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Cloning of oxidation reduction enzyme gene and the same gene and production manner null of the same

机译:氧化还原酶基因的克隆及同一基因及其生产方式的取消

摘要

PROBLEM TO BE SOLVED: To obtain a new oligonucleotide, to provide a method for amplification and cloning of a new oxydoreductase gene using the oligonucleotide as a primer, to obtain a recombinant vector containing the gene and a transformant transformed by the recombinant vector, and to provide a method for producing an oxydoreductase using the transformant.;SOLUTION: The oligonucleotide is synthesized based on an oxydoreductase gene of Bacillus cereus FERM P-14210 that is provided by the inventors in the Patent Application Number 2000-257829, the new oxydoreductase gene is amplified by the PCR method using the oligonucleotide as a primer, and the recombinant vector containing the amplified product obtained by amplifying the new oxydoreductase gene by the PCR method is produced. Next, the transformant transformed by using the recombinant vector is cultured and the oxydoreductase is obtained by collection of the oxydoreductase from the culture.;COPYRIGHT: (C)2002,JPO
机译:解决的问题:为了获得新的寡核苷酸,提供使用该寡核苷酸作为引物来扩增和克隆新的氧化还原酶基因的方法,获得包含该基因的重组载体和被该重组载体转化的转化体,并且提供一种使用该转​​化体生产氧化还原酶的方法。解决方案:该寡核苷酸基于蜡状芽孢杆菌FERM P-14210的氧化还原酶基因合成,该基因由发明人在专利申请号2000-257829中提供,新的氧化还原酶基因为使用寡核苷酸作为引物,通过PCR法进行扩增,得到含有通过PCR法扩增新的氧化还原酶基因而得到的扩增产物的重组载体。接下来,培养通过重组载体转化的转化体,并通过从培养物中收集氧化还原酶来获得氧化还原酶。;版权所有:(C)2002,JPO

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