Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

40 results about "Genus Escherichia" patented technology

L-cysteine producing bacterium and method for producing L-cysteine

L-Cysteine is produced by culturing a bacterium belonging to the genus Escherichia having an L-cysteine producing ability and modified so that cystathionine-β-lyase activity or cystathionine-β-lyase activity and tryptophanase activity should be reduced or eliminated in a medium to produce and accumulate L-cysteine in the medium and collecting the L-cysteine from the medium.
Owner:AJINOMOTO CO INC

Method for producing 2'-fucosyllactose by using escherichia coli

The invention discloses use of Escherichia coli S17-3 for the production of 2'-fucosyllactose. The preservation number of the Escherichia coli S17-3 is CCTCC 2018200. The Escherichia coli S17-3 with high yield of colanicacid is used for denovo synthesizing of 2'-fucosyllactose by using lactose as a sole substrate, and no synthetic route for exogenously expressing GDP-L-fucose exists. According toa fermentation method of recombinant escherichia coli for producing 2'-fucosyllactose, the fermentation output is increased by more than 10 times, the highest output reaches 617.0 mg / L, and the outputis greatly increased.
Owner:SHANGHAI ADVANCED RES INST CHINESE ACADEMY OF SCI

Method for producing purine nucleosides and nucleotides by fermentation using bacterium belonging to the genus bacillus or escherichia

The invention provides methods for producing purine base analogues, purine nucleosides, and purine nucleotides, such as inosine and 5'-inosinic acid, which include using a bacterium belonging to the genus Bacillus or to the genus Escherichia wherein the purine productivity of said bacterium is enhanced by increasing an activity of the YdhL protein. The invention also provides the amino acid sequence of the YdhL protein from Bacillus amyloliquefaciens and the gene encoding it.
Owner:AJINOMOTO CO INC

Method for producing L-threonine

The present invention describes a method for producing L-threonine, which comprises the steps of: culturing a microorganism belonging to the genus Escherichia having the ability to produce L-threonine in an environment containing a carbon source, a nitrogen source, and a sulfur source fermentation medium, and collecting L-threonine, wherein the sulfur concentration in the medium is adjusted so as to be at a predetermined level or lower.
Owner:AJINOMOTO CO INC

Methods for identifying species of Shigella and E. coli using operon sequence analysis

A method for comparing the variable reactivity of multiple, differentially mutated copies of 16S subsequences found in a number of ribosomal RNA operons of a single bacterial cell is described. The application of this method for distinguishing between closely related organisms, such as the genera Escherichia and Shigella, and between species of Shigella including S. boydii, S. dysenteriae, S. flexneri, and S. sonnei using nucleic acid probes is also presented.
Owner:CABTECH

Microorganism of the Genus Escherichia Having Enhanced L-Tryptophan Productivity and a Method for Producing L-Tryptophan Using the Same

The present invention relates to microorganisms of Escherichia coli having enhanced L-tryptophan productivity and to a method for producing L-tryptophan using the same. More particularly, the present invention relates to an Escherichia coli variant in which repression and attenuation control of the tryptophan operon is released and accumulation of anthranilate is reduced and thereby enhancing L-tryptophan productivity. The present invention also relates to a method for producing L-tryptophan using the Escherichia coli variant.
Owner:CJ CHEILJEDANG CORP

Mutant carbamoylphosphate synthetase and method for producing compounds derived from carbamoylphosphate

L-arginine, citrulline and pyrimidine derivatives including orotic acid, uridine, uridine 5'-monophosphate (UMP), cytidine and cytidine 5'-monophosphate (CMP) are produced using a bacterium belonging to the genus Escherichia harboring a mutant carbamoylphosphate synthetase in which the amino acid sequence corresponding to positions from 947 to 951 in a wild type carbamoylphosphate synthetase is replaced with any one of amino acid sequences of SEQ ID NOS: 1 to 9, and feedback inhibition by uridine 5'-monophosphate in the bacterium is desensitized.
Owner:AJINOMOTO CO INC

