{"title":"氧化应激增加缺氧大肠杆菌和鼠伤寒沙门氏菌细胞的易变性:突变体在非选择性培养基上生长时克隆发生","authors":"Manuel Blanco, Guadalupe Herrera, Amparo Urios","doi":"10.1016/0165-7992(95)90038-1","DOIUrl":null,"url":null,"abstract":"<div><p><em>Escherichia coli</em> and <em>Salmonella typhimurium</em> strains decifient in the OxyR-regulated adaptive response to oxidative stress were used to study the mode in which spontaneous SOS-dependent mutations are generated in a distressed bacterial population. When assayed on supplemented selective medium, the <em>E. coli</em> strain IC3821 (<em>trpE65</em>), carrying the Δ<em>oxyR30</em> mutation and containing the plasmid pRW144 (mucA/B), showed a frequency of spontaneous Trp<sup>+</sup> revertants similar to that of the <em>oxyR</em><sup>+</sup> control. Instead, the IC3821 strain exhibited an enhancement in the clonal occurrence of spontaneous revertants arising at random during growth on a nonselective medium. A similar enhancement was observed for the <em>S. typhimurium</em> strain TA4125 (<em>hisG428 ΔoxyR2</em>). The mutator effect observed in <em>oxyR<sup>−</sup></em> cells would be induced by an increased background of reactive oxygen species; it provides a model for studying the mutability of a cell population constantly exposed to mutation-inducing agents. In the IC3821 strain, revertants were induced by <em>f</em>-butyl hydroperoxide with higher efficiency than in <em>oxyR</em><sup>+</sup>. We suggest that strain IC3821 could be useful for the detection of SOS-dependent mutagenesis induced by chemical oxidants.</p></div>","PeriodicalId":100934,"journal":{"name":"Mutation Research Letters","volume":"346 4","pages":"Pages 215-220"},"PeriodicalIF":0.0000,"publicationDate":"1995-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0165-7992(95)90038-1","citationCount":"26","resultStr":"{\"title\":\"Increased mutability by oxidative stress in OxyR-deficient Escherichia coli and Salmonella typhimurium cells: clonal occurrence of the mutants during growth on nonselective media\",\"authors\":\"Manuel Blanco, Guadalupe Herrera, Amparo Urios\",\"doi\":\"10.1016/0165-7992(95)90038-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Escherichia coli</em> and <em>Salmonella typhimurium</em> strains decifient in the OxyR-regulated adaptive response to oxidative stress were used to study the mode in which spontaneous SOS-dependent mutations are generated in a distressed bacterial population. When assayed on supplemented selective medium, the <em>E. coli</em> strain IC3821 (<em>trpE65</em>), carrying the Δ<em>oxyR30</em> mutation and containing the plasmid pRW144 (mucA/B), showed a frequency of spontaneous Trp<sup>+</sup> revertants similar to that of the <em>oxyR</em><sup>+</sup> control. Instead, the IC3821 strain exhibited an enhancement in the clonal occurrence of spontaneous revertants arising at random during growth on a nonselective medium. A similar enhancement was observed for the <em>S. typhimurium</em> strain TA4125 (<em>hisG428 ΔoxyR2</em>). The mutator effect observed in <em>oxyR<sup>−</sup></em> cells would be induced by an increased background of reactive oxygen species; it provides a model for studying the mutability of a cell population constantly exposed to mutation-inducing agents. In the IC3821 strain, revertants were induced by <em>f</em>-butyl hydroperoxide with higher efficiency than in <em>oxyR</em><sup>+</sup>. We suggest that strain IC3821 could be useful for the detection of SOS-dependent mutagenesis induced by chemical oxidants.</p></div>\",\"PeriodicalId\":100934,\"journal\":{\"name\":\"Mutation Research Letters\",\"volume\":\"346 4\",\"pages\":\"Pages 215-220\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0165-7992(95)90038-1\",\"citationCount\":\"26\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mutation Research Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0165799295900381\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mutation Research Letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0165799295900381","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Increased mutability by oxidative stress in OxyR-deficient Escherichia coli and Salmonella typhimurium cells: clonal occurrence of the mutants during growth on nonselective media
Escherichia coli and Salmonella typhimurium strains decifient in the OxyR-regulated adaptive response to oxidative stress were used to study the mode in which spontaneous SOS-dependent mutations are generated in a distressed bacterial population. When assayed on supplemented selective medium, the E. coli strain IC3821 (trpE65), carrying the ΔoxyR30 mutation and containing the plasmid pRW144 (mucA/B), showed a frequency of spontaneous Trp+ revertants similar to that of the oxyR+ control. Instead, the IC3821 strain exhibited an enhancement in the clonal occurrence of spontaneous revertants arising at random during growth on a nonselective medium. A similar enhancement was observed for the S. typhimurium strain TA4125 (hisG428 ΔoxyR2). The mutator effect observed in oxyR− cells would be induced by an increased background of reactive oxygen species; it provides a model for studying the mutability of a cell population constantly exposed to mutation-inducing agents. In the IC3821 strain, revertants were induced by f-butyl hydroperoxide with higher efficiency than in oxyR+. We suggest that strain IC3821 could be useful for the detection of SOS-dependent mutagenesis induced by chemical oxidants.