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来自白色链霉菌G的编码细胞外β-内酰胺酶的基因在变铅青链霉菌中的克隆及扩增表达

Cloning and amplified expression in Streptomyces lividans of a gene encoding extracellular beta-lactamase from Streptomyces albus G.

作者信息

Dehottay P, Dusart J, Duez C, Lenzini M V, Martial J A, Frère J M, Ghuysen J M, Kieser T

出版信息

Gene. 1986;42(1):31-6. doi: 10.1016/0378-1119(86)90147-2.

Abstract

A 4.9-kb DNA fragment containing the bla gene for the extracellular beta-lactamase (BLA) of Streptomyces albus G was cloned in Streptomyces lividans using the conjugative, low-copy-number plasmid pIJ61 as vector. No expression of bla was observed when this DNA fragment was introduced into Escherichia coli HB101 on a plasmid vector. A 1.5-kb PstI-SstI fragment containing the bla gene was cloned in S. lividans on the nonconjugative, high-copy-number plasmid pIJ702. A tenfold higher yield of BLA was obtained from S. lividans carrying this plasmid than from S. albus G grown under optimal production conditions. The BLA from the clone reacts with beta-iodopenicillanate according to a branched pathway which is characteristic of the original S. albus G BLA enzyme.

摘要

含有白色链霉菌G细胞外β-内酰胺酶(BLA)的bla基因的4.9kb DNA片段,以接合性低拷贝数质粒pIJ61作为载体克隆到变铅青链霉菌中。当将该DNA片段通过质粒载体导入大肠杆菌HB101时,未观察到bla的表达。含有bla基因的1.5kb PstI-SstI片段,以非接合性高拷贝数质粒pIJ702克隆到变铅青链霉菌中。携带该质粒的变铅青链霉菌产生的BLA产量比在最佳生产条件下生长的白色链霉菌G高十倍。来自该克隆的BLA根据原始白色链霉菌G BLA酶特有的分支途径与β-碘青霉素酸发生反应。

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