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Degradation of Zearalenone by Essential Oils under In vitro Conditions
Essential oils are volatile compounds, extracted from plants, which have a strong odor. These compounds are known for their antibacterial and antifungal properties. However, data concerning degradation of mycotoxins by these metabolites are very limited. The aim of the present study was to investiga...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980393/ https://www.ncbi.nlm.nih.gov/pubmed/27563298 http://dx.doi.org/10.3389/fmicb.2016.01224 |
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author | Perczak, Adam Juś, Krzysztof Marchwińska, Katarzyna Gwiazdowska, Daniela Waśkiewicz, Agnieszka Goliński, Piotr |
author_facet | Perczak, Adam Juś, Krzysztof Marchwińska, Katarzyna Gwiazdowska, Daniela Waśkiewicz, Agnieszka Goliński, Piotr |
author_sort | Perczak, Adam |
collection | PubMed |
description | Essential oils are volatile compounds, extracted from plants, which have a strong odor. These compounds are known for their antibacterial and antifungal properties. However, data concerning degradation of mycotoxins by these metabolites are very limited. The aim of the present study was to investigate the effect of essential oils (cedarwood, cinnamon leaf, cinnamon bark, white grapefruit, pink grapefruit, lemon, eucalyptus, palmarosa, mint, thymic, and rosemary) on zearalenone (ZEA) reduction under various in vitro conditions, including the influence of temperature, pH, incubation time and mycotoxin and essential oil concentrations. The degree of ZEA reduction was determined by HPLC method. It was found that the kind of essential oil influences the effectiveness of toxin level reduction, the highest being observed for lemon, grapefruit, eucalyptus and palmarosa oils, while lavender, thymic and rosemary oils did not degrade the toxin. In addition, the decrease in ZEA content was temperature, pH as well as toxin and essential oil concentration dependent. Generally, higher reduction was observed at higher temperature in a wide range of pH, with clear evidence that the degradation rate increased gradually with time. In some combinations (e.g., palmarosa oil at pH 6 and 4 or 20°C) a toxin degradation rate higher than 99% was observed. It was concluded that some of the tested essential oils may be effective in detoxification of ZEA. We suggested that essential oils should be recognized as an interesting and effective means of ZEA decontamination and/or detoxification. |
format | Online Article Text |
id | pubmed-4980393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49803932016-08-25 Degradation of Zearalenone by Essential Oils under In vitro Conditions Perczak, Adam Juś, Krzysztof Marchwińska, Katarzyna Gwiazdowska, Daniela Waśkiewicz, Agnieszka Goliński, Piotr Front Microbiol Microbiology Essential oils are volatile compounds, extracted from plants, which have a strong odor. These compounds are known for their antibacterial and antifungal properties. However, data concerning degradation of mycotoxins by these metabolites are very limited. The aim of the present study was to investigate the effect of essential oils (cedarwood, cinnamon leaf, cinnamon bark, white grapefruit, pink grapefruit, lemon, eucalyptus, palmarosa, mint, thymic, and rosemary) on zearalenone (ZEA) reduction under various in vitro conditions, including the influence of temperature, pH, incubation time and mycotoxin and essential oil concentrations. The degree of ZEA reduction was determined by HPLC method. It was found that the kind of essential oil influences the effectiveness of toxin level reduction, the highest being observed for lemon, grapefruit, eucalyptus and palmarosa oils, while lavender, thymic and rosemary oils did not degrade the toxin. In addition, the decrease in ZEA content was temperature, pH as well as toxin and essential oil concentration dependent. Generally, higher reduction was observed at higher temperature in a wide range of pH, with clear evidence that the degradation rate increased gradually with time. In some combinations (e.g., palmarosa oil at pH 6 and 4 or 20°C) a toxin degradation rate higher than 99% was observed. It was concluded that some of the tested essential oils may be effective in detoxification of ZEA. We suggested that essential oils should be recognized as an interesting and effective means of ZEA decontamination and/or detoxification. Frontiers Media S.A. 2016-08-11 /pmc/articles/PMC4980393/ /pubmed/27563298 http://dx.doi.org/10.3389/fmicb.2016.01224 Text en Copyright © 2016 Perczak, Juś, Marchwińska, Gwiazdowska, Waśkiewicz and Goliński. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Perczak, Adam Juś, Krzysztof Marchwińska, Katarzyna Gwiazdowska, Daniela Waśkiewicz, Agnieszka Goliński, Piotr Degradation of Zearalenone by Essential Oils under In vitro Conditions |
title | Degradation of Zearalenone by Essential Oils under In vitro Conditions |
title_full | Degradation of Zearalenone by Essential Oils under In vitro Conditions |
title_fullStr | Degradation of Zearalenone by Essential Oils under In vitro Conditions |
title_full_unstemmed | Degradation of Zearalenone by Essential Oils under In vitro Conditions |
title_short | Degradation of Zearalenone by Essential Oils under In vitro Conditions |
title_sort | degradation of zearalenone by essential oils under in vitro conditions |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980393/ https://www.ncbi.nlm.nih.gov/pubmed/27563298 http://dx.doi.org/10.3389/fmicb.2016.01224 |
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