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首页> 外文期刊>International Journal of Tropical Agriculture >Application of Tannase in Wine Clarification Produced Under Submerged Fermentation Using Aspergillus ruber
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Application of Tannase in Wine Clarification Produced Under Submerged Fermentation Using Aspergillus ruber

机译:单宁酶在红曲霉深层发酵生产葡萄酒澄清中的应用。

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摘要

Tannase producing fungal strains were isolated from different locations including garbages, forests and orchards etc. The strain giving higher enzyme yield was identified to be Aspergillus ruber. Enzyme production was studied under submerged fermentation using tannin rich substrates ber leaves (Zyzyphus mauriiiana) and amla leaves (Phyllanthus emblica). Tannase production was optimized under submerged cultivation conditions. Aspergillus ruber produced maximum enzyme after 72 h of incubation at 30°Chaving pH 5.5, with mannitol as carbon source and sodium nitrate as nitrogen source. End product (Gallic acid) in the growth media completely inhibited the enzyme production at 0.3% concentration. Supplementation of tannic acid (0.6%) medium with Ber leaves and Amla leaves at a concentration of 0.6% (w/v) resulted in higher tannase production compared to tannic acid (2%) medium. Under optimized conditions here tlie enzyme production by Aspergillus ruber was 18 Unil' Tannase produced was used in clarification ofjamun wine and grape wine (red wine). For red wine (grape) andjamun wine 20 Uml~(-1) tannase was found enough to degrade a significant amount of tannins.
机译:从垃圾,森林和果园等不同地点分离出产生鞣酸酶的真菌菌株。酶产率较高的菌株被鉴定为曲霉。使用富含单宁的底物ber叶片(Zyzyphus mauriiiana)和amla叶片(Phyllanthus emblica)在水下发酵中研究了酶的产生。在淹没条件下优化鞣酸酶的生产。曲霉曲霉在30°C孵育pH 72的条件下孵育72小时后产生最大的酶,甘露醇为碳源,硝酸钠为氮源。生长培养基中的终产物(没食子酸)以0.3%的浓度完全抑制了酶的产生。与单宁酸(2%)培养基相比,以0.6%(w / v)的Ber叶和Amla叶补充单宁酸(0.6%)培养基导致鞣酸酶产量更高。在优化的条件下,曲霉曲霉产生的酶为18 Unil' Tannase,用于澄清果酱和葡萄酒(红葡萄酒)。对于红酒(葡萄)和茉莉酒,发现20 Uml〜(-1)鞣酸足以降解大量单宁。

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