Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology (IBB/CGB-UTAD), Universidade de Trás-os-Montes e Alto Douro, Vila Real 5001-801, Portugal.
Appl Microbiol Biotechnol. 2013 Jun;97(11):4991-5000. doi: 10.1007/s00253-013-4719-y. Epub 2013 Jan 30.
Excessive volatile acidity in wines is a major problem and is still prevalent because available solutions are nevertheless unsatisfactory, namely, blending the filter-sterilized acidic wine with other wines of lower volatile acidity or using reverse osmosis. We have previously explored the use of an empirical biological deacidification procedure to lower the acetic acid content of wines. This winemaker's enological practice, which consists in refermentation associated with acetic acid consumption by yeasts, is performed by mixing the acidic wine with freshly crushed grapes, musts, or marc from a finished wine fermentation. We have shown that the commercial strain Saccharomyces cerevisiae S26 is able to decrease the volatile acidity of acidic wines with a volatile acidity higher than 1.44 g L(-1) acetic acid, with no detrimental impact on wine aroma. In this study, we aimed to optimize the immobilization of S26 cells in alginate beads for the bioreduction of volatile acidity of acidic wines. We found that S26 cells immobilized in double-layer alginate-chitosan beads could reduce the volatile acidity of an acidic wine (1.1 g L(-1) acetic acid, 12.5 % (v/v) ethanol, pH 3.12) by 28 and 62 % within 72 and 168 h, respectively, associated with a slight decrease in ethanol concentration (0.7 %). Similar volatile acidity removal efficiencies were obtained in medium with high glucose concentration (20 % w/v), indicating that this process may also be useful in the deacidification of grape musts. We, therefore, show that immobilized S. cerevisiae S26 cells in double-layer beads are an efficient alternative to improve the quality of wines with excessive volatile acidity.
葡萄酒中过高的挥发性酸度是一个主要问题,而且仍然很普遍,因为现有的解决方案并不令人满意,即过滤消毒的酸性葡萄酒与挥发性酸度较低的其他葡萄酒混合,或使用反渗透。我们之前曾探索过使用经验性的生物脱酸程序来降低葡萄酒中的乙酸含量。这种酿酒师的酿造工艺,即通过与新鲜压碎的葡萄、葡萄汁或已完成的葡萄酒发酵的果皮混合,使酵母消耗乙酸来进行再发酵,可用于降低酸性葡萄酒的挥发性酸度。我们已经表明,商业酵母菌株 Saccharomyces cerevisiae S26 能够降低挥发性酸度高于 1.44 g/L 的酸性葡萄酒的挥发性酸度,而对葡萄酒香气没有不利影响。在这项研究中,我们旨在优化 S26 细胞在海藻酸钠珠中的固定化,以用于生物还原酸性葡萄酒的挥发性酸度。我们发现,双层海藻酸钠-壳聚糖珠固定化的 S26 细胞可分别在 72 和 168 h 内将酸性葡萄酒(1.1 g/L 乙酸、12.5%(v/v)乙醇、pH 3.12)的挥发性酸度降低 28%和 62%,同时乙醇浓度略有下降(0.7%)。在高葡萄糖浓度(20%w/v)的培养基中也获得了相似的挥发性酸度去除效率,表明该过程也可能有助于葡萄汁的脱酸。因此,我们表明双层珠固定化的 S. cerevisiae S26 细胞是改善高挥发性酸度葡萄酒质量的有效替代方法。