The objectives and methodology of metabolic studies of the gibberellins are discussed with particular reference to the rôle of gibberellins in the promotion of stem elongation in gibberellin-responding dwarf mutants of pea.

Exogenoualy applicated indol-3-ylaeetic acid (IAA) is metabolized mainly to IAA aspartate in intact plants and plant segments and to IAA glucose in suspension cultures fromBeta vulgaris andChenopodium album.
Main metabolic product of D-tryptophan is N-malonyltryptophan in both suspension cultures and hypocotyl segments of both species. The turnover rate of L-tryptophan to IAA is comparatively low (0.1 %); inBeta the turnover rate is higher than inChenopodium. In sugar beets phenmedipham leads to a decrease in the IAA. biosynthesis rate in suspension cultures of both plant species. There is, however, an increase in the IAA content in all intact plants. The metabolic activity is substantially higher in suspension cultures than in intact plants and plant segments.

In maturing fruits ofPhaseolus coccineus a soluble glucosyltransferase activity occurs which converts gibberellins into their O-glucosides. The enzyme glucosylates GA₃ and structurally closely related gibberellins (GA₇ and GA₃₀) to their 3-O-glucosides by transfer of glucose preferentially from UDP-glucose.
From cell suspension cultures ofLycopersicon peruvianum cytosolic glucosyltransferases were isolated which in the presence of UDP-glucose converted GA₇ and GA₉ to the corresponding glucosyl esters. In both cases numerous other gibberellins failed to serve as substrates. Thus, the enzymes are UDP-glucose: gibberellin glucosyltransferases of considerable substrate specificity.

In short-term (1 h) uptake experiments GA₃(10^-5M) stimulated P_i uptake into maize root cortex cells by 28.7 %, Ethrel (10^-3M) inhibited it by 18.5 % and BA, IAA, and ABA were inactive. In long-term (5 h) experiments ABA remained inactive, GA₃ lost its stimulatory effect, and BA (5. 10^-6M), IAA (10^-4 -10^-5M), and Ethrel (10^-3 -5. 10^-4M) decreased P_i uptake. When the hormones were present only during 3 h preincubation ("augmentation") period ABA was inactive, GA₃ slightly raised and BA, IAA, and Ethrel slowed down subsequent P_i uptake.
BA(10^-7 -10^-5M) decreased xylem sap volume flow and P_i translocation. ABA in all tested concentrations (10^-8 -10^-5M) reduced exudation rate and P_i translocation, its effect declining with time. IAA effect strongly depended on concentration used and on application time and varied from strong inhibition to moderate stimulation of both volume flow and P_i translocation. GA₃ (10^-7M) slightly stimulated xylem volume flow but inhibited phosphate translocation. Ethrel (10^-4 and 10^-5M) increased both parameters, but P_i transloeation much more than volume flow. IAA, BA, and ABA influenced volume flow and P transloeation to the same extent leaving P_i concentration in the xylem sap unchanged. GA₃ and Ethrel influence P_i concentration in the xylem sap and it is thus probable that these hormones regulate release of phosphate ions into the xylem sap.

Isoperoxidase B 1 isolated from winter wheat (Triticum aestivum L., cv. Jubilar) seedlings was shown to catalyze ethylene formation from α-keto, γ-methylmercaptobutyric acid (KMBA). In the presence of Mn²⁺, indole-3-acetic acid (IAA), andp-coumaric acid, the kinetics by isoperoxidase B 1 catalyzed conversion of KMBA into ethylene and other products was similar to that of IAA oxidation. The reaction rate was therefore controlled by IAA through its electrondonating properties.
Exogenous IAA induced ethylene formation in the segments of etiolated wheat coleoptiles. IAA-induced ethylene production was enhanced by L-methionine and mitomycin C. Aminoethoxy-analogue of rhizobitoxine, ferulic acid, sodium benzoate, cycloheximide and actinomyoin D exhibited significant inhibitory effects. These data indicate that the overall reaction mechanism in coleoptile segments involves RNA and protein synthesis.
The site of IAA action is not specific; 2,4-dichlorophenoxyacetic, α-naphthylacetic and indole-3-butyric acids, respectively, possessed comparable inductive effect as IAA. Indole-3-propionic acid, indole, L-tryptophan and glucobrassicin had only low inductive efficiency, and moreover indole and L-tryptophan slowed down IAA-induced ethylene formation.

