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Design and optimization of fermentation medium for enhanced bacteriocin production by probiotic bacterium enterococcus faecium MC13

机译:益生菌肠球菌MC13增强细菌素生产的发酵培养基的设计和优化

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摘要

Statistics-based experimental designs were used to develop a cost-effective medium for enhanced production of viable cells and bacteriocin by probiotic Enterococcus faecium MC13. Carbon, nitrogen, and mineral sources were first screened by one-variable-at-a-time (OVAT) methods. In order to increase yield production, the selected variables were further statistically optimized using response-surface methodology (RSM) with central composite design (CCD). The maximum and minimum levels of the selected variables were determined and a set of 34 experimental runs was performed. The optimum concentrations of the tested variables for production of viable cells (12.24 log CFU mL~(-1)) and bacteriocin activity (25,600AU mL~(-1)) were tryptone (10.0g/L), peptone (6.0g/L), maltose (3.0g/L), glucose (9.0g/L), NaCl (15.0g/L), sodium citrate (2.5g/L), sodium acetate (1.0g/L), and dipotassium PO4 (0.1g/L). Threefold increased yield of bacteriocin was achieved in optimized medium compared to the unoptimized counterpart, and this was two times less cost than commercial MRS medium.
机译:基于统计的实验设计用于开发一种成本有效的培养基,以通过益生菌粪肠球菌MC13增强活细胞和细菌素的生产。首先通过一次可变(OVAT)方法筛选碳,氮和矿物质来源。为了提高产量,使用响应面方法(RSM)和中央复合设计(CCD)对所选变量进行了进一步的统计优化。确定所选变量的最大和最小水平,并进行了34组实验运行。产生活细胞的最佳测试变量浓度(12.24 log CFU mL〜(-1))和细菌素活性(25,600AU mL〜(-1))分别为胰蛋白((10.0g / L),蛋白ept(6.0g / L)。 L),麦芽糖(3.0g / L),葡萄糖(9.0g / L),NaCl(15.0g / L),柠檬酸钠(2.5g / L),乙酸钠(1.0g / L)和二钾PO4(0.1 g / L)。与未优化的培养基相比,在优化的培养基中细菌素的产量增加了三倍,这比商业MRS培养基的成本低两倍。

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