Ensemble Modeling for Robustness Analysis in engineering non-native metabolic pathways

被引:72
作者
Lee, Yun [1 ]
Rivera, Jimmy G. Lafontaine [1 ]
Liao, James C. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, UCLA DOE Inst Genom & Proteom, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
Metabolic engineering; Synthetic biology; Ensemble Modeling; Robustness; ESCHERICHIA-COLI; PHOSPHOROLYTIC CLEAVAGE; EXPANDING METABOLISM; MICROBIAL-PRODUCTION; NETWORKS; CHEMICALS; FUELS; FRUCTOSE-6-PHOSPHATE; PHOSPHOKETOLASE; BIOSYNTHESIS;
D O I
10.1016/j.ymben.2014.06.006
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
Metabolic pathways in cells must be sufficiently robust to tolerate fluctuations in expression levels and changes in environmental conditions. Perturbations in expression levels may lead to system failure due to the disappearance of a stable steady state. Increasing evidence has suggested that biological networks have evolved such that they are intrinsically robust in their network structure. In this article, we presented Ensemble Modeling for Robustness Analysis (EMRA), which combines a continuation method with the Ensemble Modeling approach, for investigating the robustness issue of non-native pathways. EMRA investigates a large ensemble of reference models with different parameters, and determines the effects of parameter drifting until a bifurcation point, beyond which a stable steady state disappears and system failure occurs. A pathway is considered to have high bifurcational robustness if the probability of system failure is low in the ensemble. To demonstrate the utility of EMRA, we investigate the bifurcational robustness of two synthetic central metabolic pathways that achieve carbon conservation: non-oxidative glycolysis and reverse glyoxylate cycle. With EMRA, we determined the probability of system failure of each design and demonstrated that alternative designs of these pathways indeed display varying degrees of bifurcational robustness. Furthermore, we demonstrated that target selection for flux improvement should consider the trade-offs between robustness and performance. (C) 2014 The Authors. Published by Elsevier Inc. On behalf of International Metabolic Engineering Society.
引用
收藏
页码:63 / 71
页数:9
相关论文
共 39 条
[1]  
Allgower Eugene L, 2003, Classics in Applied Mathematics
[2]   Robustness in bacterial chemotaxis [J].
Alon, U ;
Surette, MG ;
Barkai, N ;
Leibler, S .
NATURE, 1999, 397 (6715) :168-171
[3]   Systemic properties of ensembles of metabolic networks: application of graphical and statistical methods to simple unbranched pathways [J].
Alves, R ;
Savageau, MA .
BIOINFORMATICS, 2000, 16 (06) :534-547
[4]   Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels [J].
Atsumi, Shota ;
Hanai, Taizo ;
Liao, James C. .
NATURE, 2008, 451 (7174) :86-U13
[5]   Robustness in simple biochemical networks [J].
Barkai, N ;
Leibler, S .
NATURE, 1997, 387 (6636) :913-917
[6]   Synthetic non-oxidative glycolysis enables complete carbon conservation [J].
Bogorad, Igor W. ;
Lin, Tzu-Shyang ;
Liao, James C. .
NATURE, 2013, 502 (7473) :693-+
[7]   Glycolytic Oscillations and Limits on Robust Efficiency [J].
Chandra, Fiona A. ;
Buzi, Gentian ;
Doyle, John C. .
SCIENCE, 2011, 333 (6039) :187-192
[8]   Microbial production of short-chain alkanes [J].
Choi, Yong Jun ;
Lee, Sang Yup .
NATURE, 2013, 502 (7472) :571-+
[9]   Engineering dynamic pathway regulation using stress-response promoters [J].
Dahl, Robert H. ;
Zhang, Fuzhong ;
Alonso-Gutierrez, Jorge ;
Baidoo, Edward ;
Batth, Tanveer S. ;
Redding-Johanson, Alyssa M. ;
Petzold, Christopher J. ;
Mukhopadhyay, Aindrila ;
Lee, Taek Soon ;
Adams, Paul D. ;
Keasling, Jay D. .
NATURE BIOTECHNOLOGY, 2013, 31 (11) :1039-+
[10]   Sustained oscillations in living cells [J].
Dano, S ;
Sorensen, PG ;
Hynne, F .
NATURE, 1999, 402 (6759) :320-322