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PMID: 2834821 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Toxic DNA damage by hydrogen peroxide through the Fenton reaction in vivo and in vitro.

Science (New York, N.Y.) ·Vol. 240 ·No. 4852 ·1988-04-29 ·Pages 640-2

Imlay JA, Chin SM, Linn S

Abstract

Exposure of Escherichia coli to low concentrations of hydrogen peroxide results in DNA damage that causes mutagenesis and kills the bacteria, whereas higher concentrations of peroxide reduce the amount of such damage. Earlier studies indicated that the direct DNA oxidant is a derivative of hydrogen peroxide whose formation is dependent on cell metabolism. The generation of this oxidant depends on the availability of both reducing equivalents and an iron species, which together mediate a Fenton reaction in which ferrous iron reduces hydrogen peroxide to a reactive radical. An in vitro Fenton system was established that generates DNA strand breaks and inactivates bacteriophage and that also reproduces the suppression of DNA damage by high concentrations of peroxide. The direct DNA oxidant both in vivo and in this in vitro system exhibits reactivity unlike that of a free hydroxyl radical and may instead be a ferryl radical.

MeSH Terms
Bacteriophage lambda Chemical Phenomena Chemistry DNA Damage DNA Repair DNA, Bacterial/drug effects Escherichia coli/drug effects,genetics Ferrous Compounds Free Radicals Hydrogen Peroxide/administration & dosage,pharmacology Hydrogen-Ion Concentration Hydroxides Hydroxyl Radical Oxidation-Reduction
Chemicals
DNA, Bacterial Ferrous Compounds Free Radicals Hydroxides Hydroxyl Radical Hydrogen Peroxide
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Imlay J A
Department of Biochemistry, University of California, Berkeley 94720.
Chin S M
Linn S
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-04-29
Pages
640-2
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM19020 · United States
NIEHS NIH HHS · P30ES01896 · United States
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