• Title of article

    Mitochondrial transporters involved in oleic acid utilization and glutamate metabolism in yeast

  • Author/Authors

    Trotter، نويسنده , , Pamela J. and Adamson، نويسنده , , Amy L. and Ghrist، نويسنده , , Angela C. and Rowe، نويسنده , , Lindsay and Scott، نويسنده , , Lori R. and Sherman، نويسنده , , Matthew P. and Stites، نويسنده , , Nicole C. and Sun، نويسنده , , Yue and Tawiah-Boateng، نويسنده , , Mary Anne and Tibbetts، نويسنده , , Anne S. and C. Wadington، نويسنده , , Megan and West، نويسنده , , Aaron C.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2005
  • Pages
    12
  • From page
    21
  • To page
    32
  • Abstract
    Utilization of fatty acids such as oleic acid as sole carbon source by the yeast Saccharomyces cerevisiae requires coordinated function of peroxisomes, where the fatty acids are degraded, and the mitochondria, where oxidation is completed. We identified two mitochondrial oxodicarboxylate transporters, Odc1p and Odc2p, as important in efficient utilization of oleic acid in yeast [Tibbetts et al., Arch. Biochem. Biophys. 406 (2002) 96–104]. Yet, the growth phenotype of odc1Δodc2Δ strains indicated that additional transporter(s) were also involved. Here, we identify two putative transporter genes, YMC1 and YMC2, as able to suppress the odc1Δodc2Δ growth phenotype. The mRNA levels for both are elevated in the presence of glycerol or oleic acid, as compared to glucose. Ymc1p and Ymc2p are localized to the mitochondria in oleic acid-grown cells. Deletion of all four transporters (quad mutant) prevents growth on oleic acid as sole carbon source, while growth on acetate is retained. It is known that the glutamate-sensitive retrograde signaling pathway is important for upregulation of peroxisomal function in response to oleic acid and the oxodicarboxylate α-ketoglutarate is transported out of the mitochondria for synthesis of glutamate. So, citric acid cycle function and glutamate synthesis were examined in transporter mutants. The quad mutant has significantly decreased citrate synthase activity and whole cell α-ketoglutarate levels, while isocitrate dehydrogenase activity is unaffected and glutamate dehydrogenase activity is increased 10-fold. Strains carrying only two or three transporter deletions exhibit intermediate affects. 13C NMR metabolic enrichment experiments confirm a defect in glutamate biosynthesis in the quad mutant and, in double and triple mutants, suggest increased cycling of the glutamate backbone in the mitochondria before export. Taken together these studies indicate that these four transporters have overlapping activity, and are important not only for utilization of oleic acid, but also for glutamate biosynthesis.
  • Keywords
    Mitochondria , transport , fatty acid , Citric acid cycle , peroxisome , glutamate , Yeast
  • Journal title
    Archives of Biochemistry and Biophysics
  • Serial Year
    2005
  • Journal title
    Archives of Biochemistry and Biophysics
  • Record number

    1627547