Olschläger T, Schramm E, Braun V
Mol Gen Genet. 1984;196(3):482-7. doi: 10.1007/BF00436196.
The activity and immunity genes for colicins B and M on two conjugative ColBM plasmids, pCl139 and pF166, were cloned into pBR322 and pACYC184, respectively. The colicin regions on both recombinant plasmids were identical with regard to restriction endonuclease sites and the arrangement of the genes. They map close to each other in the order cmi cma cbi cba, where cmi denotes the locus that determines immunity to colicin M, cma the structural gene for colicin M, cbi immunity to colicin B, and cba the structural gene for colicin B. With the use of mutants obtained by insertion of the transposon Tn5, and by translation in minicells, the transcriptional polarity of cma and cba was found to be from right to left. cma and cba code for polypeptides with molecular weights of 27,000 and 58,000, respectively. No evidence of biosynthetic precursors was obtained.
两种接合型ColBM质粒pCl139和pF166上的大肠杆菌素B和M的活性及免疫基因分别被克隆到pBR322和pACYC184中。两种重组质粒上的大肠杆菌素区域在限制性内切酶位点和基因排列方面是相同的。它们彼此紧密连锁,顺序为cmi cma cbi cba,其中cmi表示决定对大肠杆菌素M免疫的位点,cma是大肠杆菌素M的结构基因,cbi是对大肠杆菌素B的免疫基因,cba是大肠杆菌素B的结构基因。利用通过转座子Tn5插入获得的突变体以及在微小细胞中的翻译,发现cma和cba的转录极性是从右到左。cma和cba分别编码分子量为27,000和58,000的多肽。未获得生物合成前体的证据。