Winans S C, Walker G C
J Bacteriol. 1985 Jan;161(1):402-10. doi: 10.1128/jb.161.1.402-410.1985.
The conjugal transfer system of the broad-host range IncN plasmid pKM101 was analyzed genetically. Its organization differed significantly from that of the F plasmid. The tra genes are located in three regions, each between 3 and 4 kilobases in length. All of the genes in the first two regions are required for sensitivity to "donor-specific" phage which bind to the plasmid-mediated sex pilus, and these genes therefore are involved in the synthesis, and possibly retraction, of the sex pilus. The plasmid's origin of transfer was localized to a 1.2-kilobase region at an extreme end of the transfer region. Using two different methods, we have identified 11 complementation groups required for transfer. One of these, traC, is of special interest in that mutations at this locus can be partially suppressed if, prior to mating, cells carrying a traC mutant plasmid are incubated with cells which elaborate sex pili but are unable to transfer their plasmids. One possible explanation for this is that pilus-elaborating cells can donate traC gene product to a traC mutant in a form that can be reused.
对广宿主范围的IncN质粒pKM101的接合转移系统进行了遗传学分析。其结构与F质粒的结构有显著差异。tra基因位于三个区域,每个区域长度在3至4千碱基之间。前两个区域中的所有基因对于对结合到质粒介导的性菌毛上的“供体特异性”噬菌体的敏感性都是必需的,因此这些基因参与性菌毛的合成,可能还参与性菌毛的缩回。该质粒的转移起始点定位于转移区域一端的一个1.2千碱基区域。使用两种不同的方法,我们鉴定出了转移所需的11个互补群。其中之一traC特别令人感兴趣,因为如果在交配前,携带traC突变体质粒的细胞与能形成性菌毛但不能转移其质粒的细胞一起培养,该位点的突变可以得到部分抑制。对此的一种可能解释是,能形成菌毛的细胞可以将traC基因产物以可再利用的形式提供给traC突变体。