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Genetic Optimization Algorithm for Metabolic Engineering Revisited

To date, several independent methods and algorithms exist for exploiting constraint-based stoichiometric models to find metabolic engineering strategies that optimize microbial production performance. Optimization procedures based on metaheuristics facilitate a straightforward adaption and expansion...

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Autores principales: Alter, Tobias B., Blank, Lars M., Ebert, Birgitta E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027426/
https://www.ncbi.nlm.nih.gov/pubmed/29772713
http://dx.doi.org/10.3390/metabo8020033
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author Alter, Tobias B.
Blank, Lars M.
Ebert, Birgitta E.
author_facet Alter, Tobias B.
Blank, Lars M.
Ebert, Birgitta E.
author_sort Alter, Tobias B.
collection PubMed
description To date, several independent methods and algorithms exist for exploiting constraint-based stoichiometric models to find metabolic engineering strategies that optimize microbial production performance. Optimization procedures based on metaheuristics facilitate a straightforward adaption and expansion of engineering objectives, as well as fitness functions, while being particularly suited for solving problems of high complexity. With the increasing interest in multi-scale models and a need for solving advanced engineering problems, we strive to advance genetic algorithms, which stand out due to their intuitive optimization principles and the proven usefulness in this field of research. A drawback of genetic algorithms is that premature convergence to sub-optimal solutions easily occurs if the optimization parameters are not adapted to the specific problem. Here, we conducted comprehensive parameter sensitivity analyses to study their impact on finding optimal strain designs. We further demonstrate the capability of genetic algorithms to simultaneously handle (i) multiple, non-linear engineering objectives; (ii) the identification of gene target-sets according to logical gene-protein-reaction associations; (iii) minimization of the number of network perturbations; and (iv) the insertion of non-native reactions, while employing genome-scale metabolic models. This framework adds a level of sophistication in terms of strain design robustness, which is exemplarily tested on succinate overproduction in Escherichia coli.
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spelling pubmed-60274262018-07-13 Genetic Optimization Algorithm for Metabolic Engineering Revisited Alter, Tobias B. Blank, Lars M. Ebert, Birgitta E. Metabolites Article To date, several independent methods and algorithms exist for exploiting constraint-based stoichiometric models to find metabolic engineering strategies that optimize microbial production performance. Optimization procedures based on metaheuristics facilitate a straightforward adaption and expansion of engineering objectives, as well as fitness functions, while being particularly suited for solving problems of high complexity. With the increasing interest in multi-scale models and a need for solving advanced engineering problems, we strive to advance genetic algorithms, which stand out due to their intuitive optimization principles and the proven usefulness in this field of research. A drawback of genetic algorithms is that premature convergence to sub-optimal solutions easily occurs if the optimization parameters are not adapted to the specific problem. Here, we conducted comprehensive parameter sensitivity analyses to study their impact on finding optimal strain designs. We further demonstrate the capability of genetic algorithms to simultaneously handle (i) multiple, non-linear engineering objectives; (ii) the identification of gene target-sets according to logical gene-protein-reaction associations; (iii) minimization of the number of network perturbations; and (iv) the insertion of non-native reactions, while employing genome-scale metabolic models. This framework adds a level of sophistication in terms of strain design robustness, which is exemplarily tested on succinate overproduction in Escherichia coli. MDPI 2018-05-16 /pmc/articles/PMC6027426/ /pubmed/29772713 http://dx.doi.org/10.3390/metabo8020033 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alter, Tobias B.
Blank, Lars M.
Ebert, Birgitta E.
Genetic Optimization Algorithm for Metabolic Engineering Revisited
title Genetic Optimization Algorithm for Metabolic Engineering Revisited
title_full Genetic Optimization Algorithm for Metabolic Engineering Revisited
title_fullStr Genetic Optimization Algorithm for Metabolic Engineering Revisited
title_full_unstemmed Genetic Optimization Algorithm for Metabolic Engineering Revisited
title_short Genetic Optimization Algorithm for Metabolic Engineering Revisited
title_sort genetic optimization algorithm for metabolic engineering revisited
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027426/
https://www.ncbi.nlm.nih.gov/pubmed/29772713
http://dx.doi.org/10.3390/metabo8020033
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