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An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
BACKGROUND: Yersinia pestis is a gram-negative bacterium that causes plague, a disease linked historically to the Black Death in Europe during the Middle Ages and to several outbreaks during the modern era. Metabolism in Y. pestis displays remarkable flexibility and robustness, allowing the bacteriu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220653/ https://www.ncbi.nlm.nih.gov/pubmed/21995956 http://dx.doi.org/10.1186/1752-0509-5-163 |
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author | Charusanti, Pep Chauhan, Sadhana McAteer, Kathleen Lerman, Joshua A Hyduke, Daniel R Motin, Vladimir L Ansong, Charles Adkins, Joshua N Palsson, Bernhard O |
author_facet | Charusanti, Pep Chauhan, Sadhana McAteer, Kathleen Lerman, Joshua A Hyduke, Daniel R Motin, Vladimir L Ansong, Charles Adkins, Joshua N Palsson, Bernhard O |
author_sort | Charusanti, Pep |
collection | PubMed |
description | BACKGROUND: Yersinia pestis is a gram-negative bacterium that causes plague, a disease linked historically to the Black Death in Europe during the Middle Ages and to several outbreaks during the modern era. Metabolism in Y. pestis displays remarkable flexibility and robustness, allowing the bacterium to proliferate in both warm-blooded mammalian hosts and cold-blooded insect vectors such as fleas. RESULTS: Here we report a genome-scale reconstruction and mathematical model of metabolism for Y. pestis CO92 and supporting experimental growth and metabolite measurements. The model contains 815 genes, 678 proteins, 963 unique metabolites and 1678 reactions, accurately simulates growth on a range of carbon sources both qualitatively and quantitatively, and identifies gaps in several key biosynthetic pathways and suggests how those gaps might be filled. Furthermore, our model presents hypotheses to explain certain known nutritional requirements characteristic of this strain. CONCLUSIONS: Y. pestis continues to be a dangerous threat to human health during modern times. The Y. pestis genome-scale metabolic reconstruction presented here, which has been benchmarked against experimental data and correctly reproduces known phenotypes, provides an in silico platform with which to investigate the metabolism of this important human pathogen. |
format | Online Article Text |
id | pubmed-3220653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32206532011-11-21 An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 Charusanti, Pep Chauhan, Sadhana McAteer, Kathleen Lerman, Joshua A Hyduke, Daniel R Motin, Vladimir L Ansong, Charles Adkins, Joshua N Palsson, Bernhard O BMC Syst Biol Research Article BACKGROUND: Yersinia pestis is a gram-negative bacterium that causes plague, a disease linked historically to the Black Death in Europe during the Middle Ages and to several outbreaks during the modern era. Metabolism in Y. pestis displays remarkable flexibility and robustness, allowing the bacterium to proliferate in both warm-blooded mammalian hosts and cold-blooded insect vectors such as fleas. RESULTS: Here we report a genome-scale reconstruction and mathematical model of metabolism for Y. pestis CO92 and supporting experimental growth and metabolite measurements. The model contains 815 genes, 678 proteins, 963 unique metabolites and 1678 reactions, accurately simulates growth on a range of carbon sources both qualitatively and quantitatively, and identifies gaps in several key biosynthetic pathways and suggests how those gaps might be filled. Furthermore, our model presents hypotheses to explain certain known nutritional requirements characteristic of this strain. CONCLUSIONS: Y. pestis continues to be a dangerous threat to human health during modern times. The Y. pestis genome-scale metabolic reconstruction presented here, which has been benchmarked against experimental data and correctly reproduces known phenotypes, provides an in silico platform with which to investigate the metabolism of this important human pathogen. BioMed Central 2011-10-13 /pmc/articles/PMC3220653/ /pubmed/21995956 http://dx.doi.org/10.1186/1752-0509-5-163 Text en Copyright ©2011 Charusanti 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 Article Charusanti, Pep Chauhan, Sadhana McAteer, Kathleen Lerman, Joshua A Hyduke, Daniel R Motin, Vladimir L Ansong, Charles Adkins, Joshua N Palsson, Bernhard O An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 |
title | An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 |
title_full | An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 |
title_fullStr | An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 |
title_full_unstemmed | An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 |
title_short | An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 |
title_sort | experimentally-supported genome-scale metabolic network reconstruction for yersinia pestis co92 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220653/ https://www.ncbi.nlm.nih.gov/pubmed/21995956 http://dx.doi.org/10.1186/1752-0509-5-163 |
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