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PMID: 7215339 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

The activation of ox-brain NAD+-dependent isocitrate dehydrogenase by magnesium ions.

European journal of biochemistry ·Vol. 113 ·No. 3 ·1981-01-00 ·Pages 477-83

Willson VJ, Tipton KF

Abstract

Two independent methods were used to assess the dependence of the activity of ox brain NAD+-dependent isocitrate dehydrogenase on the concentration of magnesium ions. The results indicated the complex between magnesium and isocitrate to be the true substrate for the enzyme. Free isocitrate is neither a substrate nor an inhibitor of the enzyme but free magnesium ions inhibit competitively with respect to the magnesium-isocitrate complex. The inhibition of the enzyme by ATP and citrate appears to be largely explicable in terms of their effects on the concentration of the complex between Mg2+ and isocitrate. The dependence of the activation of the enzyme by ADP on the concentration of magnesium ions suggests that free ADP, rather than its complex with Mg2+, is the activator.

MeSH Terms
Adenosine Diphosphate/pharmacology Adenosine Triphosphate/pharmacology Animals Brain/enzymology Cattle Citrates/pharmacology Enzyme Activation/drug effects In Vitro Techniques Isocitrate Dehydrogenase/antagonists & inhibitors,metabolism Magnesium/pharmacology Male NAD/pharmacology Substrate Specificity
Chemicals
Citrates NAD Adenosine Diphosphate Adenosine Triphosphate Isocitrate Dehydrogenase Magnesium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Willson V J
Tipton K F
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1981-01-00
Pages
477-83
Language
English
Region
England
NLM ID
0107600
Subset
IM
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