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filingDate 2014-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_110147abafa74ec73b4b7450dd9e026b
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publicationDate 2014-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104087601-A
titleOfInvention Method for producing chirally pure S-acetoin
abstract The invention relates to a method for producing chirally pure S-acetoin. The method comprises the following steps: carrying out coexpression on a gene of diacetyl reductase (dar) and a gene of glucose dehydrogenase (gdh) in Escherichia coli, converting and producing chirally pure S-acetoin in the presence of a recombinant Escherichia coli rest cell used as a biocatalyst and diacetyl and glucose used as substrates. The diacetyl reductase has the characteristic that diacetyl is catalytically produced into the chirally pure S-acetoin, and the glucose dehydrogenase can provide the coenzyme NADH required for the diacetyl reductase, the yield of S-acetoin can reach up to 28g / L and the optical purity of S-acetoin is 99.7%. The method disclosed by the invention has the advantages of simple medium, convenience in operation process and low cost, the product S-acetoin is conveniently separated, the complex chiral separation step does not be needed, the intracellular coenzyme regeneration is achieved and the method has industrial application prospects.
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