Adsorption, absorption and translocation of sodium were compared in three species showing an ascending degree in tolerance to salinity: red cabbage (tolerant) shows higher Root Cationic Exchange Capacity than tomato (sensitive) or radish (intermediate). At low NaCl concentrations, tomato accumulates the greatest quantities of sodium; but Na⁺ translocation remains proportional to the quantity absorbed in the three plants. At high salt concentrations, diffusive phenomena explain similar accumulation in every plant, but red cabbage quickly localises 50% of Na⁺ amount in cotyledons, while this element stays stored in tomato roots. The consequence of these three nutrition phases was discussed in relation to the behaviour observed at the germination time of these same plants.

The overall washing out of ions, especially⁸⁶Rb⁺ (as the tracer for K⁺), from hypocotyl segments of pumpkin (Cucurbita pepo L.) into distilled water or a CaCl₂ solution was studied, during plasmolysis with a saccharose solution and during deplasmolysis. Compartimental analysis was used to evaluate the⁸⁶Rb⁺ washing out kinetics. During plasmolysis, the washing out of⁸⁶Rb⁺ increases, due to two processes whose half-times are lower than those during washing out into the CaCl₂ solution. During deplasmolysis, the permeability of plasmalemma and tonoplast is substantially descreased, leading to washing out of most⁸⁶Rb⁺ from the cells. Plasmolysis differs from a mere decrease in the turgor pressure in the fact that after exchange for a hypotonic solution the membranes are irreversibly damaged.
The aim of this work was to monitor the changes in the cell membrane permeability due to a change in the water potential of the cells, especially during plasmolysis and deplasmolysis.

Cholinesterase activity was studied in 2 to 10-week-old pea plants cultivated under artificial illumination. Free and membrane-bound forms of the enzyme were separated by extracting the enzyme from pea shoots with buffers differing in ionic strength. The ratio of the free cholinesterase to the membrane-bound one fluctuated between 1 : 1 and 1 : 2.5. The free cholinesterase was inhibited by neostigmine (0.1mmoll^-1) by 50%, the membrane-bound enzyme by 90%. The pH optimum of cholinesterase activity was 8.5, the temperature optimum 37 °C. The enzyme activity was increased by some cations in this order: Mg²⁺ < < K⁺. The K^m value for the substrate S-acetylthiocholine iodide was 250 μmoll^-1, the enzyme activity being inhibited by concentrations higher than 3 mmoll^-1 of this substrate.
The activity of the membrane-bound enzyme was demonstrated in the roots, leaves, stems, fruits, seeds and carpels, but could not be reliably detected in the blossoms. The highest activity expressed per fresh matter was found in older leaves and in the fruits, the lowest in the roots and stems. Cholinesterase activity in plant parts markedly varied during the investigated growth period.

Proteins of protein bodies from lupin cotyledons were subjected to affinity chromatography on a column of Con A-Sepharose. About 42% of them contained sugar component. Globulin fractions soluble and precipitated at pH 4.4 contained 77% and 66% of glycoprotein, respectively.

The growth ofArabidopsis thaliana calli on media without growth regulators was studied Calli under study showed autonomy for cytokmms independently whether cultivated on the light or m the dark When cultivated in intense light, they were able to grow, either transiently or permanently, on the medium without any growth regulators In the dark, they were strictly dependent on 2,4 D m the medium Both the intensity of growth and the duration of the transient growth on the medium without growth regulators m the light decreased with the duration of the previous cultivation on the medium with growth regulators The intensity of growth on the medium without grow th regulators was best and the growth was permanent m the callus clone of spontaneous origin which was never treated by growth regulators The degree of chromosomal variability (assessed as the number of chromocentres) m this callus line was lower than that in calli induced on media with growth regulators and then transferred onto medium without growth regulatois.

