Fujimoto S, Tomita H, Wakamatsu E, Tanimoto K, Ike Y
Department of Microbiology, Gunma University School of Medicine, Japan.
J Bacteriol. 1995 Oct;177(19):5574-81. doi: 10.1128/jb.177.19.5574-5581.1995.
The pheromone-responding conjugative bacteriocin plasmid pPD1 (59 kb) of Enterococcus faecalis was mapped physically by using a relational clone approach, and transposon analysis with Tn917 (Emr) or Tn916 (Tcr) facilitated the location of the bacteriocin-related genes in a segment of about 6.7 kb. Tn917 insertions within a 3-kb region resulted in constitutive clumping. The nucleotide sequence of the region that included the insertions giving rise to constitutive clumping was determined. The region of pPD1 spanned about 8 kb and was found to contain a number of open reading frames, some of which were named on the basis of homologies with two other pheromone-responding plasmids, pAD1 and pCF10. The genes were arranged in the sequence repB-repA-traC-traB-traA-ipd-traE-traF- orfY-sea-1 with all but repB and traA oriented in the same (left-to-right) direction. traC and traB corresponded, respectively, to traC and traB of pAD1 and to prgY and prgZ of pCF10.
利用关联克隆方法对粪肠球菌的信息素响应性接合细菌素质粒pPD1(59 kb)进行了物理图谱绘制,并且使用Tn917(Emr)或Tn916(Tcr)进行转座子分析有助于将细菌素相关基因定位在约6.7 kb的片段中。在一个3 kb区域内的Tn917插入导致组成型聚集。测定了包含导致组成型聚集的插入片段的区域的核苷酸序列。pPD1的该区域跨度约8 kb,发现包含许多开放阅读框,其中一些是根据与另外两个信息素响应性质粒pAD1和pCF10的同源性命名的。这些基因按repB-repA-traC-traB-traA-ipd-traE-traF-orfY-sea-1的顺序排列,除repB和traA外,所有基因均沿相同(从左到右)方向排列。traC和traB分别对应于pAD1的traC和traB以及pCF10的prgY和prgZ。