Dynamic mathematical models of batch experiments and fed-batch cultures for cyclic adenosine monophosphate production by Arthrobacter A302

被引:0
作者
Lei Li
Xiaochun Chen
Huajing Ren
Jiaming Cao
Jian Xiong
Jianxin Bai
Hanjie Ying
机构
[1] Nanjing University of Technology,State Key Laboratory of Materials
来源
World Journal of Microbiology and Biotechnology | 2011年 / 27卷
关键词
A302; Cyclic adenosine monophosphate; Fed-batch; Kinetic model;
D O I
暂无
中图分类号
学科分类号
摘要
A glucose utilizing strain, Arthrobacter A302 was used for cyclic adenosine monophosphate (cAMP) production in batch modes. The non-structured model in a 5 l stirred tank bioreactor for understanding, controlling, and optimizing the fermentation process was proposed using the logistic equation for microbial growth, the Luedeking-Piret equation for product formation and Luedeking-Piret-like equation for substrate uptake, respectively. The production of cAMP was a mixed-growth-associated pattern. Based on model prediction, a comparison of calculated value using the parameters evaluated above with another experimental data in 30 l bioreactor was used to test the model. The results predicted from the model were in good agreement with the experimental observations in 30 l bioreactor, which demonstrated that the model might be useful for the development and optimization of production of cAMP in industrial scale. Based on estimated kinetic parameters, three different fed-batch modes, constant rate and intermittent (once and repeated), were adopted in order to obtain more cAMP accumulation. Furthermore, the final production of cAMP reached 11.24 g l−1 after 72 h incubation using three stages feeding strategy. In particular, the cAMP productivity (0.156 g l−1 h−1) was successfully improved by 22.83, 11.43 and 9.86%, respectively, compared with the modes of the batch, constant rate fed-batch and intermittent fed-batch once.
引用
收藏
页码:2379 / 2385
页数:6
相关论文
共 93 条
[1]  
Aborhey S(1977)Modeling of lactic acid production by Streptococcus cremoris hp J Gen Appl Microbiol 23 7-21
[2]  
Williamson D(2000)Molecular diversity of cyclic AMP signalling Front Neuroendocrin 21 103-110
[3]  
Antoni FA(2007)A generalised unstructured model for batch cultures of Enzyme Microbial Technol 41 377-382
[4]  
Bouguettoucha A(2009)Medium optimization for the production of cyclic adenosine 3′, 5′- monophosphate by Microbacterium sp. no. 205 using response surface methodology Bioresour Technol 100 919-924
[5]  
Balannec B(2010)Enhanced cyclic adenosine monophosphate production by Bioresour Technol 101 3159-3163
[6]  
Nacef S(2003) A302 through rational redistribution of metabolic flux Biotechnol Lett 25 1143-1146
[7]  
Chen XC(1999)Kinetics of β-mannanase fermentation by Enzyme Microb Technol 25 613-621
[8]  
Bai JX(1996)Unstructured kinetic model for sophorolipid production by Candida bombicola Chin J Biotechnol 12 219-225
[9]  
Cao JM(2006)The kinetics of lysine batch fermentation Proc Biochem 41 1908-1912
[10]  
Li ZJ(2003)Kinetics of Chin Pharmacol Bull 19 940-943