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filingDate 2018-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e730c6a039acdd442e110d4829c2e88
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publicationDate 2019-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2708556-C1
titleOfInvention RECOMBINANT PLASMID DNA p280_2GM CODING POLYPEPTIDE WITH PROPERTIES OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR OF HUMAN, STRAIN ESCHERICHIA COLI SG 20050/p280_2GM - PRODUCER OF POLYPEPTIDE WITH PROPERTIES OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR OF HUMAN AND METHOD OF OBTAINING OF SAID POLYPEPTIDE
abstract FIELD: biotechnology.SUBSTANCE: invention relates to biotechnology, particularly to genetic engineering, and is an in vitro constructed recombinant plasmid DNA containing two copies of a human granulocyte-macrophage colony-stimulating factor (GM-CSF) synthetic gene, Escherichia coli strain SG20050/p280_2GM is a producer of said polypeptide and a method of producing a polypeptide with GM-CSF properties. Recombinant plasmid DNA p280_2GM codes a polypeptide with properties of granulocyte-macrophage colony-stimulating factor (GM-CSF) of a person characterized by the following features: codes the amino acid sequence of the mature human GM-CSF; has molecular weight of 2.95 MDa (4,422 base pairs); consists of: PsTI/BamHI(pol)-fragment of plasmid DNA p280GM (1,484 base pairs) containing C-terminal part of beta-lactamase gene, tandem of promoters of tryptophan operon E. coli and synthetic gene GM-CSF of human, as well as EcoRI(pol)/PstI (2,938 base pairs) – a fragment of the same plasmid containing the synthetic human GM-CSF gene and the N-terminal portion of the beta-lactamase gene; contains: – tandem promoters of tryptophan operon E. coli; two copies of human synthetic GM-CSF gene; transcription terminator t0 of lambda phage; as a genetic marker, a beta-lactamase gene determining the resistance of E. coli transformed plasmid p280_2GM to ampicillin antibiotics; unique recognition sites by restriction endonucleases located at the following distances to the right from EcoRI site (279 base pairs) – BamHI – 912 nucleotides; PstI – 3,396 nucleotides.EFFECT: invention increases output of polypeptide with properties of granulocyte-macrophage colony-stimulating factor.3 cl, 8 dwg, 4 tbl, 15 ex
priorityDate 2018-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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