Consiglio per la Ricerca in Agricoltura e l'Analisi dell'Economia agraria, Centro di Ricerca Viticoltura ed Enologia, Via Pietro Micca 35, 14100 Asti, Italy; Università di Torino - Dipartimento di Scienze della Vita e Biologia dei Sistemi, Via Accademia Albertina.13, 10123 Torino, Italy.
Università di Torino - Dipartimento di Scienze della Vita e Biologia dei Sistemi, Via Accademia Albertina.13, 10123 Torino, Italy.
Food Res Int. 2018 Mar;105:1011-1018. doi: 10.1016/j.foodres.2017.12.004. Epub 2017 Dec 6.
A strain of Saccharomyces (S) cerevisiae (ISE19), which displayed an initial good adaptation to a high sugar medium with increased acetate and glycerol production but weak overall growth/fermentation performances, was selected during the alcoholic fermentation of Cortese grape must. To obtain insights into the metabolic changes that occur in the must during growth in particular conditions (high ethanol, high residual sugars and low nitrogen availability) leading to a sluggish fermentation or even fermentation arrest, comparative in-gel proteomic analyses were performed on cells grown in media containing 200g/L and 260g/L of glucose, respectively, while the YAN (Yeast Assimilable Nitrogen) concentration was maintained as it was. Two post-translationally different arginine synthases (pI 5.6 and 5.8) were found in higher abundances in the high glucose-grown cells, together with an increased abundance of a glycosyltransferase involved in cell-wall mannans synthesis, and of two regulatory proteins (K7_Bmh1p and K7_Bmh2p) that control membrane transport. In parallel, a proteinase K-like proteolytic enzyme and three other protein fragments (Indolepyruvate decarboxylase 1, Fba1p and Eno1p) were present in lower abundances in the high glucose condition, where oxidative stress and cell cycle involved enzymes were also found to be less abundant. The overall results suggest that in stationary phase stress conditions, leading to stuck fermentation, S. cerevisiae ISE19 decreases cell replication, oxidative stress responses and proteolytic activity, while induces other metabolic modifications that are mainly based on cell-wall renewal, regulation of the solute transport across the cell membrane and de novo arginine synthesis.
一株酿酒酵母(Saccharomyces cerevisiae)(ISE19)在科蒂埃葡萄汁的酒精发酵过程中被选中,该酵母菌株在初始阶段能够很好地适应高糖培养基,同时增加了乙酸和甘油的产量,但整体生长/发酵性能较弱。为了深入了解在特定条件(高乙醇、高残余糖和低氮供应)下生长过程中葡萄汁中发生的代谢变化,导致发酵缓慢甚至发酵停止,对细胞在含有 200g/L 和 260g/L 葡萄糖的培养基中生长时进行了比较凝胶内蛋白质组学分析,而酵母可同化氮(YAN)浓度保持不变。在高葡萄糖生长的细胞中发现了两种翻译后具有不同等电点的精氨酸合成酶(pI 5.6 和 5.8),同时还发现了一种参与细胞壁甘露聚糖合成的糖基转移酶的丰度增加,以及两种调节蛋白(K7_Bmh1p 和 K7_Bmh2p),它们控制膜转运。同时,在高葡萄糖条件下,一种蛋白酶 K 样蛋白水解酶和另外三个蛋白质片段(吲哚丙酮酸脱羧酶 1、Fba1p 和 Eno1p)的丰度降低,其中还发现氧化应激和细胞周期相关酶的丰度也降低。总体结果表明,在导致发酵停滞的静止期应激条件下,酿酒酵母 ISE19 减少细胞复制、氧化应激反应和蛋白水解活性,同时诱导其他代谢修饰,主要基于细胞壁更新、调节溶质跨细胞膜运输和从头精氨酸合成。