Kitagaki Hiroshi, Araki Yoshio, Funato Kouichi, Shimoi Hitoshi
National Research Institute of Brewing, 3-7-1 Kagamiyama, Higashi-hiroshima City, Hiroshima 739-0046, Japan.
FEBS Lett. 2007 Jun 26;581(16):2935-42. doi: 10.1016/j.febslet.2007.05.048. Epub 2007 May 29.
Cell death in yeast (Saccharomyces cerevisiae) involves several apoptotic processes. Here, we report the first evidence of the following processes, which are also characteristic of apoptosis, in ethanol-induced cell death in yeast: chromatin condensation and fragmentation, DNA cleavage, and a requirement for de novo protein synthesis. Mitochondrial fission protein, Fis1, appears to mediate ethanol-induced apoptosis and ethanol-induced mitochondrial fragmentation. However, mitochondrial fragmentation in response to elevated ethanol levels was not correlated with cell death. Further, in the presence of ethanol, generation of reactive oxygen species was elevated in mutant fis1Delta cells. Our characterization of ethanol-induced cell death in yeast as being Fis1-mediated apoptosis is likely to pave the way to overcoming limitations in large-scale fermentation processes, such as those employed in the production of alcoholic beverages and ethanol-based biofuels.
酵母(酿酒酵母)中的细胞死亡涉及多个凋亡过程。在此,我们报告了在酵母乙醇诱导的细胞死亡中首次出现以下也是凋亡特征的过程的证据:染色质浓缩和碎片化、DNA 裂解以及对从头蛋白质合成的需求。线粒体分裂蛋白 Fis1 似乎介导乙醇诱导的凋亡和乙醇诱导的线粒体碎片化。然而,对升高的乙醇水平作出反应的线粒体碎片化与细胞死亡并无关联。此外,在有乙醇存在的情况下,突变体 fis1Delta 细胞中活性氧的生成增加。我们将酵母中乙醇诱导的细胞死亡表征为 Fis1 介导的凋亡,这可能为克服大规模发酵过程中的限制铺平道路,例如用于生产酒精饮料和乙醇基生物燃料的那些过程。