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Characterization of a K. lactis mutant with altered regulation of mitochondrial alcohol dehydrogenases

机译:线粒体酒精脱氢酶调控变化的乳酸克鲁维酵母突变体的表征

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摘要

KlADH3 and KlADH4 are Kluyveromyces lactis genes encoding the two mitochondrial alcohol dehydrogenase activities located within mitochondria. In this yeast, ethanol induces the transcription of KlADH4 and, conversely, represses that of KlADH3. In this study, we describe the effects of the aar900 mutation on such regulation. This mutation, firstly isolated in a strain devoid of alcohol dehydrogenase genes except KlADH4, conferred to cells resistance to allyl alcohol because of the absence of the KlAdh4p activity. When the mutation was transferred by crosses to an isogenic strain containing all the alcohol dehydrogenase genes, we found that the KlADH3 gene was highly expressed even in the presence of ethanol. In addition, we observed that the absence of KlAdh4p resulted from a post-transcriptional control in that KlADH4 was transcriptionally induced by ethanol. We also found that KlPDC1, another ethanol-repressible gene, was not transcribed in the mutant in the presence of this carbon source, indicating that the escape of KlADH3 from ethanol repression was a peculiar feature of this gene. Genetic analysis showed a Mendelian segregation of the mutation that was mapped in a region of chromosome III close to the ade1 locus. Interestingly, the aar900 mutants had a pleiotropic phenotype and showed increased resistance to monovalent cations and benomyl, suggesting that the mutation could also affect genes other than the alcohol dehydrogenase ones. Strains carrying the aar900 mutation could represent useful tools to unravel the peculiar regulation of KlADH3 and KlADH4 by ethanol.
机译:KlADH3和KlADH4是乳酸克鲁维酵母基因,编码位于线粒体内的两个线粒体醇脱氢酶活性。在该酵母中,乙醇诱导K1ADH4的转录,反之则抑制K1ADH3的转录。在这项研究中,我们描述了aar900突变对这种调节的影响。该突变首先分离于除了K1ADH4之外没有酒精脱氢酶基因的菌株中,由于缺乏K1Adh4p活性,赋予细胞对烯丙醇的抗性。当通过杂交将突变转移到包含所有酒精脱氢酶基因的同基因菌株中时,我们发现即使在乙醇存在下,KlADH3基因也高度表达。此外,我们观察到KlAdh4p的缺失是由转录后控制引起的,因为KlADH4是由乙醇转录诱导的。我们还发现,在存在该碳源的情况下,突变体中没有转录出另一种可抑制乙醇的基因KlPDC1,这表明从乙醇抑制中逃逸的KlADH3是该基因的独特特征。遗传分析显示该突变的孟德尔分离,定位在靠近ade1基因座的III号染色体区域。有趣的是,aar900突变体具有多效性表型,并且对单价阳离子和苯菌灵的抵抗力增强,表明该突变还可能影响除酒精脱氢酶基因以外的其他基因。携带aar900突变的菌株可能代表有用的工具,以阐明乙醇对KlADH3和KlADH4的特殊调节。

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