Ott R W, Barnes M H, Brown N C, Ganesan A T
J Bacteriol. 1986 Mar;165(3):951-7. doi: 10.1128/jb.165.3.951-957.1986.
The polC gene of Bacillus subtilis is defined by five temperature-sensitive mutations and the 6-(p-hydroxyphenylazo)-uracil (HPUra) resistance mutation azp-12. Biochemical evidence suggests that polC codes for the 160-kilodalton DNA polymerase III. A recombinant plasmid, p154t, was isolated and found to contain the azp-12 marker and one end of the polC gene (N. C. Brown and M. H. Barnes, J. Cell. Biochem. 78 [Suppl.]: 116, 1983). The azp-12 marker was localized to a 1-kilobase DNA segment which was used as a probe to isolate recombinant lambda phages containing polC region sequences. A complete polC gene was constructed by in vitro ligation of DNA segments derived from two of the recombinant phages. The resulting plasmid, pRO10, directed the synthesis of four proteins of 160, 76, 39, and 32 kilodaltons in Escherichia coli maxicells. Recombination-deficient (recE) B. subtilis PSL1 containing pRO10 produced an HPUra-resistant polymerase III activity which was lost when the strain was cured of pRO10. In vivo, the HPUra resistance of the plasmid-encoded polymerase III appeared to be recessive to the resident HPUra-sensitive polymerase III enzyme.
枯草芽孢杆菌的polC基因由五个温度敏感突变和6-(对羟基苯偶氮)尿嘧啶(HPUra)抗性突变azp-12定义。生化证据表明polC编码160千道尔顿的DNA聚合酶III。分离出一个重组质粒p154t,发现它含有azp-12标记和polC基因的一端(N.C.布朗和M.H.巴恩斯,《细胞生物化学杂志》78[增刊]:116,1983)。azp-12标记定位于一个1千碱基的DNA片段,该片段用作探针来分离含有polC区域序列的重组λ噬菌体。通过体外连接来自两个重组噬菌体的DNA片段构建了一个完整的polC基因。所得质粒pRO10在大肠杆菌大细胞中指导合成了四种蛋白质,分子量分别为160、76、39和32千道尔顿。含有pRO10的重组缺陷型(recE)枯草芽孢杆菌PSL1产生了一种对HPUra有抗性的聚合酶III活性,当该菌株去除pRO10时,这种活性丧失。在体内,质粒编码的聚合酶III对HPUra的抗性似乎对驻留的对HPUra敏感的聚合酶III酶呈隐性。