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首页> 外文期刊>Biosciences Biotechnology Research Asia >Medium Formulation and its Optimization to Enhance Protease Production by Streptomyces sp. Isolated from Mangroves
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Medium Formulation and its Optimization to Enhance Protease Production by Streptomyces sp. Isolated from Mangroves

机译:培养基配方及其优化,以增强链霉菌SP增强蛋白酶生产。 与红树植物隔绝

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Streptomyces sp. LCJ12A was isolated from the soil and sediments of Pichavaram Mangrove Forest, Tamil Nadu, India. Production of protease from the Streptomyces sp. LCJ12A was carried out by using submerged fermentation. To enhance the protease production, the fermentation medium was formulated and optimized. Different carbon, nitrogen and inducer sources were used for the optimization. In that fructose, sodium nitrate and red gram husk showed greater quantity of protease production and their different concentrations were optimized in Protease production broth (PPB). Response surface methodology (RSM) was employed fof the medium optimization at a low cost for the production of industrially important enzyme. The optimized values showed that fructose at 2.0 g/L enhances the yield of protease up to 120.08±2.2 U/mL, sodium nitrate at 2.0 g/L maximize the protease production up to 180.35±1.9 U/mL and red gram husk at 2.0 g/L yields 194.16±2.2 U/mL which was 1.6 times higher when compared to the unoptimized medium. Statistical optimization by using RSM predicted that 327.16 U/mL of protease enzyme can be produced. Through experimentation based on RSM, tbe protease yield reached up to 323.4 U/mL. When compared to unoptimized medium, the statistically optimized medium produced 3 times higher yield. As a result of the optimization studies, an increase in protease activity was reached compared to the unoptimized conditions and thus offers a new approach for industrial enzyme production.
机译:streptomyces sp。 LCJ12A是从印度泰米尔纳德邦的Pichavaram美洲红树森林的土壤和沉积物中分离出来的。从Streptomyces SP生产蛋白酶。通过使用浸没式发酵进行LCJ12A。为了增强蛋白酶生产,配制和优化发酵培养基。使用不同的碳,氮和诱导物来源进行优化。在这种果糖,硝酸钠和红革克壳中显示出更多的蛋白酶生产,并且它们的不同浓度在蛋白酶生产肉汤(PPB)中进行了优化。应对表面方法(RSM)以低成本用于生产工业上重要的酶的低优化FOF。优化值表明,2.0g / L的果糖增强了蛋白酶的产率至120.08±2.2u / ml,硝酸钠在2.0g / l最大化蛋白酶生产高达180.35±1.9 U / ml和红色革兰克的蛋白酶产生。与未优化的培养基相比,G / L产量194.16±2.2 U / mL的1.6倍。通过使用RSM的统计优化预测,可以生产327.16 U / mL蛋白酶酶。通过基于RSM的实验,TBE蛋白酶产率达到323.4U / mL。与未优化的培养基相比,统计上优化的培养基产量高出3倍。由于优化研究,与未优化的条件相比,达到蛋白酶活性的增加,并为工业酶生产提供了一种新方法。

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