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Production of Sweet Table Wine by Termination of Alcohol Fermentation Using an Antimicrobial Substance from Paprika Seed

机译:通过使用辣椒粉种子中的抗微生物物质终止酒精发酵来生产甜食酒

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摘要

Sweet table wine was produced by a combination of fermentation using free or immobilized yeast cells and termination of the fermentation using an antimicrobial substance that was extracted with 50% aqueous ethanol solution from paprika seeds, followed by fractionation with octadecylsilyl gel. The paprika seed antimicrobial substance (PSAS) obtained exhibited strong antimicrobial activity against wine yeast, Saccharomyces cerevisiae W-3 (minimum inhibitory concentration = approximately 16 mg/L). Alcohol fermentation could be terminated immediately after the addition of PSAS to give a concentration of 100mg/L to the fermenting must whenever desired (at any ethanol concentration of fermenting must). The number of free viable yeast cells in the must gradually decreased during storage after the addition of PSAS. Regardless of whether free or immobilized yeast cells were used as biocatalyst, free viable yeast cells of approximately 10 cfu/mL were counted on day 4 after the addition of PSAS, and no viable cells were detected on day 7.
机译:通过使用游离或固定的酵母细胞进行发酵与使用抗微生物物质终止发酵相结合来生产甜食酒,该抗微生物物质用从辣椒粉种子中提取的50%乙醇水溶液萃取,然后用十八烷基硅烷基凝胶进行分馏。获得的辣椒粉种子抗微生物物质(PSAS)对酿酒酵母Saccharomyces cerevisiae W-3表现出较强的抗微生物活性(最低抑菌浓度=约16 mg / L)。加入PSAS后,可以随时终止酒精发酵,使发酵液的浓度达到100mg / L(在任何乙醇浓度下都必须发酵)。添加PSAS后,在储存过程中必须逐渐减少游离酵母细胞的数量。无论使用游离的还是固定的酵母细胞作为生物催化剂,添加PSAS后第4天都计数了大约10 cfu / mL的游离活酵母细胞,而在第7天没有检测到活细胞。

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