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首页> 外文期刊>Biotechnology & Biotechnological Equipment >Soy Meal Waste Extract as Cultivation Medium for Production of Extracellular ???±-Galactosidase from the Fungus Humicola Lutea 120?¢????5
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Soy Meal Waste Extract as Cultivation Medium for Production of Extracellular ???±-Galactosidase from the Fungus Humicola Lutea 120?¢????5

机译:大豆粕废物提取物作为从真菌腐质霉Lutea 120中产生细胞外β-半乳糖苷酶的培养基5

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Soy meal extract presenting a waste product from soy protein concentrate manufacture was applied as cultivation medium for the production of extracellular ???±-galactosidase in submerged fermentation of the filamentous fungus Humicola lutea 120?¢????5. Maximum enzyme activity (2000 U.l ?¢????1 ) was produced when the soy meal extract containing 5% dry substances (?¢????1% raffinose oligosaccharides) was used at 120th h cultivation and 35???°C. Chromatography on Sephadex G-100 and DEAE-cellulose resulted in a purified ???±-galactosidase fraction with specific enzyme activity of 37 U.mg ?¢????1 . The optimum conditions for the enzyme reaction were pH 4.0 to 4.5 at 50???°C. The partially purified enzyme was stable up to 40???°C at pH 2.0 to 7.5. The crude enzyme preparation readily hydrolyzes raffinose according HPLC analysis, but no activity against disaccharides as sucrose and melibiose was observed. The soy meal waste extract can be recommended as a suitable medium for the industrial cultivation of strains producing ???±-galactosidase for food and fodder purposes.
机译:呈现来自大豆浓缩蛋白生产的废品的豆粕提取物用作培养基,用于丝状真菌腐质霉Humicola lutea 120 5的深层发酵中生产细胞外β-半乳糖苷酶。当在第120小时培养和35°C培养中使用含有5%干燥物质(≥1%棉子糖寡糖)的豆粕提取物时,可产生最大的酶活性(2000 Ul -1)。 C。在Sephadex G-100和DEAE-纤维素上进行色谱分离,得到纯化的β-半乳糖苷酶级分,其比酶活性为37μg·mg-1-1。酶反应的最佳条件是在50℃下pH为4.0至4.5。该部分纯化的酶在pH 2.0至7.5至40℃稳定。根据HPLC分析,粗制酶制剂易于水解棉子糖,但是未观察到针对二糖的蔗糖和蜜三糖的活性。可以推荐将豆粕废物提取物用作工业生产食品和饲料用β-半乳糖苷酶菌株的合适培养基。

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