Canosi U, Siccardi A G, Falaschi A, Mazza G
J Bacteriol. 1976 Apr;126(1):108-21. doi: 10.1128/jb.126.1.108-121.1976.
Two inhibitors of replicative deoxyribonucleic acid (DNA) synthesis, nalidixic acid (NAL) and 6-(p-hydroxyphenylazo)-uracil (HPUra), showed different effects on genetic recombination and DNA repair in Bacillus subtilis. Previous work (Pedrini et al., 1972) showed that NAL does not interfere with the transformation process of B. subtilis. The results reported in this work demonstrated that the drug was also without effect on the transfection by SPP1 or SPO-1 phage DNA (a process that requires a recombination event). The drug was also ineffective on the host cell reactivation of ultraviolet-irradiated SPP1 phage, as well as on transfection with ultraviolet-irradiated DNA of the same phage. HPUra instead markedly reduced the transformation process, as well as transfection, by SPO-1 DNA, but it did not affect the host cell reactivation of SPO-1 phage. In conclusion, whereas the NAL target seems to be specific for replicative DNA synthesis, the HPUra target (i.e., the DNA polymerase III of B. subtilis) seems to be involved also in recombination, but not in the excision repair process. The mutations conferring NAL and HPUra resistance used in this work were mapped by PBS-1 transduction.
两种复制性脱氧核糖核酸(DNA)合成抑制剂,萘啶酸(NAL)和6-(对羟基苯偶氮)尿嘧啶(HPUra),对枯草芽孢杆菌的基因重组和DNA修复表现出不同的作用。先前的研究(Pedrini等人,1972年)表明,NAL不干扰枯草芽孢杆菌的转化过程。本研究报告的结果表明,该药物对SPP1或SPO-1噬菌体DNA的转染也没有影响(该过程需要重组事件)。该药物对紫外线照射的SPP1噬菌体的宿主细胞再活化也无效,对用同一噬菌体的紫外线照射DNA进行转染也无效。相反,HPUra显著降低了SPO-1 DNA的转化过程以及转染,但它不影响SPO-1噬菌体的宿主细胞再活化。总之,虽然NAL的作用靶点似乎对复制性DNA合成具有特异性,但HPUra的作用靶点(即枯草芽孢杆菌的DNA聚合酶III)似乎也参与重组,但不参与切除修复过程。本研究中使用的赋予NAL和HPUra抗性的突变通过PBS-1转导进行定位。