Mitochondrial malate dehydrogenase of bovine cerebrum. Characterization and mechanisms of inhibition by silver ions

J Biochem. 1975 Nov;78(5):989-99. doi: 10.1093/oxfordjournals.jbchem.a131006.

Abstract

Attempts were made to characterize mitochondrial malate dehydrogenase [L-malate: NAD+ oxidoreductase, EC 1.1.1.37] (M-MDH) purified from bovine cerebrum and to elucidate the mechanisms responsible for inhibition of the enzymic activity by Ag+. The molecular weights of the native enzyme and its subunits were 54,000-55,000 and 30,000-32,000, respectively. In general, the physiochemical and catalytic properties of bovine cerebral M-MDH was not very different from those of other corresponding mammalian enzymes. Incubation of the enzyme with Ag+ caused the loss of equivalent amounts of sulfhydryls with a parallel decrease of the enzymic activity. When the enzyme was exposed to 2-, 3.5-, and 5-fold molar excesses of Ag+, the enzymic activity showed an initial rapid fall and a subsequent slow restoration to a partially inactivated level (60-70, 45-50, and 15-20% of an untreated control, respectively), while the alpha-helical content of the enzyme fell exponentially with time. A 7-fold molar excess of Ag+ reduced both the enzymic activity and the alpha-helical content to a much greater degree and no restoration of the enzymic activity was observed. The Km values of Ag+-inactivated enzyme for NADH and oxaloacetate were the same as those of the native enzyme. The data suggest that Ag+ could inhibit enzymic activity both by reducing the structural regularity of the enzyme molecule and by attacking sulfhydryl groups necessary for the catalytic activity of bovine cerebral M-MDH.

MeSH terms

  • Amino Acids / analysis
  • Animals
  • Brain / enzymology*
  • Cattle
  • Dose-Response Relationship, Drug
  • Hydrogen-Ion Concentration
  • Kinetics
  • Macromolecular Substances
  • Malate Dehydrogenase / antagonists & inhibitors*
  • Mitochondria / enzymology*
  • Molecular Weight
  • NAD / pharmacology
  • Oxaloacetates / pharmacology
  • Silver / pharmacology*
  • Sulfhydryl Reagents / pharmacology

Substances

  • Amino Acids
  • Macromolecular Substances
  • Oxaloacetates
  • Sulfhydryl Reagents
  • NAD
  • Silver
  • Malate Dehydrogenase