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Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal
Energy metabolism is central to cellular biology. Thus, genome-scale models of heterotrophic unicellular species must account appropriately for the utilization of external nutrients to synthesize energy metabolites such as ATP. However, metabolic models designed for flux-balance analysis (FBA) may c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413070/ https://www.ncbi.nlm.nih.gov/pubmed/28419089 http://dx.doi.org/10.1371/journal.pcbi.1005494 |
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author | Fritzemeier, Claus Jonathan Hartleb, Daniel Szappanos, Balázs Papp, Balázs Lercher, Martin J. |
author_facet | Fritzemeier, Claus Jonathan Hartleb, Daniel Szappanos, Balázs Papp, Balázs Lercher, Martin J. |
author_sort | Fritzemeier, Claus Jonathan |
collection | PubMed |
description | Energy metabolism is central to cellular biology. Thus, genome-scale models of heterotrophic unicellular species must account appropriately for the utilization of external nutrients to synthesize energy metabolites such as ATP. However, metabolic models designed for flux-balance analysis (FBA) may contain thermodynamically impossible energy-generating cycles: without nutrient consumption, these models are still capable of charging energy metabolites (such as ADP→ATP or NADP(+)→NADPH). Here, we show that energy-generating cycles occur in over 85% of metabolic models without extensive manual curation, such as those contained in the ModelSEED and MetaNetX databases; in contrast, such cycles are rare in the manually curated models of the BiGG database. Energy generating cycles may represent model errors, e.g., erroneous assumptions on reaction reversibilities. Alternatively, part of the cycle may be thermodynamically feasible in one environment, while the remainder is thermodynamically feasible in another environment; as standard FBA does not account for thermodynamics, combining these into an FBA model allows erroneous energy generation. The presence of energy-generating cycles typically inflates maximal biomass production rates by 25%, and may lead to biases in evolutionary simulations. We present efficient computational methods (i) to identify energy generating cycles, using FBA, and (ii) to identify minimal sets of model changes that eliminate them, using a variant of the GlobalFit algorithm. |
format | Online Article Text |
id | pubmed-5413070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54130702017-05-14 Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal Fritzemeier, Claus Jonathan Hartleb, Daniel Szappanos, Balázs Papp, Balázs Lercher, Martin J. PLoS Comput Biol Research Article Energy metabolism is central to cellular biology. Thus, genome-scale models of heterotrophic unicellular species must account appropriately for the utilization of external nutrients to synthesize energy metabolites such as ATP. However, metabolic models designed for flux-balance analysis (FBA) may contain thermodynamically impossible energy-generating cycles: without nutrient consumption, these models are still capable of charging energy metabolites (such as ADP→ATP or NADP(+)→NADPH). Here, we show that energy-generating cycles occur in over 85% of metabolic models without extensive manual curation, such as those contained in the ModelSEED and MetaNetX databases; in contrast, such cycles are rare in the manually curated models of the BiGG database. Energy generating cycles may represent model errors, e.g., erroneous assumptions on reaction reversibilities. Alternatively, part of the cycle may be thermodynamically feasible in one environment, while the remainder is thermodynamically feasible in another environment; as standard FBA does not account for thermodynamics, combining these into an FBA model allows erroneous energy generation. The presence of energy-generating cycles typically inflates maximal biomass production rates by 25%, and may lead to biases in evolutionary simulations. We present efficient computational methods (i) to identify energy generating cycles, using FBA, and (ii) to identify minimal sets of model changes that eliminate them, using a variant of the GlobalFit algorithm. Public Library of Science 2017-04-18 /pmc/articles/PMC5413070/ /pubmed/28419089 http://dx.doi.org/10.1371/journal.pcbi.1005494 Text en © 2017 Fritzemeier 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 Fritzemeier, Claus Jonathan Hartleb, Daniel Szappanos, Balázs Papp, Balázs Lercher, Martin J. Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal |
title | Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal |
title_full | Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal |
title_fullStr | Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal |
title_full_unstemmed | Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal |
title_short | Erroneous energy-generating cycles in published genome scale metabolic networks: Identification and removal |
title_sort | erroneous energy-generating cycles in published genome scale metabolic networks: identification and removal |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413070/ https://www.ncbi.nlm.nih.gov/pubmed/28419089 http://dx.doi.org/10.1371/journal.pcbi.1005494 |
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