Abstract

Aim: The addition of SO2 is a common technique for stopping alcoholic fermentation by Saccharomyces cerevisiae and producing beverages with residual sugar. However, SO2 causes a metabolic shift in active yeast leading to the formation of acetaldehyde and resulting in higher preservative SO2 requirements in the final product. The current work investigated the effects of stopping alcoholic fermentation using two industrial strains of Saccharomyces cerevisiae, by means of cooling and/or addition of SO2, on the kinetics of hexoses and acetaldehyde.Methods and results: Alcoholic fermentation was conducted by inoculating natural Chardonnay grape must with two commonly used strains of Saccharomyces cerevisiae (CY3079 and EC1118). Ten days after inoculation, cooling (to 4 °C) and/or addition of SO2 (50-350 mg/L) were applied to stop fermentations at approximately 70-90 g/L of residual sugar. Incubations were carried out in an anaerobic chamber to prevent the formation of acetalhdeyde resulting from chemical oxidation. Samples were taken regularly and analysed for glucose, fructose and acetalhdyde levels.In this work, addition of SO2 to 150 mg/L or more were effective in inhibiting further and practically relevant degradation of hexoses even in non-cooled control treatments. With concurrent cooling, an addition to 50 mg/L was sufficient. Addition of SO2always led to a slow increase in yeast acetaldehyde formation over time, regardless of cooling or the apparent inhibition of yeast sugar metabolism. Acetaldehyde increases were reduced with larger SO2 additions.Conclusions: When using SO2 to stop alcoholic fermentations, large doses should be used and wines separated from the sedimented biomass soon thereafter. Nevertheless, rapid cooling remains preferable to SO2 addition and can prevent further microbial formation of acetaldehyde.Significance and impact of the study: Results from the current work show that acetaldehyde, and therefore bound SO2formation, can be reduced when alcoholic fermentation is halted to obtain wines with residual sweetness.

Highlights

  • During alcoholic fermentation in grape wine production, it may be desirable to conserve residual sugar in order to balance high acidity, which is more common in cool climates, or achieve sweet wine styles that are appreciated by some consumers (Fischer and Wilke, 2000)

  • After 25 d an average of only 40 % (CY3079) and 26 % (EC1118) of the residual sugar content at d=10 remained in the wines

  • The data from our study showed that an apparent lack of sugar degradation, as quantified within the limits of the analytical technique applied and relevant in practical terms, did not preclude yeast acetaldehyde formation

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Summary

Introduction

During alcoholic fermentation in grape wine production, it may be desirable to conserve residual sugar in order to balance high acidity, which is more common in cool climates, or achieve sweet wine styles that are appreciated by some consumers (Fischer and Wilke, 2000). Residual sugar can be conserved by stopping alcoholic fermentation (AF) before the natural sugar is depleted by yeast metabolism (Boulton et al, 1996). This can be achieved by removing the yeast biomass (by filtration or centrifugation) or by inhibiting its metabolism by adding distillates (in the production of special fortified wines), cooling or adding SO2 (Bird, 2010). By strongly binding acetaldehyde (the terminal electron acceptor of alcoholic fermentation) (Gottschalk, 1986), the biosynthesis of glycerol intensifies as an alternative pathway for the regeneration of reduced dinucleotides (Remize et al, 2000) and, concurrently, yeast acetaldehyde formation increases (Jackowetz et al, 2011)

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