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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-01
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-21
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filingDate 2013-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7674e3482b60edfd0c8ba7d2634cbcc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c650174516a2146b48b842e3182fe9a1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c68bdcf9aeb69312e2da2c0d52a6efe6
publicationDate 2015-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103571784-B
titleOfInvention Engineering bacteria of special lipase for expressing biodiesel and fermenting process of engineering bacteria
abstract The invention provides engineering bacteria of special lipase for expressing biodiesel and fermenting process of engineering bacteria. The fermenting process comprises the following steps: by using onion Burkholderia GJ (B.cenocepacia) as original bacteria, screening constitutive strong promoter Pcon from the original bacteria through a fluorescent promoter probe carrier, cloning T7RNA polymerase gene not containing promoter in the promoter Pcon, feeding the promoter Pcon and the T7RNA polymerase gene into the original through electro-transformation to obtain host bacterial, cloning the lipase gene in a general carrier pBBR22b to obtain lipase expression plasmid, feeding the lipase expression plasmid into the host bacteria through the electro-transformation to obtain lipase engineering bacteria Burkholderiacenocepacia MTPF), CCTCC NO: M2O13229. The expression quantity of the lipase is greatly improved, and the produced lipase has good catalytic activity, low carbon alcohol tolerance and high temperature resistance.
priorityDate 2013-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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