The involvement of the bridging imidazolate in the catalytic mechanism of action of bovine superoxide dismutase

Biochem J. 1977 Oct 1;167(1):271-4. doi: 10.1042/bj1670271.

Abstract

The pulse-radiolysis method has been used to study the catalytic mechanism of O2 leads to dismutation by the Co(II)-substituted bovine erythrocuprein (superoxide dismutase, EC 1.15.1.1). Catalysis is accompanied by spectral changes that may be interpreted in terms of rapid protonation and deprotonation of the Cu-facing nitrogen atom of the imidazolate that bridges the Cu(II) and the Co(II) [or Zn(II)] in the oxidized enzyme. This rapid change permits the possibility that the imidazole is a proton donor in the catalytic reduction of O2 leads to.

MeSH terms

  • Animals
  • Cattle
  • Imidazoles*
  • Kinetics
  • Protons
  • Pulse Radiolysis
  • Superoxide Dismutase / metabolism*

Substances

  • Imidazoles
  • Protons
  • Superoxide Dismutase