Effect of indoleacetic acid on the growth ofRhizobium in culture

After inoculation ofRhizobium lupini strain A98 andR. leguminosarum strain PRE into a medium containing IAA, growth was initially suppressed. However, when IAA was added in the course of the logarithmic phase, growth was not inhibited. Apparently, IAA affects primarily the lag phase cells.Neither adaptation ofRhizobium to IAA was observed, nor spontaneous breakdown or biological degradation of IAA.The lag phase prolongation depended on the ratio: amount of IA A/number of cells.The authors wish to thank Professor Dr. A. Quispel for his interest and valuable discussions.     

Absence of biological activity in oxidation products of indoleacetic acid

The main enzymatic oxidation products of IAA have been tested for biological activity, using as bioassay the straight-growth test ofAvena coleoptile. After being purified by rechromatography, none of these products (including methyleneoxindole) exhibited biological activity within the wide range of concentrations employed; consequently, the results accord with the evidence that IAA is the true hormone of plant growth.     

Transport of auxin (indoleacetic acid) through lipid bilayer membranes

Summary Diffusion of auxin (indole-3-acetic acid) through planar lipid bilayer membranes was studied as a function of pH and auxin concentration. Membranes were made of egg or soybean lecithin or phosphatidyl serine inn-decane (25–35 mg/ml). Tracer and electrical techniques were used to estimate the permeabilities to nonionized (HA) and ionized (A^–) auxin. The auxin tracer flux is unstirred layer limited at low pH and membrane limited at high pH, i.e., when [A^–][HA]. The tracer flux is not affected by the transmembrane voltage and is much higher than the flux predicted from the membrane conductance. Thus, only nonionized auxin crosses the membrane at a significant rate. Auxin transport shows saturation kinetics, but this is due entirely to unstirred layer effects rather than to the existence of an auxin carrier in the membrane. A rapid interconversion of A^– and HA at the membrane surface allows A^– to facilitate the auxin flux through the unstirred layer. Thus, the total flux is higher than that expected for the simple diffusion of HA alone. The relation between flux (J _A), concentrations and permeabilities is: 1/J _A=1/P ^UL([A^–]+[HA])+1/P _HA ^M [HA]. By fitting this equation to our data we find thatP ^UL=6.9×10^–4 cm/sec andP _HA ^M =3.3×10^–3 cm/sec for egg lecithin-decane bilayers. Similar membrane permeabilities were observed with phosphatidyl serine or soybean lipids. Thus, auxin permeability is not affected by a net surface charge on the membrane. Our model describing diffusion and reaction in the unstirred layers can explain the anomolous relationship between pH and weak acid (or weak base) uptake observed in many plant cells.     

Effect of indoleacetic acid on the metabolic activity oftaraxacum root segments

Inoubation of thin slioes ofTaraxacum root segments in 3-indoleaoetic acid solutions enhanced the level of total proteins, RNA, DNA and a number of enzymes reaching an optimum at 0.01 mg 1^-1. It has been shown that the auxin promotes the synthesis of DNA, again with an optimum promotion at 0.01 mg 1^-1 IAA. This work was carried out at the Department of Botany, University of Sheffield, Sheffield, England. The author wishes to thank Dr. A. Booth for taking a keen interest in this work.     

The effect of kinetin on the indoleacetic acid level and indoleacetic acid oxidase activity in roots of young plants

Kinetin treatment increased the extractable IAA content in roots of young plants of Phaseolus vulgaris L., Zea mays L. and Avena sativa L. The highest increase was obtained with roots of beans and the lowest with oat roots. Maize was intermediate between these two species. Kinetin treatment decreased the activity of IAA-oxidase but the correlation between the decrease of the activity of this enzyme and the increase in the level of IAA was not good. The decrease of the oxidase activity was greatest in oat roots where kinetin had very little effect on the IAA level, and was rather small in bean roots, where kinetin treatment significantly increased the IAA level.     

Effect of chinoform on the function of biological membranes.

