Xie L, Nyberg G, Gu X, Li H, Möllborn F, Wang D I
Biotechnology Process Engineering Center, Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139; telephone: (617)-253-2126; fax: (617)-253-2400.
Biotechnol Bioeng. 1997 Dec 5;56(5):577-82. doi: 10.1002/(SICI)1097-0290(19971205)56:5<577::AID-BIT11>3.0.CO;2-9.
The application of a stoichiometric medium design approach was studied in fed-batch cultivation of Chinese hamster ovary (CHO) cells. A serum-free medium containing a very low protein concentration (2 mg/L insulin) was developed. A supplemental medium was formulated according to the stoichiometric equation governing cell growth using cell composition obtained from hybridoma cells. Fed-batch culture was conducted in spinner flasks using the supplemental medium for feeding. Significant improvement in cell growth, by-product reduction, and Gamma-Interferon (IFN-gamma) production was achieved as compared to a typical batch culture. Results indicate that the stoichiometric approach, originally developed for hybridoma cultures, is a fast and effective method for cell culture process design and improvement. The glycosylation of IFN-gamma was monitored off-line during the culture process. The accumulative IFN-gamma glycosylation efficiency was slightly improved as compared to that of the batch culture, due to the nutritional control through the stoichiometric feeding. Periodic glucose starvation was observed during the fed-batch culture as a result of the manual feeding. Pulse-chase radiolabeling assay shows that glucose starvation leads to a deteriorated IFN-gamma glycosylation efficiency. (c) 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 56: 577-582, 1997.
在中国仓鼠卵巢(CHO)细胞的补料分批培养中研究了化学计量培养基设计方法的应用。开发了一种蛋白质浓度极低(2 mg/L胰岛素)的无血清培养基。根据控制细胞生长的化学计量方程,利用从杂交瘤细胞获得的细胞组成来配制补充培养基。使用补充培养基进行补料分批培养,在转瓶中进行补料。与典型的分批培养相比,细胞生长、副产物减少以及γ-干扰素(IFN-γ)产量都有显著提高。结果表明,最初为杂交瘤培养开发的化学计量方法是一种快速有效的细胞培养工艺设计和改进方法。在培养过程中离线监测IFN-γ的糖基化。由于通过化学计量补料进行营养控制,与分批培养相比,IFN-γ的累积糖基化效率略有提高。由于手动补料,在补料分批培养过程中观察到周期性的葡萄糖饥饿。脉冲追踪放射性标记分析表明,葡萄糖饥饿会导致IFN-γ糖基化效率下降。(c) 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 56: 577 - 582, 1997。