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Carrier-Mediated Uptake and Phloem Systemy of a 350-Dalton Chlorinated Xenobiotic with an α-Amino Acid Function1

By Céline Delétage-Grandon, Jean-François Chollet, Mireille Faucher, Francoise Rocher, Ewald Komor and Jean-Louis Bonnemain

Abstract

In a previous paper we have shown that ε-(phenoxyalkanecarboxylyl)-l-Lys conjugates are potent inhibitors of amino acid transport systems and that it is possible to modulate the uptake inhibition by hydrophobic or hydrophilic additions in the 4-position of the aromatic ring (J.F. Chollet, C. Delétage, M. Faucher, L. Miginiac, J.L. Bonnemain [1997] Biochem Biophys Acta 1336: 331–341). In this report we demonstrate that ε-(2,4-dichlorophenoxyacetyl)-l-Lys (2,4D-Lys), one of the largest molecules of the series and one of the most potent inhibitors, is a highly permeant conjugate. Uptake of 2,4D-Lys by broad bean (Vicia faba) leaf discs is mediated by an active carrier system (Km1 = 0.2 mm; Vmax1 = 2.4 nmol cm−2 h−1 at pH 5.0) complemented by an important diffusive component. Among the compounds tested (neutral, basic, and acidic amino acids, auxin, glutathione, and sugars), only the aromatic amino acids clearly compete with 2,4D-Lys. The conjugate accumulates in the vein network, is exported toward the growing organs, and exhibits a distribution pattern different from that of the herbicide moiety. However, over time 2,4D-Lys progressively splits into 2,4D and lysine. Analyses by high-performance liquid chromatography and liquid scintillation spectrometry of the phloem sap collected from the castor bean system, used as a systemy test, indicate decreasing capacities of 2,4D, 2,4D-Lys, and glyphosate, respectively, to move from the epidermis cell wall to the sieve element. Our results show that it is possible to design synthesis of large-size xenobiotics (approximately 350 D) with a lipophilic pole, exhibiting high mobility within the vascular system

Topics: Research Article
Publisher: American Society of Plant Physiologists
Year: 2001
OAI identifier: oai:pubmedcentral.nih.gov:88820
Provided by: PubMed Central
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