To investigate the mechanism by which the toxic effect of chinoform (5-chloro-7-iodo-8-quinolinol) develops, its action on the function of biological membranes was examined. Findings were: 1. Chinoform induced K+ release from red cells. This effect was increased by prior addition of Mg2+ and decreased by albumin, ruthenium red, or lanthanum chloride. 2. Chinoform induced K+ release from isolated rat liver mitochondria more effectively in the presence of Mg2+ or other bivalent cations, and a chinoform-Mg chelate was more effective than chinoform alone. The K+ release from mitochondria was protected by albumin and to a certain extent by lanthanum chloride. 3. The change in the ion permeability of mitochondrial membrane induced by chinoform in the presence of Mg2+ was accompanied by uncoupling of the oxidative phosphorylation. These results suggest that chinoform interacts with membranes more effectively as a metal chelate, producing conformational and functional changes in those membranes.     

Fluorescence and photoinactivation of indoleacetic acid

These results indicate quite clearly that the induction of the photoinactivation of indoleacetic acid (IAA) is by no means a peculiarity of riboflavin but is a property common to many fluorescent substances. It is not essential that the compounds be colored. Colorless materials are also able to bring about IAA photoinactivation provided that they absorb ultraviolet light.After exposure to light, the reaction mixture becomes turbid and develops a light-pink coloration. Experiments are being performed to elucidate the nature of the reaction product.It is suggested that besides riboflavin other naturally occurring fluorescent substances in plants may play a role in light-induced growth reactions.     

Effect of glycerol on the capacity and conductivity of lipid bilayer membranes

It is shown that glycerol addition to one side of BLM containing cholesterol leads to a significant decrease of its capacity, and the decrease rate is in indirect proportion to glycerol concentration. Washing out or addition of glycerol to another side results in a full or partial reconstitution of the capacity. The effect of glycerol on the BLM conductivity is manifested in its increase for membranes having specific conductivity above 2.10(-7) Om-1 X cm2. The peculiarity of glycerol is manifested in the fact that during definite period of time (20 +/- 30 min) the membrane is under "stress" condition with the characteristic current fluctuations, which may be compared with its medium meaning. Such condition is preserved up to the moment of BLM rupture. It is supposed that such effects are due to the big-scale reconstructions of membrane structure under the influence of glycerol.     

Effect of dicyclohexylcarbodiimide on the proton conductance of thylakoid membranes in intact chloroplast

The effects of dicyclohexylcarbodiimide, a potent inhibitor of chloroplast ATPase, on the light-induced electric potential changes in intact chloroplasts of Peperomia metallica and of a hornwort Anthoceros sp. were investigated by means of glass microcapillary electrodes. The characteristics of potential changes induced by flashes or continuous light in chloroplasts of both species are similar except for the phase of potential rise in continuous light, which is clearly biphasic in Anthoceros chloroplasts. Dicyclohexylcarbodiimide at concentration 5 · 10⁻⁵ M completely abolishes the transient potential undershoot in the light-off reaction but has little effect on the peak value of the photoelectric response. The membrane conductance in the light and in the dark was tested by measuring the decay kinetics of flash-generated potential in dark-adapted and preilluminated chloroplasts. In the absence of dicyclohexylcarbodiimide, preillumination causes a significant acceleration of the potential decay. The light-induced changes in the decay kinetics of flash-induced responses were abolished in the presence of dicyclohexylcarbodiimide, whereas the rate of potential decay in dark-adapted chloroplasts was not altered by dicyclohexylcarbodiimide. The results are consistent with the notion that dicyclohexylcarbodiimide diminishes H⁺ conductance of energized thylakoid membranes by interacting with the H⁺ channel of ATPase. The occurrence of a lag (approx. 300 ms) on the plot of potential undershoot (diffusion potential) versus illumination time might suggest the increase in H⁺ permeability coefficient of thylakoid membrane during illumination.     

