首页> 外国专利> METHOD FOR ISOLATING PROTEIN FROM WASTE CULTURE SOLUTION AFTER SHORT PERIOD CULTURE OF BCG BACTERIA AND MEASURING REAGENT FOR DELAYED HYPERSENSITIVITY REACTION

METHOD FOR ISOLATING PROTEIN FROM WASTE CULTURE SOLUTION AFTER SHORT PERIOD CULTURE OF BCG BACTERIA AND MEASURING REAGENT FOR DELAYED HYPERSENSITIVITY REACTION

机译:BCG细菌短期培养后从废水培养液中分离蛋白质的方法及超敏反应的测定试剂

摘要

PROBLEM TO BE SOLVED: To provide a method for efficiently recover a useful protein excreted by BCG bacteria in a culture medium and provide the recovered protein as a reagent, by using a waste culture medium from a short period culture of the BCG bacteria which is discharged in large amount as an industrial waste. ;SOLUTION: The subject protein is obtained by heating a waste culture medium at 40-45°C, successively filtering BCG bacteria cells and small molecular weight culture medium components to obtain a concentrated protein and carrying out an affinity purification of the protein successively by a phenylsepharose CL-4B column, a DEAE-sepharose column using urea, a sephacryl S200HR column and finally a DEAE-sepharose CL-6B column without using urea. The protein is used as a reagent.;COPYRIGHT: (C)1997,JPO
机译:解决的问题:提供一种方法,该方法通过使用从排出的BCG细菌的短期培养中得到的废培养基,有效地回收培养基中BCG细菌分泌的有用蛋白,并提供回收的蛋白作为试剂。作为工业废物大量使用。 ;解决方案:通过在40-45°C下加热废培养基,依次过滤BCG细菌细胞和小分子量培养基成分以获得浓缩的蛋白质,并通过连续的蛋白质亲和纯化来获得目标蛋白质。苯基琼脂糖CL-4B色谱柱,使用尿素的DEAE-琼脂糖色谱柱,sephacryl S200HR色谱柱以及最后不使用尿素的DEAE-琼脂糖CL-6B色谱柱。该蛋白质用作试剂。;版权:(C)1997,JPO

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