http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1205764-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-62
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-00
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filingDate 1983-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1986-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_621bf7b3a8001d7c0d5f5f4cac9b0e74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_178a99edfda65059d232736d58c9ab35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7cef7a2f8dd47b431931e7db3f851dd
publicationDate 1986-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1205764-A
titleOfInvention Cloning vectors for polypeptide expression in microbial hosts
abstract Abstract The invention relates to a novel class of plasmid cloning vehicles which include a DNA sequence coding for the desired polypeptide linked for tran-scriptional expression in reading phase with one or more functional fragments derived from an outer membrane protein gene of a gram-negative bacterium. The plasmids also include an inducible promoter sequence positioned in the proper orientation for transcriptional expression of the desired polypeptide, as well as a separate DNA sequence coding for a repressor protein which can interact with the inducible promoter to prevent tran-scription therefrom. The repressor protein can be selectively inactivated by means of an inducer molecule to permit transcriptional expression of the desired polypeptide. Such plasmids may be used to introduce genetic capability into micro-organisms for the pro-duction of proteins, such as medically or commercially useful hormones, enzymes, immunogenic proteins, or intermediates therefor, but only in the presence of an appropriate inducer.
priorityDate 1982-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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