Abstract. Mutual effects between Mn. Ca, and Mg were studied during steady-state absorption experiments with excised barley roots. Calcium appeared to enhance the rate of Mn absorption; whereas, Mg had a highly depressive effect. The combination of both Ca and Mg was even more inhibitory to Mn absorption than Mg alone. Manganese had no effect on the usual negligible Ca absorption by this tissue, but effectively inhibited the absorption of Mg. Although divalent cation absorption from the Ca-Mg-Mn system was essentially nil, K absorption was greatly stimulated in the presence of these cations.These mutual effects and others reported in the literature are explained by the hypothesis that selectivity in ion absorption results from cation-induced conformational changes in the structure of the carrier molecule.In a previous paper (10), evidence was presented for the metabolic transport of Mn into excised barley roots. Absorption was relatively rapid and was affected bv concentration, pH, etc., much as that of other inorganic cations. To further study the mechanism of Mn absorption and its similarities to that of other metabolically absorbed cations, the influence of several monovalent, divalent and trivalent cations on the absorption of Mn was examined. The effects of 2 of these cations, Ca and Mg, are discussed here.The role of Ca in regulating the absorption of ions is well recognized. Its effects on the uptake of the monovalent, al,kali cations range from highly stimulatorv to strongly inhibitory, depending on the ion and the H+ concentration (8). Furthermore, Ca has been found to be highly effective in controlling the relative selectivity of absorption of these ions from mixed solutions (4, 7). involves configurational changes, the hypothesis is promoted that selectivity in ion transport results from cation-induced conforniational changes in the structure of the membrane or ion carrier(s).
Materials and MethodsExcised roots of 5-day-old barley seedlings (Hordeum zulgare L., var. Trebi) were used in all experiments. The planits were growwn and the roots were prepared and treated as described previously (10). The experimlental temperature was 25 ± 0.50 and the pH was 5.0 ± 0.2 maintained by small additions of 0.1 N HCl. Distilled water and analvzed reagent-grade chloride salts were used in all experiments. Absorption periods of 1 and 6 hr were chosen oIn the basis of the previous work so that rates of metabolic absorption occurring during the steady-state phase could be measured (10