ABSTRACIThe uptake of 15-3Hlindoleacetic acid (IAA) by Zea mays L. root segments involves nonsaturable and saturable processes. The pH optimum of the saturable component was found to be 5.0. The proton ionophore carbonylcyanidep-trifluoromethoxyphenylhydrazone inhibited at 100 micromolar the saturable component of IAA uptake but had no effect on non-saturable uptake. This indicates that the saturable component of IAA uptake is dependent on the proton gradient across the plasmalemma. The high level of proton extrusion in the elongation zone of the root will stimulate nonsaturable and saturable uptake of IAA in that zone.The movement of IAA involves both diffusion and carriermediated transport. It was suggested (18) that the polarity of auxin transport is brought about by the asymmetrical distribution, on the plasmalemma, of a carrier for the efflux of IAA. Jacobs and Gilbert (6) provided evidence that this carrier is located, in pea stems, preferentially at the basal end of certain cells. This would lead to basipetal polarity of IAA transport in the stem, whereas in the root auxin transport is preferentially acropetal (8,12,20 Incubation. The medium contained 2% (w/v) glucose, and IAA*I at 5 nM and was buffered using Na2HPO4/citric acid (sum of concentrations sodium phosphate plus citric acid: 10 mM). Groups of 20 segments were incubated for 4 min at 20.0 ± 0.2°C in tubes containing 1.0 ml of medium and shaken at 150 r.p.m.Use of FCCP. This protonophore was dissolved in ethanol and added to the medium just before use. To test the effect of FCCP on IAA uptake, segments were first pre-treated in medium, buffered at pH 5.0, without IAA, and containing or not (control) FCCP at 100 tM. The final concentration of ethanol in the medium was 0.5% (v/v). Control media were prepared using an equal quantity of ethanol. No difference was observed between controls with and without ethanol (0.5%). Segments were then transferred to uptake medium (also at pH 5.0) containing IAA* at 5 nm with or without nonradioactive IAA at 10 gM. FCCP (100 Mm) was present in the uptake medium (FCCP-treated) or absent (control).Radioactivity Determination. Segments were rapidly rinsed using distilled water, and placed, 4 per vial, with 4 ml scintillation fluid ('Optifluor,' Packard Instruments). Radioactivity was determined by liquid scintillation counting as previously described (10) using a Kontron 'BETAmatic II' liquid scintillation spectrometer.Replication. Experiments were performed twice, and no significant difference between the two experiments was observed, so treatment means and SE were calculated from 10 scintillation vials, each containing 4 segments. Results were expressed as Bq per segment.
RESULTS AND DISCUSSIONIt has previously been shown (10) that after 4 min incubation of maize root segments in medium containing IAA*, radioactivity in the tissue was almost exclusively in the IAA molecule (only about 5% had been metabolized). Therefore, under the present experimental conditions, the radioactivity taken up can be used as a measure ...