Catalase catalyzes of peroxynitrite-mediated phenolic nitration

Biosci Biotechnol Biochem. 1998 Mar;62(3):448-52. doi: 10.1271/bbb.62.448.

Abstract

Catalase catalyzed the peroxynitrite-mediated nitration of 4-hydroxyphenylacetic acid. The curve for the pH dependence of nitration was similar to that for the reaction between peroxynitrite and phenol. Cyanide, azide, and 3-amino-1,2,4-triazole inhibited the nitration in a dose-dependent way. When catalase was mixed with peroxynitrite, Compound I was detected as an intermediate. Because azide was an electron donor for the peroxidatic action of catalase, and because 3-amino-1,2,4-triazole inhibited catalase activity by binding with Compound I, peroxynitrite-mediated phenolic nitration was probably accompanied by Compound I formation. Both catalase and superoxide dismutase protected Escherichia coli from peroxynitrite toxicity.

MeSH terms

  • Animals
  • Catalase / metabolism*
  • Catalysis
  • Cattle
  • Escherichia coli / drug effects
  • Hydrogen-Ion Concentration
  • Kinetics
  • Microbial Sensitivity Tests
  • Nitrates / metabolism*
  • Nitrates / pharmacology
  • Oxidants / metabolism*
  • Oxidants / pharmacology
  • Phenylacetates / metabolism*
  • Superoxide Dismutase / metabolism

Substances

  • Nitrates
  • Oxidants
  • Phenylacetates
  • peroxynitric acid
  • 4-hydroxyphenylacetic acid
  • Catalase
  • Superoxide Dismutase