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Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer
Microbial biomineralization sometimes leads to periplasmic encrustation, which is predicted to enhance microorganism preservation in the fossil record. Mineral precipitation within the periplasm is, however, thought to induce death, as a result of permeability loss preventing nutrient and waste tran...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562303/ https://www.ncbi.nlm.nih.gov/pubmed/26441847 http://dx.doi.org/10.3389/fmicb.2015.00879 |
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author | Miot, Jennyfer Remusat, Laurent Duprat, Elodie Gonzalez, Adriana Pont, Sylvain Poinsot, Mélanie |
author_facet | Miot, Jennyfer Remusat, Laurent Duprat, Elodie Gonzalez, Adriana Pont, Sylvain Poinsot, Mélanie |
author_sort | Miot, Jennyfer |
collection | PubMed |
description | Microbial biomineralization sometimes leads to periplasmic encrustation, which is predicted to enhance microorganism preservation in the fossil record. Mineral precipitation within the periplasm is, however, thought to induce death, as a result of permeability loss preventing nutrient and waste transit across the cell wall. This hypothesis had, however, never been investigated down to the single cell level. Here, we cultured the nitrate reducing Fe(II) oxidizing bacteria Acidovorax sp. strain BoFeN1 that have been previously shown to promote the precipitation of a diversity of Fe minerals (lepidocrocite, goethite, Fe phosphate) encrusting the periplasm. We investigated the connection of Fe biomineralization with carbon assimilation at the single cell level, using a combination of electron microscopy and Nano-Secondary Ion Mass Spectrometry. Our analyses revealed strong individual heterogeneities of Fe biomineralization. Noteworthy, a small proportion of cells remaining free of any precipitate persisted even at advanced stages of biomineralization. Using pulse chase experiments with (13)C-acetate, we provide evidence of individual phenotypic heterogeneities of carbon assimilation, correlated with the level of Fe biomineralization. Whereas non- and moderately encrusted cells were able to assimilate acetate, higher levels of periplasmic encrustation prevented any carbon incorporation. Carbon assimilation only depended on the level of Fe encrustation and not on the nature of Fe minerals precipitated in the cell wall. Carbon assimilation decreased exponentially with increasing cell-associated Fe content. Persistence of a small proportion of non-mineralized and metabolically active cells might constitute a survival strategy in highly ferruginous environments. Eventually, our results suggest that periplasmic Fe biomineralization may provide a signature of individual metabolic status, which could be looked for in the fossil record and in modern environmental samples. |
format | Online Article Text |
id | pubmed-4562303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45623032015-10-05 Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer Miot, Jennyfer Remusat, Laurent Duprat, Elodie Gonzalez, Adriana Pont, Sylvain Poinsot, Mélanie Front Microbiol Microbiology Microbial biomineralization sometimes leads to periplasmic encrustation, which is predicted to enhance microorganism preservation in the fossil record. Mineral precipitation within the periplasm is, however, thought to induce death, as a result of permeability loss preventing nutrient and waste transit across the cell wall. This hypothesis had, however, never been investigated down to the single cell level. Here, we cultured the nitrate reducing Fe(II) oxidizing bacteria Acidovorax sp. strain BoFeN1 that have been previously shown to promote the precipitation of a diversity of Fe minerals (lepidocrocite, goethite, Fe phosphate) encrusting the periplasm. We investigated the connection of Fe biomineralization with carbon assimilation at the single cell level, using a combination of electron microscopy and Nano-Secondary Ion Mass Spectrometry. Our analyses revealed strong individual heterogeneities of Fe biomineralization. Noteworthy, a small proportion of cells remaining free of any precipitate persisted even at advanced stages of biomineralization. Using pulse chase experiments with (13)C-acetate, we provide evidence of individual phenotypic heterogeneities of carbon assimilation, correlated with the level of Fe biomineralization. Whereas non- and moderately encrusted cells were able to assimilate acetate, higher levels of periplasmic encrustation prevented any carbon incorporation. Carbon assimilation only depended on the level of Fe encrustation and not on the nature of Fe minerals precipitated in the cell wall. Carbon assimilation decreased exponentially with increasing cell-associated Fe content. Persistence of a small proportion of non-mineralized and metabolically active cells might constitute a survival strategy in highly ferruginous environments. Eventually, our results suggest that periplasmic Fe biomineralization may provide a signature of individual metabolic status, which could be looked for in the fossil record and in modern environmental samples. Frontiers Media S.A. 2015-09-08 /pmc/articles/PMC4562303/ /pubmed/26441847 http://dx.doi.org/10.3389/fmicb.2015.00879 Text en Copyright © 2015 Miot, Remusat, Duprat, Gonzalez, Pont and Poinsot. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Miot, Jennyfer Remusat, Laurent Duprat, Elodie Gonzalez, Adriana Pont, Sylvain Poinsot, Mélanie Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer |
title | Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer |
title_full | Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer |
title_fullStr | Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer |
title_full_unstemmed | Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer |
title_short | Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer |
title_sort | fe biomineralization mirrors individual metabolic activity in a nitrate-dependent fe(ii)-oxidizer |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562303/ https://www.ncbi.nlm.nih.gov/pubmed/26441847 http://dx.doi.org/10.3389/fmicb.2015.00879 |
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