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Autophagic Proteome in Two Saccharomyces cerevisiae Strains during Second Fermentation for Sparkling Wine Elaboration

机译:酿酒酵母的第二次发酵过程中两个酿酒酵母菌株的自噬蛋白质组。

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摘要

A correlation between autophagy and autolysis has been proposed in order to accelerate the acquisition of wine organoleptic properties during sparkling wine elaboration. In this context, a proteomic analysis was carried out in two industrial strains (P29, conventional sparkling wine strain and G1, implicated in sherry wine elaboration) with the aim of studying the autophagy-related proteome and comparing the effect of CO overpressure during sparkling wine elaboration. In general, a detrimental effect of pressure and second fermentation development on autophagy-related proteome was observed in both strains, although it was more pronounced in flor yeast strain G1. Proteins mainly involved in autophagy regulation and autophagosome formation in flor yeast G1, and those required for vesicle nucleation and expansion in P29 strain, highlighted in sealed bottle. Proteins Sec2 and Sec18 were detected 3-fold under pressure conditions in P29 and G1 strains, respectively. Moreover, ‘fingerprinting’ obtained from multivariate data analysis established differences in autophagy-related proteome between strains and conditions. Further research is needed to achieve more solid conclusions and design strategies to promote autophagy for an accelerated autolysis, thus reducing cost and time production, as well as acquisition of good organoleptic properties.
机译:自噬和自溶之间的相关性已被提出,以加速起泡酒加工过程中对酒感官特性的获取。在此背景下,对两种工业菌株(P29,传统的起泡酒菌株和G1,与雪利酒的加工有关)进行了蛋白质组学分析,目的是研究自噬相关的蛋白质组,并比较起泡酒过程中CO超压的影响。阐述。通常,在两个菌株中都观察到压力和二次发酵发展对自噬相关蛋白质组的有害影响,尽管在花酵母菌株G1中更为明显。在密封瓶中突出显示了主要在花酵母G1中参与自噬调节和自噬体形成的蛋白质,以及在P29菌株中囊泡成核和扩增所需的蛋白质。在压力条件下,分别在P29和G1菌株中检测到蛋白质Sec2和Sec18的3倍。此外,通过多变量数据分析获得的“指纹图谱”确定了菌株和条件之间自噬相关蛋白质组的差异。需要做进一步的研究以获得更可靠的结论和设计策略,以促进自噬以加速自溶,从而降低成本和时间,并获得良好的感官特性。

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