp for homologous recombination knockout vector with high efficiency, not only laid a good foundation for genetic modification of Bacillus siamensis, and has an important significance for accelerating its application in industrial production, but also provided an important reference for genetictransformation of other Bacillus spp.

The invention belongs to the technical field of microbial genetic engineering, specifically relates to a construction method of a complete mycobacterium tuberculosis H37Rv genome ORF bacterial two-hybrid clone library and application thereof. The construction method is characterized by comprising the following steps: preparing a bacterial two-hybrid carrier pTRG-MCM delta suitable for constructing the complete mycobacterium tuberculosis H37Rv genome ORF clone library; obtaining all encoded genes of the mycobacterium tuberculosis H37Rv by a PCR reaction; accurately cloning all encoded genes of the mycobacterium tuberculosis H37Rv into the constructed bacterial two-hybrid carrier pTRG-MCM delta; and transforming Escherichia coli DH10B to obtain the complete mycobacterium tuberculosis H37Rv genome ORF bacterial two-hybrid clone library.