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

Chestnut ( 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-...

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Published inMolecules (Basel, Switzerland) Vol. 24; no. 2; p. 302
Main Authors Esposito, Tiziana, Celano, Rita, Pane, Catello, Piccinelli, Anna Lisa, Sansone, Francesca, Picerno, Patrizia, Zaccardelli, Massimo, Aquino, Rita P, Mencherini, Teresa
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 15.01.2019
MDPI
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Summary:Chestnut ( 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 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 6.04⁻15.51 mg/mL) and spore germination (EC 2.22⁻11.17 mg/mL) of and . At the highest concentration, CSB-M was also active against both in mycelium and spore form (EC 64.98 and 16.33 mg/mL). The EA contributed to the antifungal activity of extracts (EC 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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These two authors contributed equally to this work.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules24020302