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Five control systems preventing transfer of Escherichia coli K-12 sex factor F.

机译:五个防止大肠杆菌K-12性因子F转移的控制系统。

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摘要

The transfer inhibition systems of 28 Fin+ plasmids have been characterized, using Flac mutants insensitive to inhibition by R100 or R62. All F-like plasmids (except R455) and one N group plasmid determined systems analogous to that of R100; this is designated the FinOP system. None of these plasmids could supply a FinP component of the transfer inhibitor able to replace that of F itself. In addition to the FinOP and R62 transfer inhibition systems described previously, new systems were encoded by the F-like plasmid R455, the I-like plasmid JR66a, and the group X plasmid R485. Besides inhibiting F transfer, JR66a also inhibited F pilus formation and surface exclusion, whereas R485 inhibited only pilus formation and R455 inhibited neither. All three R factors inhibited transfer of J-independent Flac elements, indicating that they act directly on one or more genes (or products) of the transfer operon, rather than directly via traJ. The tral products and transfer origin sequences of two Fin+ F-like plasmids, ColB2 and R124, appear to have similar specificities to those of F itself.
机译:使用对R100或R62的抑制不敏感的Flac突变体,已鉴定了28种Fin +质粒的转移抑制系统。所有F样质粒(R455除外)和一个N基团质粒确定的系统类似于R100;这被称为FinOP系统。这些质粒均不能提供能够取代F本身的转移抑制剂的FinP成分。除先前描述的FinOP和R62转移抑制系统外,新系统还由F样质粒R455,I样质粒JR66a和X组质粒R485编码。除抑制F转移外,JR66a还抑制F菌毛的形成和表面排斥,而R485仅抑制菌毛的形成,R455均不抑制菌毛的形成。所有这三个R因子均抑制J非依赖性Flac元素的转移,表明它们直接作用于转移操纵子的一个或多个基因(或产物),而不是直接通过traJ。两个Fin + F样质粒ColB2和R124的tral产物和转移起点序列似乎具有与F本身相似的特异性。

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