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一种允许两个F因子复制的大肠杆菌突变体。

A mutant of Escherichia coli permitting replication of two F factors.

作者信息

Maas W K, Goldschmidt A D

出版信息

Proc Natl Acad Sci U S A. 1969 Mar;62(3):873-80. doi: 10.1073/pnas.62.3.873.

Abstract

Control mechanisms of replication of bacterial genetic elements are poorly understood at present. We have studied one such mechanism involving replication of the F factor in Escherichia coli. The F factor can replicate either autonomously in F(+) or F' strains, or as an integral part of the chromosome in Hfr strains. We have shown that presence of either an integrated F factor or a free F factor prevents replication of a second free F factor. Two integrated F factors can replicate in the same cell. The present experiments show that when a F'lac element was transferred by mating into an Hfr strain, it had to become integrated into the chromosome in order to persist. With a recombination-deficient (recA) Hfr strain as recipient, the frequency of F'lac integration was greatly reduced. This permitted us to isolate a mutant Hfr strain in which the F'lac element was able to replicate autonomously. The mutation has most likely occurred in the integrated F factor itself. Availability of this new recA mutant Hfr strain facilitates genetic analysis of the F factor, since in recA(+) Hfr strains frequent integration of a free F factor into the chromosome obscures recognition of complementation and recombination between two free F factors.

摘要

目前,对细菌遗传元件复制的控制机制了解甚少。我们研究了一种涉及大肠杆菌中F因子复制的机制。F因子既可以在F(+)或F'菌株中自主复制,也可以作为Hfr菌株染色体的一个组成部分进行复制。我们已经表明,整合的F因子或游离的F因子的存在都会阻止第二个游离F因子的复制。两个整合的F因子可以在同一细胞中复制。目前的实验表明,当通过交配将F'lac元件转移到Hfr菌株中时,它必须整合到染色体中才能持续存在。以重组缺陷型(recA)Hfr菌株作为受体,F'lac整合的频率大大降低。这使我们能够分离出一种突变Hfr菌株,其中F'lac元件能够自主复制。该突变很可能发生在整合的F因子本身。这种新的recA突变Hfr菌株的可用性有助于对F因子进行遗传分析,因为在recA(+) Hfr菌株中,游离F因子频繁整合到染色体中会掩盖对两个游离F因子之间互补和重组的识别。

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本文引用的文献

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Sex Compatibility in Escherichia Coli.大肠杆菌中的性别兼容性
Genetics. 1952 Nov;37(6):720-30. doi: 10.1093/genetics/37.6.720.
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EXCLUSION OF A FLAC EPISOME BY AN HFR GENE.高频重组(Hfr)基因对游离基因的排除
Proc Natl Acad Sci U S A. 1963 Dec;50(6):1051-5. doi: 10.1073/pnas.50.6.1051.

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