ABSTRACT(22S,23S)-Homobrassinolide was tested for its effect on the electric cell potential, proton extrusion, ferricyanide reduction, and amino acid and sucrose uptake of leaves of Egeria densa Planchon. In the light, (22S,23S)-homobrassinolide and its derivative, 2a-3a-dihydroxy-5a-stigmast-22-en-6-one, were similar to each other and similar to fusicoccin in causing hyperpolarization and proton extrusion, whereas stigmasterol was less effective. In darkness, the three sterols showed comparable effects.(22S,23S)-Homobrassinolide slightly stimulated ferricyanide reduction and promoted uptake of sucrose and a-aminoisobutyric acid. The results are compatible with a stimulation of an electrogenic proton pump mechanism at the plasmalemma by (22S,23S)-homobrassinolide.behavior to auxin in corn roots (14) suggests an FC3-like mechanism of action for this compound. Unfortunately, the structural requirements of the steroid backbone, responsible for the stimulation of transport by brassinosteroids, is not yet clear, although some work was dedicated to this issue (10). In order to characterize further the role of the steroid structure in modifying transport on the cellular level, we here describe the effects of another potent synthetic analog, SSHB (1 in Fig. 1), on the membrane potential and on proton and solute transport of Egeria densa, a submerged aquatic weed well characterized in this respect (5, 6, 12), and we compare the SSHB effect with those induced by related substances and FC.
MATERIALS AND METHODS
Plant CultivationBrassinosteroids are a new class of growth regulators found in many plants (1, 10). Among them brassinolide, (22R,23R,24S)-2a,3a,22,23-tetrahydroxy-24-methyl-Bhomo-7-oxa-5a-cholestan-6-one, is the best characterized and causes the highest growth promotion. The comparison with other plant hormones in a series of bioassays revealed auxinlike properties, albeit a powerful synergism between brassinolide and IAA was reported (1 1, 15