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Molecular cloning of Bacillus sphaericus penicillin V amidase gene and its expression in Escherichia coli and Bacillus subtilis.

机译:球形芽孢杆菌青霉素V酰胺酶基因的分子克隆及其在大肠杆菌和枯草芽孢杆菌中的表达。

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摘要

The Bacillus sphaericus gene coding for penicillin V amidase, which catalyzes the hydrolysis of penicillin V to yield 6-aminopenicillanic acid and phenoxyacetic acid, has been isolated by molecular cloning in Escherichia coli. The gene is contained within a 2.2-kilobase HindIII-PstI fragment and is expressed when transferred into E. coli and Bacillus subtilis. The expression in B. subtilis carrying the recombinant plasmid is approximately two times higher than in the original B. sphaericus strain. A comparison of the purified enzyme from B. sphaericus and the expressed gene product in E. coli minicells suggests that the native enzyme consists of four identical subunits, each with a molecular weight of 35,000.
机译:通过在大肠杆菌中的分子克隆已经分离出编码青霉素V酰胺酶的球形芽孢杆菌基因,该基因催化青霉素V的水解以产生6-氨基青霉酸和苯氧乙酸。该基因包含在一个2.2千碱基的HindIII-PstI片段中,并在转移到大肠杆菌和枯草芽孢杆菌中时表达。携带重组质粒的枯草芽孢杆菌中的表达比原始球形芽孢杆菌菌株中的表达高大约两倍。从球形芽孢杆菌中纯化的酶与大肠杆菌小细胞中表达的基因产物的比较表明,天然酶由四个相同的亚基组成,每个亚基的分子量为35,000。

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