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The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei

Inorganic polyphosphate (polyP) is ubiquitous across all forms of life, but the study of its metabolism has been mainly confined to bacteria and yeasts. Few reports detail the presence and accumulation of polyP in Archaea, and little information is available on its functions and regulation. Here, we...

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Autores principales: Paula, Fabiana S., Chin, Jason P., Schnürer, Anna, Müller, Bettina, Manesiotis, Panagiotis, Waters, Nicholas, Macintosh, Katrina A., Quinn, John P., Connolly, Jasmine, Abram, Florence, McGrath, John W., O’Flaherty, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864096/
https://www.ncbi.nlm.nih.gov/pubmed/31745137
http://dx.doi.org/10.1038/s41598-019-53168-4
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author Paula, Fabiana S.
Chin, Jason P.
Schnürer, Anna
Müller, Bettina
Manesiotis, Panagiotis
Waters, Nicholas
Macintosh, Katrina A.
Quinn, John P.
Connolly, Jasmine
Abram, Florence
McGrath, John W.
O’Flaherty, Vincent
author_facet Paula, Fabiana S.
Chin, Jason P.
Schnürer, Anna
Müller, Bettina
Manesiotis, Panagiotis
Waters, Nicholas
Macintosh, Katrina A.
Quinn, John P.
Connolly, Jasmine
Abram, Florence
McGrath, John W.
O’Flaherty, Vincent
author_sort Paula, Fabiana S.
collection PubMed
description Inorganic polyphosphate (polyP) is ubiquitous across all forms of life, but the study of its metabolism has been mainly confined to bacteria and yeasts. Few reports detail the presence and accumulation of polyP in Archaea, and little information is available on its functions and regulation. Here, we report that homologs of bacterial polyP metabolism proteins are present across the major taxa in the Archaea, suggesting that archaeal populations may have a greater contribution to global phosphorus cycling than has previously been recognised. We also demonstrate that polyP accumulation can be induced under strictly anaerobic conditions, in response to changes in phosphate (Pi) availability, i.e. Pi starvation, followed by incubation in Pi replete media (overplus), in cells of the methanogenic archaeon Methanosarcina mazei. Pi-starved M. mazei cells increased transcript abundance of the alkaline phosphatase (phoA) gene and of the high-affinity phosphate transport (pstSCAB-phoU) operon: no increase in polyphosphate kinase 1 (ppk1) transcript abundance was observed. Subsequent incubation of Pi-starved M. mazei cells under Pi replete conditions, led to a 237% increase in intracellular polyphosphate content and a > 5.7-fold increase in ppk1 gene transcripts. Ppk1 expression in M. mazei thus appears not to be under classical phosphate starvation control.
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spelling pubmed-68640962019-12-03 The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei Paula, Fabiana S. Chin, Jason P. Schnürer, Anna Müller, Bettina Manesiotis, Panagiotis Waters, Nicholas Macintosh, Katrina A. Quinn, John P. Connolly, Jasmine Abram, Florence McGrath, John W. O’Flaherty, Vincent Sci Rep Article Inorganic polyphosphate (polyP) is ubiquitous across all forms of life, but the study of its metabolism has been mainly confined to bacteria and yeasts. Few reports detail the presence and accumulation of polyP in Archaea, and little information is available on its functions and regulation. Here, we report that homologs of bacterial polyP metabolism proteins are present across the major taxa in the Archaea, suggesting that archaeal populations may have a greater contribution to global phosphorus cycling than has previously been recognised. We also demonstrate that polyP accumulation can be induced under strictly anaerobic conditions, in response to changes in phosphate (Pi) availability, i.e. Pi starvation, followed by incubation in Pi replete media (overplus), in cells of the methanogenic archaeon Methanosarcina mazei. Pi-starved M. mazei cells increased transcript abundance of the alkaline phosphatase (phoA) gene and of the high-affinity phosphate transport (pstSCAB-phoU) operon: no increase in polyphosphate kinase 1 (ppk1) transcript abundance was observed. Subsequent incubation of Pi-starved M. mazei cells under Pi replete conditions, led to a 237% increase in intracellular polyphosphate content and a > 5.7-fold increase in ppk1 gene transcripts. Ppk1 expression in M. mazei thus appears not to be under classical phosphate starvation control. Nature Publishing Group UK 2019-11-19 /pmc/articles/PMC6864096/ /pubmed/31745137 http://dx.doi.org/10.1038/s41598-019-53168-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Paula, Fabiana S.
Chin, Jason P.
Schnürer, Anna
Müller, Bettina
Manesiotis, Panagiotis
Waters, Nicholas
Macintosh, Katrina A.
Quinn, John P.
Connolly, Jasmine
Abram, Florence
McGrath, John W.
O’Flaherty, Vincent
The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei
title The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei
title_full The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei
title_fullStr The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei
title_full_unstemmed The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei
title_short The potential for polyphosphate metabolism in Archaea and anaerobic polyphosphate formation in Methanosarcina mazei
title_sort potential for polyphosphate metabolism in archaea and anaerobic polyphosphate formation in methanosarcina mazei
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864096/
https://www.ncbi.nlm.nih.gov/pubmed/31745137
http://dx.doi.org/10.1038/s41598-019-53168-4
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