Menezes J C, Alves S S, Lemos J M, de Azevedo S F
Department of Chemical Engineering, Technical University of Lisbon, Portugal.
J Chem Technol Biotechnol. 1994 Oct;61(2):123-38. doi: 10.1002/jctb.280610207.
Penicillin-G fermentation with industrial media in 1 m3 stirred tank bioreactors was studied. A model based on the Bajpai-Reuss model structure was developed. Under typical production conditions catabolite repression is nonidentifiable and extensive mycelium differentiation occurs. Thus, the original model was reformulated, neglecting glucose repression of penicillin production and including biomass autolysis. The multi-substrate nature of industrial media was critically analysed. By combining the two most important carbon substrates present, a simple and applicable model was obtained. Model predictions agreed well with experimental data and reproduced the general characteristics observed in the fermentations. The predictive power of the model was tested for fermentations with different sugar feed rate profiles and raw materials (corn-steep liquor and sugar syrup). Several aspects of parameter estimation and model development are discussed on the basis of direct experimental data inspection and a sensitivity analysis of model parameters.
研究了在1立方米搅拌罐式生物反应器中使用工业培养基进行青霉素G发酵的过程。基于Bajpai-Reuss模型结构开发了一个模型。在典型的生产条件下,分解代谢物阻遏难以识别,且会发生广泛的菌丝体分化。因此,对原始模型进行了重新构建,忽略了葡萄糖对青霉素生产的阻遏作用,并纳入了生物质自溶的情况。对工业培养基的多底物性质进行了严格分析。通过结合存在的两种最重要碳底物,得到了一个简单且适用的模型。模型预测与实验数据吻合良好,并重现了发酵过程中观察到的一般特征。针对不同糖进料速率曲线和原料(玉米浆和糖浆)的发酵过程,测试了该模型的预测能力。基于直接的实验数据检查和模型参数的敏感性分析,讨论了参数估计和模型开发的几个方面。