发明名称 |
METHOD OF BACTERIOCINS ISOLATION |
摘要 |
FIELD: biotechnology.SUBSTANCE: culture fluid of producer strain is concentrated on hollow fibers truncating macromolecules with a molecular weight higher than 15 kDa. The cell concentrate is added to dry NaCl in a final concentration of 0.5 M. Mixed on a shaker for 20 min. The suspension is centrifuged for 15 min at 10000 g and the supernatant is separated, the supernatant pH is made up to 3.0 by four-molar solution of HCl. The suspension is centrifuged. The residue is added to water in a volume of 0.1% of the initial volume of the culture fluid, the residue is suspended and alcohol is added in amount of 0.1% of the initial volume of the culture fluid. Ethanol or propanol or isopropanol is used as alcohol. Exposed for 30 minutes at 0°C and centrifuged. The alcohol is removed from the solution by evaporation. The peptide fraction is purified. Water is added to 0.1% of the initial volume of the culture fluid, active carbon is added in an amount of 0.5% w/v (v - water volume). Centrifuged removing impurities adsorbed on the carbon. The aqueous solution is passed through the membrane truncating macromolecules with a molecular weight more than 10 kDa.EFFECT: invention enables to accelerate preparation of bacteriocin and to increase the degree of purification of the resulting product in a yield of 90% of the total activity in the culture fluid.1 dwg, 1 tbl, 4 ex |
申请公布号 |
RU2492231(C2) |
申请公布日期 |
2013.09.10 |
申请号 |
RU20110131558 |
申请日期 |
2011.07.28 |
申请人 |
FEDERAL'NOE BJUDZHETNOE UCHREZHDENIE NAUKI GOSUDARSTVENNYJ NAUCHNYJ TSENTR PRIKLADNOJ MIKROBIOLOGIII BIOTEKHNOLOGII (FBUN GNTS PMB) |
发明人 |
SUROVTSEV VLADIMIR IVANOVICH;BORZENKOV VALERIJ MIKHAJLOVICH;KHATJUSHIN JURIJ IVANOVICH;VEREVKIN VLADIMIR VASIL'EVICH;KRASIL'NIKOVA VALENTINA MIKHAJLOVNA |
分类号 |
C12N1/20;C07K1/20;C12P1/04;C12P21/00 |
主分类号 |
C12N1/20 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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