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Application of Response Surface Methodology for Optimizing Arginine Deiminase Production Medium for Enterococcus faecium sp. GR7

机译:响应面法在粪肠球菌精氨酸脱亚氨酶生产培养基优化中的应用。 GR7

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摘要

Arginine metabolism in Enterococcus faecium sp. GR7 was enhanced via arginine deiminase pathway. Process parameters including fermentation media and environmental conditions were optimized using independent experiments and response surface methodology (central composite design). Fermentation media (EAPM) were optimized using independent experiments which resulted in 4-fold increase in arginine deiminase specific activity as compared to basal medium. To further enhance arginine deiminase activity in E. faecium sp. GR7 and biomass production including a five-level central composite design (CCD) was employed to study the interactive effect of three-process variables. Response surface methodology suggested a quadratic model which was further validated experimentally where it showed approximately 15-fold increase in arginine metabolism (in terms of arginine deiminase specific activity) over basal medium. By solving the regression equation and analyzing the response surface cartons, optimal concentrations of the media components (g/L) were determined as arginine 20.0; tryptone 15.0; lactose 10.0; K2HPO4 3.0; NaCl 1.0, MnSO4 0.6 mM; Tween 80 1%; pH 6.0 for achieving specific arginine deiminase activity of 4.6 IU/mG with concomitant biomass production of 12.1 mg/L. The model is significant as the coefficient of determination (R 2) was 0.87 to 0.90 for all responses. Enhanced arginine deiminase yield from E. faecium, a GRAS lactic acid bacterial strain, is desirable to explore in vitro therapeutic potential of the arginine metabolizing E. faecium sp. GR7.
机译:粪肠球菌中的精氨酸代谢。通过精氨酸脱亚氨酶途径增强了GR7。使用独立的实验和响应面方法(中央复合设计)对包括发酵培养基和环境条件在内的工艺参数进行了优化。发酵培养基(EAPM)使用独立实验进行了优化,与基础培养基相比,精氨酸脱亚氨酶的比活性提高了4倍。为了进一步增强粪肠球菌中的精氨酸脱亚氨酶活性。 GR7和包括五级中央复合设计(CCD)的生物量生产用于研究三过程变量的交互作用。响应面分析法提出了一个二次模型,该模型在实验上得到了进一步验证,该模型显示精氨酸代谢量(基于精氨酸脱亚氨酶的比活性)比基础培养基提高了约15倍。通过求解回归方程并分析响应纸箱,确定培养基成分的最佳浓度(g / L)为精氨酸20.0;胰蛋白1 15.0;乳糖10.0; K2HPO4 3.0; NaCl 1.0,MnSO4 0.6 mM;吐温80 1%; pH 6.0,精氨酸脱亚氨酶的特定活性为4.6 IU / mG,同时产生的生物量为12.1 mg / L。该模型具有重要意义,因为所有响应的确定系数(R 2 )为0.87至0.90。为了探索精氨酸代谢屎肠球菌的体外治疗潜力,期望从粪便大肠杆菌(一种GRAS乳酸菌)中提高精氨酸脱亚氨酶的产量。 GR7。

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