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Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies

The aim was to study the inhibitory effects of coumarin derivatives on the plant pathogenic fungi, as well as beneficial bacteria and nematodes. The antifungal assay was performed on four cultures of phytopathogenic fungi by measuring the radial growth of the fungal colonies. Antibacterial activity...

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Autores principales: Rastija, Vesna, Vrandečić, Karolina, Ćosić, Jasenka, Majić, Ivana, Šarić, Gabriella Kanižai, Agić, Dejan, Karnaš, Maja, Lončarić, Melita, Molnar, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303553/
https://www.ncbi.nlm.nih.gov/pubmed/34298898
http://dx.doi.org/10.3390/ijms22147283
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author Rastija, Vesna
Vrandečić, Karolina
Ćosić, Jasenka
Majić, Ivana
Šarić, Gabriella Kanižai
Agić, Dejan
Karnaš, Maja
Lončarić, Melita
Molnar, Maja
author_facet Rastija, Vesna
Vrandečić, Karolina
Ćosić, Jasenka
Majić, Ivana
Šarić, Gabriella Kanižai
Agić, Dejan
Karnaš, Maja
Lončarić, Melita
Molnar, Maja
author_sort Rastija, Vesna
collection PubMed
description The aim was to study the inhibitory effects of coumarin derivatives on the plant pathogenic fungi, as well as beneficial bacteria and nematodes. The antifungal assay was performed on four cultures of phytopathogenic fungi by measuring the radial growth of the fungal colonies. Antibacterial activity was determined by the broth microdilution method performed on two beneficial soil organisms. Nematicidal activity was tested on two entomopathogenic nematodes. The quantitative structure-activity relationship (QSAR) model was generated by genetic algorithm, and toxicity was estimated by T.E.S.T. software. The mode of inhibition of enzymes related to the antifungal activity is elucidated by molecular docking. Coumarin derivatives were most effective against Macrophomina phaseolina and Sclerotinia sclerotiorum, but were not harmful against beneficial nematodes and bacteria. A predictive QSAR model was obtained for the activity against M. phaseolina (R(2)(tr) = 0.78; R(2)(ext) = 0.67; Q(2)(loo) = 0.67). A QSAR study showed that multiple electron-withdrawal groups, especially at position C-3, enhanced activities against M. phaseolina, while the hydrophobic benzoyl group at the pyrone ring, and –Br, –OH, –OCH(3), at the benzene ring, may increase inhibition of S. sclerotiourum. Tested compounds possibly act inhibitory against plant wall-degrading enzymes, proteinase K. Coumarin derivatives are the potentially active ingredient of environmentally friendly plant-protection products.
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spelling pubmed-83035532021-07-25 Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies Rastija, Vesna Vrandečić, Karolina Ćosić, Jasenka Majić, Ivana Šarić, Gabriella Kanižai Agić, Dejan Karnaš, Maja Lončarić, Melita Molnar, Maja Int J Mol Sci Article The aim was to study the inhibitory effects of coumarin derivatives on the plant pathogenic fungi, as well as beneficial bacteria and nematodes. The antifungal assay was performed on four cultures of phytopathogenic fungi by measuring the radial growth of the fungal colonies. Antibacterial activity was determined by the broth microdilution method performed on two beneficial soil organisms. Nematicidal activity was tested on two entomopathogenic nematodes. The quantitative structure-activity relationship (QSAR) model was generated by genetic algorithm, and toxicity was estimated by T.E.S.T. software. The mode of inhibition of enzymes related to the antifungal activity is elucidated by molecular docking. Coumarin derivatives were most effective against Macrophomina phaseolina and Sclerotinia sclerotiorum, but were not harmful against beneficial nematodes and bacteria. A predictive QSAR model was obtained for the activity against M. phaseolina (R(2)(tr) = 0.78; R(2)(ext) = 0.67; Q(2)(loo) = 0.67). A QSAR study showed that multiple electron-withdrawal groups, especially at position C-3, enhanced activities against M. phaseolina, while the hydrophobic benzoyl group at the pyrone ring, and –Br, –OH, –OCH(3), at the benzene ring, may increase inhibition of S. sclerotiourum. Tested compounds possibly act inhibitory against plant wall-degrading enzymes, proteinase K. Coumarin derivatives are the potentially active ingredient of environmentally friendly plant-protection products. MDPI 2021-07-06 /pmc/articles/PMC8303553/ /pubmed/34298898 http://dx.doi.org/10.3390/ijms22147283 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rastija, Vesna
Vrandečić, Karolina
Ćosić, Jasenka
Majić, Ivana
Šarić, Gabriella Kanižai
Agić, Dejan
Karnaš, Maja
Lončarić, Melita
Molnar, Maja
Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies
title Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies
title_full Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies
title_fullStr Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies
title_full_unstemmed Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies
title_short Biological Activities Related to Plant Protection and Environmental Effects of Coumarin Derivatives: QSAR and Molecular Docking Studies
title_sort biological activities related to plant protection and environmental effects of coumarin derivatives: qsar and molecular docking studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303553/
https://www.ncbi.nlm.nih.gov/pubmed/34298898
http://dx.doi.org/10.3390/ijms22147283
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