Molecular characterization of Saccharomyces cerevisiae Delta3, Delta2-enoyl-CoA isomerase

J Biol Chem. 1998 Dec 11;273(50):33184-91. doi: 10.1074/jbc.273.50.33184.

Abstract

We report here the identification of the Saccharomyces cerevisiae peroxisomal Delta3,Delta2-enoyl-CoA isomerase, an enzyme that is essential for the beta-oxidation of unsaturated fatty acids. The yeast gene YLR284C was identified in an in silico screen for genes that contain an oleate response element, a transcription factor-binding site common to most fatty acid-induced genes. Growth on oleic acid resulted in a significant increase in YLR284C mRNA, demonstrating that it is indeed an oleate-induced gene. The deduced product of YLR284C contains a type 1 peroxisomal targeting signal-like sequence at its C terminus and localizes to the peroxisome in a PEX8-dependent manner. Removal of YLR284C from the S. cerevisiae genome eliminated growth on oleic acid, but had no effect on peroxisome biogenesis, indicating a role for YLR284C in fatty acid metabolism. Cells lacking YLR284C had no detectable Delta3,Delta2-enoyl-CoA isomerase activity, and a bacterially expressed form of this protein catalyzed the isomerization of 3-cis-octenoyl-CoA to 2-trans-octenoyl-CoA with a specific activity of 16 units/mg. We conclude that YLR284C encodes the yeast peroxisomal Delta3,Delta2-enoyl-CoA isomerase and propose a new name, ECI1, to reflect its enoyl-CoA isomerase activity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Carbon-Carbon Double Bond Isomerases / chemistry
  • Carbon-Carbon Double Bond Isomerases / genetics*
  • Carbon-Carbon Double Bond Isomerases / metabolism
  • DNA, Fungal
  • Dodecenoyl-CoA Isomerase
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Expression Regulation, Fungal / drug effects
  • Microbodies / enzymology
  • Molecular Sequence Data
  • Oleic Acid / pharmacology
  • Promoter Regions, Genetic
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Saccharomyces cerevisiae / enzymology*

Substances

  • DNA, Fungal
  • Recombinant Proteins
  • Oleic Acid
  • Carbon-Carbon Double Bond Isomerases
  • Dodecenoyl-CoA Isomerase

Associated data

  • GENBANK/AF090442