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F质粒功能表达缺陷的大肠杆菌K-12染色体突变体的遗传分析:cpxA和cpxB基因的鉴定

Genetic analysis of Escherichia coli K-12 chromosomal mutants defective in expression of F-plasmid functions: identification of genes cpxA and cpxB.

作者信息

McEwen J, Silverman P

出版信息

J Bacteriol. 1980 Oct;144(1):60-7. doi: 10.1128/jb.144.1.60-67.1980.

Abstract

Two temperature-sensitive, chromosomal mutants of Escherichia coli were selected for their inability to express deoxyribonucleic acid donor activity and other activities associated with the conjugative plasmid F. These mutants were also auxotrophic for isoleucine and valine at 41 degrees C. Each mutant strain contained two altered genes: cpxA, located at 88 min on the E. coli K-12 genetic map, and cpxB, located at 41 min. Mutations in both genes were required for maximal expression of mutant phenotypes. The parent strain of mutants KN401 and KN312 already contained the cpxB mutation that is present in both mutants (cpxB1). This mutation by itself was cryptic. The cpxA mutations represent different mutant alleles since they are of independent origin. A cpxA mutation by itself significantly affected the expression of plasmid functions and growth at 41 degrees C in the absence of isoleucine and valine, but strains containing both a cpxA and cpxB mutation were more severely affected. Along with the observation that both cpxA mutations were revertable, the temperature sensitivity of cpxA cpxB+ cells suggests that both cpxA alleles contain point mutations that do not completely destroy the activity of the cpxA gene product.

摘要

选择了两株大肠杆菌的温度敏感型染色体突变体,它们无法表达脱氧核糖核酸供体活性以及与接合质粒F相关的其他活性。这些突变体在41℃时对异亮氨酸和缬氨酸也是营养缺陷型。每个突变菌株都包含两个改变的基因:位于大肠杆菌K-12遗传图谱88分钟处的cpxA和位于41分钟处的cpxB。两个基因的突变都是突变表型最大表达所必需的。突变体KN401和KN312的亲本菌株已经含有两个突变体中都存在的cpxB突变(cpxB1)。这个突变本身是隐性的。cpxA突变代表不同的突变等位基因,因为它们起源独立。单独的cpxA突变在缺乏异亮氨酸和缬氨酸的情况下显著影响质粒功能的表达和41℃时的生长,但同时含有cpxA和cpxB突变的菌株受到的影响更严重。连同两个cpxA突变都是可回复的这一观察结果,cpxA cpxB+细胞的温度敏感性表明两个cpxA等位基因都包含点突变,这些点突变不会完全破坏cpxA基因产物的活性。

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