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首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Optimization of alkaline protease production by batch culture of Bacillus sp RKY3 through Plackett-Burman and response surface methodological approaches
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Optimization of alkaline protease production by batch culture of Bacillus sp RKY3 through Plackett-Burman and response surface methodological approaches

机译:通过Plackett-Burman分批培养芽孢杆菌RKY3的碱性蛋白酶生产和响应面方法

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The proteolytic enzymes are the most important group of commercially produced enzymes. The production of alkaline protease was optimized using a newly isolated Bacillus sp. RKY3. The fermentation variables were selected in accordance with the Plackett-Burman design and were further optimized via response surface methodological approach. Four significant variables (corn starch, yeast extract, corn steep liquor, and inoculum size) were selected for the optimization studies. The statistical model was constructed via central composite design (CCD) using three screened variables (corn starch, corn steep liquor, and inoculum size). An overall 2.3-fold increase in protease production was achieved in the optimized medium as compared with the unoptimized basal medium. Enzyme activity increased significantly with optimized medium (939 u ml(-1)) when compared with unoptimized medium (417 u ml(-1)). (C) 2007 Elsevier Ltd. All rights reserved.
机译:蛋白水解酶是商业生产的酶中最重要的组。使用新分离的芽孢杆菌属菌株优化了碱性蛋白酶的生产。 RKY3。根据Plackett-Burman设计选择发酵变量,并通过响应面方法学进一步优化发酵变量。选择了四个重要变量(玉米淀粉,酵母提取物,玉米浆和接种量)进行优化研究。通过中央复合设计(CCD)使用三个筛选变量(玉米淀粉,玉米浆和接种量)构建统计模型。与未优化的基础培养基相比,在优化的培养基中蛋白酶产量总体提高了2.3倍。与未优化的培养基(417 u ml(-1))相比,优化的培养基(939 u ml(-1))的酶活性显着增加。 (C)2007 Elsevier Ltd.保留所有权利。

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