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Antifungal Effect of Chitosan as Ca(2+) Channel Blocker

The aim of this study was to investigate antifungal activity of a range of different molecular weight (MW) chitosan against Penicillium italicum. Our results demonstrate that the antifungal activity was dependent both the MW and concentration of the chitosan. Among a series of chitosan derived from...

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Autores principales: Lee, Choon Geun, Koo, Ja Choon, Park, Jae Kweon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Plant Pathology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892820/
https://www.ncbi.nlm.nih.gov/pubmed/27298599
http://dx.doi.org/10.5423/PPJ.OA.08.2015.0162
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author Lee, Choon Geun
Koo, Ja Choon
Park, Jae Kweon
author_facet Lee, Choon Geun
Koo, Ja Choon
Park, Jae Kweon
author_sort Lee, Choon Geun
collection PubMed
description The aim of this study was to investigate antifungal activity of a range of different molecular weight (MW) chitosan against Penicillium italicum. Our results demonstrate that the antifungal activity was dependent both the MW and concentration of the chitosan. Among a series of chitosan derived from the hydrolysis of high MW chitosan, the fractions containing various sizes of chitosan ranging from 3 to 15 glucosamine units named as chitooligomers-F2 (CO-F2) was found to show the highest antifungal activity against P. italicum. Furthermore, the effect of CO-F2 toward this fungus was significantly reduced in the presence of Ca(2+), whereas its effect was recovered by ethylenediaminetetraacetic acid, suggesting that the CO-F2 acts via disruption of Ca(2+) gradient required for survival of the fungus. Our results suggest that CO-F2 may serve as potential compounds to develop alternatives to synthetic fungicides for the control of the postharvest diseases.
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spelling pubmed-48928202016-06-13 Antifungal Effect of Chitosan as Ca(2+) Channel Blocker Lee, Choon Geun Koo, Ja Choon Park, Jae Kweon Plant Pathol J Research Article The aim of this study was to investigate antifungal activity of a range of different molecular weight (MW) chitosan against Penicillium italicum. Our results demonstrate that the antifungal activity was dependent both the MW and concentration of the chitosan. Among a series of chitosan derived from the hydrolysis of high MW chitosan, the fractions containing various sizes of chitosan ranging from 3 to 15 glucosamine units named as chitooligomers-F2 (CO-F2) was found to show the highest antifungal activity against P. italicum. Furthermore, the effect of CO-F2 toward this fungus was significantly reduced in the presence of Ca(2+), whereas its effect was recovered by ethylenediaminetetraacetic acid, suggesting that the CO-F2 acts via disruption of Ca(2+) gradient required for survival of the fungus. Our results suggest that CO-F2 may serve as potential compounds to develop alternatives to synthetic fungicides for the control of the postharvest diseases. Korean Society of Plant Pathology 2016-06 2016-06-01 /pmc/articles/PMC4892820/ /pubmed/27298599 http://dx.doi.org/10.5423/PPJ.OA.08.2015.0162 Text en © The Korean Society of Plant Pathology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lee, Choon Geun
Koo, Ja Choon
Park, Jae Kweon
Antifungal Effect of Chitosan as Ca(2+) Channel Blocker
title Antifungal Effect of Chitosan as Ca(2+) Channel Blocker
title_full Antifungal Effect of Chitosan as Ca(2+) Channel Blocker
title_fullStr Antifungal Effect of Chitosan as Ca(2+) Channel Blocker
title_full_unstemmed Antifungal Effect of Chitosan as Ca(2+) Channel Blocker
title_short Antifungal Effect of Chitosan as Ca(2+) Channel Blocker
title_sort antifungal effect of chitosan as ca(2+) channel blocker
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892820/
https://www.ncbi.nlm.nih.gov/pubmed/27298599
http://dx.doi.org/10.5423/PPJ.OA.08.2015.0162
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