期刊文献+

利用代谢网络模型和线性规划法在线预测谷氨酸发酵中产物浓度 被引量:10

On-Line Prediction of Product Concentrations in Glutamate Fermentation Using Metabolic Network Model and Linear Programming
在线阅读 下载PDF
导出
摘要 在好氧型的谷氨酸发酵实验中发现,溶解氧(DO)对发酵性能有很大的影响,谷氨酸的生成方式也因此有很大不同:较低的DO水平能够延长产酸期、提高谷氨酸的最终浓度,但是代谢副产物———乳酸也有较大程度的积蓄;而DO水平过高,虽然代谢副产物不会生成积蓄,但菌体消亡过快导致产酸期缩短、谷氨酸的最终浓度降低.同时,谷氨酸的生成方式与发酵过程中摄氧率(OUR)和CO2的释放率(CER)有着非常紧密的关联.作者利用代谢网络模型并结合使用线性规划优化法,通过在线测定OUR和CER,比较准确地在线推定出发酵过程中谷氨酸的质量浓度变化.与传统的非构造式动力学模型相比,上述预测方法具有建模简单、模型物理意义明确、通用性能好等优点,为后续过程的在线控制和优化提供一种全新和有效的途径. The experimental data showed that, in aerobic glutamate fermentation with strain C. glutamicum S9114, glutamate produced in different ways with different patterns of O2 uptake rate (OUR), CO2 evolution rate (CER) and by-products accumulation at different dissolved oxygen (DO) levels: glutamate production could be prolonged but with higher lactate accumulation at a lower DO level; while glutamate production stopped at low concentration level with a quick decline of both OUR and CER when controlling DO at a higher level. In this study, a metabolic network model combined with the linear programming optimization was used to online predict the glutamate production under different DO levels, with only OUR and CER be online measured. The results indicated the power and advantages of the metabolic network model over the traditional unstructured dynamic models, in terms of easy parameter identification, clear biochemical interpreting of data, as well as prediction performance. The proposed method supplies a novel and alternative way for on-line control and optimization of fermentation processes.
出处 《食品与生物技术学报》 CAS CSCD 北大核心 2005年第4期31-37,41,共8页 Journal of Food Science and Biotechnology
基金 江苏省自然科学基金资助项目(BK-2003021)资助课题.
关键词 代谢网络 谷氨酸发酵 数学模型 线性规划 在线预测 metabolic network glutamate fermentation mathematical model linearprogramming on-line prediction
  • 相关文献

参考文献9

  • 1唐军,蔡水洪,叶勤.克鲁斯假丝酵母分批发酵生产甘油的代谢流分布[J].高校化学工程学报,2002,16(1):58-63. 被引量:24
  • 2杨艳,陈奎发,李春,刘雨磊,曹竹安.谷氨酰胺产生菌NS611的代谢流分析[J].无锡轻工大学学报(食品与生物技术),2003,22(2):38-43. 被引量:5
  • 3张嗣良.发酵过程多水平问题及其生物反应器装置技术研究——基于过程参数相关的发酵过程优化与放大技术[J].中国工程科学,2001,3(8):37-45. 被引量:46
  • 4Jin S, Ye K, Shimizu K. Metabolic pathway analysis of recombinant saccharomyces cerevisiae with a galactose-inducible promotor based on a signal flow model approach[J]. J Biosci & Bioeng, 1995, 80:541-551.
  • 5Takiguchi N, Shimizu H, Shioya S. An on-line physiological state recognition system for the lysine fermentation process based on a metabolic reaction model[J]. Biotechnol Bioeng, 1997, 55:170-181.
  • 6Shimizu H, Takiguchi N, Tanaka H. A maximum production strategy of lysine based on a simplified model derived from a metabolic reaction network[J]. Metabolic Engineering, 1999, 1 :299-308.
  • 7Savinell J M, Palsson B O. Network analysis of intermediary metabolism using linear optimization-I. Development of mathematical formalism[J]. J Theor Biol, 1992, 154:421-454.
  • 8Atkinson K.Elementary numerical analysis[M].New York:Wiley&Johnsons,1985.
  • 9Park S M, Sinskey A J, Stephanopoulos G. Metabolic and physiological studies of Corynebacterium glutamicum mutants[J]. Biotechnol Bioeng, 1997, 55..864-879.

二级参考文献13

共引文献70

同被引文献70

引证文献10

二级引证文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部