Copper, Zinc Superoxide Dismutase and H2O2

  • Liochev S
  • Fridovich I
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Abstract

Copper,zinc superoxide dismutase (Cu,Zn-SOD) catalyzes the HCO3--dependent oxidation of diverse substrates. The mechanism of these oxidations involves the generation of a strong oxidant, derived from H2O2, at the active site copper. This bound oxidant then oxidizes HCO3- to a strong and diffusible oxidant, presumably the carbonate anion radical that leaves the active site and then oxidizes the diverse substrates. Cu,Zn-SOD is also subject to inactivation by H2O2. It is now demonstrated that the rates of HCO3--dependent oxidations of NADPH and urate exceed the rate of inactivation of the enzyme by ∼100-fold. Cu,Zn-SOD is also seen to catalyze a HCO3--dependent consumption of the H2O2 and that HCO3- does not protect Cu,Zn-SOD against inactivation by H2O2. A scheme of reactions is offered in explanation of these observations.

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Liochev, S. I., & Fridovich, I. (2002). Copper, Zinc Superoxide Dismutase and H2O2. Journal of Biological Chemistry, 277(38), 34674–34678. https://doi.org/10.1074/jbc.m204726200

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