An intermediate of ubiquinone biosynthesis exists in the microsomal fraction of HepG2 cells

J Biochem. 1990 Dec;108(6):893-5. doi: 10.1093/oxfordjournals.jbchem.a123308.

Abstract

We analyzed lipids extracted from human hepatoma HepG2 cells using a high performance liquid chromatograph equipped with a reversed phase column and found a compound with a mass spectrum showing certain diagnostic ion fragments of 1-methoxy-5-polyprenyl-phenol, a known intermediate of ubiquinone biosynthesis. Universally radiolabeled [14C]-p-hydroxybenzoate, a precursor of ubiquinone, was incorporated into the compound on incubation with the cells, suggesting that the compound is a precursor of ubiquinone. The presence of the compound in the microsomal fraction of HepG2 cells was not due to contamination by the mitochondrial fraction because the activity of succinate-cytochrome c reductase in the microsomal fraction was below 1% of that in the mitochondrial fraction, whereas the contents of ubiquinone and the compound in the former were 4.6 and 7.8% of those in the latter, respectively. These results support the hypothesis that ubiquinone biosynthesis might occur in microsomes as well as mitochondria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Humans
  • Microsomes, Liver / metabolism*
  • Mitochondria, Liver / enzymology
  • Succinate Cytochrome c Oxidoreductase / metabolism
  • Tumor Cells, Cultured
  • Ubiquinone / biosynthesis*

Substances

  • Ubiquinone
  • Succinate Cytochrome c Oxidoreductase