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Oxidative mutagenesis in Escherichia coli strains lacking ROS‐scavenging enzymes and/or 8‐oxoguanine defenses
Author(s) -
RuizLaguna Julia,
PrietoÁlamo MaríaJosé,
Pueyo Carmen
Publication year - 2000
Publication title -
environmental and molecular mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1
H-Index - 87
eISSN - 1098-2280
pISSN - 0893-6692
DOI - 10.1002/(sici)1098-2280(2000)35:1<22::aid-em4>3.0.co;2-x
Subject(s) - mutagenesis , superoxide dismutase , catalase , escherichia coli , reactive oxygen species , oxidative stress , biochemistry , bacteria , biology , oxidative phosphorylation , mutation , microbiology and biotechnology , gene , chemistry , genetics
Abstract Escherichia coli strains with different combinations of null mutations in the katG , katE, sodA , sodB , fpg, and mutY genes were constructed to compare their spontaneous mutation frequencies and sensitivities to various oxidants with those of bacteria solely deficient in catalase ( katG katE ) or cytosolic superoxide dismutase ( sodA sodB ) and the parental strain possessing a full complement of these enzymes. The MutY DNA glycosylase represented the major protection against the mutagenic consequences of processes associated with normal aerobic metabolism. Spontaneous mutagenesis in MutY‐lacking bacteria was not influenced by the absence of (A)BC excinuclease or the presence of MucAB proteins, a result consistent with 8‐oxoguanine being a principal premutational lesion. In contrast, catalase and SOD represented the major protection against the genotoxic consequences of bursts of oxidative stress caused by reactive‐oxygen‐generating compounds. Therefore, only bacteria simultaneously defective in both katG and katE or sodA and sodB genes were hypersensitive with respect to mutability by peroxide and superoxide, respectively. These data suggest that oxidative lesions other than 8‐oxoguanine contribute to mutagenesis by hydrogen peroxide and redox‐cycling chemicals. Environ. Mol. Mutagen. 35:22–30, 2000 © 2000 Wiley‐Liss, Inc.