Literature DB >> 3308921

Toxicity, mutagenesis and stress responses induced in Escherichia coli by hydrogen peroxide.

S Linn1, J A Imlay.   

Abstract

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.

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Year:  1987        PMID: 3308921     DOI: 10.1242/jcs.1984.supplement_6.19

Source DB:  PubMed          Journal:  J Cell Sci Suppl        ISSN: 0269-3518


  20 in total

Review 1.  Historical overview: searching for replication help in all of the rec places.

Authors:  M M Cox
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

2.  Regulation of katF and katE in Escherichia coli K-12 by weak acids.

Authors:  H E Schellhorn; V L Stones
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

3.  Radicals in Berkeley?

Authors:  Stuart Linn
Journal:  J Biol Chem       Date:  2015-02-24       Impact factor: 5.157

4.  Transcriptional regulation of katE in Escherichia coli K-12.

Authors:  H E Schellhorn; H M Hassan
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

5.  Global genome removal of thymine glycol in Escherichia coli requires endonuclease III but the persistence of processed repair intermediates rather than thymine glycol correlates with cellular sensitivity to high doses of hydrogen peroxide.

Authors:  Mohammed Alanazi; Steven A Leadon; Isabel Mellon
Journal:  Nucleic Acids Res       Date:  2002-11-01       Impact factor: 16.971

6.  Escherichia coli genes and pathways involved in surviving extreme exposure to ionizing radiation.

Authors:  Rose T Byrne; Stefanie H Chen; Elizabeth A Wood; Eric L Cabot; Michael M Cox
Journal:  J Bacteriol       Date:  2014-07-21       Impact factor: 3.490

7.  Effects of metal ion chelators on DNA strand breaks and inactivation produced by hydrogen peroxide in Escherichia coli: detection of iron-independent lesions.

Authors:  N R Asad; A C Leitão
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

8.  Molecular cloning and nucleotide sequencing of oxyR, the positive regulatory gene of a regulon for an adaptive response to oxidative stress in Escherichia coli: homologies between OxyR protein and a family of bacterial activator proteins.

Authors:  K Tao; K Makino; S Yonei; A Nakata; H Shinagawa
Journal:  Mol Gen Genet       Date:  1989-09

9.  Superoxide and the production of oxidative DNA damage.

Authors:  K Keyer; A S Gort; J A Imlay
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

10.  Induction of manganese-containing superoxide dismutase in anaerobic Escherichia coli by diamide and 1,10-phenanthroline: sites of transcriptional regulation.

Authors:  C T Privalle; S E Kong; I Fridovich
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-15       Impact factor: 11.205

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