Dynamic optimization of metabolic networks coupled with gene expression

被引:70
作者
Waldherr, Steffen [1 ]
Oyarzun, Diego A. [2 ]
Bockmayr, Alexander [3 ]
机构
[1] Univ Magdeburg, Inst Automat Engn, D-39106 Magdeburg, Germany
[2] Univ London Imperial Coll Sci Technol & Med, Dept Math, London SW7 2AZ, England
[3] Free Univ Berlin, DFG Res Ctr Matheon, D-14195 Berlin, Germany
关键词
Flux optimization; Constraint-based methods; Metabolic genetic networks; Bacterial growth; ESCHERICHIA-COLI METABOLISM; FLUX BALANCE ANALYSIS; NUMERICAL-SOLUTION; GROWTH; MODELS; SEQUENCE; SYSTEMS; DESIGN;
D O I
10.1016/j.jtbi.2014.10.035
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The regulation of metabolic activity by tuning enzyme expression levels is crucial to sustain cellular growth in changing environments. Metabolic networks are often studied at steady state using constraint-based models and optimization techniques. However, metabolic adaptations driven by changes in gene expression cannot be analyzed by steady state models, as these do not account for temporal changes in biomass composition. Here we present a dynamic optimization framework that integrates the metabolic network with the dynamics of biomass production and composition. An approximation by a timescale separation leads to a coupled model of quasi-steady state constraints on the metabolic reactions, and differential equations for the substrate concentrations and biomass composition. We propose a dynamic optimization approach to determine reaction fluxes for this model, explicitly taking into account enzyme production costs and enzymatic capacity. In contrast to the established dynamic flux balance analysis, our approach allows predicting dynamic changes in both the metabolic fluxes and the biomass composition during metabolic adaptations. Discretization of the optimization problems leads to a linear program that can be efficiently solved. We applied our algorithm in two case studies: a minimal nutrient uptake network, and an abstraction of core metabolic processes in bacteria. In the minimal model, we show that the optimized uptake rates reproduce the empirical Monod growth for bacterial cultures. For the network of core metabolic processes, the dynamic optimization algorithm predicted commonly observed metabolic adaptations, such as a diauxic switch with a preference ranking for different nutrients, re-utilization of waste products after depletion of the original substrate, and metabolic adaptation to an impending nutrient depletion. These examples illustrate how dynamic adaptations of enzyme expression can be predicted solely from an optimization principle. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:469 / 485
页数:17
相关论文
共 60 条
[1]   Sequence-based analysis of metabolic demands for protein synthesis in prokaryotes [J].
Allen, TE ;
Palsson, BO .
JOURNAL OF THEORETICAL BIOLOGY, 2003, 220 (01) :1-18
[2]   The Moderately Efficient Enzyme: Evolutionary and Physicochemical Trends Shaping Enzyme Parameters [J].
Bar-Even, Arren ;
Noor, Elad ;
Savir, Yonatan ;
Liebermeister, Wolfram ;
Davidi, Dan ;
Tawfik, Dan S. ;
Milo, Ron .
BIOCHEMISTRY, 2011, 50 (21) :4402-4410
[3]   Intracellular crowding defines the mode and sequence of substrate uptake by Escherichia coli and constrains its metabolic activity [J].
Beg, Q. K. ;
Vazquez, A. ;
Ernst, J. ;
de Menezes, M. A. ;
Bar-Joseph, Z. ;
Barabasi, A.-L. ;
Oltvai, Z. N. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (31) :12663-12668
[4]   A quantitative approach to catabolite repression in Escherichia coli [J].
Bettenbrock, K ;
Fischer, S ;
Kremling, A ;
Jahreis, K ;
Sauter, T ;
Gilles, ED .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (05) :2578-2584
[5]   An overview of simultaneous strategies for dynamic optimization [J].
Biegler, Lorenz T. .
CHEMICAL ENGINEERING AND PROCESSING-PROCESS INTENSIFICATION, 2007, 46 (11) :1043-1053
[6]   Complexity in bacterial cell-cell communication: Quorum signal integration and subpopulation signaling in the Bacillus subtilis phosphorelay [J].
Bischofs, Ilka B. ;
Hug, Joshua A. ;
Liu, Aiwen W. ;
Wolf, Denise M. ;
Arkin, Adam P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (16) :6459-6464
[7]   Protein length in eukaryotic and prokaryotic proteomes [J].
Brocchieri, L ;
Karlin, S .
NUCLEIC ACIDS RESEARCH, 2005, 33 (10) :3390-3400
[8]   Minimal reaction sets for Escherichia coli metabolism under different growth requirements and uptake environments [J].
Burgard, AP ;
Vaidyaraman, S ;
Maranas, CD .
BIOTECHNOLOGY PROGRESS, 2001, 17 (05) :791-797
[9]   Carbon nutrition of Escherichia coli in the mouse intestine [J].
Chang, DE ;
Smalley, DJ ;
Tucker, DL ;
Leatham, MP ;
Norris, WE ;
Stevenson, SJ ;
Anderson, AB ;
Grissom, JE ;
Laux, DC ;
Cohen, PS ;
Conway, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) :7427-7432
[10]   Integrating metabolic, transcriptional regulatory and signal transduction models in Escherichia coli [J].
Covert, Markus W. ;
Xiao, Nan ;
Chen, Tiffany J. ;
Karr, Jonathan R. .
BIOINFORMATICS, 2008, 24 (18) :2044-2050