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Optimization of biotechnological systems through geometric programming
BACKGROUND: In the past, tasks of model based yield optimization in metabolic engineering were either approached with stoichiometric models or with structured nonlinear models such as S-systems or linear-logarithmic representations. These models stand out among most others, because they allow the op...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2231360/ https://www.ncbi.nlm.nih.gov/pubmed/17897440 http://dx.doi.org/10.1186/1742-4682-4-38 |
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author | Marin-Sanguino, Alberto Voit, Eberhard O Gonzalez-Alcon, Carlos Torres, Nestor V |
author_facet | Marin-Sanguino, Alberto Voit, Eberhard O Gonzalez-Alcon, Carlos Torres, Nestor V |
author_sort | Marin-Sanguino, Alberto |
collection | PubMed |
description | BACKGROUND: In the past, tasks of model based yield optimization in metabolic engineering were either approached with stoichiometric models or with structured nonlinear models such as S-systems or linear-logarithmic representations. These models stand out among most others, because they allow the optimization task to be converted into a linear program, for which efficient solution methods are widely available. For pathway models not in one of these formats, an Indirect Optimization Method (IOM) was developed where the original model is sequentially represented as an S-system model, optimized in this format with linear programming methods, reinterpreted in the initial model form, and further optimized as necessary. RESULTS: A new method is proposed for this task. We show here that the model format of a Generalized Mass Action (GMA) system may be optimized very efficiently with techniques of geometric programming. We briefly review the basics of GMA systems and of geometric programming, demonstrate how the latter may be applied to the former, and illustrate the combined method with a didactic problem and two examples based on models of real systems. The first is a relatively small yet representative model of the anaerobic fermentation pathway in S. cerevisiae, while the second describes the dynamics of the tryptophan operon in E. coli. Both models have previously been used for benchmarking purposes, thus facilitating comparisons with the proposed new method. In these comparisons, the geometric programming method was found to be equal or better than the earlier methods in terms of successful identification of optima and efficiency. CONCLUSION: GMA systems are of importance, because they contain stoichiometric, mass action and S-systems as special cases, along with many other models. Furthermore, it was previously shown that algebraic equivalence transformations of variables are sufficient to convert virtually any types of dynamical models into the GMA form. Thus, efficient methods for optimizing GMA systems have multifold appeal. |
format | Text |
id | pubmed-2231360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22313602008-02-06 Optimization of biotechnological systems through geometric programming Marin-Sanguino, Alberto Voit, Eberhard O Gonzalez-Alcon, Carlos Torres, Nestor V Theor Biol Med Model Research BACKGROUND: In the past, tasks of model based yield optimization in metabolic engineering were either approached with stoichiometric models or with structured nonlinear models such as S-systems or linear-logarithmic representations. These models stand out among most others, because they allow the optimization task to be converted into a linear program, for which efficient solution methods are widely available. For pathway models not in one of these formats, an Indirect Optimization Method (IOM) was developed where the original model is sequentially represented as an S-system model, optimized in this format with linear programming methods, reinterpreted in the initial model form, and further optimized as necessary. RESULTS: A new method is proposed for this task. We show here that the model format of a Generalized Mass Action (GMA) system may be optimized very efficiently with techniques of geometric programming. We briefly review the basics of GMA systems and of geometric programming, demonstrate how the latter may be applied to the former, and illustrate the combined method with a didactic problem and two examples based on models of real systems. The first is a relatively small yet representative model of the anaerobic fermentation pathway in S. cerevisiae, while the second describes the dynamics of the tryptophan operon in E. coli. Both models have previously been used for benchmarking purposes, thus facilitating comparisons with the proposed new method. In these comparisons, the geometric programming method was found to be equal or better than the earlier methods in terms of successful identification of optima and efficiency. CONCLUSION: GMA systems are of importance, because they contain stoichiometric, mass action and S-systems as special cases, along with many other models. Furthermore, it was previously shown that algebraic equivalence transformations of variables are sufficient to convert virtually any types of dynamical models into the GMA form. Thus, efficient methods for optimizing GMA systems have multifold appeal. BioMed Central 2007-09-26 /pmc/articles/PMC2231360/ /pubmed/17897440 http://dx.doi.org/10.1186/1742-4682-4-38 Text en Copyright © 2007 Marin-Sanguino et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Marin-Sanguino, Alberto Voit, Eberhard O Gonzalez-Alcon, Carlos Torres, Nestor V Optimization of biotechnological systems through geometric programming |
title | Optimization of biotechnological systems through geometric programming |
title_full | Optimization of biotechnological systems through geometric programming |
title_fullStr | Optimization of biotechnological systems through geometric programming |
title_full_unstemmed | Optimization of biotechnological systems through geometric programming |
title_short | Optimization of biotechnological systems through geometric programming |
title_sort | optimization of biotechnological systems through geometric programming |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2231360/ https://www.ncbi.nlm.nih.gov/pubmed/17897440 http://dx.doi.org/10.1186/1742-4682-4-38 |
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