Indole-3-acetic acid (IAA) is known to induce slow oscillations of the bioelectric potential (BEP) in plant tissues, which can be measured with extracellular and intracellular electrodes. Oscillations on the cell surface correspond to those of the membrane potential in auxin-treated cells [3]. Newman concluded that auxindependent BEP oscillations were related to the mechanism of the auxin polar transport [8, 9], which occurs through the living phloem and xylem tissues in stems and roots [6, 7]. However, it is only one aspect of the phytohormone action. The IAA effects on plant growth, movements, and other processes of vital activity, including the auxin transport, are mediated by the same mechanism of the hormonal signal perception and transduction with participation of membranes [3]. The objective of this work was to investigate the influence of the local treatment of conducting and peripheral tissues with IAA on BEP generation. The segments excised from burdock ( Arctium lappa L.) petioles and dandelion ( Taraxacum officinale L.) roots were used. Surface BEP were measured using EVL-1MZ AgCl electrodes with a micropipette filled with 3% agar and 0.1 M KCl and a pH-340 amplifier of the constant current. Two-cm-long segments were excised from basal parts of burdock petioles. They were incubated in 10 - 3 M CaCl 2 at room temperature and illumination for 2 h, rinsed with distilled water, and fixed vertically (with apical cut upward) in petri dishes filled with 10 - 3 M CaCl 2 so that the solution covered the 0.5-cm basal parts of the segments. On the cut surface, two symmetrical conducting bundles or parenchymal regions were selected, and small cotton clumps (1.5 mm in diameter) moistened with distilled water were placed on. They exerted a contact between plant tissues and electrodes. The difference of potentials between two bundles or parenchymal zones was measured three times at intervals of 10 min to obtain stable values. Thereafter, the cotton clump under the measuring electrode was replaced by that moistened with IAA (10 or 100 mg/l) and cotton clumps moistened with distilled water under the reference electrodes and under both electrodes of control segments were refreshed. The difference of potentials was monitored for 2 h. Periodically, drying cotton clumps were moistened with distilled water or auxin solutions. Five experiments were carried out with five replicates in each. The control values were subtracted, and the means with their confidence intervals at p = 0.05 are presented.
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