The mature nodules ofLens esculenta Moench. contained higher levels of indolyl acetic acid (IAA), cytokinins (CK), gibberellic acid (GA)-like substances and more active in nitrogenase (N₂-ase) activity than young or old ones. Synthesis of IAA and its metabolism was found to be controlled by tryptophan (tryp) and phenol metabolism, respectively, in nodules of different ages. An abscisic acid (ABA)-like substance being a 'late growth phase' hormone, was highest in old nodules.
IAA and CK were highest in winter when N₂-ase activity was also highest but then GA and ABA were low. The IAA metabolic pattern of both roots and nodules was regulated by phenols. The hormones hardly changed seasonally in the roots and showed higher activities of IAA oxidase, MeOx reductase, peroxidase and polyphenol oxidase than nodules.
The nodular anabolic changes are more pronounced in winter as lentil is a winter crop. The size of nodules at a particular age was the same in different seasons, even though their hormone content varied with the season showing that the nodular hormones were not solely utilized for nodule development and growth.

Effects of cyclic AMP and traumatic acid on adventitious bud initiation inTorenia stem segments culturedin vitro were examined. Both the compounds stimulated bud initiation at relatively low concentrations. Simultaneous addition of an anticytokinin did not counteract the stimulatory action of the 2 chemicals. Their stimulatory effects were also clear when expiants were pre-incubated for 2 h with 1 μM of either of the 2 substances. The treatment with cyclic AMP and traumatic acid may favourably modify some physiological process which is triggered by excising expiants (wounding) and leads to adventitious bud initiation.

At pollination of maize plants, the old leaves, those of medium age, and young leaves, cut into segments transversally (10 segments) and longitudinally (8 segments and main vein), were sampled and concentrations of N, P, K, Ca, and Mg were determined. Then concentration gradients of these elements in maize leaves of different age were evaluated. The results obtained show that concentration gradient of N was the most evident in transversal segments of leaves of different ages, in particular in young leaves, that of K in the old leaves, and the Ca concentration gradient in leaves of medium age. The phosphorus concentration gradient was weakly expressed and in the young leaves not recorded at all. In longitudinal segments, concentration gradients of elements varied in leaves of different ages.

The increase in epidermal conductance of primary bean leaves started within 10 min after irradiation by 1200 μmol m^-2 s^-1 of darkened plants. The rate of stomatal opening increased toa maximum and then decreased till a steady-state value of epidermal conductance was reached. Stomata on the abaxial epidermis always started to open sooner and opened faster than stomata on adaxial epidermis. Both water stress and ageing of leaves delayed the beginning of opening and decreased the opening rate as well as the steady-state values of epidermal conductance.

Ethanol can influence germination of seeds ofPinus halepensis. When supplied by the appropriate procedure, the anaesthetic is able to mimic light in stimulating seed germination. This action is interpreted in terms of changes in membrane properties.

The interaction of senescence and phosphorus deficiency in determining phosphatase activities ofLemna minor has been examined in axenic cultures. Acid phosphatase activity increased in phosphorus deficiency, alkaline pyrophosphatase activity decreased during senescence and this decrease was exaggerated by phosphorus deficiency. The results are discussed in relation to possible functional significance of the enzyme activities.

The LpDH and NpDH activities in crown gall tumors incited byAgrobacterium tumefaciens strain C58 were followed in 7 plant species and 100 tumors were assayed in each experimental variant. The NpDH activity was found in 790 out of 800 crown galls observed. The LpDH activity was tested, after induction of tumors withA. tumefaciens strain B6-806 and 37400, in three experimental variants. The LpDH activity was found in 290 out of 300 crown galls. In the small fraction of the LpDH and NpDH negative tumors, the activity was possibly actually present, but it was below the limits of the sensitivity of the detection technique used.

The mechanism of uptake of sulfate by excised maize roots (Zea mays L. cv. Ganga-5) was investigated. It was found that in the concentration range l × 10^-9 M - 5 × 10^-2 M, the sulfate uptake could be represented by a single multiphasic isotherm having four phases. Each phase covered a limited concentration range and obeyed Michaelis-Menten kinetics, which indicates mediation in sulfate uptake by a structure which changes characteristics (kinetic constants) at certain discrete salts concentrations (transition points).