Kamisaka Yasushi, Noda Naomi, Tomita Nao, Kimura Kazuyoshi, Kodaki Tsutomu, Hosaka Kohei
Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology (AIST), Ibaraki, Japan.
Biosci Biotechnol Biochem. 2006 Mar;70(3):646-53. doi: 10.1271/bbb.70.646.
Genes involved in lipid accumulation were identified in Saccharomyces cerevisiae using transposon insertion mutagenesis. Five ORFs, such as SNF2, IRA2, PRE9, PHO90, and SPT21 were found from the analysis of the insertion sites in transposon insertion mutants with higher lipid content. Since these ORFs are not directly involved in storage lipid biosynthesis, we speculate that they are involved in carbon fluxes into storage lipids in response to nutrient conditions. Lipid analysis of disruptants of these ORFs indicated that the Deltasnf2, and Deltaira2 disruptants had significantly higher lipid content. Cultivation in a nitrogen-limited medium increased the lipid content in all disruptants, among which the Deltapre9 disruptant was the most sensitive to nitrogen limitation. We then focused on the Deltasnf2 disruptant due to its higher lipid content and its function as a regulator of phospholipid synthesis. Lipid class analysis indicated that triacylglycerol and free fatty acids contributed to the increase in total lipids of the Deltasnf2 disruptant. The addition of exogenous fatty acids was not so effective at increasing the lipid content in the Deltasnf2 disruptant as it was in the wild type. It should be noticed that exogenous free linoleic acid was much higher in the Deltasnf2 disruptant than in the wild type, as in the case of endogenous free fatty acids. In addition, the incorporation of exogenous fatty acids into cells increased in the disruptant, suggesting that fatty acid transporters were regulated by SNF2. The results suggest that metabolic fluxes into storage lipids, which are activated in the Deltasnf2 disruptant, is repressed by the incorporation of exogenous fatty acids. They provide new insight into the biosynthesis of storage lipids in yeast.
利用转座子插入诱变技术在酿酒酵母中鉴定出参与脂质积累的基因。通过对脂质含量较高的转座子插入突变体的插入位点分析,发现了5个开放阅读框,如SNF2、IRA2、PRE9、PHO90和SPT21。由于这些开放阅读框不直接参与储存脂质的生物合成,我们推测它们参与了在营养条件响应下进入储存脂质的碳通量。对这些开放阅读框缺失突变体的脂质分析表明,Δsnf2和Δira2缺失突变体的脂质含量显著更高。在氮限制培养基中培养增加了所有缺失突变体中的脂质含量,其中Δpre9缺失突变体对氮限制最为敏感。然后,由于其较高的脂质含量及其作为磷脂合成调节因子的功能,我们将重点放在了Δsnf2缺失突变体上。脂质类别分析表明,三酰甘油和游离脂肪酸导致了Δsnf2缺失突变体总脂质的增加。添加外源脂肪酸在增加Δsnf2缺失突变体的脂质含量方面不如在野生型中有效。应该注意的是,与内源性游离脂肪酸的情况一样,Δsnf2缺失突变体中外源游离亚油酸的含量比野生型高得多。此外,缺失突变体中外源脂肪酸进入细胞的量增加,表明脂肪酸转运蛋白受SNF2调节。结果表明,在Δsnf2缺失突变体中被激活的进入储存脂质的代谢通量受到外源脂肪酸掺入的抑制。它们为酵母中储存脂质的生物合成提供了新的见解。