Pshennikova E S, Lipasova V A, Kolot M N, Khmel' I A
Genetika. 1986 May;22(5):733-40.
Organization of genes for colicin, immunity and lysis and regulation of their expression in colicinogenic plasmid ColD-CA23 were studied. The polypeptides synthesised in minicells carrying the ColD plasmid, its Tn5 mutants and the recombinant plasmids constructed by cloning the ColD EcoRV fragments on pBR325 were analysed. The position of the colicin gene promotor is established and direction of the gene transcription determined. The immunity gene was shown to be expressed independently of the gene coding for colicin and believed to have its own SOS-independent promotor. Treatment with mitomycin C of the ColD-carrying cells leads to induction of the synthesis both of colicin and of a 10 KD protein responsible for cell killing and lysis. This protein can be detected in a cultural medium under lysis. Plasmid mutations abolishing synthesis of the lysis protein prevent release of colicin. The colicin and lysis genes are arranged in an operon, the lysis gene being situated next to that of colicin. The ColD genetic map is suggested.
对产大肠杆菌素质粒ColD-CA23中大肠杆菌素、免疫和裂解基因的组织及其表达调控进行了研究。分析了在携带ColD质粒、其Tn5突变体以及通过将ColD EcoRV片段克隆到pBR325上构建的重组质粒的小细胞中合成的多肽。确定了大肠杆菌素基因启动子的位置并测定了基因转录方向。免疫基因被证明独立于编码大肠杆菌素的基因表达,并被认为有其自身不依赖SOS的启动子。用丝裂霉素C处理携带ColD的细胞会导致大肠杆菌素和一种负责细胞杀伤和裂解的10 KD蛋白质的合成诱导。这种蛋白质在裂解时可在培养基中检测到。消除裂解蛋白合成的质粒突变会阻止大肠杆菌素的释放。大肠杆菌素和裂解基因排列在一个操纵子中,裂解基因位于大肠杆菌素基因旁边。提出了ColD遗传图谱。