Healthy human intestinal escherichia coli and application thereof

The invention discloses healthy human intestinal escherichia coli and application thereof and relates to the field of microbial technology. The escherichia coli JL-3 belongs to Escherichia, and the preservation number is CGMCC No. 14074. The escherichia coli can remarkably prolong average lifetime of caenorhabditis elegans, can remarkably enhance heat-stress resistance of caenorhabditis elegans, can be settled in caenorhabditis elegans, has good gastrointestinal operation endurance ability, can generate nitric oxide signal molecule, and has a wide prospect of being developed into health food or medicines.
Owner:HEBEI AGRICULTURAL UNIV.

Method for producing l-amino acid using bacteria belonging to the genus escherichia

There is provided a method for producing L-threonine, L-valine, L-proline, L-leucine, L-methionine and L-arginine using bacterium belonging to the genus Escherichia wherein L-amino acid productivity of the bacterium is enhanced by enhancing an activity of proteins coded by b2682 and b2683 genes, or protein coded by b1242 or b3434 gene.
Owner:AJINOMOTO CO INC

Method for producing L-threonine using bacteria belonging to the genus escherichia

The invention represents a method for preparing amino acid L-threonine by using bacterium belonging to Escherichia genus. This bacterium shows ability for production of L-threonine and modified by so manner that expression of gene chosen from the group glk, pgi, pfkA, tpiA, gapA, pgk, eno and pykA encoding glycogenolysis enzyme is enhanced.
Owner:AJINOMOTO CO INC

Process for producing L-threonine with the use of bacterium belonging to the genus escherichia

There is disclosed a method for producing L-threonine using bacterium belonging to the genus Escherichia wherein the bacterium has L- theonine productivity and has been modified to enhance an activity of aspartate aminotransferase.
Owner:AJINOMOTO CO INC

DNA encoding dipeptide-synthesizing enzyme (variants), bacterium belonging to the genus escherichia, and methods for producing dipeptides using thereof

The present invention describes novel bacterial L-amino acids α-ligases, which catalyzing reaction of dipeptide formation having an acidic L-amino acid such as L-Asp or L-Glu at the N-terminus. The method for producing dipeptides using said L-amino acids α-ligases and a bacterium of the family Enterobacteriaceae, particularly a bacterium belonging to the genus Escherichia, which has been modified to contain the DNA encoding said L-amino acids α-ligases, is described.
Owner:AJINOMOTO CO INC

Modified Escherichia coli engineering bacterium and method for producing citramalic acid by using modified Escherichia coli engineering bacterium

ActiveCN114806987AHigh glucose conversion efficiencyImprove conversion efficiencyBacteriaTransferasesEscherichia coliEnterobacter species
The invention discloses a modified Escherichia coli engineering bacterium and a method for producing citramalic acid by using the modified Escherichia coli engineering bacterium. According to the method, Escherichia coli S17-3 is taken as an original strain, and a T7 RNA polymerase gene for identifying a T7 promoter is inserted into a genome of the original strain, so that the modified escherichia coli engineering strain is obtained. The modified escherichia coli engineering bacteria further highly express citramalic acid synthase genes and one or more functional proteins of an inactivation auxiliary response factor RcsA, a response regulation factor RcsB, transmembrane sensing kinase RcsC, phosphate transporter RcsD and outer membrane lipoprotein RcsF. The invention provides novel industrial escherichia coli and a fermentation culture method, the strain is easy to culture, citramalic acid can be efficiently biosynthesized by using a cheap carbon source, and the production efficiency is higher than that of the existing biosynthesis method.
Owner:SHANGHAI ADVANCED RES INST CHINESE ACADEMY OF SCI

