Synergy between 13C-metabolic flux analysis and flux balance analysis for understanding metabolic adaption to anaerobiosis in E. coli

被引:111
作者
Chen, Xuewen [1 ]
Alonso, Ana P. [1 ]
Allen, Doug K. [2 ]
Reed, Jennifer L. [3 ,4 ]
Shachar-Hill, Yair [1 ]
机构
[1] Michigan State Univ, Dept Plant Biol, Great Lakes Bioenergy Res Ctr, E Lansing, MI 48824 USA
[2] USDA ARS, Plant Genet Res Unit, Donald Danforth Plant Sci Ctr, St Louis, MO 63132 USA
[3] Univ Wisconsin, Chem & Biol Engn Dept, Madison, WI 53706 USA
[4] Univ Wisconsin, Great Lakes Bioenergy Res Ctr, Madison, WI 53706 USA
关键词
E; coli; Metabolic flux analysis; Flux balance analysis; Maintenance ATP utilization; Formate hydrogen lyase; Incomplete TCA cycle; BIDIRECTIONAL REACTION STEPS; ESCHERICHIA-COLI; MASS-SPECTROMETRY; BIOCHEMICAL NETWORKS; HYDROGEN-PRODUCTION; EVOLUTION; MODELS; RESPONSES; KNOCKOUT; GROWTH;
D O I
10.1016/j.ymben.2010.11.004
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Genome-based Flux Balance Analysis (FBA) and steady-state isotopic-labeling-based Metabolic Flux Analysis (MFA) are complimentary approaches to predicting and measuring the operation and regulation of metabolic networks. Here, genome-derived models of Escherichia coli (E. coli) metabolism were used for FBA and C-13-MFA analyses of aerobic and anaerobic growths of wild-type E. coli (K-12 MG1655) cells. Validated MFA flux maps reveal that the fraction of maintenance ATP consumption in total ATP production is about 14% higher under anaerobic (51.1%) than aerobic conditions (37.2%). FBA revealed that an increased ATP utilization is consumed by ATP synthase to secrete protons from fermentation. The TCA cycle is shown to be in complete in aerobically growing cells and submaximal grow this due to limited oxidative phosphorylation. An FBA was successful in predicting product secretion rates in aerobic culture if both glucose and oxygen up take measurement were constrained, but the most-frequently predicted values of internal fluxes yielded from sampling the feasible space differ substantially from MFA-derived fluxes. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:38 / 48
页数:11
相关论文
共 81 条
[1]
Compartment-specific labeling information in 13C metabolic flux analysis of plants [J].
Allen, Doug K. ;
Shachar-Hill, Yalr ;
Ohlrogge, John B. .
PHYTOCHEMISTRY, 2007, 68 (16-18) :2197-2210
[2]
The role of light in soybean seed filling metabolism [J].
Allen, Doug K. ;
Ohlrogge, John B. ;
Shachar-Hill, Yair .
PLANT JOURNAL, 2009, 58 (02) :220-234
[3]
Alonso A.P., 2010, PLANT PHYSL IN PRESS
[4]
[Anonymous], 2012, Molecular Cloning: A Laboratory Manual
[5]
Metabolic flux analysis in a nonstationary system:: Fed-batch fermentation of a high yielding strain of E. coli producing 1,3-propanediol [J].
Antoniewicz, Maciek R. ;
Kraynie, David F. ;
Laffend, Lisa A. ;
Gonzalez-Lergier, Joanna ;
Kelleher, Joanne K. ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (03) :277-292
[6]
Elementary metabolite units (EMU): A novel framework for modeling isotopic distributions [J].
Antoniewicz, Maciek R. ;
Kelleher, Joanne K. ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (01) :68-86
[7]
Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox [J].
Becker, Scott A. ;
Feist, Adam M. ;
Mo, Monica L. ;
Hannum, Gregory ;
Palsson, Bernhard O. ;
Herrgard, Markus J. .
NATURE PROTOCOLS, 2007, 2 (03) :727-738
[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]
Sampling for metabolome analysis of microorganisms [J].
Bolten, Christoph J. ;
Kiefer, Patrick ;
Letisse, Fabien ;
Portais, Jean-Charles ;
Wittmann, Christoph .
ANALYTICAL CHEMISTRY, 2007, 79 (10) :3843-3849
[10]
Identification of flux control in metabolic networks using non-equilibrium thermodynamics [J].
Bordel, Sergio ;
Nielsen, Jens .
METABOLIC ENGINEERING, 2010, 12 (04) :369-377