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Disruption of the Gene Encoding the Acyl-CoA-binding Protein ( ) Perturbs Acyl-CoA Metabolism in
- Source :
- Journal of Biological Chemistry. 271:22514-22521
- Publication Year :
- 1996
- Publisher :
- Elsevier BV, 1996.
-
Abstract
- The ACB1 gene encoding the acyl-CoA-binding protein (ACBP) was disrupted in Saccharomyces cerevisiae. The disruption did not affect the growth rate on glucose but reduced the growth rate on ethanol slightly. Although the growth rate of the acb1-disrupted cells was unaffected or only slightly affected, the acb1-disrupted strain was unable to compete with wild type cells when grown in mixed culture. The acyl-CoA level in the disrupted cells was increased from 1.5- to 2.5-fold during exponential growth. The increase in the acyl-CoA level was caused solely by an increase in de novo synthesized stearoyl-CoA. Experiments with purified yeast fatty acid synthetase show that it will synthesize long chain acyl-CoAs in the absence of acyl-CoA-binding protein. The addition of ACBP to the incubation medium resulted in a dramatic decrease in the chain length of the synthesized acyl-CoA esters. Despite the fact that the stearoyl-CoA concentration was increased 7-fold and the Δ9-desaturase mRNA level was increased 3-fold, the synthesis of oleic acid was unchanged in the acb1-disrupted strain. The results strongly indicate that ACBP in yeast is involved in the transport of newly synthesized acyl-CoA esters from the fatty acid synthetase to acyl-CoA-consuming processes.
- Subjects :
- chemistry.chemical_classification
Ethanol
biology
Saccharomyces cerevisiae
Wild type
Fatty acid
Cell Biology
biology.organism_classification
Biochemistry
Yeast
Oleic acid
chemistry.chemical_compound
chemistry
Acyl-CoA-binding protein
lipids (amino acids, peptides, and proteins)
Molecular Biology
Gene
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 271
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi...........83a28912c430b972158ea109d99f57e3
- Full Text :
- https://doi.org/10.1074/jbc.271.37.22514