http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20180113469-A

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filingDate 2018-04-05^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a5e52d73129c78306d10e61b7f4e521
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publicationDate 2018-10-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20180113469-A
titleOfInvention Modulation of plasmid copy number in antibiotics-free plasmid maintenance system
abstract The present invention relates to a synthetic 5 'untranslated region (UTR), a gene expression cassette comprising a promoter and regulatory gene, a replication origin and a recombinant vector comprising said gene expression cassette, an improved segregational instability in which said recombinant vector is introduced A method for producing a recombinant microorganism having improved separation anxiety by introducing the recombinant vector, and a method for quantitatively controlling the number of plasmid copies in a recombinant microorganism. The gene encoding the translation initiation factor necessary for the cell according to the present invention, infA And Escherichia coli as a host are introduced into a gene expression cassette containing the regulatory gene to remove the efp encoding the protein elongation factor (EF-P) from the chromosome of the microorganism, and the plasmid can be isolated from the antibiotic- It can be stably maintained. Further, in the recombinant microorganism, infA And efp When the expression level is precisely controlled through a promoter, PCN can also be quantitatively controlled with high efficiency, and can be widely applied in various industries for producing recombinant proteins.
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priorityDate 2017-04-06^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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