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PMID: 11032827 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Peroxisomal degradation of trans-unsaturated fatty acids in the yeast Saccharomyces cerevisiae.

The Journal of biological chemistry ·Vol. 276 ·No. 2 ·2001-01-12 ·Pages 895-903

Gurvitz A, Hamilton B, Ruis H, Hartig A

Abstract

Degradation of trans-unsaturated fatty acids was studied in the yeast Saccharomyces cerevisiae. Propagation of yeast cells on trans-9 elaidic acid medium resulted in transcriptional up-regulation of the SPS19 gene, whose promoter contains an oleate response element. This up-regulation depended on the Pip2p-Oaf1p transcription factor and was accompanied by induction of import-competent peroxisomes. Utilization of trans fatty acids as a single carbon and energy source was evaluated by monitoring the formation of clear zones around cell growth on turbid media containing fatty acids dispersed with Tween 80. For metabolizing odd-numbered trans double bonds, cells required the beta-oxidation auxiliary enzyme Delta(3)-Delta(2)-enoyl-CoA isomerase Eci1p. Metabolism of the corresponding even-numbered double bonds proceeded in the absence of Sps19p (2,4-dienoyl-CoA reductase) and Dci1p (Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase). trans-2,trans-4-Dienoyl-CoAs could enter beta-oxidation directly via Fox2p (2-enoyl-CoA hydratase 2 and d-specific 3-hydroxyacyl-CoA dehydrogenase) without the involvement of Sps19p, whereas trans-2,cis-4-dienoyl-CoAs could not. This reductase-independent metabolism of trans-2,trans-4-dienoyl-CoAs resembled the situation postulated for mammalian mitochondria in which oleic acid is degraded through a di-isomerase-dependent pathway. In this hypothetical process, trans-2,trans-4-dienoyl-CoA metabolites are generated by Delta(3)-Delta(2)-enoyl-CoA isomerase and Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase and are degraded by 2-enoyl-CoA hydratase 1 in the absence of 2,4-dienoyl-CoA reductase. Growth of a yeast fox2sps19Delta mutant in which Fox2p was exchanged with rat peroxisomal multifunctional enzyme type 1 on trans-9,trans-12 linolelaidic acid medium gave credence to this theory. We propose an amendment to the current scheme of the carbon flux through beta-oxidation taking into account the dispensability of beta-oxidation auxiliary enzymes for metabolizing trans double bonds at even-numbered positions.

MeSH Terms
Acyl Coenzyme A/metabolism Carbon-Carbon Double Bond Isomerases/metabolism Cloning, Molecular Enoyl-CoA Hydratase/metabolism Escherichia coli Fatty Acids, Unsaturated/chemistry,metabolism Genes, Reporter Genotype Isomerism Kinetics Peroxisomes/enzymology Plasmids Recombinant Proteins/metabolism Saccharomyces cerevisiae/enzymology,genetics,growth & development Structure-Activity Relationship Substrate Specificity
Chemicals
Acyl Coenzyme A Fatty Acids, Unsaturated Recombinant Proteins Enoyl-CoA Hydratase long-chain-enoyl-CoA hydratase Carbon-Carbon Double Bond Isomerases delta(3,5),delta(2,4)-dienoyl-CoA isomerase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Gurvitz A
Institut für Biochemie und Molekulare Zellbiologie der Universität Wien and Ludwig Boltzmann-Forschungsstelle für Biochemie, Vienna Biocenter, Dr Bohrgasse 9, A-1030 Vienna, Austria. [email protected]
Hamilton B
Ruis H
Hartig A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-01-12
Pages
895-903
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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