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Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis

BACKGROUND: Methanogenic Archaea play key metabolic roles in anaerobic ecosystems, where they use H(2 )and other substrates to produce methane. Methanococcus maripaludis is a model for studies of the global response to nutrient limitations. RESULTS: We used high-coverage quantitative proteomics to d...

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Autores principales: Xia, Qiangwei, Wang, Tiansong, Hendrickson, Erik L, Lie, Thomas J, Hackett, Murray, Leigh, John A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723118/
https://www.ncbi.nlm.nih.gov/pubmed/19627604
http://dx.doi.org/10.1186/1471-2180-9-149
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author Xia, Qiangwei
Wang, Tiansong
Hendrickson, Erik L
Lie, Thomas J
Hackett, Murray
Leigh, John A
author_facet Xia, Qiangwei
Wang, Tiansong
Hendrickson, Erik L
Lie, Thomas J
Hackett, Murray
Leigh, John A
author_sort Xia, Qiangwei
collection PubMed
description BACKGROUND: Methanogenic Archaea play key metabolic roles in anaerobic ecosystems, where they use H(2 )and other substrates to produce methane. Methanococcus maripaludis is a model for studies of the global response to nutrient limitations. RESULTS: We used high-coverage quantitative proteomics to determine the response of M. maripaludis to growth-limiting levels of H(2), nitrogen, and phosphate. Six to ten percent of the proteome changed significantly with each nutrient limitation. H(2 )limitation increased the abundance of a wide variety of proteins involved in methanogenesis. However, one protein involved in methanogenesis decreased: a low-affinity [Fe] hydrogenase, which may dominate over a higher-affinity mechanism when H(2 )is abundant. Nitrogen limitation increased known nitrogen assimilation proteins. In addition, the increased abundance of molybdate transport proteins suggested they function for nitrogen fixation. An apparent regulon governed by the euryarchaeal nitrogen regulator NrpR is discussed. Phosphate limitation increased the abundance of three different sets of proteins, suggesting that all three function in phosphate transport. CONCLUSION: The global proteomic response of M. maripaludis to each nutrient limitation suggests a wider response than previously appreciated. The results give new insight into the function of several proteins, as well as providing information that should contribute to the formulation of a regulatory network model.
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spelling pubmed-27231182009-08-08 Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis Xia, Qiangwei Wang, Tiansong Hendrickson, Erik L Lie, Thomas J Hackett, Murray Leigh, John A BMC Microbiol Research article BACKGROUND: Methanogenic Archaea play key metabolic roles in anaerobic ecosystems, where they use H(2 )and other substrates to produce methane. Methanococcus maripaludis is a model for studies of the global response to nutrient limitations. RESULTS: We used high-coverage quantitative proteomics to determine the response of M. maripaludis to growth-limiting levels of H(2), nitrogen, and phosphate. Six to ten percent of the proteome changed significantly with each nutrient limitation. H(2 )limitation increased the abundance of a wide variety of proteins involved in methanogenesis. However, one protein involved in methanogenesis decreased: a low-affinity [Fe] hydrogenase, which may dominate over a higher-affinity mechanism when H(2 )is abundant. Nitrogen limitation increased known nitrogen assimilation proteins. In addition, the increased abundance of molybdate transport proteins suggested they function for nitrogen fixation. An apparent regulon governed by the euryarchaeal nitrogen regulator NrpR is discussed. Phosphate limitation increased the abundance of three different sets of proteins, suggesting that all three function in phosphate transport. CONCLUSION: The global proteomic response of M. maripaludis to each nutrient limitation suggests a wider response than previously appreciated. The results give new insight into the function of several proteins, as well as providing information that should contribute to the formulation of a regulatory network model. BioMed Central 2009-07-23 /pmc/articles/PMC2723118/ /pubmed/19627604 http://dx.doi.org/10.1186/1471-2180-9-149 Text en Copyright ©2009 Xia 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
Xia, Qiangwei
Wang, Tiansong
Hendrickson, Erik L
Lie, Thomas J
Hackett, Murray
Leigh, John A
Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis
title Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis
title_full Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis
title_fullStr Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis
title_full_unstemmed Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis
title_short Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis
title_sort quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen methanococcus maripaludis
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723118/
https://www.ncbi.nlm.nih.gov/pubmed/19627604
http://dx.doi.org/10.1186/1471-2180-9-149
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