http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2014065699-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_41583b9989764ebec3d9b73aa2ea1278
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-62
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-71
filingDate 2012-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_007b66937fce320afd548591cd45b31d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70d9d05cf26cb5e27d4a347f59275441
publicationDate 2014-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2014065699-A1
titleOfInvention Novel bacterial expression plasmid
abstract The present invention provides expression vectors useful for high-throughput screening of gene libraries. In a specific embodiment, an expression vector comprising (a) the Rop gene operatively linked to the trp promoter-operator; (b) a purification tag sequence and a protease cleavage site downstream of the Rop gene; and (d) a multiple cloning site downstream of the protease cleavage site, wherein the insertion of a heterologous gene of interest into the multiple cloning site and subsequent expression thereof in a host cell produces a high yield of a fusion protein comprising the Rop protein and the protein encoded by the heterologous gene of interest without the need of chemical inducers, temperature shifts, or growth medium alterations to initiate protein synthesis, and wherein the fusion protein controls plasmid replication at temperatures below about 30° C. but exhibits runaway plasmid replication when cultured at about 37° C.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111621854-A
priorityDate 2011-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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