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Strategies for fed-batch cultivation of t-PA producing CHO cells: substitution of glucose and glutamine and rational design of culture medium

机译:分批培养生产t-PA的CHO细胞的策略:葡萄糖和谷氨酰胺的替代及培养基的合理设计

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A strategy for fed-batch cultivation of t-PA producing recombinant CHO cells is presented, based on the substitution of glucose and glutamine for slowly metabolized nutrients and in a rational design of the medium. Media for the batch and fed stages were based on the cell specific amino acid requirements, which allowed a more accurate determination of the initiation of the fed stage and the frequency of nutrient addition from then on. Salt concentration was also reduced in both media to avoid an increase in osmolality. As a consequence of this rational design, most amino acid did not accumulate significantly during the fed stage, as usually occurs when their supply is not based on cell requirements; also, lower amounts of by-products were obtained when osmolality level was kept low, that altogether increased viability, longevity and t-PA production when compared with a reference batch culture. Alternating glucose and galactose during the fed stage, allowed lactate detoxification of the cells through their own metabolism. This allowed an increase in cell growth and cell viability with respect to a fed-batch culture in which only glucose was used in the fed stage
机译:基于葡萄糖和谷氨酰胺替代缓慢代谢的营养素,并在合理设计培养基的基础上,提出了分批培养t-PA产生重组CHO细胞的策略。分批和进料阶段的培养基基于细胞特定的氨基酸要求,从而可以更准确地确定进料阶段的开始以及从那时起添加营养物的频率。两种培养基中的盐浓度也均降低,以避免渗透压升高。由于这种合理的设计,大多数氨基酸在进食阶段没有显着积累,通常是在其供应不基于细胞需求的情况下发生的。同样,当重量摩尔渗透压浓度保持在较低水平时,获得的副产物量也较少,与参考分批培养相比,它们的生存力,寿命和t-PA产量均增加。在进食阶段交替改变葡萄糖和半乳糖,可以通过细胞自身的代谢使乳酸排毒。相对于在补料阶段仅使用葡萄糖的补料分批培养,这可以提高细胞生长和细胞活力。

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