首页> 外文期刊>The Journal of biological chemistry >ATP Synthesis-coupled and -uncoupled Acetate Production from Acetyl-CoA by Mitochondrial Acetate:Succinate CoA-transferase and Acetyl-CoA Thioesterase in Trypanosoma
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ATP Synthesis-coupled and -uncoupled Acetate Production from Acetyl-CoA by Mitochondrial Acetate:Succinate CoA-transferase and Acetyl-CoA Thioesterase in Trypanosoma

机译:ATP合成耦合和醋酸乙烯酸酯的醋酸乙酸醋酸酯,通过线粒体乙酸酯:琥珀酸盐COA转移酶和乙酰-COA硫代酯酶在脑瘤中

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Insect stage trypanosomes use an “acetate shuttle” to transfer mitochondrial acetyl-CoA to the cytosol for the essential fatty acid biosynthesis. The mitochondrial acetate sources are acetate:succinate CoA-transferase (ASCT) and an unknown enzymatic activity. We have identified a gene encoding acetyl-CoA thioesterase (ACH) activity, which is shown to be the second acetate source. First, RNAi-mediated repression of ASCT in the ACH null background abolishes acetate production from glucose, as opposed to both single ASCT and ACH mutants. Second, incorporation of radiolabeled glucose into fatty acids is also abolished in this ACH/ASCT double mutant. ASCT is involved in ATP production, whereas ACH is not, because the ASCT null mutant is ~1000 times more sensitive to oligomycin, a specific inhibitor of the mitochondrial F0/F1-ATP synthase, than wild-type cells or the ACH null mutant. This was confirmed by RNAi repression of the F0/F1-ATP synthase F1β subunit, which is lethal when performed in the ASCT null background but not in the wild-type cells or the ACH null background. We concluded that acetate is produced from both ASCT and ACH; however, only ASCT is responsible, together with the F0/F1-ATP synthase, for ATP production in the mitochondrion.
机译:昆虫阶段锥虫使用“醋酸醋酸醋酸”,将线粒体乙酰-CoA转移到胞质溶胶中,用于必需脂肪酸生物合成。线粒体乙酸盐源是乙酸酯:琥珀酸盐COA转移酶(ASCT)和未知的酶活性。我们已经鉴定了编码乙酰-Coa硫代酯酶(ACH)活性的基因,其显示为第二乙酸源。首先,RNAi介导的ASCT在ACH零背景中的抑制废除了葡萄糖的醋酸盐,而不是单一ASCT和ACH突变体。其次,在该ACH / ASCT双突变体中也消除了放射性标记的葡萄糖将放射性标记的葡萄糖掺入脂肪酸中。 ASCT涉及ATP生产,而ACH不是,因为ASCT NULL突变体对寡霉素的敏感性比野生型细胞或ACH空突变体比寡霉素更敏感,是对线粒体F0 / F1-ATP合酶的特异性抑制剂。这通过F0 / F1-ATP合酶F1β亚基的RNAi抑制证实,当在ASCT空背景中进行但不在野生型单元或ACH空背景中进行时,这是致命的。我们得出结论,醋酸酯是由ASCT和ACH产生的;然而,仅ASCT负责,与F0 / F1-ATP合成酶一起进行ATP在线粒体中的ATP生产。

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