创新技术生产的红甜酒中的酚类抗氧化剂

I. Kekelidze , N. Ebelashvili , M. Japaridze , B. Chankvetadze , L. Chankvetadze
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引用次数: 10

摘要

红葡萄酒中的酚类化合物、儿茶素、黄酮醇、酚碳酸、花青素、白藜芦醇具有高抗氧化活性,可显著降低许多疾病的风险。如今,世界市场对红葡萄酒的需求日益增长,这是由于其抗氧化作用。然而,根据抗氧化活性,可以区分出酚类化合物含量高的红葡萄酒。它们在葡萄酒中的浓度取决于葡萄种植地点、葡萄品种、发酵浸渍技术。我们开发了创新的红甜酒技术,目的是富集抗氧化酚类化合物。本研究的目的:对以萨佩拉维葡萄品种为原料制备的红甜酒样品进行控制和检验。对照样品按现有工艺制备;试验-分别使用浸渍技术和组合浸渍技术,即:发酵,浆干发酵,发酵浆强化至16%(体积),并保持一周。采用高效液相色谱法测定酚类物质的含量。经观察,酚类抗氧化剂的浓度在混合使用浸渍技术时增加最多。浸渍技术是:对剩余的纸浆进行干燥发酵。与对照相比,酚类物质含量增加了(−)-表儿茶素、槲皮素- 3 -葡萄糖苷和咖啡酸- 5倍;鞣花酸- 4倍;t-羧酸- 2倍;丁香酸-减少65%;(+) -儿茶素-减少40%。
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Phenolic antioxidants in red dessert wine produced with innovative technology

Phenolic compounds of red wines, catechins, flavonols, phenolcarbonic acids, anthocyanins, resveratrol are characterized by high antioxidanat activity and sharply reduce the risk of numerous diseases. Nowadays an increasing demand on red wines in the world market is conditioned by their antioxidant effect. However, according to antioxidanat activity those red wines are distinguished which are characterized with high content of phenolic compounds. Their concentration in wine depends on the vine growing place, grape cultivar, techniques of fermentative maceration. We have developed innovative technology for red dessert wine, with the aim of enrichment with antioxidant phenolic compounds. Object for the study: Control and test red dessert wine samples prepared from Saperavi grape cultivar. Control sample were prepared according to the existing technology; test – using maceration techniques in separately and combination, that are: saignée, dry fermentation of the pulp, fortification of the fermented pulp up to 16% (vol.) and staying for a week. By means of the HPLC analysis we determined the amount of phenolics. It has been observed that the concentration of phenolic antioxidants is most of all increased by in the test sample when combination use of maceration techniques: saignée and dry fermentation of the remaining pulp. In comparison with the control increases content phenolics: (−)–epicatechin, quercetin–3–glucoside and caffeic acid – 5–times; ellagic acid – 4–times; t-caftaric acid – 2– times; syringic acid – by 65%; (+)–catechin – by 40%.

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