A flexible state-space approach for the modeling of metabolic networks I: Development of mathematical methods

被引:5
作者
Baughman, Adam C. [1 ,2 ]
Sharfstein, Susan T. [1 ,2 ,3 ]
Martin, Lealon L. [1 ,2 ]
机构
[1] Rensselaer Polytech Inst, Dept Chem & Biol Engn, Troy, NY 12180 USA
[2] Rensselaer Polytech Inst, Ctr Biotechnol & Interdisciplinary Studies, Troy, NY 12180 USA
[3] Rensselaer Polytech Inst, Dept Biol, Troy, NY 12180 USA
关键词
Metabolic modeling; Network topology; Global optimization; FLUX BALANCE ANALYSIS; ESCHERICHIA-COLI; HYBRIDOMA CELLS; INTRACELLULAR FLUXES; ANTIBODY-PRODUCTION; HYDROGEN-PRODUCTION; OBJECTIVE FUNCTION; MASS-SPECTROMETRY; MURINE HYBRIDOMA; IDEAS APPROACH;
D O I
10.1016/j.ymben.2010.12.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We introduce a novel, flexible, optimization-based mathematical frame work for the modeling of arbitrarily complex metabolic networks: topological metabolic analysis (TMA). The framework is adapted from state-space approaches used by Manousiouthakis and co-workers for the representation of complex heat- and mass-exchanger networks. We offer a thorough discussion of the mathematics and general theory underlying the framework, and discuss certain mathematical advantages of our modeling representation in comparison with other commonly used techniques (MFA and FBA). We employ a novel aggregate objective function for use with our basic constraint model, including a generalized least-squares term (for fitting available experimental measurements) and a linear design term (for representing biological or engineering goals). Using a case-study taken from recent literature (McKinlay et al., 2007), we demonstrate (among other benefits) the ability of this objective to identify alternate distinct-yet-equally optimal solutions for a given modeling problem. We also show that these solutions, obtained using only external metabolite uptake and secretion measurements, provide useful biological insights and compare favorably with solutions obtained on thebasisof C-13 isotopetracing data. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:125 / 137
页数:13
相关论文
共 72 条
[1]   Decoupling cell growth and product formation in Chinese hamster ovary cells through metabolic control [J].
Altamirano, C ;
Cairó, JJ ;
Gòdia, F .
BIOTECHNOLOGY AND BIOENGINEERING, 2001, 76 (04) :351-360
[2]  
[Anonymous], 2003, AMPL: A Modeling Language for Mathematical Programming
[3]   On the state space approach to mass/heat exchanger network design [J].
Bagajewicz, MJ ;
Pham, R ;
Manousiouthakis, V .
CHEMICAL ENGINEERING SCIENCE, 1998, 53 (14) :2595-2621
[4]   MASS HEAT-EXCHANGE NETWORK REPRESENTATION OF DISTILLATION NETWORKS [J].
BAGAJEWICZ, MJ ;
MANOUSIOUTHAKIS, V .
AICHE JOURNAL, 1992, 38 (11) :1769-1800
[5]   Inverse metabolic engineering: A strategy for directed genetic engineering of useful phenotypes [J].
Bailey, JE ;
Sburlati, A ;
Hatzimanikatis, V ;
Lee, K ;
Renner, WA ;
Tsai, PS .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 79 (05) :568-579
[6]   Absolute metabolite concentrations and implied enzyme active site occupancy in Escherichia coli [J].
Bennett, Bryson D. ;
Kimball, Elizabeth H. ;
Gao, Melissa ;
Osterhout, Robin ;
Van Dien, Stephen J. ;
Rabinowitz, Joshua D. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (08) :593-599
[7]  
BIANCONI G, 2008, PHYS REV E, V78
[8]   Metabolic flux analysis and pharmaceutical production [J].
Boghigian, Brett A. ;
Seth, Gargi ;
Kiss, Robert ;
Pfeifer, Blaine A. .
METABOLIC ENGINEERING, 2010, 12 (02) :81-95
[9]  
Bonarius HPJ, 1996, BIOTECHNOL BIOENG, V50, P299, DOI 10.1002/(SICI)1097-0290(19960505)50:3<299::AID-BIT9>3.0.CO
[10]  
2-B