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Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes
Azole antifungal agents are widely used as active ingredients in antifungal pharmaceuticals and agricultural fungicides. An increase in the use of azole antifungals has resulted in an increase in the concentration of these compounds in wastewater and surface water, with potential implications for ag...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509311/ https://www.ncbi.nlm.nih.gov/pubmed/31093477 http://dx.doi.org/10.1007/s13205-019-1733-5 |
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author | Kryczyk-Poprawa, Agata Żmudzki, Paweł Maślanka, Anna Piotrowska, Joanna Opoka, Włodzimierz Muszyńska, Bożena |
author_facet | Kryczyk-Poprawa, Agata Żmudzki, Paweł Maślanka, Anna Piotrowska, Joanna Opoka, Włodzimierz Muszyńska, Bożena |
author_sort | Kryczyk-Poprawa, Agata |
collection | PubMed |
description | Azole antifungal agents are widely used as active ingredients in antifungal pharmaceuticals and agricultural fungicides. An increase in the use of azole antifungals has resulted in an increase in the concentration of these compounds in wastewater and surface water, with potential implications for agriculture. In the present study, bifonazole (BIF) and clotrimazole (CTZ) were selected for investigation because of their widespread use in topical formulations and persistence in the environment. The mycoremediation capacity of BIF and CTZ by mycelia of Lentinula edodes in in vitro culture was evaluated. The main aim of this study was to identify the presumable biodegradation products of the investigated active pharmaceutical substances using the LC/MS/MS method. For this purpose, the media were enriched with the following active pharmaceutical ingredients selected for this study: BIF powder, CTZ powder, and BIF cream, each of them at the same concentration of 0.1 mg/mL. Subsequently, thin-layer chromatography coupled with densitometry was used to evaluate the content of BIF and CTZ in mycelium from in vitro cultures of L. edodes. The degradation process was found to affect primarily the imidazole moiety of both investigated compounds. In addition, the amounts of undegraded investigated compounds were found to be 4.98, 9.26, and 4.56 mg/g dry weight for BIF powder, CTZ powder, and BIF cream, respectively. Therefore, the findings of this study revealed that L. edodes could be considered for remediation of pollution caused by azole antifungal agents. |
format | Online Article Text |
id | pubmed-6509311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-65093112019-05-15 Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes Kryczyk-Poprawa, Agata Żmudzki, Paweł Maślanka, Anna Piotrowska, Joanna Opoka, Włodzimierz Muszyńska, Bożena 3 Biotech Original Article Azole antifungal agents are widely used as active ingredients in antifungal pharmaceuticals and agricultural fungicides. An increase in the use of azole antifungals has resulted in an increase in the concentration of these compounds in wastewater and surface water, with potential implications for agriculture. In the present study, bifonazole (BIF) and clotrimazole (CTZ) were selected for investigation because of their widespread use in topical formulations and persistence in the environment. The mycoremediation capacity of BIF and CTZ by mycelia of Lentinula edodes in in vitro culture was evaluated. The main aim of this study was to identify the presumable biodegradation products of the investigated active pharmaceutical substances using the LC/MS/MS method. For this purpose, the media were enriched with the following active pharmaceutical ingredients selected for this study: BIF powder, CTZ powder, and BIF cream, each of them at the same concentration of 0.1 mg/mL. Subsequently, thin-layer chromatography coupled with densitometry was used to evaluate the content of BIF and CTZ in mycelium from in vitro cultures of L. edodes. The degradation process was found to affect primarily the imidazole moiety of both investigated compounds. In addition, the amounts of undegraded investigated compounds were found to be 4.98, 9.26, and 4.56 mg/g dry weight for BIF powder, CTZ powder, and BIF cream, respectively. Therefore, the findings of this study revealed that L. edodes could be considered for remediation of pollution caused by azole antifungal agents. Springer International Publishing 2019-05-09 2019-06 /pmc/articles/PMC6509311/ /pubmed/31093477 http://dx.doi.org/10.1007/s13205-019-1733-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Kryczyk-Poprawa, Agata Żmudzki, Paweł Maślanka, Anna Piotrowska, Joanna Opoka, Włodzimierz Muszyńska, Bożena Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes |
title | Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes |
title_full | Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes |
title_fullStr | Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes |
title_full_unstemmed | Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes |
title_short | Mycoremediation of azole antifungal agents using in vitro cultures of Lentinula edodes |
title_sort | mycoremediation of azole antifungal agents using in vitro cultures of lentinula edodes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509311/ https://www.ncbi.nlm.nih.gov/pubmed/31093477 http://dx.doi.org/10.1007/s13205-019-1733-5 |
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