Fatty acid synthesis in mitochondria of Euglena gracilis

Eur J Biochem. 1984 Jul 2;142(1):121-6. doi: 10.1111/j.1432-1033.1984.tb08258.x.

Abstract

A malonyl-CoA-independent fatty acid synthetic system, different from the systems in other subcellular fractions, occurred in mitochondria of Euglena gracilis. The system had ability to synthesize fatty acids directly from acetyl-CoA as both primer and C2 donor using NADH as an electron donor. Fatty acids were synthesized by reversal of beta-oxidation with the exception that enoyl-CoA reductase functioned instead of acyl-CoA dehydrogenase in degradation system. A fairly high activity of enoyl-CoA reductase was found on various enoyl-CoA substrates (C4-C12) with NADH or NADPH. Three species of enoyl-CoA reductase, distinct from each other by their chain-length specificity, were found in Euglena mitochondria, and one of them was highly specific for crotonyl-CoA. It is also discussed that the mitochondrial fatty-acid synthetic system contributes to wax ester fermentation, the anaerobic energy-generating system found in the organism.

MeSH terms

  • Acetyl Coenzyme A / metabolism
  • Acetyl-CoA Carboxylase / metabolism
  • Acyl-CoA Dehydrogenases / metabolism
  • Adenosine Triphosphate / metabolism
  • Chromatography, DEAE-Cellulose
  • Cytosol / enzymology
  • Cytosol / metabolism
  • Euglena gracilis / enzymology
  • Euglena gracilis / metabolism*
  • Euglena gracilis / ultrastructure
  • Fatty Acids / biosynthesis*
  • Kinetics
  • Malonyl Coenzyme A / metabolism
  • Microsomes / enzymology
  • Microsomes / metabolism
  • Mitochondria / enzymology
  • Mitochondria / metabolism*
  • NAD / metabolism
  • NADP / metabolism
  • Substrate Specificity

Substances

  • Fatty Acids
  • NAD
  • Malonyl Coenzyme A
  • NADP
  • Acetyl Coenzyme A
  • Adenosine Triphosphate
  • Acyl-CoA Dehydrogenases
  • Acetyl-CoA Carboxylase