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Production and characterization of a thermo-pH stable pectinase from Bacillus licheniformis UNP-1: A novel strain isolated from Unapdev hot spring

机译:来自芽孢杆菌UNP-1的热pH稳定果胶酶的生产与表征:unapdev温泉分离的新菌株

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摘要

An efficient thermostable pectinase producer was isolated from the hot water spring of Unapdev and identified as Bacillus licheniformis UNP-1 using culture-dependent techniques by its morphological, microscopic, biochemical, physiological and molecular characteristics. Thermostable pectinase production was optimized in a submerged fermentation system using modified fermentation medium (MFM). The optimized components of MFM performed by changing one parameter at a time were pectinase defined liquid medium containing (g/L) 10 pure Pectin, 2.0 KH2PO4, 6.0 K2HPO4, 2.0 MgSO4 center dot 7H(2)O Optimized culture conditions were used for thermostable pectinase production. Bacillus licheniformis UNP-1 produced 55.2 U/mL of pectinase. Optimum pH and temperature for the production were 9 and 60 degrees C, respectively with 48 hours of incubation. The pectinase enzyme showed maximum activity at pH 11 and at 80 degrees C. Pectinolytic activity was the highest in the presence of Fe3+ metal ion. Optimum catalytic activity was recorded at substrate concentration of polygalacturonic acid of 3.5% after 90 min of incubation. The molecular mass of the dialyzed thermostable pectinase was 35 kDa. Partially purified pectinase enzyme was used for fruit juice extraction and clarification.
机译:从UNAPDEV的热水果酶中分离出一种有效的热稳定果胶酶生产者,并使用其形态学,微观,生物化学,生理学和分子特性,使用培养基依赖于培养基的技术鉴定为芽孢杆菌。使用改性发酵培养基(MFM)在浸没式发酵系统中优化了热稳定果胶酶生产。通过在时间改变一个参数的MFM的优化组分是含有(G / L)10纯果胶,2.0kH2PO4,6.0K2HPO4,2.0mgSO 4中心点7h(2)O优化培养条件的果胶酶定义的液体培养基用于热稳定性果胶酶生产。芽孢杆菌的嗜睡UNP-1产生55.2u / ml果胶酶。为生产的最佳pH和温度分别为9℃和60℃,孵育48小时。果胶酶酶在pH 11和80℃下显示最大活性,在Fe3 +金属离子存在下果胶溶液活性最高。在孵育90分钟后,在3.5%的polygalactuon酸的底物浓度下记录最佳催化活性。透析的热稳定果胶酶的分子量为35kDa。部分纯化的果胶酶用于果汁提取和澄清。

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