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In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure

Following observations of survival of microbes and other life forms in deep subsurface environments it is necessary to understand their biological functioning under high pressure conditions. Key aspects of biochemical reactions and transport processes within cells are determined by the intracellular...

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Autores principales: Foglia, Fabrizia, Hazael, Rachael, Meersman, Filip, Wilding, Martin C., Sakai, Victoria García, Rogers, Sarah, Bove, Livia E., Koza, Michael Marek, Moulin, Martine, Haertlein, Michael, Forsyth, V. Trevor, McMillan, Paul F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581952/
https://www.ncbi.nlm.nih.gov/pubmed/31213614
http://dx.doi.org/10.1038/s41598-019-44704-3
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author Foglia, Fabrizia
Hazael, Rachael
Meersman, Filip
Wilding, Martin C.
Sakai, Victoria García
Rogers, Sarah
Bove, Livia E.
Koza, Michael Marek
Moulin, Martine
Haertlein, Michael
Forsyth, V. Trevor
McMillan, Paul F.
author_facet Foglia, Fabrizia
Hazael, Rachael
Meersman, Filip
Wilding, Martin C.
Sakai, Victoria García
Rogers, Sarah
Bove, Livia E.
Koza, Michael Marek
Moulin, Martine
Haertlein, Michael
Forsyth, V. Trevor
McMillan, Paul F.
author_sort Foglia, Fabrizia
collection PubMed
description Following observations of survival of microbes and other life forms in deep subsurface environments it is necessary to understand their biological functioning under high pressure conditions. Key aspects of biochemical reactions and transport processes within cells are determined by the intracellular water dynamics. We studied water diffusion and rotational relaxation in live Shewanella oneidensis bacteria at pressures up to 500 MPa using quasi-elastic neutron scattering (QENS). The intracellular diffusion exhibits a significantly greater slowdown (by −10–30%) and an increase in rotational relaxation times (+10–40%) compared with water dynamics in the aqueous solutions used to resuspend the bacterial samples. Those results indicate both a pressure-induced viscosity increase and slowdown in ionic/macromolecular transport properties within the cells affecting the rates of metabolic and other biological processes. Our new data support emerging models for intracellular organisation with nanoscale water channels threading between macromolecular regions within a dynamically organized structure rather than a homogenous gel-like cytoplasm.
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spelling pubmed-65819522019-06-26 In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure Foglia, Fabrizia Hazael, Rachael Meersman, Filip Wilding, Martin C. Sakai, Victoria García Rogers, Sarah Bove, Livia E. Koza, Michael Marek Moulin, Martine Haertlein, Michael Forsyth, V. Trevor McMillan, Paul F. Sci Rep Article Following observations of survival of microbes and other life forms in deep subsurface environments it is necessary to understand their biological functioning under high pressure conditions. Key aspects of biochemical reactions and transport processes within cells are determined by the intracellular water dynamics. We studied water diffusion and rotational relaxation in live Shewanella oneidensis bacteria at pressures up to 500 MPa using quasi-elastic neutron scattering (QENS). The intracellular diffusion exhibits a significantly greater slowdown (by −10–30%) and an increase in rotational relaxation times (+10–40%) compared with water dynamics in the aqueous solutions used to resuspend the bacterial samples. Those results indicate both a pressure-induced viscosity increase and slowdown in ionic/macromolecular transport properties within the cells affecting the rates of metabolic and other biological processes. Our new data support emerging models for intracellular organisation with nanoscale water channels threading between macromolecular regions within a dynamically organized structure rather than a homogenous gel-like cytoplasm. Nature Publishing Group UK 2019-06-18 /pmc/articles/PMC6581952/ /pubmed/31213614 http://dx.doi.org/10.1038/s41598-019-44704-3 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
Foglia, Fabrizia
Hazael, Rachael
Meersman, Filip
Wilding, Martin C.
Sakai, Victoria García
Rogers, Sarah
Bove, Livia E.
Koza, Michael Marek
Moulin, Martine
Haertlein, Michael
Forsyth, V. Trevor
McMillan, Paul F.
In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure
title In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure
title_full In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure
title_fullStr In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure
title_full_unstemmed In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure
title_short In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure
title_sort in vivo water dynamics in shewanella oneidensis bacteria at high pressure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581952/
https://www.ncbi.nlm.nih.gov/pubmed/31213614
http://dx.doi.org/10.1038/s41598-019-44704-3
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