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Bioactive Secondary Metabolites Produced by the Oak Pathogen Diplodia corticola

Academic Article
Publication Date:
2016
Short description:
Bioactive Secondary Metabolites Produced by the Oak Pathogen Diplodia corticola / Masi, M., Maddau, L., Linaldeddu, B.T., Cimmino, A., D'Amico, W., Scanu, B., Evidente, M., Tuzi, A., Evidente, A.. - In: JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY. - ISSN 0021-8561. - 64:1(2016), pp. 217-225. [10.1021/acs.jafc.5b05170]
abstract:
Three new lactones and a new fatty acid ester, named sapinofuranones C and D, diplopyrone B, and diplobifuranylone C, respectively, were isolated from Diplodia corticola, together with sphaeropsidins A and C, diplopyrone, diplobifuranylones A and B, diplofuranone A, and the (S,S)-enantiomer of sapinofuranone B. Sapinofuranones C and D, diplopyrone B, and diplobifuranylone C were characterized as (5S)-5-((1,S-1,6-dihydroxyhexa-2,4-dienyl)-dihydrofuran-2-one, 4,5-dihydroxy-deca-6,8-dienoic acid methyl ester, (5S)-5-hydroxy-6-(penta-1,3-dienyl)-5,6-dihydro-pyran-2-one, and 5′-((1R)-1-hydroxyethyl)-2′,5′-dihydro-2H-[2,2′]bifuranyl-5-one by spectroscopic and chemical methods, respectively. The relative configuration of sapinofuranone C was assigned by X-ray diffraction analysis, whereas its absolute configuration was determined by applying the advanced Mosher's method to its 11-O-p-bromobenzoyl derivative. The same method was used to assign the absolute configuration to C-5 of diplopyrone B and to that of the hydroxyethyl of the side chain of diplobifuranylone C, respectively. The metabolites isolated were tested at 1 mg/mL on leaves of cork oak, grapevine cv. 'Cannonau', and tomato using the leaf puncture assay. They were also tested on tomato cuttings at 0.2, 0.1, and 0.05 mg/mL. Each compound was tested for zootoxic activity on Artemia salina L. larvae. The efficacy of sapinofuranone C and diplopyrone B on three plant pathogens, namely, Athelia rolfsii, Fusarium avenaceum, and Phytophthora nicotianae was also evaluated. In all phytotoxic assays only diplopyrone B was found to be active. It also showed strong inhibition on the vegetative growth of A. rolfsii and P. nicotianae. All metabolites were inactive in the assay performed for the zootoxic activity (A. salina) even at the highest concentration used (200 μg/mL). Diplopyrone B showed a promising antioomycete activity for the control of Phytophthora spp. also taking into account the absence of zootoxic activity.
Iris type:
1.1 Articolo in rivista
Keywords:
Botryosphaeriaceae; diplobifuranylone C; diplopyrone B; furanones; phytotoxins; sapinofuranones C and D; unsaturated carboxylic acids; α-pyrone; Ascomycota; Lactones; Molecular Structure; Plant Diseases; Quercus; Secondary Metabolism; Chemistry (all); Agricultural and Biological Sciences (all)
List of contributors:
Masi, Marco; Maddau, Lucia; Linaldeddu, Benedetto Teodoro; Cimmino, Alessio; D'Amico, Wanda; Scanu, Bruno; Evidente, Marco; Tuzi, Angela; Evidente, Antonio
Authors of the University:
MADDAU Lucia
SCANU Bruno
Handle:
https://iris.uniss.it/handle/11388/168084
Published in:
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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