Carnitine-dependent metabolic activities in Saccharomyces cerevisiae: Three carnitine acetyltransferases are essential in a carnitine-dependent strain
dc.contributor.author | Swiegers, J. H. | en_ZA |
dc.contributor.author | Dippenaar, N. | en_ZA |
dc.contributor.author | Pretorius, I. S. | en_ZA |
dc.contributor.author | Bauer, Florian | en_ZA |
dc.date.accessioned | 2011-05-15T16:05:34Z | |
dc.date.available | 2011-05-15T16:05:34Z | |
dc.date.issued | 2001 | |
dc.description.abstract | L-Carnitine is required for the transfer of activated acyl-groups across intracellular membranes in eukaryotic organisms. In Saccharomyces cerevisiae, peroxisomal membranes are impermeable to acetyl-CoA, which is produced in the peroxisome when cells are grown on fatty acids as carbon source. In a reversible reaction catalysed by carnitine acetyltransferases (CATs), activated acetyl groups are transferred to carnitine to form acetylcarnitine which can be shuttled across membranes. Here we describe a mutant selection strategy that specifically selects for mutants affected in carnitine-dependent metabolic activities. Complementation of three of these mutants resulted in the cloning of three CAT encoding genes: CAT2, coding for the carnitine acetyltransferase associated with the peroxisomes and the mitochondria; YAT1, coding for the carnitine acetyltransferase, which is presumably associated with the outer mitochondrial membrane, and YER024w (YAT2), which encodes a third, previously unidentified carnitine acetyltransferase. The data also show that (a) L-carnitine and all three CATs are essential for growth on non-fermentable carbon sources in a strain with a disrupted CIT2 gene; (b) Yat2p contributes significantly to total CAT activity when cells are grown on ethanol; and that (c) the carnitine-dependent transfer of activated acetyl groups plays a more important role in cellular processes than previously realised. Copyright © 2001 John Wiley & Sons, Ltd. | en_ZA |
dc.description.version | Article | |
dc.identifier.citation | Yeast | |
dc.identifier.citation | 18 | |
dc.identifier.citation | 7 | |
dc.identifier.issn | 0749503X | |
dc.identifier.other | 10.1002/yea.712 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/13193 | |
dc.subject | acetyl coenzyme A | |
dc.subject | acetylcarnitine | |
dc.subject | carbon | |
dc.subject | carnitine | |
dc.subject | carnitine acetyltransferase | |
dc.subject | fatty acid | |
dc.subject | article | |
dc.subject | catalysis | |
dc.subject | cell growth | |
dc.subject | cell membrane transport | |
dc.subject | chemical reaction | |
dc.subject | controlled study | |
dc.subject | enzyme activity | |
dc.subject | eukaryote | |
dc.subject | fermentation | |
dc.subject | fungus growth | |
dc.subject | fungus mutant | |
dc.subject | gene disruption | |
dc.subject | genetic complementation | |
dc.subject | intracellular membrane | |
dc.subject | metabolic activation | |
dc.subject | mitochondrial membrane | |
dc.subject | mitochondrion | |
dc.subject | molecular cloning | |
dc.subject | nonhuman | |
dc.subject | outer membrane | |
dc.subject | peroxisome | |
dc.subject | priority journal | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | Carnitine | |
dc.subject | Carnitine Acyltransferases | |
dc.subject | Carnitine O-Acetyltransferase | |
dc.subject | Cloning, Molecular | |
dc.subject | DNA, Fungal | |
dc.subject | Ethanol | |
dc.subject | Genetic Complementation Test | |
dc.subject | Membrane Proteins | |
dc.subject | Mutagenesis | |
dc.subject | Plasmids | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | Saccharomyces cerevisiae Proteins | |
dc.subject | Sequence Analysis, DNA | |
dc.subject | Eukaryota | |
dc.subject | Felis catus | |
dc.subject | Saccharomyces cerevisiae | |
dc.title | Carnitine-dependent metabolic activities in Saccharomyces cerevisiae: Three carnitine acetyltransferases are essential in a carnitine-dependent strain | |
dc.type | Article |