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filingDate 2018-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3189f6f1ecb82936446676dc9586d89
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publicationDate 2018-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109022472-A
titleOfInvention The construction of recombinant vector of -1 α '-hydroxylase gene of 25(OH)VD containing reinder and expression, isolation and purification method
abstract It the present invention relates to the recombinant vector of -1 α '-hydroxylase gene of 25(OH)VD containing reinder and its encodes the expression of albumen, isolate and purify the method with determination of activity: 1) according to -1 α '-hydroxylase gene of 25(OH)VD and e. coli codon Preference annotated out from the genome of reinder, -1 α '-hydroxylase gene sequence of reinder 25(OH)VD after being optimized, -1 α '-hydroxylase gene sequence of 25(OH)VD for similarly obtaining the roe deer after optimizing according to e. coli codon Preference and sheep, to as control;2) primer of design is utilized, pass through gibson connection method, reinder, roe deer, -1 α '-hydroxylase gene of sheep 25(OH)VD, cortex ferredoxin gene and NADPH- cortex ferredoxin reductase gene after optimization is implemented in coli expression carrier pET-28a respectively, obtains recombinant vector.Final detection, the catalytic activity of the bacterial strain expression acquisition enzyme of -1 α '-hydroxylase gene of 25(OH)VD containing reinder are 2 times of sheep, are 1.5 times of roe deer.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021147857-A1
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