Spectral characterization and chemical modification of catalase-peroxidase from Streptomyces sp

J Biol Chem. 1995 Jun 9;270(23):13740-7. doi: 10.1074/jbc.270.23.13740.

Abstract

Catalase-peroxidase was purified to near homogeneity from Streptomyces sp. The enzyme was composed of two subunits with a molecular mass of 78 kDa and contained 1.05 mol of protoporphyrin IX/mol of dimeric protein. The absorption and resonance Raman spectra of the native and its cyano-enzyme were closely similar to those of other heme proteins with a histidine as the fifth ligand. However, the peak from tyrosine ring at approximately 1612 cm-1, which is unique in catalases, was not found in resonance Raman spectra of catalase-peroxidase. The electron paramagnetic resonance spectrum of the native enzyme revealed uniquely two sets of rhombic signals, which were converted to a single high spin, hexacoordinate species after the addition of sodium formate. Cyanide bound to the sixth coordination position of the heme iron, thereby converting the enzyme to a low spin, hexacoordinate species. The time-dependent inactivation of the enzyme with diethyl pyrocarbonate and its kinetic analysis strongly suggested the occurrence of histidine residue. From the above-mentioned spectroscopic results and chemical modification, it was deduced that the native enzyme is predominantly in the high spin, ferric form and has a histidine as the fifth ligand.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalase / chemistry*
  • Catalase / isolation & purification
  • Diethyl Pyrocarbonate / pharmacology
  • Electron Spin Resonance Spectroscopy
  • Molecular Weight
  • Peroxidases / chemistry*
  • Peroxidases / isolation & purification
  • Spectrum Analysis
  • Streptomyces / enzymology*
  • Structure-Activity Relationship

Substances

  • Peroxidases
  • Catalase
  • Diethyl Pyrocarbonate