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Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds
Twelve methylenedioxy-containing compounds including piperine and 10 piperine-like synthetic compounds were assessed to determine their antifungal and antiaflatoxigenic activities against Aspergillus flavus ATCC 22546 in terms of their structure–activity relationships. Piperonal and 1,3-benzodioxole...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999856/ https://www.ncbi.nlm.nih.gov/pubmed/27537912 http://dx.doi.org/10.3390/toxins8080240 |
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author | Moon, Young-Sun Choi, Won-Sik Park, Eun-Sil Bae, In Kyung Choi, Sung-Deuk Paek, Ockjin Kim, Sheen-Hee Chun, Hyang Sook Lee, Sung-Eun |
author_facet | Moon, Young-Sun Choi, Won-Sik Park, Eun-Sil Bae, In Kyung Choi, Sung-Deuk Paek, Ockjin Kim, Sheen-Hee Chun, Hyang Sook Lee, Sung-Eun |
author_sort | Moon, Young-Sun |
collection | PubMed |
description | Twelve methylenedioxy-containing compounds including piperine and 10 piperine-like synthetic compounds were assessed to determine their antifungal and antiaflatoxigenic activities against Aspergillus flavus ATCC 22546 in terms of their structure–activity relationships. Piperonal and 1,3-benzodioxole had inhibitory effects against A. flavus mycelial growth and aflatoxin B(1) production up to a concentration of 1000 μg/mL. Ten piperine-like synthetic compounds were synthesized that differed in terms of the carbon length in the hydrocarbon backbone and the presence of the methylenedioxy moiety. In particular, 1-(2-methylpiperidin-1-yl)-3-phenylprop-2-en-1-one had potent antifungal and antiaflatoxigenic effects against A. flavus up to a concentration of 1 μg/mL. This synthetic compound was remarkable because the positive control thiabendazole had no inhibitory effect at this concentration. Reverse transcription-PCR analysis showed that five genes involved in aflatoxin biosynthesis pathways were down-regulated in A. flavus, i.e., aflD, aflK, aflQ, aflR, and aflS; therefore, the synthetic compound inhibited aflatoxin production by down-regulating these genes. |
format | Online Article Text |
id | pubmed-4999856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-49998562016-09-01 Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds Moon, Young-Sun Choi, Won-Sik Park, Eun-Sil Bae, In Kyung Choi, Sung-Deuk Paek, Ockjin Kim, Sheen-Hee Chun, Hyang Sook Lee, Sung-Eun Toxins (Basel) Article Twelve methylenedioxy-containing compounds including piperine and 10 piperine-like synthetic compounds were assessed to determine their antifungal and antiaflatoxigenic activities against Aspergillus flavus ATCC 22546 in terms of their structure–activity relationships. Piperonal and 1,3-benzodioxole had inhibitory effects against A. flavus mycelial growth and aflatoxin B(1) production up to a concentration of 1000 μg/mL. Ten piperine-like synthetic compounds were synthesized that differed in terms of the carbon length in the hydrocarbon backbone and the presence of the methylenedioxy moiety. In particular, 1-(2-methylpiperidin-1-yl)-3-phenylprop-2-en-1-one had potent antifungal and antiaflatoxigenic effects against A. flavus up to a concentration of 1 μg/mL. This synthetic compound was remarkable because the positive control thiabendazole had no inhibitory effect at this concentration. Reverse transcription-PCR analysis showed that five genes involved in aflatoxin biosynthesis pathways were down-regulated in A. flavus, i.e., aflD, aflK, aflQ, aflR, and aflS; therefore, the synthetic compound inhibited aflatoxin production by down-regulating these genes. MDPI 2016-08-16 /pmc/articles/PMC4999856/ /pubmed/27537912 http://dx.doi.org/10.3390/toxins8080240 Text en © 2016 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 (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Moon, Young-Sun Choi, Won-Sik Park, Eun-Sil Bae, In Kyung Choi, Sung-Deuk Paek, Ockjin Kim, Sheen-Hee Chun, Hyang Sook Lee, Sung-Eun Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds |
title | Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds |
title_full | Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds |
title_fullStr | Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds |
title_full_unstemmed | Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds |
title_short | Antifungal and Antiaflatoxigenic Methylenedioxy-Containing Compounds and Piperine-Like Synthetic Compounds |
title_sort | antifungal and antiaflatoxigenic methylenedioxy-containing compounds and piperine-like synthetic compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999856/ https://www.ncbi.nlm.nih.gov/pubmed/27537912 http://dx.doi.org/10.3390/toxins8080240 |
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