FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to the biotechnologies. The invention represents the recombinant strain of bacteria E. coli FM-IFN, which is produced by means of the successive transformation of the strain cells E. coli BL21 by recombinant plasmid DNA pFM-AP and pFM-IFN-17, recombinant plasmid DNA pFM-AP with the size of 4,582 b.p., which encodes the inducible synthesis of the enzyme methionine-aminopeptidase E.coli under the control of a lactose promoter and contains the gene cm, which determines the resistances to chloramphenicol, as a genetic marker, recombinant plasmid DNA pFM-IFN-17 with the size of 3,215 b.p., which encodes the synthesis of the interferon alpha-2b of a human under the control the lactose and tryptophanic promotor and terminator of the transcription rrnBT1T2 and contains the synthetic gene km, which determines the resistances to kanamycin, as a genetic marker.
EFFECT: production of recombinant interferon aplpha-2b of a human free from methionine on the N-end with the high output and following the simplified technology.
4 cl, 8 dwg, 1 tbl, 6 ex
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Authors
Dates
2017-02-08—Published
2016-03-30—Filed