Identification of membrane-bound phosphoglucomutase and glucose-6 phosphatase by 32P-labeling of rat liver microsomal membrane proteins with 32P-glucose-6 phosphate

J Biochem. 1995 Apr;117(4):908-14. doi: 10.1093/oxfordjournals.jbchem.a124795.

Abstract

Three recent reports have suggested that rat liver microsomal glucose-6 phosphatase (Glc6Pase) should be a 62-64 kDa polypeptide. In this work, we examine the possibility that the 62-64 kDa could represent a functional dimeric form of the 36.5 kDa glucose-6 phosphate (Glc6P)-phosphohydrolase, previously identified [Countaway et al. (1988) J. Biol. Chem. 263, 2672-2678]. From 32P-labeling experiments with 32P-Glc6P and analysis of 32P-labeled protein by SDS-PAGE and autoradiography, we show that three different rat liver microsomal polypeptides, the apparent molecular masses of which are 62, 54, and 37 kDa, may be specifically labeled with 32P-Glc6P. We demonstrate that the 62 kDa polypeptide is a microsome-bound form of cytosolic phosphoglucomutase, by combining labeling competition experiments and enzymatic assay. It should likely not account for a putative dimeric form of Glc6P-phosphohydrolase. The 37 kDa polypeptide fulfills the criteria of Glc6P-phosphohydrolase. We have not obtained any definitive evidence for its assembly as a dimer under functioning conditions. The 32P-Glc6P-labeling characteristics of the 54 kDa polypeptide are those expected for a protein displaying affinity in the millimolar range of concentration and a high binding capacity for Glc6P. They are consistent with those of a 54 kDa microsomal polypeptide, previously suggested to be involved in Glc6Pase activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cholic Acid
  • Cholic Acids / pharmacology
  • Disulfides / analysis
  • Disulfides / metabolism
  • Glucose-6-Phosphatase / analysis*
  • Glucose-6-Phosphatase / metabolism
  • Glucose-6-Phosphate
  • Glucosephosphates / metabolism*
  • Kinetics
  • Membrane Proteins / metabolism*
  • Membranes / enzymology
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology*
  • Phosphoglucomutase / analysis*
  • Phosphoglucomutase / metabolism
  • Phosphorus Radioisotopes
  • Rats
  • Substrate Specificity

Substances

  • Cholic Acids
  • Disulfides
  • Glucosephosphates
  • Membrane Proteins
  • Phosphorus Radioisotopes
  • Glucose-6-Phosphate
  • Glucose-6-Phosphatase
  • Phosphoglucomutase
  • Cholic Acid