Siegwart P, Côté J, Male K, Luong J H, Perrier M, Kamen A
Biotechnology Research Institute, National Research Council Canada, 6100 Royalmount Avenue, Montréal, Québec, Canada, H4P 2R2, Département de génie chimique, Ecole Polytechnique, Université de Montréal, Case Postale 6079, Succursale centr.
Biotechnol Prog. 1999 Jul-Aug;15(4):608-16. doi: 10.1021/bp990077v.
Fed-batch cultures were implemented to study the metabolism of HEK-293 cells. Glucose, measured every 30 min by a FIA biosensor system, was maintained at 1 mM throughout the culture using an adaptive nonlinear controller based on minimal process modeling. The controller performed satisfactorily at both low and high cell concentrations without the need for retuning between different culture phases. Overall, lactate production was significantly reduced by maintaining a low glucose concentration, thus decreasing the rate of glycolysis. The rates of glucose and glutamine uptake as well as the lactate and ammonia production were compared to those obtained in batch mode with an initial glucose concentration of 21 mM. Basically, three phases were observed in both culture modes. The metabolic shift from the first to the second phase was characterized by a significant reduction in glucose consumption and lactate production while maximum growth rate was maintained. The specific respiration rate appeared unchanged during the first two phases, suggesting that no change occurred in the oxidative pathway capacity. In the third phase, cell growth became slower very likely due to glutamine limitation.
采用补料分批培养法研究人胚肾细胞(HEK - 293)的代谢。使用基于最小过程建模的自适应非线性控制器,通过流动注射分析(FIA)生物传感器系统每30分钟测量一次葡萄糖,并在整个培养过程中将其维持在1 mM。该控制器在低细胞浓度和高细胞浓度下均表现良好,无需在不同培养阶段进行重新调整。总体而言,通过维持低葡萄糖浓度可显著降低乳酸生成,从而降低糖酵解速率。将葡萄糖和谷氨酰胺的摄取速率以及乳酸和氨的生成速率与初始葡萄糖浓度为21 mM的分批培养模式下获得的速率进行比较。基本上,在两种培养模式下均观察到三个阶段。从第一阶段到第二阶段的代谢转变的特征是葡萄糖消耗和乳酸生成显著减少,同时维持最大生长速率。在前两个阶段,比呼吸速率似乎保持不变,这表明氧化途径能力没有变化。在第三阶段,细胞生长很可能由于谷氨酰胺限制而变慢。