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A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli
Nitric oxide (NO•) is generated by the innate immune response to neutralize pathogens. NO• and its autoxidation products have an extensive biochemical reaction network that includes reactions with iron-sulfur clusters, DNA, and thiols. The fate of NO• inside a pathogen depends on a kinetic competiti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642044/ https://www.ncbi.nlm.nih.gov/pubmed/23658508 http://dx.doi.org/10.1371/journal.pcbi.1003049 |
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author | Robinson, Jonathan L. Brynildsen, Mark P. |
author_facet | Robinson, Jonathan L. Brynildsen, Mark P. |
author_sort | Robinson, Jonathan L. |
collection | PubMed |
description | Nitric oxide (NO•) is generated by the innate immune response to neutralize pathogens. NO• and its autoxidation products have an extensive biochemical reaction network that includes reactions with iron-sulfur clusters, DNA, and thiols. The fate of NO• inside a pathogen depends on a kinetic competition among its many targets, and is of critical importance to infection outcomes. Due to the complexity of the NO• biochemical network, where many intermediates are short-lived and at extremely low concentrations, several species can be measured, but stable products are non-unique, and damaged biomolecules are continually repaired or regenerated, kinetic models are required to understand and predict the outcome of NO• treatment. Here, we have constructed a comprehensive kinetic model that encompasses the broad reactivity of NO• in Escherichia coli. The incorporation of spontaneous and enzymatic reactions, as well as damage and repair of biomolecules, allowed for a detailed analysis of how NO• distributes in E. coli cultures. The model was informed with experimental measurements of NO• dynamics, and used to identify control parameters of the NO• distribution. Simulations predicted that NO• dioxygenase (Hmp) functions as a dominant NO• consumption pathway at O(2) concentrations as low as 35 µM (microaerobic), and interestingly, loses utility as the NO• delivery rate increases. We confirmed these predictions experimentally by measuring NO• dynamics in wild-type and mutant cultures at different NO• delivery rates and O(2) concentrations. These data suggest that the kinetics of NO• metabolism must be considered when assessing the importance of cellular components to NO• tolerance, and that models such as the one described here are necessary to rigorously investigate NO• stress in microbes. This model provides a platform to identify novel strategies to potentiate the effects of NO•, and will serve as a template from which analogous models can be generated for other organisms. |
format | Online Article Text |
id | pubmed-3642044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36420442013-05-08 A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli Robinson, Jonathan L. Brynildsen, Mark P. PLoS Comput Biol Research Article Nitric oxide (NO•) is generated by the innate immune response to neutralize pathogens. NO• and its autoxidation products have an extensive biochemical reaction network that includes reactions with iron-sulfur clusters, DNA, and thiols. The fate of NO• inside a pathogen depends on a kinetic competition among its many targets, and is of critical importance to infection outcomes. Due to the complexity of the NO• biochemical network, where many intermediates are short-lived and at extremely low concentrations, several species can be measured, but stable products are non-unique, and damaged biomolecules are continually repaired or regenerated, kinetic models are required to understand and predict the outcome of NO• treatment. Here, we have constructed a comprehensive kinetic model that encompasses the broad reactivity of NO• in Escherichia coli. The incorporation of spontaneous and enzymatic reactions, as well as damage and repair of biomolecules, allowed for a detailed analysis of how NO• distributes in E. coli cultures. The model was informed with experimental measurements of NO• dynamics, and used to identify control parameters of the NO• distribution. Simulations predicted that NO• dioxygenase (Hmp) functions as a dominant NO• consumption pathway at O(2) concentrations as low as 35 µM (microaerobic), and interestingly, loses utility as the NO• delivery rate increases. We confirmed these predictions experimentally by measuring NO• dynamics in wild-type and mutant cultures at different NO• delivery rates and O(2) concentrations. These data suggest that the kinetics of NO• metabolism must be considered when assessing the importance of cellular components to NO• tolerance, and that models such as the one described here are necessary to rigorously investigate NO• stress in microbes. This model provides a platform to identify novel strategies to potentiate the effects of NO•, and will serve as a template from which analogous models can be generated for other organisms. Public Library of Science 2013-05-02 /pmc/articles/PMC3642044/ /pubmed/23658508 http://dx.doi.org/10.1371/journal.pcbi.1003049 Text en © 2013 Robinson, Brynildsen 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 Robinson, Jonathan L. Brynildsen, Mark P. A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli |
title | A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli
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title_full | A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli
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title_fullStr | A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli
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title_full_unstemmed | A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli
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title_short | A Kinetic Platform to Determine the Fate of Nitric Oxide in Escherichia coli
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title_sort | kinetic platform to determine the fate of nitric oxide in escherichia coli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642044/ https://www.ncbi.nlm.nih.gov/pubmed/23658508 http://dx.doi.org/10.1371/journal.pcbi.1003049 |
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