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Taylor and Francis Group, Journal of Plant Interactions, 3(2), p. 185-193, 2007

DOI: 10.1080/17429140701596349

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Effect of benzoic acid hydroxyl- and methoxy-ring substituents on cucumber (Cucumis sativusL.) root membrane potential

Journal article published in 2007 by Wanda Camusso, Silvano Sacco, Massimo Maffei ORCID, Cinzia M. Bertea
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The allelopathic effect of some benzoic acid (BA) OH- and OCH3-ring substituents was studied on cucumber root transmembrane potential difference (Vm). Most of the methoxy-BAs induced a rapid Vm depolarization, followed by a Vm hyperpolarization, with the only exception for p-anisic acid (pA). On the other hand, salicylic acid (SA) and 3,4-dimethoxybenzoic acid (DHB) strongly depolarized Vm. A positive correlation was found between Vm hyperpolarization and lipophilicity of methoxylated BAs, whereas a positive correlation was found between lipophilicity and Vm depolarization of hydroxylated BAs. The influence of BAs on K was studied by means of specific blocking with Cs indicating a possible direct interaction of SA, gallic acid (GA), vanillic acid (VA) and 3,4-dimethoxybenzoic acid (DMB). Interference of BAs with the Vm hyperpolarizing effect of root perfusion with the fungal toxin fusicoccin were also observed.