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Optimization of Cyclodextrin Glucanotransferase Production From Bacillus clausii E16 in Submerged Fermentation Using Response Surface Methodology

机译:使用响应表面方法从浸没式发酵中优化来自枯草芽孢杆菌E16的环糊精葡聚糖转移酶生产

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Cyclodextrin glucanotransferase production from Bacillus clausii E16, a new bacteria isolated from Brazilian soil samples was optimized in shake-flask cultures. A 2~4 full-factorial central composite design was performed to optimize the culture conditions, using a response surface methodology. The combined effect among the soluble starch concentration, the peptone concentration, the yeast extract concentration, and the initial pH value of the culture medium was investigated. The optimum concentrations of the components, determined by a 2~4 full-factorial central composite design, were 13.4 g/L soluble starch, 4.9 g/L peptone, 5.9 g/L yeast extract, and initial pH 10.1. Under these optimized conditions, the maximum cyclodextrin glucanotransferase activity was 5.9 U/mL after a 48-h fermentation. This yield was 68% higher than that obtained when the microorganism was cultivated in basal culture medium.
机译:来自巴西土壤样品中分离的新细菌的Bacillus Clausii E16的环糊精葡聚糖转移酶产生在摇瓶培养上进行了优化。 使用响应面方法进行2〜4个全因子中央复合设计以优化培养条件。 研究了培养基的可溶性淀粉浓度,蛋白胨浓度,酵母提取物浓度和初始pH值的综合作用。 由2〜4个全因子中央复合设计确定的组分的最佳浓度为13.4g / l可溶性淀粉,4.9g / l蛋白胨,5.9g / L酵母提取物和初始pH 10.1。 在这些优化条件下,在48小时发酵后,最大环糊精葡聚糖转移酶活性为5.9u / ml。 当在基础培养基中培养微生物时,该产率高出68%。

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