http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108048438-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P13-004
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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-70
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filingDate 2018-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108048438-B
titleOfInvention Halohydrin dehalogenase mutant and application thereof
abstract The invention discloses a halohydrin dehalogenase mutant and application thereof in synthesis of atorvastatin key intermediate (3R,5R) 6-nitrile-3, 5-tert-butyl dihydroxyhexanoate, wherein the halohydrin dehalogenase mutant Hhec-A has an amino acid sequence shown in SEQ ID No. 2. Compared with wild enzyme, the catalytic activity of the 1 halogenated alcohol dehalogenase mutant provided by the invention is improved by 22 times, and the specific activity is improved by about 20 times. When the mutant HheC-A is used for catalyzing the reaction process of converting D3 into A7 in a whole cell manner, when the input amount of D3 is 50g/L, the conversion rate of D3 is 92% in 9 hours, and the yield of A7 is 72%. The yield of the product of the mutant HheC-A catalyzing the conversion of D3 into A7 is 4.8 times that of the wild enzyme HheC.
priorityDate 2018-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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