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首页> 外文期刊>Environmental Science and Pollution Research >Production of alpha-1,4-glucosidase from Bacillus licheniformis KIBGE-IB4 by utilizing sweet potato peel
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Production of alpha-1,4-glucosidase from Bacillus licheniformis KIBGE-IB4 by utilizing sweet potato peel

机译:通过利用甘薯剥离,从芽孢杆菌的芽孢杆菌的α-1,4-葡糖苷酶生产

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摘要

In the current study, sweet potato peel (Ipomoea batatas) was observed as the most favorable substrate for the maximum synthesis of alpha-1,4-glucosidase among various agro-industrial residues. Bacillus licheniformis KIBGE-IB4 produced 6533.0 U ml(-1) of alpha-1,4-glucosidase when growth medium was supplemented with 1% dried and crushed sweet potato peel. It was evident from the results that bacterial isolate secreted 6539.0 U ml(-1) of alpha-1,4-glucosidase in the presence of 0.4% peptone and meat extract with 0.1% yeast extract. B. licheniformis KIBGE-IB4 released 6739.0 and 7190.0 U ml(-1) of enzyme at 40 degrees C and pH 7.0, respectively. An improved and cost-effective growth medium design resulted 8590.0 U ml-1 of alpha-1,4-glucosidase with 1.3-fold increase as compared to initial amount from B. licheniformis KIBGE-IB4. This enzyme can be used to fulfill the accelerating demand of food and pharmaceutical industries. Further purification and immobilization of this enzyme can also enhance its utility for various commercial applications.
机译:在目前的研究中,将甘薯果皮剥离(IPOMOEA Batatas)视为最有利的基材,用于最大限度地合成各种农业工业残留物中的α-1,4-葡糖苷酶。芽孢杆菌Licheniformis Kibge-Ib4在加入1%干燥和粉碎的甘薯果皮中时产生6533.0uml(-1)α-1,4-葡糖苷酶。从结果中显而易见的是,在0.4%蛋白胨和0.1%酵母提取物的情况下,细菌分离物分泌6539.0uml(-1)α-1,4-葡糖苷酶。 B. Licheniformis Kibge-IB4分别在40℃和pH 7.0下释放6739.0和7190.0uml(-1)酶。与来自B.Hisheniformis kibge-Ib4的初始量相比,改善和经济高效的生长培养基设计产生了8590.0uml-1的α-1,4-葡糖苷酶,增加1.3倍。该酶可用于满足食品和制药行业的加速需求。进一步纯化和固定该酶也可以增强其用于各种商业应用的效用。

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