Higareda A E, Possani L D, Ramírez O T
Department of Bioengineering, Universidad Nacional Autónoma de México, Morelos.
Cytotechnology. 1994;15(1-3):73-86. doi: 10.1007/BF00762381.
Exponentially fed-batch cultures (EFBC) of a murine hybridoma in T-flasks were explored as a simple alternative experimental tool to chemostats for the study of metabolism, growth and monoclonal antibody (MAb) production kinetics. EFBC were operated in the variable volume mode using an exponentially increasing and predetermined stepwise feeding profile of fresh complete medium. The dynamic and steady-state behaviors of the EFBC coincided with those reported for chemostats at dilution rates below the maximum growth rate. In particular, steady-state for growth rate and concentration of viable cells, glucose, and lactate was attained at different dilution rates between 0.005 and 0.05 h-1. For such a range, the glucose and lactate metabolic quotients and the steady-state glucose concentration increased, whereas total MAb, volumetric, and specific MAb production rates decreased 65-, 6-, and 3-fold, respectively, with increasing dilution rates. The lactate from glucose yield remained relatively constant for dilution rates up to 0.03 h-1, where it started to decrease. In contrast, viability remained above 80% at high dilution rates but rapidly decreased at dilution rates below 0.02 h-1. No true washout occurred during operation above the maximum growth, as concluded from the constant viable cell number. However, growth rate decreased to as low as 0.01 h-1, suggesting the requirement of a minimum cell density, and concomitant autocrine growth factors, for growth. Chemostat operation drawbacks were avoided by EFBC in T-flasks. Namely, simple and stable operation was obtained at dilution rates ranging from very low to above the maximum growth rate. Furthermore, simultaneous operation of multiple experiments in reduced size was possible, minimizing start-up time, media and equipment costs.
研究了在T型烧瓶中对小鼠杂交瘤进行指数补料分批培养(EFBC),作为一种简单的替代实验工具,用于替代恒化器来研究代谢、生长和单克隆抗体(MAb)生产动力学。EFBC采用可变体积模式运行,使用新鲜完全培养基按指数增加且预先确定的逐步补料曲线。在低于最大生长速率的稀释率下,EFBC的动态和稳态行为与恒化器报道的一致。特别是,在0.005至0.05 h-1之间的不同稀释率下,实现了生长速率、活细胞浓度、葡萄糖和乳酸的稳态。对于这样的范围,随着稀释率增加,葡萄糖和乳酸代谢商以及稳态葡萄糖浓度增加,而总单克隆抗体、体积单克隆抗体和比单克隆抗体生产率分别下降65倍、6倍和3倍。对于高达0.03 h-1的稀释率,葡萄糖生成乳酸的产率保持相对恒定,之后开始下降。相比之下,在高稀释率下活力保持在80%以上,但在低于0.02 h-1的稀释率下迅速下降。从恒定的活细胞数可以得出结论,在高于最大生长速率的操作过程中没有发生真正的洗出。然而,生长速率降至低至0.01 h-1,这表明生长需要最低细胞密度以及伴随的自分泌生长因子。T型烧瓶中的EFBC避免了恒化器操作的缺点。即,在从非常低到高于最大生长速率的稀释率范围内获得了简单且稳定的操作。此外,可以同时进行多个缩小规模的实验,从而将启动时间、培养基和设备成本降至最低。