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Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin
Glycerol/diol dehydratases catalyze the conversion of glycerol to 3-hydroxypropionaldehyde (3-HPA), the basis of a multi-component system called reuterin. Reuterin has antimicrobial properties and undergoes chemical conjugation with dietary heterocyclic amines (HCAs). In aqueous solution reuterin is...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098142/ https://www.ncbi.nlm.nih.gov/pubmed/27819285 http://dx.doi.org/10.1038/srep36246 |
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author | Engels, Christina Schwab, Clarissa Zhang, Jianbo Stevens, Marc J. A. Bieri, Corinne Ebert, Marc-Olivier McNeill, Kristopher Sturla, Shana J. Lacroix, Christophe |
author_facet | Engels, Christina Schwab, Clarissa Zhang, Jianbo Stevens, Marc J. A. Bieri, Corinne Ebert, Marc-Olivier McNeill, Kristopher Sturla, Shana J. Lacroix, Christophe |
author_sort | Engels, Christina |
collection | PubMed |
description | Glycerol/diol dehydratases catalyze the conversion of glycerol to 3-hydroxypropionaldehyde (3-HPA), the basis of a multi-component system called reuterin. Reuterin has antimicrobial properties and undergoes chemical conjugation with dietary heterocyclic amines (HCAs). In aqueous solution reuterin is in dynamic equilibrium with the toxicant acrolein. It was the aim of this study to investigate the extent of acrolein formation at various physiological conditions and to determine its role in biological and chemical activities. The application of a combined novel analytical approach including IC-PAD, LC-MS and NMR together with specific acrolein scavengers suggested for the first time that acrolein, and not 3-HPA, is the active compound responsible for HCA conjugation and antimicrobial activity attributed to reuterin. As formation of the HCA conjugate was observed in vivo, our results imply that acrolein is formed in the human gut with implications on detoxification of HCAs. We propose to re-define the term reuterin to include acrolein. |
format | Online Article Text |
id | pubmed-5098142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50981422016-11-10 Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin Engels, Christina Schwab, Clarissa Zhang, Jianbo Stevens, Marc J. A. Bieri, Corinne Ebert, Marc-Olivier McNeill, Kristopher Sturla, Shana J. Lacroix, Christophe Sci Rep Article Glycerol/diol dehydratases catalyze the conversion of glycerol to 3-hydroxypropionaldehyde (3-HPA), the basis of a multi-component system called reuterin. Reuterin has antimicrobial properties and undergoes chemical conjugation with dietary heterocyclic amines (HCAs). In aqueous solution reuterin is in dynamic equilibrium with the toxicant acrolein. It was the aim of this study to investigate the extent of acrolein formation at various physiological conditions and to determine its role in biological and chemical activities. The application of a combined novel analytical approach including IC-PAD, LC-MS and NMR together with specific acrolein scavengers suggested for the first time that acrolein, and not 3-HPA, is the active compound responsible for HCA conjugation and antimicrobial activity attributed to reuterin. As formation of the HCA conjugate was observed in vivo, our results imply that acrolein is formed in the human gut with implications on detoxification of HCAs. We propose to re-define the term reuterin to include acrolein. Nature Publishing Group 2016-11-07 /pmc/articles/PMC5098142/ /pubmed/27819285 http://dx.doi.org/10.1038/srep36246 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Engels, Christina Schwab, Clarissa Zhang, Jianbo Stevens, Marc J. A. Bieri, Corinne Ebert, Marc-Olivier McNeill, Kristopher Sturla, Shana J. Lacroix, Christophe Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
title | Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
title_full | Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
title_fullStr | Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
title_full_unstemmed | Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
title_short | Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
title_sort | acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098142/ https://www.ncbi.nlm.nih.gov/pubmed/27819285 http://dx.doi.org/10.1038/srep36246 |
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