http://www.cnr.it/ontology/cnr/individuo/prodotto/ID197663
Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea (Articolo in rivista)
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- Label
- Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.phytochem.2012.01.011 (literal)
- Alternative label
Evidente, A., Masi, M., Linaldeddu, B. T., Franceschini, A., Scanu, B., Cimmino, A., Andolfi, A., Motta, A. Maddau, L. (2012)
Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea
in Phytochemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Evidente, A., Masi, M., Linaldeddu, B. T., Franceschini, A., Scanu, B., Cimmino, A., Andolfi, A., Motta, A. Maddau, L. (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Scienze del Suolo, della Pianta, dell'Ambiente e delle Produzioni Animali, Università di Napoli Federico II, 80055 Portici, Italy
Dipartimento di Protezione delle Piante - sezione di Patologia vegetale, Università di Sassari, via E. De Nicola 1, 07100 Sassari, Italy
Istituto di Chimica Biomolecolare, CNR, Comprensorio Olivetti, Edificio 70, Via Campi Flegrei 34, 80078 Pozzuoli, Italy (literal)
- Titolo
- Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea (literal)
- Abstract
- Two phytotoxic dihydrofuropyran-2-ones, named afritoxinones A and B, were isolated from liquid culture
of Diplodia africana, a fungal pathogen responsible for branch dieback of Phoenicean juniper in Italy.
Additionally, six others known metabolites were isolated and characterized: oxysporone, sphaeropsidin
A, epi-sphaeropsidone, R-(?)-mellein, (3R,4R)-4-hydroxymellein and (3R,4S)-4-hydroxymellein. The structures
of afritoxinones A and B were established by spectroscopic and optical methods and determined to be
as (3aS/,6R/,7aS)-6-methoxy-3a,7a-dihydro-3H,6H-furo[2,3-b]pyran-2-one and (3aR/,6R/,7aS)-6-methoxy-
3a,7a-dihydro-3H,6H-furo[2,3-b]pyran-2-one, respectively. The phytotoxic activity of afritoxinones
A and B and oxysporone was evaluated on host (Phoenicean juniper) and non-host plant (holm oak, cork
oak and tomato) by cutting and leaf puncture assay. Oxysporone proved to be the most phytotoxic
compound. This study represents the first report of secondary metabolites produced by D. africana. In
addition, the taxonomic implications of secondary metabolites in Botryosphaeriaceae family studies are
discussed. (literal)
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