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1.
Food Microbiol ; 92: 103556, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32950150

RESUMO

Rotting caused by grey mould (Botrytis cinerea) is a concerning disease for numerous crops both pre- and postharvest stages. Application of antagonistic yeasts is a promising strategy for controlling grey mould incidence which could mitigate undesirable consequences of using synthetic fungicides. In this work, a screening for detection of yeasts isolated from figs producers of antifungal volatile organic compounds (VOCs) were performed by confrontation in double dishes systems. Eleven out of 34 yeasts confronted reduced B. cinerea growth parameter in vitro. This reduction was correlated (p ≤ 0.050) with the production of 10 volatile compounds: two acids (acetic acid and octanoic acid), 7 esters (Ethyl propionate, n-Propyl acetate, Isobutyl acetate, 2-methylbutyl acetate, furfuryl acetate, phenylmethyl acetate, 2-phenylethyl acetate) and one ketone (Heptan-2-one). In bases on in vitro assay, Hanseniaspora uvarum 793 was applied to in vivo assays with strawberries and cherries. The reduction of incidence of B. cinerea in strawberries at 7 °C and 25 °C was 54.9 and 72.1% after 6 and 3 days, respectively. The reduction of incidence of B. cinerea in cherries at 7 °C and 25 °C was 48.9 and 45.6% after 5 and 4 days, respectively. These results showed that VOCs produced by Hanseniaspora uvarum 793 are effective in the control of incidence of Botrytis cinerea in fruits, being a potential alternative to chemical fungicide.


Assuntos
Botrytis/efeitos dos fármacos , Frutas/microbiologia , Fungicidas Industriais/farmacologia , Doenças das Plantas/microbiologia , Compostos Orgânicos Voláteis/farmacologia , Leveduras/química , Botrytis/crescimento & desenvolvimento , Ficus/microbiologia , Fragaria/microbiologia , Fungicidas Industriais/química , Fungicidas Industriais/metabolismo , Hanseniaspora/efeitos dos fármacos , Hanseniaspora/crescimento & desenvolvimento , Doenças das Plantas/prevenção & controle , Prunus avium/microbiologia , Compostos Orgânicos Voláteis/química , Compostos Orgânicos Voláteis/metabolismo , Leveduras/genética , Leveduras/isolamento & purificação , Leveduras/metabolismo
2.
Pest Manag Sci ; 64(2): 203-7, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18069657

RESUMO

BACKGROUND: In order to understand the bioactivity of Myoporum bontioides A. Gray against plant pathogens and determine its active ingredients, the inhibitory activities of methanol extracts from M. bontioides against Fusarium oxysporum f. sp. niveum (E. F. Smith) Snyder & Hansen, Pestalotia mangiferae P. Henn., Thielaviopsis paradoxa (De Seynes) v. Hohnel, Colletotrichum musae (Berk. & M. A. Curtis) v. Arx, Alternaria alternata (Fr.) Keissler, Mycosphaerella sentina (Fr.) Schroter and Sphaceloma fawcettii Jenk. were evaluated using a growth rate method, and the active ingredient was isolated by activity-directed isolation and identified by determination and analysis of IR, (1)H NMR, (13)C NMR and mass spectra and correlative physical constants. RESULTS: The results showed that the extracts from stems and leaves of M. bontioides exhibited inhibitory activity against the seven fungi, with > 58% inhibition at 10 g L(-1) after 72 h. The active compound was isolated and identified as (-)-epingaione, and showed inhibitory activity against the above seven fungi. The inhibitory activity against P. mangiferae was the highest, with an EC(50) value of 77 mg L(-1). The EC(50) values against the other six fungi were 147-245 mg L(-1). (-)-Epingaione also inhibited spore germination of F. oxysporum f. sp. niveum, T. paradoxa and S. fawcettii. CONCLUSION: (-)-Epingaione demonstrated broad-spectrum inhibitory activity against plant pathogenic fungi and is promising for exploitation as a fungicide.


Assuntos
Fungos/efeitos dos fármacos , Furanos/química , Furanos/farmacologia , Myoporum/química , Pentanonas/química , Pentanonas/farmacologia , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Fungicidas Industriais/química , Fungicidas Industriais/farmacologia , Estrutura Molecular
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