4.7 Article

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

Journal

METABOLIC ENGINEERING
Volume 25, Issue -, Pages 63-71

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymben.2014.06.006

Keywords

Metabolic engineering; Synthetic biology; Ensemble Modeling; Robustness

Funding

  1. National Science Foundation [MCB-1139318]
  2. UCLA-DOE Institute for Genomics and Proteomics
  3. Office of Science (BER), U.S. Department of Energy [DE-SC0008744, DE-SC0006698]
  4. U.S. Department of Energy (DOE) [DE-SC0006698] Funding Source: U.S. Department of Energy (DOE)
  5. Direct For Biological Sciences
  6. Div Of Molecular and Cellular Bioscience [1139318] Funding Source: National Science Foundation

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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.

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