ABSTRACT
Potential oxygen consumption by lees, more precisely by nonviable yeasts, during wine aging was recently described. Additionally, yeast autolysis is described as the main mechanism of degradation of lees during wine aging. Thus, to understand the effect of oxygen consumption by yeast lees during wine aging, an accelerated wine aging methodology was tested. Wine aging in the presence of yeast lees was studied both in the presence and in the absence of oxygen. Different markers of yeast autolysis were followed to find a relationship between oxygen consumption by yeast lees and changes in the final wine composition after aging. No differences for compounds tested were found in the wine and in the lees except among sterol compounds in lees: in the presence of oxygen, the concentration of ergosterol in lees was significantly lower than that in the absence of oxygen. It was hypothesized that ergosterol could be oxidized under the influence of oxygen, but none of the known products of ergosterol oxidation were recovered in the corresponding yeast lees. In addition, the decrease of ergosterol content in yeast lees cannot account for the total amount of oxygen consumed by yeast lees during such wine aging.
Subject(s)
Oxygen Consumption/physiology , Saccharomyces cerevisiae/metabolism , Wine/microbiology , Biodegradation, Environmental , Ergosterol/metabolism , Hydrolysis , Lipid Metabolism , Sterols/metabolism , Time FactorsABSTRACT
During enological fermentations, superfluous oxygen consumption by yeast cells is observed. The superfluous oxygen consumed by the yeast cells is mainly related to the operation of non-respiratory oxygen consumption pathways resulting in an overall decrease in the total sterol fraction in yeast. On the other hand, yeast lees remaining at the end of alcoholic fermentations exhibit specific oxygen utilization rates ranging from 1 to 4 micromol O2 h- 10(-10) cells from the second to the thirteenth month of wine aging. This oxygen consumption capacity of yeast lees was independent of residual cell viability. In this study, we investigated the potential relationship between the oxygen added to commercial yeast strains during enological fermentation and the capacity of the corresponding yeast lees to interact with oxygen. Additions of low (7 mg l(-)) and excess (37 mg l(-1)) amounts of oxygen at the end of the cell growth phase were compared in terms of repercussions on the oxygen consumption activity of the corresponding yeast lees. As expected, the superfluous oxygen consumption by yeast cells during fermentation had a positive influence on the fermentation kinetics and increased cell biomass formation. Oxygen consumption rates and the total capacity of oxygen consumption by the corresponding yeast lees clearly decreased when oxygen was added during fermentation. This marked decrease in yeast lees reactivity towards oxygen was concomitantly related to an increase in ergosterol synthesis and to oxygen-dependent sterol degradation. Such degradation occurred when oxygen was added in excess. Therefore, oxygenation control during fermentation appears to be a potential way to optimize both the fermentation kinetics and control yeast lees reactivity towards oxygen. For practical applications, oxygenation control during alcoholic fermentation may be considered as a general tool for decreasing the highly reductive effect of yeast lees during wine aging.
ABSTRACT
Under anaerobic conditions, yeast growth normally requires oxygen in order to favour the synthesis of sterols and unsaturated fatty acids. However, in such conditions, superfluous oxygen consumption by yeast cells is observed. The superfluous oxygen consumed by the yeast cells appears to be not related to classical respiration, but mainly to the operation of several alternative oxygen consumption pathways. In this study, the potential relationship between this superfluous oxygen consumption and the yeast sterol synthesis pathway was investigated during enological fermentation. Additions of small (7 mg l(-1)) and excess (37 mg l(-1)) amounts of oxygen at the end of cell growth phase were used as a method of comparing oxygen consumption by normal synthetic pathways with that by alternative respiration pathways. The superfluous oxygen consumption by yeast cells during fermentation seemed not to alter and strongly favoured fermentation kinetics and cell biomass formation. However, a marked decrease of the orderliness of the membrane phospholipids is observed, which is not related to the drop of cell viability. After oxygen additions, squalene contents of the cells decreased, while the relative proportions of ergosterol or its precursors in the total sterol fraction did not correlatively increase. It was further found that an oxygen-dependent sterol degradation occurred when oxygen was added in excess amounts with respect to the cellular requirements for sterol synthesis. At present, this modification of the sterol contents of yeast membranes has not been related to any physiological parameters.
