Laboratory of Microbial Technology, Graduate School of Science and Technology, Kyoto Institute of Technologygrid.419025.b, Kyoto, Japan.
Laboratory of Food Manufacturing and Microbiology, Graduate School of Life and Environmental Sciences, University of Yamanashi, Kofu, Yamanashi, Japan.
Microbiol Spectr. 2022 Oct 26;10(5):e0090122. doi: 10.1128/spectrum.00901-22. Epub 2022 Aug 30.
Under laboratory conditions, acute 10% (vol/vol) ethanol stress causes protein denaturation and accumulation of insoluble proteins in yeast cells. However, yeast cells can acquire resistance to severe ethanol stress by pretreatment with mild ethanol stress (6% vol/vol) and mitigate insoluble protein accumulation under subsequent exposure to 10% (vol/vol) ethanol. On the other hand, protein quality control (PQC) of yeast cells during winemaking remains poorly understood. Ethanol concentrations in the grape must increase gradually, rather than acutely, to more than 10% (vol/vol) during the winemaking process. Gradual increases in ethanol evoke two possibilities for yeast PQC under high ethanol concentrations in the must: suppression of insoluble protein accumulation through the acquisition of resistance or the accumulation of denatured insoluble proteins. We examined these two possibilities by conducting alcoholic fermentation tests at 15°C that mimic white winemaking using synthetic grape must (SGM). The results obtained revealed the negligible accumulation of insoluble proteins in wine yeast cells throughout the fermentation process. Furthermore, wine yeast cells in fermenting SGM did not accumulate insoluble proteins when transferred to synthetic defined (SD) medium containing 10% (vol/vol) ethanol. Conversely, yeast cells cultured in SD medium accumulated insoluble proteins when transferred to fermented SGM containing 9.8% (vol/vol) ethanol. Thus, wine yeast cells acquire resistance to the cellular impact of severe ethanol stress during fermentation and mitigate the accumulation of insoluble proteins. This study provides novel insights into the PQC and robustness of wine yeast during winemaking. Winemaking is a dynamic and complex process in which ethanol concentrations gradually increase to reach >10% (vol/vol) through alcoholic fermentation. However, there is little information on protein damage in wine yeast during winemaking. We investigated the insoluble protein levels of wine yeast under laboratory conditions in SD medium and during fermentation in SGM. Under laboratory conditions, wine yeast cells, as well as laboratory strain cells, accumulated insoluble proteins under acute 10% (vol/vol) ethanol stress, and this accumulation was suppressed by pretreatment with 6% (vol/vol) ethanol. During the fermentation process, insoluble protein levels were maintained at low levels in wine yeast even when the SGM ethanol concentration exceeded 10% (vol/vol). These results indicate that the progression of wine yeast through fermentation in SGM results in stress tolerance, similar to the pretreatment of cells with mild ethanol stress. These findings further the understanding of yeast cell physiology during winemaking.
在实验室条件下,急性 10%(体积/体积)乙醇应激会导致酵母细胞中的蛋白质变性和不溶性蛋白质的积累。然而,酵母细胞可以通过用温和的乙醇应激(6%体积/体积)预处理来获得对严重乙醇应激的抗性,并减轻随后暴露于 10%(体积/体积)乙醇时不溶性蛋白质的积累。另一方面,在酿酒过程中酵母细胞的蛋白质质量控制(PQC)仍然知之甚少。在酿酒过程中,葡萄汁中的乙醇浓度逐渐升高,而不是急性升高到 10%(体积/体积)以上。乙醇浓度的逐渐升高引发了酵母 PQC 在高乙醇浓度下的两种可能性:通过获得抗性抑制不溶性蛋白质的积累或积累变性的不溶性蛋白质。我们通过在 15°C 下进行模拟白葡萄酒酿造的酒精发酵试验来研究这两种可能性,使用合成葡萄汁(SGM)。结果表明,在整个发酵过程中,葡萄酒酵母细胞中不溶性蛋白质的积累可忽略不计。此外,当将酵母细胞从含有 10%(体积/体积)乙醇的合成定义(SD)培养基转移到含有 10%(体积/体积)乙醇的发酵 SGM 时,葡萄酒酵母细胞中不会积累不溶性蛋白质。相反,当将酵母细胞从含有 9.8%(体积/体积)乙醇的发酵 SGM 转移到含有 9.8%(体积/体积)乙醇的发酵 SGM 时,酵母细胞会在 SD 培养基中积累不溶性蛋白质。因此,葡萄酒酵母细胞在发酵过程中获得了对严重乙醇应激的细胞影响的抗性,并减轻了不溶性蛋白质的积累。这项研究为酿酒过程中葡萄酒酵母的 PQC 和稳健性提供了新的见解。酿酒是一个动态而复杂的过程,其中乙醇浓度通过酒精发酵逐渐升高至>10%(体积/体积)。然而,关于酿酒过程中葡萄酒酵母中的蛋白质损伤知之甚少。我们在 SD 培养基中研究了实验室条件下葡萄酒酵母的不溶性蛋白质水平和 SGM 中的发酵。在实验室条件下,葡萄酒酵母细胞和实验室菌株细胞在急性 10%(体积/体积)乙醇应激下积累不溶性蛋白质,而用 6%(体积/体积)乙醇预处理可抑制这种积累。在发酵过程中,即使 SGM 中的乙醇浓度超过 10%(体积/体积),葡萄酒酵母中的不溶性蛋白质水平仍保持在低水平。这些结果表明,葡萄酒酵母通过 SGM 发酵的进展导致了应激耐受性,类似于用温和的乙醇应激预处理细胞。这些发现进一步加深了对酿酒过程中酵母细胞生理学的理解。