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Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi

Chestnut (Castanea sativa Miller.) burs (CSB) represent a solid waste produced during the edible fruit harvesting. Their usual disposal in the field increases the environmental and economic impact of the agricultural process. HPLC-UV-HRMS profiling revealed that CSB organic and aqueous extracts (CSB...

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Autores principales: Esposito, Tiziana, Celano, Rita, Pane, Catello, Piccinelli, Anna Lisa, Sansone, Francesca, Picerno, Patrizia, Zaccardelli, Massimo, Aquino, Rita Patrizia, Mencherini, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359146/
https://www.ncbi.nlm.nih.gov/pubmed/30650628
http://dx.doi.org/10.3390/molecules24020302
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author Esposito, Tiziana
Celano, Rita
Pane, Catello
Piccinelli, Anna Lisa
Sansone, Francesca
Picerno, Patrizia
Zaccardelli, Massimo
Aquino, Rita Patrizia
Mencherini, Teresa
author_facet Esposito, Tiziana
Celano, Rita
Pane, Catello
Piccinelli, Anna Lisa
Sansone, Francesca
Picerno, Patrizia
Zaccardelli, Massimo
Aquino, Rita Patrizia
Mencherini, Teresa
author_sort Esposito, Tiziana
collection PubMed
description Chestnut (Castanea sativa Miller.) burs (CSB) represent a solid waste produced during the edible fruit harvesting. Their usual disposal in the field increases the environmental and economic impact of the agricultural process. HPLC-UV-HRMS profiling revealed that CSB organic and aqueous extracts (CSB-M, CSB-H, CSB-A) contain several hydrolyzable tannins, mainly ellagitannins, and glycoside flavonols. Ellagic acid (EA) and chestanin are predominant components (5–79 and 1–13 mg/g dry extract, respectively). NMR analysis confirmed the chemical structures of the major constituents from CSB-M. The extracts displayed a significant scavenging activity against DPPH(•) (EC(50) 12.64–24.94 µg/mL) and ABTS(•+) radicals (TEAC value 2.71–3.52 mM Trolox/mg extract). They were effective in inhibiting the mycelial growth (EC(50) 6.04–15.51 mg/mL) and spore germination (EC(50) 2.22–11.17 mg/mL) of Alternaria alternata and Fusarium solani. At the highest concentration, CSB-M was also active against Botrytis cinerea both in mycelium and spore form (EC(50) 64.98 and 16.33 mg/mL). The EA contributed to the antifungal activity of extracts (EC(50) on spore germination 13.33–112.64 µg/mL). Our results can support the upgrading of chestnut burs from agricultural wastes to a resource of natural fungicides for managing fruit and vegetable diseases.
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spelling pubmed-63591462019-02-06 Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi Esposito, Tiziana Celano, Rita Pane, Catello Piccinelli, Anna Lisa Sansone, Francesca Picerno, Patrizia Zaccardelli, Massimo Aquino, Rita Patrizia Mencherini, Teresa Molecules Article Chestnut (Castanea sativa Miller.) burs (CSB) represent a solid waste produced during the edible fruit harvesting. Their usual disposal in the field increases the environmental and economic impact of the agricultural process. HPLC-UV-HRMS profiling revealed that CSB organic and aqueous extracts (CSB-M, CSB-H, CSB-A) contain several hydrolyzable tannins, mainly ellagitannins, and glycoside flavonols. Ellagic acid (EA) and chestanin are predominant components (5–79 and 1–13 mg/g dry extract, respectively). NMR analysis confirmed the chemical structures of the major constituents from CSB-M. The extracts displayed a significant scavenging activity against DPPH(•) (EC(50) 12.64–24.94 µg/mL) and ABTS(•+) radicals (TEAC value 2.71–3.52 mM Trolox/mg extract). They were effective in inhibiting the mycelial growth (EC(50) 6.04–15.51 mg/mL) and spore germination (EC(50) 2.22–11.17 mg/mL) of Alternaria alternata and Fusarium solani. At the highest concentration, CSB-M was also active against Botrytis cinerea both in mycelium and spore form (EC(50) 64.98 and 16.33 mg/mL). The EA contributed to the antifungal activity of extracts (EC(50) on spore germination 13.33–112.64 µg/mL). Our results can support the upgrading of chestnut burs from agricultural wastes to a resource of natural fungicides for managing fruit and vegetable diseases. MDPI 2019-01-15 /pmc/articles/PMC6359146/ /pubmed/30650628 http://dx.doi.org/10.3390/molecules24020302 Text en © 2019 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
Esposito, Tiziana
Celano, Rita
Pane, Catello
Piccinelli, Anna Lisa
Sansone, Francesca
Picerno, Patrizia
Zaccardelli, Massimo
Aquino, Rita Patrizia
Mencherini, Teresa
Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi
title Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi
title_full Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi
title_fullStr Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi
title_full_unstemmed Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi
title_short Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi
title_sort chestnut (castanea sativa miller.) burs extracts and functional compounds: uhplc-uv-hrms profiling, antioxidant activity, and inhibitory effects on phytopathogenic fungi
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359146/
https://www.ncbi.nlm.nih.gov/pubmed/30650628
http://dx.doi.org/10.3390/molecules24020302
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