López P, Martinez S, Diaz A, Espinosa M
Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
J Bacteriol. 1987 Oct;169(10):4869-71. doi: 10.1128/jb.169.10.4869-4871.1987.
The Streptococcus pneumoniae polA+ gene was introduced into Escherichia coli on the recombinant plasmid pSM31, which is based on the pSC101 replicon. Extracts of E. coli polA5 mutants containing pSM31 showed DNA polymerase activity, indicating that the pneumococcal DNA polymerase I was expressed in the heterospecific host. Complete complementation of the E. coli polA5 mutation by the pneumococcal polA+ gene was detected in excision repair of DNA damage.
肺炎链球菌polA+基因通过基于pSC101复制子的重组质粒pSM31导入大肠杆菌。含有pSM31的大肠杆菌polA5突变体提取物显示出DNA聚合酶活性,这表明肺炎球菌DNA聚合酶I在异种宿主中得到了表达。在DNA损伤的切除修复过程中,检测到肺炎球菌polA+基因对大肠杆菌polA5突变的完全互补作用。