Mito S, Zhang Q M, Yonei S
Laboratory of Radiation Biology, Faculty of Science, Kyoto University, Japan.
J Bacteriol. 1993 May;175(9):2645-51. doi: 10.1128/jb.175.9.2645-2651.1993.
Gene fusions in Escherichia coli that showed increased beta-galactosidase expression in response to treatment with a superoxide radical (O2-) generator, methyl viologen (MV), were obtained. These fusions were constructed by using a Mud(Ap lac) phage to insert the lactose structural genes randomly into the E. coli chromosome. Ampicillin-resistant colonies were screened for increased expression of beta-galactosidase on X-Gal (5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside) plates containing MV at 1.25 micrograms/ml. Other O2- generators, menadione and plumbagin, also induced beta-galactosidase activity in these fusion strains. The induction by these drugs occurred only under aerobic conditions. Hyperoxygenation also elicited an induction of the fusions. On the other hand, no significant induction was observed with hydrogen peroxide and cumene hydroperoxide. The induction of these fusions by MV was not dependent on the peroxide stress control mediated by the oxyR gene or on the recA-dependent SOS system. These fusions were named soi (superoxide inducible)::lacZ. The induction of beta-galactosidase was significantly reduced by introducing a soxS::Tn10 locus into the fusion strains, indicating that the soi genes are members of the soxRS regulon. Five of the fusions were located in 6 to 26 min of the E. coli genetic map, while three fusions were located in 26 to 36 min, indicating that these fusions are not related to genes already known to be inducible by O2- under the control of soxRS. At least five mutants containing the soi::lacZ fusion were more sensitive to MV and menadione than the wild-type strain, suggesting that the products of these soi genes play an important role in protection against oxidative stress.
获得了在超氧阴离子(O2-)发生器甲基紫精(MV)处理下β-半乳糖苷酶表达增加的大肠杆菌基因融合体。这些融合体是通过使用Mud(Ap lac)噬菌体将乳糖结构基因随机插入大肠杆菌染色体构建而成的。在含有1.25微克/毫升MV的X-Gal(5-溴-4-氯-3-吲哚基-β-D-吡喃半乳糖苷)平板上筛选对氨苄青霉素有抗性的菌落,以检测β-半乳糖苷酶表达的增加情况。其他O2-发生器甲萘醌和白花丹素也能在这些融合菌株中诱导β-半乳糖苷酶活性。这些药物的诱导作用仅在有氧条件下发生。高氧也能引发融合体的诱导。另一方面,过氧化氢和氢过氧化异丙苯未观察到明显的诱导作用。MV对这些融合体的诱导不依赖于由oxyR基因介导的过氧化物应激控制或依赖于recA的SOS系统。这些融合体被命名为soi(超氧化物诱导型)::lacZ。通过将soxS::Tn10位点引入融合菌株,β-半乳糖苷酶的诱导作用显著降低,表明soi基因是soxRS调节子的成员。其中五个融合体位于大肠杆菌遗传图谱的6至26分钟处,而三个融合体位于26至36分钟处,这表明这些融合体与已知在soxRS控制下可被O2-诱导的基因无关。至少五个含有soi::lacZ融合体的突变体对MV和甲萘醌比野生型菌株更敏感,这表明这些soi基因的产物在抵抗氧化应激中起重要作用。