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In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces

Bacterial biomineralization is a widespread process that affects cycling of metals in the environment. Functionalized bacterial cell surfaces and exopolymers are thought to initiate mineral formation, however, direct evidences are hampered by technical challenges. Here, we present a breakthrough in...

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Autores principales: Couasnon, Thaïs, Alloyeau, Damien, Ménez, Bénédicte, Guyot, François, Ghigo, Jean-Marc, Gélabert, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455489/
https://www.ncbi.nlm.nih.gov/pubmed/32923582
http://dx.doi.org/10.1126/sciadv.aaz3125
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author Couasnon, Thaïs
Alloyeau, Damien
Ménez, Bénédicte
Guyot, François
Ghigo, Jean-Marc
Gélabert, Alexandre
author_facet Couasnon, Thaïs
Alloyeau, Damien
Ménez, Bénédicte
Guyot, François
Ghigo, Jean-Marc
Gélabert, Alexandre
author_sort Couasnon, Thaïs
collection PubMed
description Bacterial biomineralization is a widespread process that affects cycling of metals in the environment. Functionalized bacterial cell surfaces and exopolymers are thought to initiate mineral formation, however, direct evidences are hampered by technical challenges. Here, we present a breakthrough in the use of liquid-cell scanning transmission electron microscopy to observe mineral growth on bacteria and the exopolymers they secrete. Two Escherichia coli mutants producing distinct exopolymers are investigated. We use the incident electron beam to provoke and observe the precipitation of Mn-bearing minerals. Differences in the morphology and distribution of Mn precipitates on the two strains reflect differences in nucleation site density and accessibility. Direct observation under liquid conditions highlights the critical role of bacterial cell surface charges and exopolymer types in metal mineralization. This has strong environmental implications because biofilms structured by exopolymers are widespread in nature and constitute the main form of microbial life on Earth.
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spelling pubmed-74554892020-09-11 In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces Couasnon, Thaïs Alloyeau, Damien Ménez, Bénédicte Guyot, François Ghigo, Jean-Marc Gélabert, Alexandre Sci Adv Research Articles Bacterial biomineralization is a widespread process that affects cycling of metals in the environment. Functionalized bacterial cell surfaces and exopolymers are thought to initiate mineral formation, however, direct evidences are hampered by technical challenges. Here, we present a breakthrough in the use of liquid-cell scanning transmission electron microscopy to observe mineral growth on bacteria and the exopolymers they secrete. Two Escherichia coli mutants producing distinct exopolymers are investigated. We use the incident electron beam to provoke and observe the precipitation of Mn-bearing minerals. Differences in the morphology and distribution of Mn precipitates on the two strains reflect differences in nucleation site density and accessibility. Direct observation under liquid conditions highlights the critical role of bacterial cell surface charges and exopolymer types in metal mineralization. This has strong environmental implications because biofilms structured by exopolymers are widespread in nature and constitute the main form of microbial life on Earth. American Association for the Advancement of Science 2020-07-03 /pmc/articles/PMC7455489/ /pubmed/32923582 http://dx.doi.org/10.1126/sciadv.aaz3125 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Couasnon, Thaïs
Alloyeau, Damien
Ménez, Bénédicte
Guyot, François
Ghigo, Jean-Marc
Gélabert, Alexandre
In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces
title In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces
title_full In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces
title_fullStr In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces
title_full_unstemmed In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces
title_short In situ monitoring of exopolymer-dependent Mn mineralization on bacterial surfaces
title_sort in situ monitoring of exopolymer-dependent mn mineralization on bacterial surfaces
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455489/
https://www.ncbi.nlm.nih.gov/pubmed/32923582
http://dx.doi.org/10.1126/sciadv.aaz3125
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