Frey J, Ghersa P, Palacios P G, Belet M
J Bacteriol. 1986 Apr;166(1):15-9. doi: 10.1128/jb.166.1.15-19.1986.
The plasmid ColD-CA23, a high-copy-number plasmid of 5.12 kilobases, encodes colicin D, a protein of approximately 87,000 daltons which inhibits bacterial protein synthesis. Colicin D production is under the control of the Escherichia coli SOS regulatory system and is released to the growth medium via the action of the lysis gene product(s). A detailed map of the ColD plasmid was established for 10 restriction enzymes. Using in vitro insertional omega mutagenesis and in vivo insertional Tn5 mutagenesis, we localized the regions of the plasmid responsible for colicin D activity (cda), for mitomycin C-induced lysis (cdl), and for colicin D immunity (cdi). These genes were all located contiguously on a 2,400-base-pair fragment similar to a large number of other Col plasmids (A, E1, E2, E3, E8, N, and CloDF). The ColD plasmid was mobilizable by conjugative transfer by helper plasmids of the IncFII incompatibility group, but not by plasmids belonging to the groups IncI-alpha or IncP. The location of the mobilization functions was determined by deletion analysis. The plasmid needs a segment of 400 base pairs, which is located between the mob genes and the gene for autolysis, for its replication.
质粒ColD-CA23是一个5.12千碱基对的高拷贝数质粒,编码大肠杆菌素D,一种约87,000道尔顿的蛋白质,它能抑制细菌蛋白质合成。大肠杆菌素D的产生受大肠杆菌SOS调节系统的控制,并通过裂解基因产物的作用释放到生长培养基中。针对10种限制性内切酶构建了ColD质粒的详细图谱。利用体外插入型ω诱变和体内插入型Tn5诱变,我们确定了质粒中负责大肠杆菌素D活性(cda)、丝裂霉素C诱导裂解(cdl)和大肠杆菌素D免疫性(cdi)的区域。这些基因都连续位于一个2400碱基对的片段上,该片段与许多其他Col质粒(A、E1、E2、E3、E8、N和CloDF)相似。ColD质粒可通过IncFII不相容群的辅助质粒进行接合转移,但不能通过属于IncI-α或IncP群的质粒进行转移。通过缺失分析确定了转移功能的位置。该质粒复制需要一段400碱基对的片段,该片段位于mob基因和自溶基因之间。