Abstract

This work was designed to identify yeast cellular functions specifically affected by the stress factors predominating during the early stages of wine fermentation, and genes required for optimal growth under these conditions. The main experimental method was quantitative fitness analysis by means of competition experiments in continuous culture of whole genome barcoded yeast knockout collections. This methodology allowed the identification of haploinsufficient genes, and homozygous deletions resulting in growth impairment in synthetic must. However, genes identified as haploproficient, or homozygous deletions resulting in fitness advantage, were of little predictive power concerning optimal growth in this medium. The relevance of these functions for enological performance of yeast was assessed in batch cultures with single strains. Previous studies addressing yeast adaptation to winemaking conditions by quantitative fitness analysis were not specifically focused on the proliferative stages. In some instances our results highlight the importance of genes not previously linked to winemaking. In other cases they are complementary to those reported in previous studies concerning, for example, the relevance of some genes involved in vacuolar, peroxisomal, or ribosomal functions. Our results indicate that adaptation to the quickly changing growth conditions during grape must fermentation require the function of different gene sets in different moments of the process. Transport processes and glucose signaling seem to be negatively affected by the stress factors encountered by yeast in synthetic must. Vacuolar activity is important for continued growth during the transition to stationary phase. Finally, reduced biogenesis of peroxisomes also seems to be advantageous. However, in contrast to what was described for later stages, reduced protein synthesis is not advantageous for the early (proliferative) stages of the fermentation process. Finally, we found adenine and lysine to be in short supply for yeast growth in some natural grape musts.

Highlights

  • Winemaking is a complex biotechnological process in which yeast cells, most commonly from the species Saccharomyces cerevisiae, play the main role by metabolizing grape must sugars into ethanol, carbon dioxide and hundreds of other secondary products

  • Yeast deletion mutants and significantly showing growth advantage or disadvantage in synthetic must under Phase I or Phase II fermentation conditions were identified by fitness analysis of the competition experiments as described above

  • Phase I growth conditions were emulated in continuous culture at a dilution rate of 0.23 h-1 using as feed the same synthetic must formulation as used in batch cultures

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Summary

Introduction

Winemaking is a complex biotechnological process in which yeast cells, most commonly from the species Saccharomyces cerevisiae, play the main role by metabolizing grape must sugars into ethanol, carbon dioxide and hundreds of other secondary products. Throughout the fermentation process, and in order to adapt to the quickly changing environmental conditions, yeasts sequentially activate or repress different sets of genes involved in several metabolic pathways. After inoculation into grape must, changes at the transcriptome and proteome levels point to the induction of the glycolytic pathway, activation of growth related biosynthetic processes, and carbon catabolite repression [2,3,4,5]. Rossouw and co-workers [11] correlated metabolite concentrations with the most significant changes in gene expression/regulation all through alcoholic fermentation. They found regulatory changes involving glycolytic metabolites during the initial stages of fermentation. By the end of fermentation, sterol metabolism appears represented, suggesting a role of lipid metabolism in membrane stabilization in the presence of high ethanol concentrations

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