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Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes

Microbial electrochemical technologies (METs) rely on the control of interactions between microorganisms and electronic devices, enabling to transform chemical energy into electricity. We report a new approach to construct ready‐to‐use artificial bioelectrodes by immobilizing Geobacter sulfurreducen...

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Autores principales: Estevez‐Canales, Marta, Pinto, David, Coradin, Thibaud, Laberty‐Robert, Christel, Esteve‐Núñez, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743811/
https://www.ncbi.nlm.nih.gov/pubmed/28401700
http://dx.doi.org/10.1111/1751-7915.12561
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author Estevez‐Canales, Marta
Pinto, David
Coradin, Thibaud
Laberty‐Robert, Christel
Esteve‐Núñez, Abraham
author_facet Estevez‐Canales, Marta
Pinto, David
Coradin, Thibaud
Laberty‐Robert, Christel
Esteve‐Núñez, Abraham
author_sort Estevez‐Canales, Marta
collection PubMed
description Microbial electrochemical technologies (METs) rely on the control of interactions between microorganisms and electronic devices, enabling to transform chemical energy into electricity. We report a new approach to construct ready‐to‐use artificial bioelectrodes by immobilizing Geobacter sulfurreducens cells in composite materials associating silica gel and carbon felt fibres. Viability test confirmed that the majority of bacteria (ca. 70 ± 5%) survived the encapsulation process in silica and that cell density did not increase in 96 h. The double entrapment within the silica–carbon composite prevented bacterial release from the electrode but allowed a suitable mass transport (ca. 5 min after electron donor pulse), making the electrochemical characterization of the system possible. The artificial bioelectrodes were evaluated in three‐electrode reactors and the maximum current displayed was ca. 220 and 150 μA cm(−3) using acetate and lactate as electron donors respectively. Cyclic voltammetry of acetate‐fed bioelectrodes revealed a sigmoidal catalytic oxidation wave, typical of more advanced‐stage biofilms. The presence of G. sulfurreducens within composites was ascertained by SEM analysis, suggesting that only part of the bacterial population was in direct contact with the carbon fibres. Preliminary analyses of the transcriptomic response of immobilized G. sulfurreducens enlightened that encapsulation mainly induces an osmotic stress to the cells. Therefore, ready‐to‐use artificial bioelectrodes represent a versatile time‐ and cost‐saving strategy for microbial electrochemical systems.
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spelling pubmed-57438112018-01-03 Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes Estevez‐Canales, Marta Pinto, David Coradin, Thibaud Laberty‐Robert, Christel Esteve‐Núñez, Abraham Microb Biotechnol Research Articles Microbial electrochemical technologies (METs) rely on the control of interactions between microorganisms and electronic devices, enabling to transform chemical energy into electricity. We report a new approach to construct ready‐to‐use artificial bioelectrodes by immobilizing Geobacter sulfurreducens cells in composite materials associating silica gel and carbon felt fibres. Viability test confirmed that the majority of bacteria (ca. 70 ± 5%) survived the encapsulation process in silica and that cell density did not increase in 96 h. The double entrapment within the silica–carbon composite prevented bacterial release from the electrode but allowed a suitable mass transport (ca. 5 min after electron donor pulse), making the electrochemical characterization of the system possible. The artificial bioelectrodes were evaluated in three‐electrode reactors and the maximum current displayed was ca. 220 and 150 μA cm(−3) using acetate and lactate as electron donors respectively. Cyclic voltammetry of acetate‐fed bioelectrodes revealed a sigmoidal catalytic oxidation wave, typical of more advanced‐stage biofilms. The presence of G. sulfurreducens within composites was ascertained by SEM analysis, suggesting that only part of the bacterial population was in direct contact with the carbon fibres. Preliminary analyses of the transcriptomic response of immobilized G. sulfurreducens enlightened that encapsulation mainly induces an osmotic stress to the cells. Therefore, ready‐to‐use artificial bioelectrodes represent a versatile time‐ and cost‐saving strategy for microbial electrochemical systems. John Wiley and Sons Inc. 2017-04-11 /pmc/articles/PMC5743811/ /pubmed/28401700 http://dx.doi.org/10.1111/1751-7915.12561 Text en © 2017 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Estevez‐Canales, Marta
Pinto, David
Coradin, Thibaud
Laberty‐Robert, Christel
Esteve‐Núñez, Abraham
Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
title Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
title_full Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
title_fullStr Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
title_full_unstemmed Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
title_short Silica immobilization of Geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
title_sort silica immobilization of geobacter sulfurreducens for constructing ready‐to‐use artificial bioelectrodes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743811/
https://www.ncbi.nlm.nih.gov/pubmed/28401700
http://dx.doi.org/10.1111/1751-7915.12561
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