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Fed-batch culture of recombinant Saccharomyces cerevisiae for glucose 6-phosphate dehydrogenase production

机译:发酵酿酒酵母的分批培养用于6-磷酸葡萄糖脱氢酶的生产

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摘要

We examined glucose 6-phosphate dehydrogenase (G6PD)production by fed-batch cultivation,using a recombinant strain of Saccharomyces cerevisiae W303-181 overexpressing this enzyme.The cultivations were carried out in a 3 L fermenter at pH 5.7,30 deg C,2.0 vvm aeration,200 rpm agitation and an inoculum concentration of 1.0 g/L.The volume of the culture medium in the fed-batch process varied from 1.333 to 2.0.L,due to the addition of 15.0 g/L glucose solution during 5 h.Different feeding rates were studied (exponentially increasing and decreasing feeding rates),and the feeding profile was determined by values of the parameter K (time constant),namely:0.2,0.5 and 0.8 h~(-1).The best enzyme production (847 U/L)was obtained with an exponentially increasing feeding rate and K=0.2 h~(-1).The results attained also showed that this process is promising for G6PD production.
机译:我们使用过量表达这种酶的酿酒酵母W303-181重组菌株分批分批培养检测了葡萄糖6-磷酸脱氢酶(G6PD)的生产。在pH 5.7,30℃,2.0的3 L发酵罐中进行培养vvm曝气,200 rpm搅拌和1.0 g / L的接种物浓度。由于在5小时内添加了15.0 g / L葡萄糖溶液,分批补料过程中培养基的体积从1.333到2.0.L不等研究了不同的进料速度(以指数方式增加和减少进料速度),并通过参数K(时间常数)的值(即0.2、0.5和0.8 h〜(-1))确定了进料曲线。进料速度以指数方式增加(K = 0.2 h〜(-1)),获得了(847 U / L)。

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