Disruption of genes encoding pyruvate dehydrogenase kinases leads to retarded growth on acetate and ethanol in Saccharomyces cerevisiae.

作者: H. Yde Steensma , Lubomir Tomaska , Peter Reuven , Jozef Nosek , Raymond Brandt

DOI: 10.1002/YEA.1543

关键词: Oxoglutarate dehydrogenase complexDihydrolipoyl transacetylaseMolecular biologyBiochemistryPyruvate decarboxylationPyruvate dehydrogenase kinaseCitric acid cycleBranched-chain alpha-keto acid dehydrogenase complexPyruvate dehydrogenase complexBiologyPyruvate dehydrogenase phosphatase

摘要: Two open reading frames, YIL042c (PKP1) and YGL059w, with 25% sequence similarity to human pyruvate dehydrogenase kinases, were shown have protein kinase activity. Using GFP fusions, it was demonstrated that the proteins localize in discrete submitochondrial regions. Strains a null mutation these loci grew poorly on acetate ethanol as carbon sources. Doubling times increased from ca. 4 h wild-type > 6 for mutants. Growth rates of mutants could be restored levels by simultaneous disruption PDA1 gene, encoding E1α subunit complex. This observation activities measured mutant strains grown glucose or suggest slow growth phenotype C2 sources is caused futile cycle which phosphoenolpyruvate converted back acetyl coenzyme A. Copyright © 2007 John Wiley & Sons, Ltd.

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