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Papers In Press, published online ahead of print September 10, 2004
Department of Microbiology, University of Illinois Urbana-Champaign, Urbana, IL 61801
Corresponding Author: jimlay{at}uiuc.edu
Endogenous H2O2 is believed to be a source of chronic damage in aerobic organisms. In order to quantify H2O2 formation, we have generated strains of Escherichia coli that lack intracellular scavenging enzymes. The H2O2 that is formed within these mutants diffuses out into the medium, where it can be measured. We sought to test the prevailing hypothesis that this H2O2 is primarily generated by the autoxidation of redox enzymes within the respiratory chain. The rate of H2O2 production increased when oxygen levels were raised, confirming that H2O2 is formed by an adventitious chemical process. However, mutants that lacked NADH dehydrogenase II and fumarate reductase--the most oxidizable components of the respiratory chain in vitro--continued to form H2O2 at normal rates. NADH dehydrogenase II did generate substantial H2O2 when it was overproduced or when quinones were absent, forcing electrons to accumulate on the enzyme. Mutants that lacked both NADH dehydrogenases respired very slowly, as expected; however, these mutants showed no diminution of H2O2 excretion, suggesting that H2O2 is primarily formed by a source outside the respiratory chain. That source has not yet been identified. In respiring cells the rate of H2O2 production was approximately 0.5% the rate of total oxygen consumption, with only modest changes when cells used different carbon sources.
J. Biol. Chem, 10.1074/jbc.M408754200
Submitted on August 2, 2004
Revised on September 9, 2004
Accepted on September 10, 2004
Are respiratory enzymes the primary sources of intracellular hydrogen peroxide
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