Hiltunen J K, Okubo F, Kursu V A S, Autio K J, Kastaniotis A J
Biocenter Oulu and Department of Biochemistry, P.O.B. 3000, University of Oulu, FIN-90014 Oulu, Finland.
Biochem Soc Trans. 2005 Nov;33(Pt 5):1162-5. doi: 10.1042/BST20051162.
Mitochondrial FAS (fatty acid synthesis) of type II is a widely conserved process in eukaryotic organisms, with particular importance for respiratory competence and mitochondrial morphology maintenance in Saccharomyces cerevisiae. The recent characterization of three missing enzymes completes the pathway. Etr1p (enoyl thioester reductase) was identified via purification of the protein followed by molecular cloning. To study the link between FAS and cell respiration further, we also created a yeast strain that has FabI enoyl-ACP (acyl-carrier protein) reductase gene from Escherichia coli engineered to carry a mitochondrial targeting sequence in the genome, replacing the endogenous ETR1 gene. This strain is respiratory competent, but unlike the ETR1 wild-type strain, it is sensitive to triclosan on media containing only non-fermentable carbon source. A colony-colour-sectoring screen was applied for cloning of YHR067w/RMD12, the gene encoding mitochondrial 3-hydroxyacyl-ACP dehydratase (Htd2/Yhr067p), the last missing component of the mitochondrial FAS. Finally, Hfa1p was shown to be the mitochondrial acetyl-CoA carboxylase.
II型线粒体脂肪酸合成(FAS)是真核生物中广泛保守的过程,对酿酒酵母的呼吸能力和线粒体形态维持尤为重要。最近对三种缺失酶的表征完善了该途径。通过蛋白质纯化随后进行分子克隆鉴定出了Etr1p(烯酰硫酯还原酶)。为了进一步研究FAS与细胞呼吸之间的联系,我们还构建了一种酵母菌株,该菌株基因组中携带来自大肠杆菌的FabI烯酰-ACP(酰基载体蛋白)还原酶基因,并经过工程改造携带线粒体靶向序列,取代了内源性ETR1基因。该菌株具有呼吸能力,但与ETR1野生型菌株不同,它在仅含有非发酵碳源的培养基上对三氯生敏感。应用菌落颜色分区筛选法克隆了YHR067w/RMD12,即编码线粒体3-羟基酰基-ACP脱水酶(Htd2/Yhr067p)的基因,这是线粒体FAS中最后一个缺失的组分。最后,Hfa1p被证明是线粒体乙酰辅酶A羧化酶。