Computing and Interpreting Specific Production Rates in a Chemostat in Steady State According to the Luedeking-Piret model

被引:7
作者
Thierie, Jacques [1 ]
机构
[1] Univ Libre Bruxelles, Fac Ecole Interfac Bioingn EIB, B-1120 Brussels, Belgium
关键词
Metabolite production; Chemostat; Continuous cultures; Bioreactor design; Bioreactor optimisation; LACTIC-ACID FERMENTATION; CONTINUOUS-CULTURE; BATCH; KINETICS;
D O I
10.1007/s12010-012-9978-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Luedeking-Piret model is an empirical relationship which is very widely used in cell cultures to evaluate specific production rates of some products (metabolites or others). It constitutes a very common method of calculation as much in fundamental as in applied research and especially for designing and optimizing industrial processes in very varied fields. However, this model appears to be frequently deficient and has to be greatly adapted, practically, one might say, for each individual case. Obviously, this is a very great drawback, requiring a great deal of time spent on it and one that greatly lessens the 'universality' of the model. This work reveals that it is possible to give the initial Luedeking-Piret model a much more general scope. The used method revealed metabolic switches that have never been suspected until now. Confirmation of the method would certainly give a precious general tool both to optimize production processes and to increase understanding of some physiological states of cells in chemostat.
引用
收藏
页码:477 / 492
页数:16
相关论文
共 22 条
[1]  
Baei MS, 2008, AFR J BIOTECHNOL, V7, P3487
[2]   Unstructured model for batch cultures without pH control of Lactobacillus helveticus -: Inhibitory effect of the undissociated lactic acid [J].
Balannec, Beatrice ;
Bouguettoucha, Abdellah ;
Amrane, Abdeltif .
BIOCHEMICAL ENGINEERING JOURNAL, 2007, 35 (03) :289-294
[3]   Batch and continuous culture of Lactococcus lactis NZ133:: experimental data and model development [J].
Boonmee, M ;
Leksawasdi, N ;
Bridge, W ;
Rogers, PL .
BIOCHEMICAL ENGINEERING JOURNAL, 2003, 14 (02) :127-135
[4]  
Bouguettoucha A, 2011, FOOD TECHNOL BIOTECH, V49, P3
[5]   The renaissance of continuous culture in the post-genomics age [J].
Bull, Alan T. .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2010, 37 (10) :993-1021
[6]   CHEMOSTAT STUDY OF KINETICS OF HUMAN LYMPHOKINE SYNTHESIS IN RECOMBINANT ESCHERICHIA-COLI [J].
CURLESS, CE ;
FORRER, PD ;
MANN, MB ;
FENTON, DM ;
TSAI, LB .
BIOTECHNOLOGY AND BIOENGINEERING, 1989, 34 (03) :415-421
[7]   Chemostat-Based Micro-Array Analysis in Baker's Yeast [J].
Daran-Lapujade, Pascale ;
Daran, Jean-Marc ;
van Maris, Antonius J. A. ;
de Winde, Johannes H. ;
Pronk, Jack T. .
ADVANCES IN MICROBIAL PHYSIOLOGY, VOL 54, 2009, 54 :257-311
[8]  
Djidel A., 2007, THESIS NANCY U
[9]   Effect of product inhibition on lactic acid fermentation: Simulation and modelling [J].
Dutta, SK ;
Mukherjee, A ;
Chakraborty, P .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1996, 46 (04) :410-413
[10]  
Ejiofor A. O., 1998, J IN DMICROBIOL, V16, P102