Silver L, Chandler M, Lane H E, Caro L
Mol Gen Genet. 1980;179(3):565-71. doi: 10.1007/BF00271746.
The drug resistance plasmid R100.1 can integrate into the E. coli chromosome at several sites on the plasmid. Many of the resulting Hfr strains continuously produce extrachromosomal circular forms of the r-determinant. These r-det 'plasmids' seem incapable of stable autonomous replication. We show that their presence in the cell requires the continuous activity of functional recA and recC genes but does not require the lexA function. The production of r-det circular forms is correlated with an increased copy number of r-det sequences, relative to RTF sequences, This copy number increase is, however, also found in a recA- background where no circular forms of r-det are found. These results show that a specific replication of r-det sequences, not present in the wild-type R100.1 plasmid, occurs in these R-Hfr strains. They suggest that a rec promoted recombination, posterior to the specific replication event, is needed for the production of circular r-det forms.
耐药质粒R100.1可在质粒上的多个位点整合到大肠杆菌染色体中。许多由此产生的高频重组(Hfr)菌株持续产生r-决定簇的染色体外环状形式。这些r-决定簇“质粒”似乎无法进行稳定的自主复制。我们发现它们在细胞中的存在需要功能性recA和recC基因的持续活性,但不需要lexA功能。r-决定簇环状形式的产生与r-决定簇序列相对于抗性转移因子(RTF)序列的拷贝数增加相关。然而,在没有发现r-决定簇环状形式的recA-背景中也发现了这种拷贝数增加。这些结果表明,在这些R-Hfr菌株中发生了野生型R100.1质粒中不存在的r-决定簇序列的特异性复制。它们表明,在特异性复制事件之后,产生环状r-决定簇形式需要rec促进的重组。