Effect of polymyxin B on the conductivity of negatively charged bilayer lipid membranes

Effect of polymyxin B on the planar bilayer lipid membranes (BLM) formed from synthetic phosphatidic acid has been studied. The addition of cholesterol to phospholipid in molar ratio 1 : 2 was followed by an increase of BLM conductance from 2 x 10(-8) to 3 x 10(-7) Ohm-1 cm-2. It was suggested that the observed increase of conductance was due to the fluidity of the membrane matrix in the presence of cholesterol. It was shown that 10(-6)--10(-5) M polymyxin slightly affected the conductance of BLM from phosphatidic acid. It was found that polymyxin increased conductance of negatively charged BLM modified by palmitic acid from 10(-8) to 10(-6) Ohm-1 cm-2.     

Effect of membrane potential on the mechanical equilibrium of biological membranes

The mechanical equilibrium of a membranous sac, whose wall is sandwiched by two oppositely charged fluid layers, is investigated as a mathematical model of a living cell. In so doing, it is assumed that the space charge density in the inner and the outer charged fluid layer is constant. It is also assumed that the fluid inside and outside of the charged fluid layer is a perfect conductor. By solving Maxwell's equation, the electric field and the thickness of the inner and the outer charged fluid layer is determined as a function of the geometry of the sac. Then, the fluid pressure in the charged fluid layer is derived by considering the body force created by the electrostatic field. The condition of mechanical equilibrium of the sac membrane yields an equation which reveals the inter-relation between the geometry, the sac fluid pressure and the membrane potential. According to this equation, the change of membrane potential causes a deformation of the sac. If the wall of the membranous sac is permeable, increase (decrease) of the absolute value of the membrane potential results in swelling (shrinking) of the sac. On the other hand, the mechanical change of the sac volume results in the change of the membrane potential. This analysis provides also an explanation of how the red blood cell maintains the biconcave shape, when the red blood cell is assumed to be a fluid filled membranous sac with non-zero membrane potential.     

Effect of PCMBS on water transfer across biological membranes

P-chloromercuriphenylsulfonate, PCMBS, and 5, 5′ dithiobis-(2-nitrobenzoic acid), DTNB at a concentration of 1 mM are found to inhibit the rate of water transport across human red cell membrane. In addition PCMBS inhibits the rates of transport of small hydrophilic but not hydrophobic nonelectrolytes. Other sulfhydryl reagents such as N-ethylmaleimide and iodoacetamide have no significant effect on the rate of water transfer in these cells. The results suggest that there are at least two populations of membrane bound SH-groups which differ in their topical location which participate in the control of water transfer. One is located closer to the outer surface of the membrane, and thus is readily accessible to PCMBS while the other component is probably located in the membrane interior. These two populations can be dissociated by pH. The effect of PCMBS on water transfer can be greatly influenced by pH and temperature. The main effect of temperature and pH is on the permeability of the membrane to the drug. The same concentration of PCMBS is also found to inhibit to a lesser degree water transfer across other biological membranes.     

Effect of indoleacetic acid on the penetration of leucine and glucose through epidermal tissue of onion bulb

The penetration of leucine-(U)-¹⁴C and glucose-(U)-¹⁴C throughthe bulb epidermal tissue of Allium cepa was examined in thepresence of indoleacetic acid (IAA). Not only the uptake ofleucine-¹⁴C and glucose-¹⁴C in epidermal tissue but also theirtranscellular penetration were accelerated by IAA treatment.N-Ethylmaleimide (NEM) inhibited their uptake and transcellularpenetration, and the inhibitory effect was relieved by additionalIAA. In the presence of IAA, leucine-¹⁴C and glucose-¹⁴C weremore penetrable by adaxial than abaxial application, but inthe absence almost no difference due to application side wasobserved. IAA appears to promote permeability of the epidermaltissue only to substances applied adaxially. N,N'-Dicyclohexylcarbodiimide(DCCD) showed a little inhibitory effect on the IAA-inducedpromotion of the uptake and penetration of leucine-¹⁴C appliedadaxially. Leucine-¹⁴C and glucose-¹⁴C penetrated more easilythrough killed than fresh tissue, with little difference betweenabaxial and adaxial applications. ¹ Present address: Department of Biology, Faculty of Science,Kochi University, Kochi 780, Japan. ² Present address: Department of Medical Zoology, Medical School,Mie University, Tsu 514, Japan. (Received October 13, 1977; )