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Carboxylate Functional Groups Mediate Interaction with Silver Nanoparticles in Biofilm Matrix
[Image: see text] Biofilms causing medical conditions or interfering with technical applications can prove undesirably resistant to silver nanoparticle (AgNP)-based antimicrobial treatment, whereas beneficial biofilms may be adversely affected by the released silver nanoparticles. Isolated biofilm m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044607/ https://www.ncbi.nlm.nih.gov/pubmed/30023786 http://dx.doi.org/10.1021/acsomega.7b00982 |
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author | Sambalova, Olga Thorwarth, Kerstin Heeb, Norbert Victor Bleiner, Davide Zhang, Yucheng Borgschulte, Andreas Kroll, Alexandra |
author_facet | Sambalova, Olga Thorwarth, Kerstin Heeb, Norbert Victor Bleiner, Davide Zhang, Yucheng Borgschulte, Andreas Kroll, Alexandra |
author_sort | Sambalova, Olga |
collection | PubMed |
description | [Image: see text] Biofilms causing medical conditions or interfering with technical applications can prove undesirably resistant to silver nanoparticle (AgNP)-based antimicrobial treatment, whereas beneficial biofilms may be adversely affected by the released silver nanoparticles. Isolated biofilm matrices can induce reduction of silver ions and stabilization of the formed nanosilver, thus altering the exposure conditions. We thus study the reduction of silver nitrate solution in model experiments under chemically defined conditions as well as in stream biofilms. Formed silver nanoparticles are characterized by state-of-the art methods. We find that isolated biopolymer fractions of biofilm organic matrix are capable of reducing ionic Ag, whereas other isolated fractions are not, meaning that biopolymer fractions contain both reducing agent and nucleation seed sites. In all of the investigated systems, we find that silver nanoparticle–biopolymer interface is dominated by carboxylate functional groups. This suggests that the mechanism of nanoparticle formation is of general nature. Moreover, we find that glucose concentration within the biofilm organic matrix correlates strongly with the nanoparticle formation rate. We propose a simple mechanistic explanation based on earlier literature and the experimental findings. The observed generality of the extracellular polymeric substance/AgNP system could be used to improve the understanding of impact of Ag(+) on aqueous ecosystems, and consequently, to develop biofilm-specific medicines and bio-inspired water decontaminants. |
format | Online Article Text |
id | pubmed-6044607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60446072018-07-16 Carboxylate Functional Groups Mediate Interaction with Silver Nanoparticles in Biofilm Matrix Sambalova, Olga Thorwarth, Kerstin Heeb, Norbert Victor Bleiner, Davide Zhang, Yucheng Borgschulte, Andreas Kroll, Alexandra ACS Omega [Image: see text] Biofilms causing medical conditions or interfering with technical applications can prove undesirably resistant to silver nanoparticle (AgNP)-based antimicrobial treatment, whereas beneficial biofilms may be adversely affected by the released silver nanoparticles. Isolated biofilm matrices can induce reduction of silver ions and stabilization of the formed nanosilver, thus altering the exposure conditions. We thus study the reduction of silver nitrate solution in model experiments under chemically defined conditions as well as in stream biofilms. Formed silver nanoparticles are characterized by state-of-the art methods. We find that isolated biopolymer fractions of biofilm organic matrix are capable of reducing ionic Ag, whereas other isolated fractions are not, meaning that biopolymer fractions contain both reducing agent and nucleation seed sites. In all of the investigated systems, we find that silver nanoparticle–biopolymer interface is dominated by carboxylate functional groups. This suggests that the mechanism of nanoparticle formation is of general nature. Moreover, we find that glucose concentration within the biofilm organic matrix correlates strongly with the nanoparticle formation rate. We propose a simple mechanistic explanation based on earlier literature and the experimental findings. The observed generality of the extracellular polymeric substance/AgNP system could be used to improve the understanding of impact of Ag(+) on aqueous ecosystems, and consequently, to develop biofilm-specific medicines and bio-inspired water decontaminants. American Chemical Society 2018-01-22 /pmc/articles/PMC6044607/ /pubmed/30023786 http://dx.doi.org/10.1021/acsomega.7b00982 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Sambalova, Olga Thorwarth, Kerstin Heeb, Norbert Victor Bleiner, Davide Zhang, Yucheng Borgschulte, Andreas Kroll, Alexandra Carboxylate Functional Groups Mediate Interaction with Silver Nanoparticles in Biofilm Matrix |
title | Carboxylate Functional Groups
Mediate Interaction
with Silver Nanoparticles in Biofilm Matrix |
title_full | Carboxylate Functional Groups
Mediate Interaction
with Silver Nanoparticles in Biofilm Matrix |
title_fullStr | Carboxylate Functional Groups
Mediate Interaction
with Silver Nanoparticles in Biofilm Matrix |
title_full_unstemmed | Carboxylate Functional Groups
Mediate Interaction
with Silver Nanoparticles in Biofilm Matrix |
title_short | Carboxylate Functional Groups
Mediate Interaction
with Silver Nanoparticles in Biofilm Matrix |
title_sort | carboxylate functional groups
mediate interaction
with silver nanoparticles in biofilm matrix |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044607/ https://www.ncbi.nlm.nih.gov/pubmed/30023786 http://dx.doi.org/10.1021/acsomega.7b00982 |
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