Kaur Baljinder, Kaur Rajinder
Department of Biotechnology, Punjabi University, Patiala 147002, Punjab, India.
ScientificWorldJournal. 2013 Dec 17;2013:892587. doi: 10.1155/2013/892587. eCollection 2013.
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.
屎肠球菌GR7菌株中的精氨酸代谢通过精氨酸脱亚胺酶途径得到增强。利用独立实验和响应面法(中心复合设计)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。通过独立实验对发酵培养基(EAPM)进行了优化,与基础培养基相比,精氨酸脱亚胺酶比活性提高了4倍。为了进一步提高屎肠球菌GR7菌株中的精氨酸脱亚胺酶活性和生物量产量,采用了五级中心复合设计(CCD)来研究三个工艺变量的交互作用。响应面法提出了一个二次模型,并通过实验进一步验证,结果表明与基础培养基相比,精氨酸代谢(以精氨酸脱亚胺酶比活性计)提高了约15倍。通过求解回归方程并分析响应面图,确定培养基成分的最佳浓度(g/L)为:精氨酸20.0;胰蛋白胨15.0;乳糖10.0;K2HPO4 3.0;NaCl 1.0;MnSO4 0.6 mM;吐温80 1%;pH 6.0,以实现精氨酸脱亚胺酶比活性为4.6 IU/mG,同时生物量产量为12.1 mg/L。该模型具有显著性,因为所有响应的决定系数(R(2))为0.87至0.90。增强来自GRAS乳酸菌屎肠球菌的精氨酸脱亚胺酶产量,有助于探索精氨酸代谢的屎肠球菌GR7菌株的体外治疗潜力。