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Production of nuclease in fed-batch culture of recombinant Escherichia coli

机译:重组大肠杆菌补料分批培养中核酸酶的产生

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Strategies for enhancing the production of Vibrio vulnificus nuclease using a recombinant Escherichia coli were explored. Using a batch culture, a maximum nuclease yield of 3500 U/mL was obtained with a complex medium characterized by high concentrations of yeast extract, tryptone and magnesium ion. The formation of acetate during fermentation was considered to be detrimental to the nuclease production. Both dissolved oxygen (DO) control and glucose feeding could suppress acetate formation, thus enhancing nuclease production, where the former was found to be more effective. Using a pH-stat fed-batch culture with the DO level maintained above 15% air saturation and with intermittent addition of nutrients, a nuclease yield of 12000 U/mL was achieved. [References: 16]
机译:探索了使用重组大肠杆菌增强创伤弧菌核酸酶生产的策略。使用分批培养,使用以高浓度酵母提取物,胰蛋白and和镁离子为特征的复杂培养基,可获得最大3500 U / mL的核酸酶产量。发酵期间乙酸盐的形成被认为不利于核酸酶的产生。溶解氧(DO)控制和葡萄糖进料都可以抑制乙酸盐的形成,从而提高核酸酶的产量,而前者被认为更有效。使用pH恒定的分批补料培养法,DO浓度保持在15%的空气饱和度以上,并间歇添加营养素,可实现12000 U / mL的核酸酶收率。 [参考:16]

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