The Phloem Translocation of Enantiomeric Pairs of Weak Acids in Ricinus communis

A possible role for specific carrier mechanisms in the phloemtranslocation of xenobiotics in Ricinus communis L. var. Gibsonii(Nichols) has been investigated by comparing the phloem transportof enantiomers of three acidic compounds. No differences intranslocation were found between the R– and S-enantiomersof phenylalanine, 2-methoxy-2-phenylpropanoic acid or 5-methyl-5-phenyloxazolidine-2,4-dione.These similarities between transport of enantiomers indicatethat stereospecific carriers do not occur, even for the endogenousamino acid phenylalanine of which only one enantiomer occursnaturally in phloem sap. Whilst transport of the enantiomerswas similar, there were differences between the mobility ofthe three compounds, and these could largely be explained interms of their physicochemical properties, without the needto invoke the existence of specific carrier mechanisms. Key words: Phloem transport, enantiomers, Ricinus communis, weak acids