Liu Xingmao, Liu Hong, Ye Lingling, Li Shichong, Wu Benchuan, Wang Qiwei, Chen Zhaolie
Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China.
Sheng Wu Gong Cheng Xue Bao. 2011 Feb;27(2):240-6.
Taking a suspension adapted recombinant CHO cell line, 11G-S expressing human Pro-urokinase (Pro-UK) as the object of study, the impacts of different feeding nutrients, the start time of feeding and cell inoculation density on the growth and Pro-UK production of 11G-S cells in serum-free fed-batch culture were evaluated in 100 mL shacking flasks. The results indicated that amino acids, serum-free supplements and inorganic salts played important role in cell growth, cell viability and protein expression. And the effects of cells fed-batch culture was much better with the initial cell inoculation density at 3 x 10(5)-4 x 10(5) cells/mL and the start time of feeding set at 72 h, a maximum viable cells density of 7.8 x 10(6) cells/mL with a peak Pro-UK activity at 8570 IU/mL was achieved during 12 d fed-batch culture. Further, the mu of the 11G-S cells at the middle phase of the fed-batch culture, and both the q(glu) and q(gln) of the 11G-S cells at the middle and later phases of the fed-batch culture was higher than that of the 11G-S cells at the same phase of the batch culture, respectively.
以表达人尿激酶原(Pro-UK)的悬浮适应重组CHO细胞系11G-S为研究对象,在100 mL摇瓶中评估了无血清补料分批培养中不同补料营养成分、补料起始时间和细胞接种密度对11G-S细胞生长及Pro-UK表达的影响。结果表明,氨基酸、无血清添加剂和无机盐对细胞生长、细胞活力及蛋白表达起重要作用。当初始细胞接种密度为3×10⁵ - 4×10⁵个细胞/mL且补料起始时间设定为72 h时,细胞补料分批培养效果更佳,在12 d的补料分批培养过程中,最大活细胞密度达到7.8×10⁶个细胞/mL,Pro-UK活性峰值为8570 IU/mL。此外,补料分批培养中期11G-S细胞的比生长速率,以及补料分批培养中后期11G-S细胞的葡萄糖比消耗速率和谷氨酰胺比消耗速率分别高于分批培养相同阶段11G-S细胞的相应指标。