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枯草芽孢杆菌mutS mutL操纵子:鉴定、核苷酸序列及诱变

Bacillus subtilis mutS mutL operon: identification, nucleotide sequence and mutagenesis.

作者信息

Ginetti F, Perego M, Albertini A M, Galizzi A

机构信息

Dipartimento di Genetica e Microbiologia, Università degli Studi di Pavia, Italy.

出版信息

Microbiology (Reading). 1996 Aug;142 ( Pt 8):2021-9. doi: 10.1099/13500872-142-8-2021.

Abstract

The Bacillus subtilis mutS and mutL genes, involved in the DNA mismatch repair system, have been cloned and characterized. From sequence analysis the two genes appear to be organized in a single operon, located immediately downstream of the cotE gene (approximately 150 degrees on the genetic map). The deduced MutS protein is 49% identical to HexA and MutL is 46% identical to HexB of Streptococcus pneumoniae. Deletion of both mutS and mutL resulted in an increase in the frequency of spontaneous mutations and abolished the marker effect observed in transformation. The expression of the mut operon was studied with the use of a mutSL-lacZ transcriptional fusion. An increase in expression was observed during late exponential growth.

摘要

参与DNA错配修复系统的枯草芽孢杆菌mutS和mutL基因已被克隆并进行了表征。通过序列分析,这两个基因似乎组织在一个单一的操纵子中,位于cotE基因的紧下游(在遗传图谱上约150度)。推导的MutS蛋白与肺炎链球菌的HexA有49%的同一性,MutL与HexB有46%的同一性。mutS和mutL的缺失导致自发突变频率增加,并消除了转化中观察到的标记效应。利用mutSL-lacZ转录融合研究了mut操纵子的表达。在指数生长后期观察到表达增加。

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