5'-Nucleotidases in rat heart. Evidence for the occurrence of two soluble enzymes with different substrate specificities

Biochem J. 1988 Jul 1;253(1):117-21. doi: 10.1042/bj2530117.

Abstract

Chromatography of soluble proteins from rat heart on phosphocellulose columns separates two 5'-nucleotidases. The first to emerge from the column shows a preference for AMP over IMP as substrate, whereas the second shows a preference for IMP over AMP. The properties of the IMP-preferring enzyme, including the conditions under which it is eluted from phosphocellulose columns, show it to be the enzyme studied by Itoh, Oka & Ozasa [Biochem. J. (1986) 235, 847-851]. The kinetic properties of the AMP-preferring enzyme indicate that it is likely to be the enzyme responsible for the production of adenosine under conditions of hypoxia and increased work load, and with metabolic stresses such as a high load of acetate.

Publication types

  • Comparative Study

MeSH terms

  • 5'-Nucleotidase
  • Adenosine Monophosphate / metabolism
  • Adenosine Triphosphate / pharmacology
  • Animals
  • Chromatography, Ion Exchange
  • Cytosol / enzymology
  • Inosine Monophosphate / metabolism
  • Isoenzymes / metabolism*
  • Myocardium / enzymology*
  • Nucleotidases / metabolism*
  • Rats
  • Solubility
  • Substrate Specificity

Substances

  • Isoenzymes
  • Inosine Monophosphate
  • Adenosine Monophosphate
  • Adenosine Triphosphate
  • Nucleotidases
  • 5'-Nucleotidase