Nicolaï B M, Van Impe J F, Vanrolleghem P A, Vandewalle J
Agricultural Engineering Department, K.U. Leuven, Heverlee, Belgium.
Antonie Van Leeuwenhoek. 1992 Nov;62(4):273-83. doi: 10.1007/BF00572595.
The mathematical model for the penicillin G fed-batch fermentation proposed by Heijnen et al. (1979) is compared with the model of Bajpai & Reuss (1980). Although the general structure of these models is similar, the difference in metabolic assumptions and specific growth and production kinetics results in a completely different behaviour towards product optimization. A detailed analysis of both models reveals some physical and biochemical shortcomings. It is shown that it is impossible to make a reliable estimation of the model parameters, only using experimental data of simple constant glucose feed rate fermentations with low initial substrate amount. However, it is demonstrated that some model parameters might be key factors in concluding whether or not altering the substrate feeding strategy has an important influence on the final amount of product. It is illustrated that feeding strategy optimization studies can be a tool in designing experiments for parameter estimation purposes.
将海涅恩等人(1979年)提出的青霉素G补料分批发酵数学模型与巴杰派和罗伊斯(1980年)的模型进行了比较。尽管这些模型的总体结构相似,但代谢假设以及特定生长和生产动力学方面的差异导致在产品优化方面表现出完全不同的行为。对这两个模型的详细分析揭示了一些物理和生化方面的缺陷。结果表明,仅使用初始底物量较低的简单恒定葡萄糖进料速率发酵的实验数据,不可能对模型参数进行可靠估计。然而,已证明某些模型参数可能是判断改变底物进料策略是否对最终产物量有重要影响的关键因素。结果表明,进料策略优化研究可以作为设计用于参数估计目的实验的一种工具。