Succinyl phosphonate inhibits alpha-ketoglutarate oxidative decarboxylation, catalyzed by alpha-ketoglutarate dehydrogenase complexes from E. coli and pigeon breast muscle

FEBS Lett. 1996 Mar 11;382(1-2):167-70. doi: 10.1016/0014-5793(96)00166-4.

Abstract

Effects of a set of alpha-ketoglutarate phosphoanalogues on the activity of alpha-ketoglutarate dehydrogenase (EC 1.2.4.2) complexes from E. coli and pigeon breast muscle, as well as on alpha-ketoglutarate dehydrogenase isolated from the pigeon breast muscle, have been studied. alpha-Ketoglutarate phosphoanalogues (succinyl phosphonate and its monomethyl ester) were found to be effective inhibitors of alpha-ketoglutarate oxidative decarboxylation, catalyzed by both muscle and bacterial alpha-ketoglutarate dehydrogenase complexes, as well as muscle alpha-ketoglutarate dehydrogenase. The ability of glutamate phosphoanalogues to inhibit alpha-ketoglutarate oxidative decarboxylation has been shown in E. coli extract and a model system.

MeSH terms

  • Animals
  • Columbidae
  • Decarboxylation
  • Enzyme Inhibitors / pharmacology*
  • Escherichia coli / enzymology*
  • Ketoglutarate Dehydrogenase Complex / antagonists & inhibitors*
  • Ketoglutaric Acids / metabolism*
  • Muscle, Skeletal / enzymology*
  • Organophosphonates / pharmacology*
  • Oxidation-Reduction
  • Succinates / pharmacology*

Substances

  • Enzyme Inhibitors
  • Ketoglutaric Acids
  • Organophosphonates
  • Succinates
  • succinyl phosphonate
  • Ketoglutarate Dehydrogenase Complex