Gilson L, Mahanty H K, Kolter R
J Bacteriol. 1987 Jun;169(6):2466-70. doi: 10.1128/jb.169.6.2466-2470.1987.
The colicin V production and immunity genes were isolated from plasmid pColV-K30. A HindIII-to-SalI fragment of 9.4 kilobases was cloned into the compatible vectors pBR322 and pACYC184. Mutants defective in colicin production were generated by Tn5 insertions and by constructing deletions in vitro. Physical analysis of these mutations identified a 4.4-kilobase region of this DNA which contains all the plasmid genes (cva) needed for the production of colicin V. The colicin V immunity determinant (cvi) is in a 700-base-pair fragment located within one end of this region. Complementation tests identified three genes, called cvaA, cvaB, and cvaC, required for colicin production. Analysis of the proteins labeled in minicells harboring various Tn5 insertions allowed us to identify protein products for the cvaA and cvaC genes. Mutations in cvaA and cvaB eliminated colicin activity in culture supernatants, but not within the cells. Mutations in cvaC, however, eliminated all detectable activity. From these results we conclude that the cvaC gene codes for the structural gene for colicin V, while cvaA and cvaB are apparently needed for the normal export of the colicin.
从质粒pColV-K30中分离出大肠杆菌素V的产生基因和免疫基因。一个9.4千碱基的HindIII至SalI片段被克隆到相容载体pBR322和pACYC184中。通过Tn5插入和体外构建缺失产生了大肠杆菌素产生缺陷的突变体。对这些突变的物理分析确定了该DNA的一个4.4千碱基区域,其包含产生大肠杆菌素V所需的所有质粒基因(cva)。大肠杆菌素V免疫决定簇(cvi)位于该区域一端内的一个700碱基对片段中。互补试验确定了大肠杆菌素产生所需的三个基因,称为cvaA、cvaB和cvaC。对含有各种Tn5插入的小细胞中标记的蛋白质进行分析,使我们能够鉴定出cvaA和cvaC基因的蛋白质产物。cvaA和cvaB中的突变消除了培养上清液中的大肠杆菌素活性,但细胞内没有。然而,cvaC中的突变消除了所有可检测到的活性。从这些结果我们得出结论,cvaC基因编码大肠杆菌素V的结构基因,而cvaA和cvaB显然是大肠杆菌素正常输出所必需的。