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Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom
Diatoms are known to produce a variety of halogenated compounds, which were recently shown to have a role in allelopathic interactions between competing species. The production of these compounds is linked to haloperoxidase activity. This research, has shown that this system may also be involved in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917277/ https://www.ncbi.nlm.nih.gov/pubmed/24445305 http://dx.doi.org/10.3390/md12010352 |
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author | Syrpas, Michail Ruysbergh, Ewout Blommaert, Lander Vanelslander, Bart Sabbe, Koen Vyverman, Wim De Kimpe, Norbert Mangelinckx, Sven |
author_facet | Syrpas, Michail Ruysbergh, Ewout Blommaert, Lander Vanelslander, Bart Sabbe, Koen Vyverman, Wim De Kimpe, Norbert Mangelinckx, Sven |
author_sort | Syrpas, Michail |
collection | PubMed |
description | Diatoms are known to produce a variety of halogenated compounds, which were recently shown to have a role in allelopathic interactions between competing species. The production of these compounds is linked to haloperoxidase activity. This research, has shown that this system may also be involved in diatom-bacteria interactions via the H(2)O(2) dependent inactivation of a type of quorum sensing (QS) molecule, i.e., N-β-ketoacylated homoserine lactones (AHLs), by a natural haloperoxidase system from the benthic diatom Nitzschia cf pellucida. The AHL degradation pathway towards corresponding halogenated derivatives was elucidated via HPLC-MS analysis and the synthesis of a broad series of novel halogenated AHL analogues as reference compounds. Furthermore, their biological activity as quorum sensing modulators was directly compared and evaluated against a series of naturally occurring β-keto-AHLs. It has been demonstrated that the loss of the QS activity results from the final cleavage of the halogenated N-acyl chain of the signal molecules. |
format | Online Article Text |
id | pubmed-3917277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-39172772014-02-10 Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom Syrpas, Michail Ruysbergh, Ewout Blommaert, Lander Vanelslander, Bart Sabbe, Koen Vyverman, Wim De Kimpe, Norbert Mangelinckx, Sven Mar Drugs Article Diatoms are known to produce a variety of halogenated compounds, which were recently shown to have a role in allelopathic interactions between competing species. The production of these compounds is linked to haloperoxidase activity. This research, has shown that this system may also be involved in diatom-bacteria interactions via the H(2)O(2) dependent inactivation of a type of quorum sensing (QS) molecule, i.e., N-β-ketoacylated homoserine lactones (AHLs), by a natural haloperoxidase system from the benthic diatom Nitzschia cf pellucida. The AHL degradation pathway towards corresponding halogenated derivatives was elucidated via HPLC-MS analysis and the synthesis of a broad series of novel halogenated AHL analogues as reference compounds. Furthermore, their biological activity as quorum sensing modulators was directly compared and evaluated against a series of naturally occurring β-keto-AHLs. It has been demonstrated that the loss of the QS activity results from the final cleavage of the halogenated N-acyl chain of the signal molecules. MDPI 2014-01-17 /pmc/articles/PMC3917277/ /pubmed/24445305 http://dx.doi.org/10.3390/md12010352 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Syrpas, Michail Ruysbergh, Ewout Blommaert, Lander Vanelslander, Bart Sabbe, Koen Vyverman, Wim De Kimpe, Norbert Mangelinckx, Sven Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom |
title | Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom |
title_full | Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom |
title_fullStr | Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom |
title_full_unstemmed | Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom |
title_short | Haloperoxidase Mediated Quorum Quenching by Nitzschia cf pellucida: Study of the Metabolization of N-Acyl Homoserine Lactones by a Benthic Diatom |
title_sort | haloperoxidase mediated quorum quenching by nitzschia cf pellucida: study of the metabolization of n-acyl homoserine lactones by a benthic diatom |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917277/ https://www.ncbi.nlm.nih.gov/pubmed/24445305 http://dx.doi.org/10.3390/md12010352 |
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