Regulation of the gastric microsomal (H+ + K+)-transporting ATPase system by the endogenous activator. Effect of phospholipase A2 treatment

Biochem J. 1983 Jun 15;212(3):887-90. doi: 10.1042/bj2120887.

Abstract

Pig gastric microsomal (H+ + K+)-stimulated ATPase activity was nearly abolished within 10 min of digestion with phospholipase A2 at room temperature. The enzyme activity could be largely restored by a cytosolic activator protein partially purified from the gastric cells. The K+ sensitivity and turnover of 32P-labelled intermediates produced by the control and the activator-reconstituted microsomal (H+ + K+)-stimulated ATPase were closely similar but were widely different to those from treated membranes without activator reconstitution. The data suggest an essential requirement for the endogenous activator for gastric (H+ + K+)-stimulated ATPase function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Enzyme Activation / drug effects
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / enzymology*
  • H(+)-K(+)-Exchanging ATPase
  • Microsomes / drug effects
  • Microsomes / enzymology*
  • Phospholipases / pharmacology*
  • Phospholipases A / pharmacology*
  • Phospholipases A2
  • Swine

Substances

  • Phospholipases
  • Phospholipases A
  • Phospholipases A2
  • Adenosine Triphosphatases
  • H(+)-K(+)-Exchanging ATPase