Linn S, Imlay J A
Department of Biochemistry, University of California, Berkeley 94720.
J Cell Sci Suppl. 1987;6:289-301. doi: 10.1242/jcs.1984.supplement_6.19.
Two modes of killing of Escherichia coli by hydrogen peroxide can be distinguished. Mode-one killing is maximal at 1-2 mM; at higher concentrations the killing rate is approximately half-maximal and is independent of H2O2 concentration but first order with respect to exposure time. Mutagenesis and induction of a phage lambda lysogen are similarly affected by H2O2 concentration, with reduced levels of response above 1-2 mM-H2O2. Mutagenesis is not affected by inactivation of umuC. Mode-one killing requires active metabolism during the H2O2 challenge and it results in sfiA-independent filamentation of both cells that survive and those that are killed by the challenge. This mode of killing is enhanced in xth, polA, recA and recB strains; however, it is unaffected by mutations in the nth, uvrA, uvrB, uvrC, uvrD, rep, gyrA, htpR and rel loci. Mode-one killing is normal in strains totally lacking catalase activity (katE, katG), glutathione reductase (gor) or glutathione synthetase (gshB), but enhanced in a strain lacking NADH dehydrogenase (ndh). Mode-one killing is accelerated by the presence of CN- or by an unidentified function that is induced by anoxic growth and is under the control of the fnr locus. A strain carrying both xth and recA mutations and certain polA mutants appear to undergo spontaneous mode-one killing only under aerobic conditions. Taken together, these observations imply that mode-one killing results from DNA damage that normally occurs at a low, non-lethal level during aerobic growth. Models for the resistance to mode-one killing at dose above 1-2 mM-H2O2 will be discussed. Mode-two killing occurs at high concentrations of H2O2 and longer times. It does not require active metabolism, and cells that are killed do not filament, although survivors demonstrate a dose-dependent growth lag followed by a period of filamentation. Mode-two killing is accompanied by enhanced mutagenesis, but strains with DNA repair defects were not observed to be especially sensitive to this mode of killing.
过氧化氢杀死大肠杆菌的两种模式可以区分。模式一的杀伤作用在1-2 mM时最大;在更高浓度下,杀伤率约为最大杀伤率的一半,且与过氧化氢浓度无关,但与暴露时间呈一级关系。诱变作用和λ噬菌体溶原菌的诱导同样受过氧化氢浓度的影响,在1-2 mM以上的过氧化氢浓度下,反应水平降低。诱变作用不受umuC失活的影响。模式一的杀伤作用在过氧化氢攻击期间需要活跃的代谢,并且它导致存活的细胞和被攻击杀死的细胞都出现与sfiA无关的丝状体形成。这种杀伤模式在xth、polA、recA和recB菌株中增强;然而,它不受nth、uvrA、uvrB、uvrC、uvrD、rep、gyrA、htpR和rel位点突变的影响。模式一的杀伤作用在完全缺乏过氧化氢酶活性(katE、katG)、谷胱甘肽还原酶(gor)或谷胱甘肽合成酶(gshB)的菌株中是正常的,但在缺乏NADH脱氢酶(ndh)的菌株中增强。模式一的杀伤作用因存在氰化物或因缺氧生长诱导且受fnr位点控制的一种未确定功能而加速。同时携带xth和recA突变的菌株以及某些polA突变体似乎仅在有氧条件下经历自发的模式一杀伤作用。综上所述,这些观察结果表明模式一的杀伤作用是由有氧生长期间通常以低的、非致死水平发生的DNA损伤导致的。将讨论在高于1-2 mM过氧化氢剂量下对模式一杀伤作用的抗性模型。模式二的杀伤作用发生在高浓度过氧化氢和较长时间时。它不需要活跃的代谢,被杀死的细胞不会形成丝状体,尽管存活者表现出剂量依赖性的生长延迟,随后是一段丝状体形成期。模式二的杀伤作用伴随着诱变作用增强,但未观察到具有DNA修复缺陷的菌株对这种杀伤模式特别敏感。