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Stability of Ensemble Models Predicts Productivity of Enzymatic Systems
Stability in a metabolic system may not be obtained if incorrect amounts of enzymes are used. Without stability, some metabolites may accumulate or deplete leading to the irreversible loss of the desired operating point. Even if initial enzyme amounts achieve a stable steady state, changes in enzyme...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786283/ https://www.ncbi.nlm.nih.gov/pubmed/26963521 http://dx.doi.org/10.1371/journal.pcbi.1004800 |
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author | Theisen, Matthew K. Lafontaine Rivera, Jimmy G. Liao, James C. |
author_facet | Theisen, Matthew K. Lafontaine Rivera, Jimmy G. Liao, James C. |
author_sort | Theisen, Matthew K. |
collection | PubMed |
description | Stability in a metabolic system may not be obtained if incorrect amounts of enzymes are used. Without stability, some metabolites may accumulate or deplete leading to the irreversible loss of the desired operating point. Even if initial enzyme amounts achieve a stable steady state, changes in enzyme amount due to stochastic variations or environmental changes may move the system to the unstable region and lose the steady-state or quasi-steady-state flux. This situation is distinct from the phenomenon characterized by typical sensitivity analysis, which focuses on the smooth change before loss of stability. Here we show that metabolic networks differ significantly in their intrinsic ability to attain stability due to the network structure and kinetic forms, and that after achieving stability, some enzymes are prone to cause instability upon changes in enzyme amounts. We use Ensemble Modelling for Robustness Analysis (EMRA) to analyze stability in four cell-free enzymatic systems when enzyme amounts are changed. Loss of stability in continuous systems can lead to lower production even when the system is tested experimentally in batch experiments. The predictions of instability by EMRA are supported by the lower productivity in batch experimental tests. The EMRA method incorporates properties of network structure, including stoichiometry and kinetic form, but does not require specific parameter values of the enzymes. |
format | Online Article Text |
id | pubmed-4786283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47862832016-03-23 Stability of Ensemble Models Predicts Productivity of Enzymatic Systems Theisen, Matthew K. Lafontaine Rivera, Jimmy G. Liao, James C. PLoS Comput Biol Research Article Stability in a metabolic system may not be obtained if incorrect amounts of enzymes are used. Without stability, some metabolites may accumulate or deplete leading to the irreversible loss of the desired operating point. Even if initial enzyme amounts achieve a stable steady state, changes in enzyme amount due to stochastic variations or environmental changes may move the system to the unstable region and lose the steady-state or quasi-steady-state flux. This situation is distinct from the phenomenon characterized by typical sensitivity analysis, which focuses on the smooth change before loss of stability. Here we show that metabolic networks differ significantly in their intrinsic ability to attain stability due to the network structure and kinetic forms, and that after achieving stability, some enzymes are prone to cause instability upon changes in enzyme amounts. We use Ensemble Modelling for Robustness Analysis (EMRA) to analyze stability in four cell-free enzymatic systems when enzyme amounts are changed. Loss of stability in continuous systems can lead to lower production even when the system is tested experimentally in batch experiments. The predictions of instability by EMRA are supported by the lower productivity in batch experimental tests. The EMRA method incorporates properties of network structure, including stoichiometry and kinetic form, but does not require specific parameter values of the enzymes. Public Library of Science 2016-03-10 /pmc/articles/PMC4786283/ /pubmed/26963521 http://dx.doi.org/10.1371/journal.pcbi.1004800 Text en © 2016 Theisen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Theisen, Matthew K. Lafontaine Rivera, Jimmy G. Liao, James C. Stability of Ensemble Models Predicts Productivity of Enzymatic Systems |
title | Stability of Ensemble Models Predicts Productivity of Enzymatic Systems |
title_full | Stability of Ensemble Models Predicts Productivity of Enzymatic Systems |
title_fullStr | Stability of Ensemble Models Predicts Productivity of Enzymatic Systems |
title_full_unstemmed | Stability of Ensemble Models Predicts Productivity of Enzymatic Systems |
title_short | Stability of Ensemble Models Predicts Productivity of Enzymatic Systems |
title_sort | stability of ensemble models predicts productivity of enzymatic systems |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786283/ https://www.ncbi.nlm.nih.gov/pubmed/26963521 http://dx.doi.org/10.1371/journal.pcbi.1004800 |
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