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Optimization of Fermentation Medium for the Production of Atrazine Degrading Strain Acinetobacter sp. DNS32 by Statistical Analysis System

机译:生产阿特拉津降解菌不动杆菌的发酵培养基的优化统计分析系统的DNS32

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摘要

Statistical experimental designs provided by statistical analysis system (SAS) software were applied to optimize the fermentation medium composition for the production of atrazine-degrading Acinetobacter sp. DNS32 in shake-flask cultures. A “Plackett-Burman Design” was employed to evaluate the effects of different components in the medium. The concentrations of corn flour, soybean flour, and K2HPO4 were found to significantly influence Acinetobacter sp. DNS32 production. The steepest ascent method was employed to determine the optimal regions of these three significant factors. Then, these three factors were optimized using central composite design of “response surface methodology.” The optimized fermentation medium composition was composed as follows (g/L): corn flour 39.49, soybean flour 25.64, CaCO3 3, K2HPO4 3.27, MgSO4·7H2O 0.2, and NaCl 0.2. The predicted and verifiable values in the medium with optimized concentration of components in shake flasks experiments were 7.079 × 108 CFU/mL and 7.194 × 108 CFU/mL, respectively. The validated model can precisely predict the growth of atrazine-degraing bacterium, Acinetobacter sp. DNS32.
机译:应用统计分析系统(SAS)软件提供的统计实验设计来优化发酵培养基的组成,以生产降解阿特拉津的不动杆菌。摇瓶文化中的DNS32。采用“ Plackett-Burman设计”来评估培养基中不同成分的影响。发现玉米粉,大豆粉和K2HPO4的浓度显着影响不动杆菌属。 DNS32生产。采用最陡上升法确定这三个重要因素的最佳区域。然后,使用“响应面方法”的中央组合设计对这三个因素进行了优化。优化的发酵培养基组成如下(g / L):玉米粉39.49,大豆粉25.64,CaCO3 3,K2HPO4 3.27,MgSO4·7H2O 0.2和NaCl 0.2。摇瓶实验中最佳成分浓度的培养基中预测值和可验证值分别为7.079×10 8 CFU / mL和7.194×10 8 CFU / mL。经过验证的模型可以准确预测阿特拉津降解细菌不动杆菌的生长。 DNS32。

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