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Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing

Microbial biosensors can be an excellent alternative to classical methods for toxicity monitoring, which are time-consuming and not sensitive enough. However, bacteria typically connect to electrodes through biofilm formation, leading to problems due to lack of uniformity or long device production t...

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Detalles Bibliográficos
Autores principales: Uria, N., Fiset, E., Pellitero, M. Aller, Muñoz, F.X., Rabaey, K., Campo, F.J.del
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488082/
https://www.ncbi.nlm.nih.gov/pubmed/36159604
http://dx.doi.org/10.1016/j.ese.2020.100053
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author Uria, N.
Fiset, E.
Pellitero, M. Aller
Muñoz, F.X.
Rabaey, K.
Campo, F.J.del
author_facet Uria, N.
Fiset, E.
Pellitero, M. Aller
Muñoz, F.X.
Rabaey, K.
Campo, F.J.del
author_sort Uria, N.
collection PubMed
description Microbial biosensors can be an excellent alternative to classical methods for toxicity monitoring, which are time-consuming and not sensitive enough. However, bacteria typically connect to electrodes through biofilm formation, leading to problems due to lack of uniformity or long device production times. A suitable immobilisation technique can overcome these challenges. Still, they may respond more slowly than biofilm-based electrodes because bacteria gradually adapt to electron transfer during biofilm formation. In this study, we propose a controlled and reproducible way to fabricate bacteria-modified electrodes. The method consists of an immobilisation step using a cellulose matrix, followed by an electrode polarization in the presence of ferricyanide and glucose. Our process is short, reproducible and led us to obtain ready-to-use electrodes featuring a high-current response. An excellent shelf-life of the immobilised electrochemically active bacteria was demonstrated for up to one year. After an initial 50% activity loss in the first month, no further declines have been observed over the following 11 months. We implemented our bacteria-modified electrodes to fabricate a lateral flow platform for toxicity monitoring using formaldehyde (3%). Its addition led to a 59% current decrease approximately 20 min after the toxic input. The methods presented here offer the ability to develop a high sensitivity, easy to produce, and long shelf life bacteria-based toxicity detectors.
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spelling pubmed-94880822022-09-23 Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing Uria, N. Fiset, E. Pellitero, M. Aller Muñoz, F.X. Rabaey, K. Campo, F.J.del Environ Sci Ecotechnol Original Research Microbial biosensors can be an excellent alternative to classical methods for toxicity monitoring, which are time-consuming and not sensitive enough. However, bacteria typically connect to electrodes through biofilm formation, leading to problems due to lack of uniformity or long device production times. A suitable immobilisation technique can overcome these challenges. Still, they may respond more slowly than biofilm-based electrodes because bacteria gradually adapt to electron transfer during biofilm formation. In this study, we propose a controlled and reproducible way to fabricate bacteria-modified electrodes. The method consists of an immobilisation step using a cellulose matrix, followed by an electrode polarization in the presence of ferricyanide and glucose. Our process is short, reproducible and led us to obtain ready-to-use electrodes featuring a high-current response. An excellent shelf-life of the immobilised electrochemically active bacteria was demonstrated for up to one year. After an initial 50% activity loss in the first month, no further declines have been observed over the following 11 months. We implemented our bacteria-modified electrodes to fabricate a lateral flow platform for toxicity monitoring using formaldehyde (3%). Its addition led to a 59% current decrease approximately 20 min after the toxic input. The methods presented here offer the ability to develop a high sensitivity, easy to produce, and long shelf life bacteria-based toxicity detectors. Elsevier 2020-07-12 /pmc/articles/PMC9488082/ /pubmed/36159604 http://dx.doi.org/10.1016/j.ese.2020.100053 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Uria, N.
Fiset, E.
Pellitero, M. Aller
Muñoz, F.X.
Rabaey, K.
Campo, F.J.del
Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
title Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
title_full Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
title_fullStr Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
title_full_unstemmed Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
title_short Immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
title_sort immobilisation of electrochemically active bacteria on screen-printed electrodes for rapid in situ toxicity biosensing
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488082/
https://www.ncbi.nlm.nih.gov/pubmed/36159604
http://dx.doi.org/10.1016/j.ese.2020.100053
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