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S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum

Allicin can be used as fumigant to protect food and cultural relics from fungal contamination because of its strong antifungal activity and the characteristics of high volatility and no residues. However, the obvious disadvantages such as high minimal inhibitory concentration and instability prevent...

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Autores principales: Qi, Feilong, Zhang, Chen, Jiang, Shanshan, Wang, Qian, Kuerban, Kudelaidi, Luo, Man, Dong, Mengxue, Zhou, Xinguang, Wu, Laiming, Jiang, Biao, Ye, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567679/
https://www.ncbi.nlm.nih.gov/pubmed/31142631
http://dx.doi.org/10.1042/BSR20190167
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author Qi, Feilong
Zhang, Chen
Jiang, Shanshan
Wang, Qian
Kuerban, Kudelaidi
Luo, Man
Dong, Mengxue
Zhou, Xinguang
Wu, Laiming
Jiang, Biao
Ye, Li
author_facet Qi, Feilong
Zhang, Chen
Jiang, Shanshan
Wang, Qian
Kuerban, Kudelaidi
Luo, Man
Dong, Mengxue
Zhou, Xinguang
Wu, Laiming
Jiang, Biao
Ye, Li
author_sort Qi, Feilong
collection PubMed
description Allicin can be used as fumigant to protect food and cultural relics from fungal contamination because of its strong antifungal activity and the characteristics of high volatility and no residues. However, the obvious disadvantages such as high minimal inhibitory concentration and instability prevent it from wide application. In this study, a stable derivative of allicin, S-ethyl ethanethiosulfinate (ALE), was synthesized. We further explored its antifungal activity and apoptosis-inducing effect, as well as the underlying mechanism. ALE had an excellent capability of inhibiting spore germination and mycelial growth of Penicillium chrysogenum observed by inverted microscope and scanning electron microscopy. XTT colorimetric assay indicated ALE could reduce the cell viability obviously and IC(50) was 0.92 μg/ml, only 1/42 of allicin (38.68 μg/ml). DHR 123 ROS Assay Kit, flow cytometry assay and confocal immunofluorescence revealed intercellular ROS generation and metacaspase-dependent apoptosis triggered by ALE, while antioxidant tocopherol could reverse ALE-induced cytotoxicity effect and metacaspase activation. These results indicate that ALE induces metacaspase-dependent apoptosis through ROS generation, thus possesses an effective antifungal activity. This new derivative of allicin might be developed as a high efficient alternative to the conventional fungicides for food storage and cultural relic protection.
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spelling pubmed-65676792019-07-02 S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum Qi, Feilong Zhang, Chen Jiang, Shanshan Wang, Qian Kuerban, Kudelaidi Luo, Man Dong, Mengxue Zhou, Xinguang Wu, Laiming Jiang, Biao Ye, Li Biosci Rep Research Articles Allicin can be used as fumigant to protect food and cultural relics from fungal contamination because of its strong antifungal activity and the characteristics of high volatility and no residues. However, the obvious disadvantages such as high minimal inhibitory concentration and instability prevent it from wide application. In this study, a stable derivative of allicin, S-ethyl ethanethiosulfinate (ALE), was synthesized. We further explored its antifungal activity and apoptosis-inducing effect, as well as the underlying mechanism. ALE had an excellent capability of inhibiting spore germination and mycelial growth of Penicillium chrysogenum observed by inverted microscope and scanning electron microscopy. XTT colorimetric assay indicated ALE could reduce the cell viability obviously and IC(50) was 0.92 μg/ml, only 1/42 of allicin (38.68 μg/ml). DHR 123 ROS Assay Kit, flow cytometry assay and confocal immunofluorescence revealed intercellular ROS generation and metacaspase-dependent apoptosis triggered by ALE, while antioxidant tocopherol could reverse ALE-induced cytotoxicity effect and metacaspase activation. These results indicate that ALE induces metacaspase-dependent apoptosis through ROS generation, thus possesses an effective antifungal activity. This new derivative of allicin might be developed as a high efficient alternative to the conventional fungicides for food storage and cultural relic protection. Portland Press Ltd. 2019-06-14 /pmc/articles/PMC6567679/ /pubmed/31142631 http://dx.doi.org/10.1042/BSR20190167 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Qi, Feilong
Zhang, Chen
Jiang, Shanshan
Wang, Qian
Kuerban, Kudelaidi
Luo, Man
Dong, Mengxue
Zhou, Xinguang
Wu, Laiming
Jiang, Biao
Ye, Li
S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum
title S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum
title_full S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum
title_fullStr S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum
title_full_unstemmed S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum
title_short S-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ROS generation in Penicillium chrysogenum
title_sort s-ethyl ethanethiosulfinate, a derivative of allicin, induces metacaspase-dependent apoptosis through ros generation in penicillium chrysogenum
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567679/
https://www.ncbi.nlm.nih.gov/pubmed/31142631
http://dx.doi.org/10.1042/BSR20190167
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