Olmos-Orizaba Berenice Eridani, Arroyo-Peñaloza José Santos, Martínez-Alcántar Lorena, Montoya-Pérez Rocío, Flores-García Alberto, Rodríguez-Orozco Alain Raimundo, Calderón-Cortés Elizabeth, Saavedra-Molina Alfredo, Campos-García Jesús, Cortés-Rojo Christian
Instituto de Investigaciones Químico-Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Morelia 58030, Mexico.
Facultad de Ciencias Médicas y Biológicas "Dr. Ignacio Chávez", Universidad Michoacana de San Nicolás de Hidalgo, Morelia 58020, Mexico.
Life (Basel). 2022 Jul 14;12(7):1052. doi: 10.3390/life12071052.
Polyunsaturated fatty acids (PUFA) hypersensitize yeast to oxidative stress. Ethanol accumulation during fermentation is another factor that induces oxidative stress via mitochondrial dysfunction and ROS overproduction. Since this microorganism has raised growing interest as a PUFA factory, we have studied if the combination of PUFA plus ethanol enhances yeast death. Respiration, ROS generation, lipid peroxidation, mitochondrial cardiolipin content, and cell death were assessed in yeast grown in the presence of 10% ethanol (ETOH) or linolenic acid (C18:3), or ethanol plus C18:3 (ETOH+C18:3). Lipid peroxidation and cardiolipin loss were several-fold higher in cells with ETOH+C18:3 than with C18:3. On the contrary, ETOH tended to increase cardiolipin content without inducing changes in lipid peroxidation. This was consistent with a remarkable diminution of cell growth and an exacerbated propidium iodide staining in cells with only ETOH+C18:3. The respiration rate decreased with all the treatments to a similar degree, and this was paralleled with similar increments in ROS between all the treatments. These results indicate that PUFA plus ethanol hypersensitize yeast to necrotic cell death by exacerbating membrane damage and mitochondrial cardiolipin loss, independent of mitochondrial dysfunction and ROS generation. The implications of these observations for some biotechnological applications in yeast and its physiology are discussed.
多不饱和脂肪酸(PUFA)会使酵母对氧化应激超敏。发酵过程中乙醇的积累是另一个通过线粒体功能障碍和活性氧(ROS)过量产生诱导氧化应激的因素。由于这种微生物作为PUFA生产工厂越来越受到关注,我们研究了PUFA与乙醇的组合是否会加剧酵母死亡。对在10%乙醇(ETOH)、亚麻酸(C18:3)或乙醇加C18:3(ETOH + C18:3)存在下生长的酵母的呼吸作用、ROS生成、脂质过氧化、线粒体心磷脂含量和细胞死亡进行了评估。与C18:3相比,ETOH + C18:3处理的细胞中脂质过氧化和心磷脂损失高出数倍。相反,ETOH倾向于增加心磷脂含量,而不引起脂质过氧化的变化。这与仅用ETOH + C18:3处理的细胞中细胞生长显著减少和碘化丙啶染色加剧一致。所有处理均使呼吸速率以相似程度下降,并且所有处理之间ROS的增加也相似。这些结果表明,PUFA与乙醇通过加剧膜损伤和线粒体心磷脂损失,使酵母对坏死性细胞死亡超敏,这与线粒体功能障碍和ROS生成无关。讨论了这些观察结果对酵母某些生物技术应用及其生理学的意义。