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Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation
Shewanellae are gram-negative facultatively anaerobic metal-reducing bacteria commonly found in chemically (i.e., redox) stratified environments. Occupying such niches requires the ability to rapidly acclimate to changes in electron donor/acceptor type and availability; hence, the ability to compete...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891590/ https://www.ncbi.nlm.nih.gov/pubmed/20589080 http://dx.doi.org/10.1371/journal.pcbi.1000822 |
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author | Pinchuk, Grigoriy E. Hill, Eric A. Geydebrekht, Oleg V. De Ingeniis, Jessica Zhang, Xiaolin Osterman, Andrei Scott, James H. Reed, Samantha B. Romine, Margaret F. Konopka, Allan E. Beliaev, Alexander S. Fredrickson, Jim K. Reed, Jennifer L. |
author_facet | Pinchuk, Grigoriy E. Hill, Eric A. Geydebrekht, Oleg V. De Ingeniis, Jessica Zhang, Xiaolin Osterman, Andrei Scott, James H. Reed, Samantha B. Romine, Margaret F. Konopka, Allan E. Beliaev, Alexander S. Fredrickson, Jim K. Reed, Jennifer L. |
author_sort | Pinchuk, Grigoriy E. |
collection | PubMed |
description | Shewanellae are gram-negative facultatively anaerobic metal-reducing bacteria commonly found in chemically (i.e., redox) stratified environments. Occupying such niches requires the ability to rapidly acclimate to changes in electron donor/acceptor type and availability; hence, the ability to compete and thrive in such environments must ultimately be reflected in the organization and utilization of electron transfer networks, as well as central and peripheral carbon metabolism. To understand how Shewanella oneidensis MR-1 utilizes its resources, the metabolic network was reconstructed. The resulting network consists of 774 reactions, 783 genes, and 634 unique metabolites and contains biosynthesis pathways for all cell constituents. Using constraint-based modeling, we investigated aerobic growth of S. oneidensis MR-1 on numerous carbon sources. To achieve this, we (i) used experimental data to formulate a biomass equation and estimate cellular ATP requirements, (ii) developed an approach to identify cycles (such as futile cycles and circulations), (iii) classified how reaction usage affects cellular growth, (iv) predicted cellular biomass yields on different carbon sources and compared model predictions to experimental measurements, and (v) used experimental results to refine metabolic fluxes for growth on lactate. The results revealed that aerobic lactate-grown cells of S. oneidensis MR-1 used less efficient enzymes to couple electron transport to proton motive force generation, and possibly operated at least one futile cycle involving malic enzymes. Several examples are provided whereby model predictions were validated by experimental data, in particular the role of serine hydroxymethyltransferase and glycine cleavage system in the metabolism of one-carbon units, and growth on different sources of carbon and energy. This work illustrates how integration of computational and experimental efforts facilitates the understanding of microbial metabolism at a systems level. |
format | Text |
id | pubmed-2891590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28915902010-06-29 Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation Pinchuk, Grigoriy E. Hill, Eric A. Geydebrekht, Oleg V. De Ingeniis, Jessica Zhang, Xiaolin Osterman, Andrei Scott, James H. Reed, Samantha B. Romine, Margaret F. Konopka, Allan E. Beliaev, Alexander S. Fredrickson, Jim K. Reed, Jennifer L. PLoS Comput Biol Research Article Shewanellae are gram-negative facultatively anaerobic metal-reducing bacteria commonly found in chemically (i.e., redox) stratified environments. Occupying such niches requires the ability to rapidly acclimate to changes in electron donor/acceptor type and availability; hence, the ability to compete and thrive in such environments must ultimately be reflected in the organization and utilization of electron transfer networks, as well as central and peripheral carbon metabolism. To understand how Shewanella oneidensis MR-1 utilizes its resources, the metabolic network was reconstructed. The resulting network consists of 774 reactions, 783 genes, and 634 unique metabolites and contains biosynthesis pathways for all cell constituents. Using constraint-based modeling, we investigated aerobic growth of S. oneidensis MR-1 on numerous carbon sources. To achieve this, we (i) used experimental data to formulate a biomass equation and estimate cellular ATP requirements, (ii) developed an approach to identify cycles (such as futile cycles and circulations), (iii) classified how reaction usage affects cellular growth, (iv) predicted cellular biomass yields on different carbon sources and compared model predictions to experimental measurements, and (v) used experimental results to refine metabolic fluxes for growth on lactate. The results revealed that aerobic lactate-grown cells of S. oneidensis MR-1 used less efficient enzymes to couple electron transport to proton motive force generation, and possibly operated at least one futile cycle involving malic enzymes. Several examples are provided whereby model predictions were validated by experimental data, in particular the role of serine hydroxymethyltransferase and glycine cleavage system in the metabolism of one-carbon units, and growth on different sources of carbon and energy. This work illustrates how integration of computational and experimental efforts facilitates the understanding of microbial metabolism at a systems level. Public Library of Science 2010-06-24 /pmc/articles/PMC2891590/ /pubmed/20589080 http://dx.doi.org/10.1371/journal.pcbi.1000822 Text en Pinchuk 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pinchuk, Grigoriy E. Hill, Eric A. Geydebrekht, Oleg V. De Ingeniis, Jessica Zhang, Xiaolin Osterman, Andrei Scott, James H. Reed, Samantha B. Romine, Margaret F. Konopka, Allan E. Beliaev, Alexander S. Fredrickson, Jim K. Reed, Jennifer L. Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation |
title | Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation |
title_full | Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation |
title_fullStr | Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation |
title_full_unstemmed | Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation |
title_short | Constraint-Based Model of Shewanella oneidensis MR-1 Metabolism: A Tool for Data Analysis and Hypothesis Generation |
title_sort | constraint-based model of shewanella oneidensis mr-1 metabolism: a tool for data analysis and hypothesis generation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891590/ https://www.ncbi.nlm.nih.gov/pubmed/20589080 http://dx.doi.org/10.1371/journal.pcbi.1000822 |
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