Altamirano C, Paredes C, Illanes A, Cairó J J, Gòdia F
Escuela de Ingeniería Bioquímica, Facultad de Ingeniería, Universidad Católica de Valparaíso, Av. Brasil 2147, Valparaíso, Chile.
J Biotechnol. 2004 May 27;110(2):171-9. doi: 10.1016/j.jbiotec.2004.02.004.
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.
本文提出了一种用于培养生产t-PA的重组CHO细胞的补料分批培养策略,该策略基于用缓慢代谢的营养物质替代葡萄糖和谷氨酰胺,并对培养基进行合理设计。分批培养阶段和补料阶段的培养基基于细胞对特定氨基酸的需求,这使得能够更准确地确定补料阶段的起始时间以及从那时起营养物质添加的频率。两种培养基中的盐浓度也有所降低,以避免渗透压升高。由于这种合理设计,在补料阶段大多数氨基酸不会像通常在供应不基于细胞需求时那样显著积累;此外,当渗透压水平保持较低时,副产物的产量也较低,与参考分批培养相比,这总体上提高了细胞活力、寿命和t-PA产量。在补料阶段交替使用葡萄糖和半乳糖,可使细胞通过自身代谢对乳酸进行解毒。与在补料阶段仅使用葡萄糖的补料分批培养相比,这使得细胞生长和细胞活力有所增加。