Zymomonas mobilis endogenous promoter mutants

The present application discloses Zymomonas mobilis endogenous promoter mutants which guide the expression of heterologous nucleic acids that can be chimeric-linked, promote the expression of heterologous nucleic acids, and at the same time, these promoter mutants are high-expression promoters having a significantly enhanced function relative to wild-type promoters, the present invention relates to chimeric genes for expressing chimeric genes in cells of Zymomonas and / or Escherichia.
Owner:HUBEI UNIV

Process for producing L-lysine by fermenting

InactiveCN100384984CBacteriaTransferasesBacteroidesDiaminopimelate dehydrogenase
A bacterium belonging to the genus Escherichia, which is transformed by introducing, into its cells, a DNA coding for a dihydrodipicolinate synthase originating from a bacterium belonging to the genus Escherichia having mutation to desensitize feedback inhibition by L-lysine and a DNA coding for an aspartokinase III originating from a bacterium belonging to the genus Escherichia having mutation to desensitize feedback inhibition by L-lysine; preferably a bacterium belonging to the genus Escherichia in which a dihydrodipicolinate reductase gene and a diaminopimelate dehydrogenase gene originating from Brevibacterium lactofermentum (or a succinyldiaminopimelate transaminase gene and a succinyldiaminopimelate deacylase gene) are further enhanced, is cultivated in an appropriate medium, L-lysine is produced and accumulated in a culture thereof, and L-lysine is collected from the culture.
Owner:AJINOMOTO CO INC

Ammonium ion resistant colibacillus for producing succinic acid and application thereof

The invention discloses an ammonium ion resistant colibacillus for producing succinic acid and application thereof and belongs to genus Escherichia. The colibacillus is named as Escherichia coli BER528, and the accession number CCTCC NO is of M2015160. On the anaerobic condition, the strain is capable of resisting high-density ammonium ions and accumulating succinic acid. During anaerobic shake flask fermentation with 0.53mol / LNH4 + added externally, 72h strain DCW is of 1.82g / L, the succinic acid yield is of 11.72g / L, but an original parent strain grows extremely slow, the 72h strain DCW is of 1.14g / L only, and the succinic acid yield is of 2.56g / L. Compared with that of the parent strain, the succinic acid yield is increased by 4.57 times. In the process of anaerobic fermentation with pH regulation through ammonia water by the aid of a 5L fermentation tank for 90h, the mutant strain DCW and final succinic acid yield are of 1.22g / L and 27.32g / L and is of 1.16 times and 1.88 times of those of the parent strain, and the mutant strain BER528 has important social benefit and economic value accordingly.
Owner:态创生物科技(广州)有限公司

A microorganism of the genus escherichia producing l-tryptophan and method for producing l-tryptophan using the same

ActiveUS20180087077A1Effectively and economically producing L-tryptophanHigh yieldBacteriaHydrolasesL-TRYPTOPHAN USEMicrobiology
The present invention relates to a microorganism of the genus Escherichia in which L-tryptophan productivity is improved by inactivating phosphatase activity. Further, the present invention relates to a method for producing L-tryptophan using the microorganism of the genus Escherichia.
Owner:CJ CHEILJEDANG CORP

Corynebacterium sp. transformed with a fructokinase gene derived from escherichia sp. and process for preparing l-amino acid using the same

ActiveUS20140099680A1Prevent unnecessary energy consumptionCost effective productionBacteriaTransferasesEscherichia coliCorynebacterium efficiens
The present invention relates to Corynebacterium sp. that is transformed with an Escherichia sp.-derived fructokinase gene to express fructokinase showing a sufficient activity of converting fructose into fructose-6-phosphate, thereby preventing unnecessary energy consumption, and a method for producing L-amino acids using the strain. The transformed Corynebacterium sp. of the present invention is able to express fructokinase from the Escherichia-derived fructokinase gene to prevent unnecessary energy consumption during fructose metabolism, leading to more cost-effective production of L-amino acids. Therefore, it can be widely used for the effective production of L-amino acids.
Owner:CJ CHEILJEDANG CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products