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lacY基因存在缺陷的大肠杆菌突变体的分离、遗传分析及特性研究

Isolation, genetic analysis, and characterization of Escherichia coli mutants with defects in the lacY gene.

作者信息

Hobson A C, Gho D, Müller-Hill B

出版信息

J Bacteriol. 1977 Sep;131(3):830-8. doi: 10.1128/jb.131.3.830-838.1977.

Abstract

Five hundred thirty-five lacY mutants were isolated from an Escherichia coli strain carrying the lactose operon on an F' factor, either without mutagenesis or after mutagenesis with 2-aminopurine or N-methyl-N'-nitro-N-nitrosoguanidine. Crosses against 48 independently isolated deletions ending in the lacY gene divided the gene into 36 deletion groups. Suppressibility studies with 7 nonsense suppressor strains classified 276 mutants as nonsense mutants and 78 as missense (or nonsuppressible) mutants. One hundred seventy-nine mutants were "leaky" and could not be so allocated, and two were found to have small internal deletions. Nonsense mutants could in many cases be subdivided even within deletion groups on the basis of their suppressibility pattern, giving a total of 70 groups of nonsense mutants. Studies of these mutants allow the following conclusions: lactose and melibiose most probably do not have separate binding sites on the permease; the lacY region most likely consists of one cistron, and so both active transport and facilitated diffusion are functions of one protein; and finally, there is probably no small defined region of the permease responsible for energy coupling of transport. Furthermore, the strains and the analysis form the basis for a future functional study of the permease by biochemical techniques.

摘要

从携带F'因子上乳糖操纵子的大肠杆菌菌株中分离出535个lacY突变体,这些突变体或是未经诱变,或是经2-氨基嘌呤或N-甲基-N'-硝基-N-亚硝基胍诱变后获得。与48个独立分离的、以lacY基因结尾的缺失突变体进行杂交,将该基因分为36个缺失组。用7种无义抑制菌株进行的抑制性研究将276个突变体归类为无义突变体,78个归类为错义(或不可抑制)突变体。179个突变体是“渗漏型”的,无法进行这样的分类,并且发现有两个突变体存在小的内部缺失。在许多情况下,无义突变体甚至可以根据其抑制模式在缺失组内进一步细分,总共得到70组无义突变体。对这些突变体的研究得出以下结论:乳糖和蜜二糖很可能在通透酶上没有单独的结合位点;lacY区域很可能由一个顺反子组成,因此主动运输和易化扩散都是一种蛋白质的功能;最后,通透酶可能没有一个负责运输能量偶联的小的特定区域。此外,这些菌株和分析为未来通过生化技术对通透酶进行功能研究奠定了基础。

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