Participation of peroxisomes in lipid biosynthesis in the harderian gland of guinea pig

Biochem J. 1989 Sep 1;262(2):677-80. doi: 10.1042/bj2620677.

Abstract

Peroxisomal enzyme activities in the guinea-pig harderian gland, which has a unique lipid composition, were studied. Activities of catalase, acyl-CoA oxidase and the cyanide-insensitive acyl-CoA beta-oxidation system in this tissue were comparable with those in rat liver. The activities of dihydroxyacetone phosphate acyltransferase (DHAPAT, EC 2.3.1.42) and alkyl-DHAP synthase (EC 2.5.1.26) were appreciable, and the distributions of both activities were consistent with that of sedimentable catalase activity. Glycerol-3-phosphate acyltransferase (GPAT, EC 2.3.1.15), which is localized in both microsomes (microsomal fractions) and mitochondria in the rat liver, was a peroxisomal enzyme in the harderian gland, though the activity was only about one-tenth of the DHAPAT activity. These enzymes had different pH profiles and substrate specificity. The existence of high activities of enzymes of the acyl-DHAP pathway in peroxisomes suggests the physiological significance of peroxisomes in the biosynthesis of glycerol ether phospholipid and 1-alkyl-2,3-diacylglycerol in the guinea-pig harderian gland.

MeSH terms

  • Acyltransferases / metabolism
  • Animals
  • Carnitine Acyltransferases / metabolism
  • Carnitine O-Acetyltransferase / metabolism
  • Glycerol-3-Phosphate O-Acyltransferase / metabolism
  • Guinea Pigs
  • Harderian Gland / enzymology*
  • Harderian Gland / ultrastructure
  • Lacrimal Apparatus / enzymology*
  • Lipids / biosynthesis*
  • Male
  • Microbodies / enzymology*

Substances

  • Lipids
  • Acyltransferases
  • Carnitine Acyltransferases
  • carnitine octanoyltransferase
  • Glycerol-3-Phosphate O-Acyltransferase
  • glycerone-phosphate O-acyltransferase
  • Carnitine O-Acetyltransferase