Haloacetophenones as newly potent nematicides against Meloidogyne incognita

TOCCO, GRAZIELLA;ELOH, KODJO;ONNIS, VALENTINA;CABONI, PIERLUIGI
2017-01-01

Abstract

Acetophenones are a class of aromatic compounds frequently produced by plants as a response to a stress or as a protection reaction against parasites or herbivors. In the present research, we investigated the role of the carbonyl moiety in a series of commercially available aromatic ketones tested for their nematicidal activity against the root-knot nematode Meloidogyne incognita (Kofoid et White) Chitwood. Interestingly, we found that the presence of electron withdrawing groups onto the aromatic ring were highly efficient in inducing nematode paralysis and death (EC50/24h between 2.5 and 54.8mg/L and EC50/72h between 2.3 and 65.6mg/L, respectively). Moreover, a chlorine atom in α-position to the carbonyl functionality emerged as a key residue in improving acetophenones activity. In this paper, the nematicidal ability of a series of differently substituted acetophenones is reported and the preliminary structure-activity relationship studies are also discussed. We also performed an in vitro GC-MS metabolomics analysis on the potato cyst nematode Globodera pallida, after treatment with 2,4'-dichloroacetophenone (6) at 100mg/L for 24h. The 1-dodecanol and talose were evidenced as the main upregulated metabolites, suggesting a possible V-ATPase dysfunction.
2017
Inglese
110
94
102
9
https://www.sciencedirect.com/science/article/pii/S0926669017303898?via=ihub
Esperti anonimi
internazionale
scientifica
1-Dodecanol; Metabolomics; Nematicidal compounds; Talose; V-ATPase; Agronomy and crop science
no
Tocco, Graziella; Eloh, Kodjo; Onnis, Valentina; Sasanelli, Nicola; Caboni, Pierluigi
1.1 Articolo in rivista
info:eu-repo/semantics/article
1 Contributo su Rivista::1.1 Articolo in rivista
262
5
reserved
File in questo prodotto:
File Dimensione Formato  
Haloacetophenones_Industrial Crops&Products_2017.pdf

Solo gestori archivio

Descrizione: articolo principale
Tipologia: versione editoriale
Dimensione 918.6 kB
Formato Adobe PDF
918.6 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Questionario e social

Condividi su:
Impostazioni cookie