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甲氧苄啶诱导的大肠杆菌K-12 DNA聚合酶I缺陷

Trimethoprim-induced DNA polymerase I deficiency in Escherichia coli K-12.

作者信息

Mukhopadhyay P, Syrowik U, Palchaudhuri S

出版信息

J Bacteriol. 1983 Jun;154(3):1098-103. doi: 10.1128/jb.154.3.1098-1103.1983.

Abstract

Curing of the mini-ColE1 plasmid pML21 was observed among cells of Escherichia coli K-12 strain C600(pML21) grown under subinhibitory conditions in the presence of trimethoprim, a specific inhibitor of dihydrofolate reductase. Some of the cured colonies showed (i) a reduction in frequency of transformation with pML21 compared with those of isogenic strains not treated with trimethoprim, (ii) loss of viability after acquisition of a recA mutation, and (iii) UV sensitivity greater than that of the original isogenic strain. These colonies therefore had PolA- phenotypes. Moreover, they were found to be deficient in DNA polymerase I activity in the in vitro assays, indicating the occurrence of a polA mutation in them. Many of the colonies with PolA- phenotypes were also thyA deoC mutants, and these mutations, in addition to the polA mutations, appeared to be involved in the expression of the PolA- phenotypes.

摘要

在二氢叶酸还原酶的特异性抑制剂甲氧苄啶存在的亚抑制条件下培养的大肠杆菌K-12菌株C600(pML21)细胞中,观察到微小ColE1质粒pML21的消除。一些消除后的菌落表现出:(i) 与未用甲氧苄啶处理的同基因菌株相比,用pML21转化的频率降低;(ii) 在获得recA突变后活力丧失;(iii) 对紫外线的敏感性高于原始同基因菌株。因此,这些菌落具有PolA-表型。此外,在体外测定中发现它们缺乏DNA聚合酶I活性,表明它们发生了polA突变。许多具有PolA-表型的菌落也是thyA deoC突变体,除了polA突变外,这些突变似乎也参与了PolA-表型的表达。

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