http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022174597-A1

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filingDate 2021-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c771689f73d0a7918df54ce8b04666d
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publicationDate 2022-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2022174597-A1
titleOfInvention Genetically engineered bacterium for producing l-sarcosine, construction method therefor and use thereof
abstract Provided are a genetically engineered bacterium for producing L-sarcosine, a construction method therefor and the use thereof. The genetically engineered bacterium takes escherichia coli as a host, and is obtained by means of integrating the following steps on the genome thereof: single copying an imine reductase gene dpkA; single copying a citrate synthase gene gltA; knocking out a glyoxylate cycle-inhibiting gene iclR; knocking out a malate synthase gene aceB; single copying an isocitrate lyase gene aceA; single copying a membrane-bound transhydrogenase gene pntAB; knocking out 2-keto acid reductase gene ycdW; single copying a phosphoenolpyruvate carboxylase gene ppc; and knocking out a pyruvate kinase gene pykF. After systemic metabolic modification is performed, the genetically engineered bacterium can be used for synthesizing L-sarcosine by means of taking glucose and methylamine as the main raw materials. After fermentation is performed in a 5 L fermentation tank for 30 h, the yield of L-sarcosine can reach 10 g/L.
priorityDate 2021-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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