Sensitivity function-based model reduction: A bacterial gene expression case study.

Mathematical models used to predict the behavior of genetically modified organisms require 1). a (rather) large number of state variables, and 2). complicated kinetic expressions containing a large number of parameters. Since these models are hardly identifiable and of limited use in model-based optimization and control strategies, a generic methodology based on sensitivity function analysis is presented to reduce the model complexity at the level of the kinetics, while maintaining high prediction power. As a case study to illustrate the method and results obtained, the influence of the dissolved oxygen concentration on the cytN gene expression in the bacterium Azospirillum brasilense Sp7 is modeled. As a first modeling approach, available mechanistic knowledge is incorporated into a mass balance equation model with 3 states and 14 parameters. The large differences in order of magnitude of the model parameters identified on the available experimental data indicate 1). possible structural problems in the kinetic model and, associated with this, 2). a possibly too high number of model parameters. A careful sensitivity function analysis reveals that a reduced model with only seven parameters is almost as accurate as the original model.

[1]  K J Versyck,et al.  On the design of optimal dynamic experiments for parameter estimation of a Ratkowsky-type growth kinetics at suboptimal temperatures. , 2000, International journal of food microbiology.

[2]  S. Park,et al.  Transcriptional regulation of the proton-translocating ATPase (atpIBEFHAGDC) operon of Escherichia coli: control by cell growth rate , 1996, Journal of bacteriology.

[3]  Hua Wu,et al.  Parametric sensitivity in chemical systems , 1999 .

[4]  B Sonnleitner,et al.  Growth of Saccharomyces cerevisiae is controlled by its limited respiratory capacity: Formulation and verification of a hypothesis , 1986, Biotechnology and bioengineering.

[5]  Jeffrey H. Miller Experiments in molecular genetics , 1972 .

[6]  J. Vanderleyden,et al.  A Cytochrome cbb3(Cytochrome c) Terminal Oxidase in Azospirillum brasilense Sp7 Supports Microaerobic Growth , 1998, Journal of bacteriology.

[7]  S. Park,et al.  Aerobic regulation of isocitrate dehydrogenase gene (icd) expression in Escherichia coli by the arcA and fnr gene products , 1997, Journal of bacteriology.

[8]  Bart De Moor,et al.  Optimal adaptive control of fed-batch fermentation processes , 1995 .

[9]  J. Michiels,et al.  Transcription of the Azospirillum brasilense nifH gene is positively regulated by NifA and NtrA and is negatively controlled by the cellular nitrogen status , 1992, Molecular and General Genetics MGG.

[10]  K. Marchal,et al.  Quantitative Analysis of Bacterial Gene Expression by Using the gusA Reporter Gene System , 2001, Applied and Environmental Microbiology.

[11]  R. Berber,et al.  Dynamic modeling, sensitivity analysis and parameter estimation of industrial yeast fermenters , 1997 .