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A Saccharomyces cerevisiae gene required for heterologous fatty acid elongase activity encodes a microsomal β-keto-reductase

  • Frédé Ric Beaudoin
  • , Ken Gable
  • , Olga Sayanova
  • , Teresa Dunn
  • , Johnathan A. Napier*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

76 Scopus citations

Abstract

A number of Saccharomyces cerevisiae membrane-bound oxidoreductases were examined for potential roles in microsomal fatty acid elongation, by assaying heterologous elongating activities in individual deletion mutants. One yeast gene, YBR159w, was identified as being required for activity of both the Caenorhabditis elegans elongase PEA1 (F56H11.4) and the Arabidopsis thaliana elongase FAE1. Ybr159p shows some limited homology to human steroid dehydrogenases and is a member of the short-chain alcohol dehydrogenase superfamily. Disruption of YBR159w is not lethal, in contrast to previous reports, although the mutants are slow growing and display high temperature sensitivity. Both Ybr159p and an Arabidopsis homologue were shown to restore heterologous elongase activities when expressed in ybr159Δ mutants. Biochemical characterization of microsomal preparations from ybr159Δ cells revealed a primary perturbation in Β-ketoacyl reduction, confirming the assignment of YBR159w as encoding a component of the microsomal elongase.

Original languageEnglish
Pages (from-to)11481-11488
Number of pages8
JournalJournal of Biological Chemistry
Volume277
Issue number13
DOIs
StatePublished - 29 Mar 2002

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