首页> 外文期刊>FEMS Yeast Research >Unsaturated fatty acids-dependent linkage between respiration and fermentation revealed by deletion of hypoxic regulatory KlMGA2 gene in the facultative anaerobe-respiratory yeast Kluyveromyces lactis
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Unsaturated fatty acids-dependent linkage between respiration and fermentation revealed by deletion of hypoxic regulatory KlMGA2 gene in the facultative anaerobe-respiratory yeast Kluyveromyces lactis

机译:通过缺血调节Klmga2基因在伴随的厌氧呼吸酵母Kluyveromyces乳房中缺血和发酵之间的不饱和脂肪酸依赖性连杆。

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摘要

In the yeast Kluyveromyces lactis, the inactivation of structural or regulatory glycolytic and fermentative genes generates obligate respiratory mutants which can be characterized by sensitivity to the mitochondrial drug antimycin A on glucose medium (Rag(-) phenotype). Rag(-) mutations can occasionally be generated by the inactivation of genes not evidently related to glycolysis or fermentation. One such gene is the hypoxic regulatory gene KlMGA2. In this work, we report a study of the many defects, in addition to the Rag- phenotype, generated by KlMGA2 deletion. We analyzed the fermentative and respiratory metabolism, mitochondrial functioning and morphology in the Klmga2 Delta strain. We also examined alterations in the regulation of the expression of lipid biosynthetic genes, in particular fatty acids, ergosterol and cardiolipin, under hypoxic and cold stress and the phenotypic suppression by unsaturated fatty acids of the deleted strain. Results indicate that, despite the fact that the deleted mutant strain had a typical glycolytic/fermentative phenotype and KlMGA2 is a hypoxic regulatory gene, the deletion of this gene generated defects linked to mitochondrial functions suggesting new roles of this protein in the general regulation and cellular fitness of K. lactis. Supplementation of unsaturated fatty acids suppressed or modified these defects suggesting that KlMga2 modulates membrane functioning or membrane-associated functions, both cytoplasmic and mitochondrial.
机译:在酵母Kluyveromyces乳房中,结构或调节糖酵解和发酵基因的灭活产生了迫使呼吸突变体,其能够通过对葡萄糖培养基(RAG( - )表型的线粒体药物抗霉素A的敏感性来表征。 rag( - )突变偶尔可以通过对糖醇分解或发酵而言的基因失活来产生。一种这样的基因是缺氧调节基因KlMGA2。在这项工作中,除了通过KLMGA2缺失产生的rag-表型之外,我们还报告了许多缺陷的研究。我们分析了KLMGA2 Delta菌株中的发酵和呼吸代谢,线粒体功能和形态。我们还在缺氧和冷应激下,通过不饱和脂肪酸的不饱和脂肪酸在缺氧和冷应激下调节脂质生物合成基因,特别是脂肪酸,Ergoster索和心脂蛋白的表达的改变。结果表明,尽管缺失的突变菌株具有典型的甘醇菌分/发酵表型和KlMGA2是一种缺氧调节基因,但该基因的缺失产生与线粒体功能相关的缺陷,这表明该蛋白在一般调节和细胞中的新作用K.乳酸的健身。补充不饱和脂肪酸抑制或修饰这些缺陷,表明KLMGA2调节膜功能或膜相关功能,包括细胞质和线粒体。

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