The lengths of roots and shoots, fresh and dry matter yield, and the contents of insoluble saccharides and free amino acids were reduced with the rise in NaCl concentration. However, under combination of NaCl with Ca²⁺ ions, these parameters generally raised. Contents of soluble saccharides, proline and quaternary ammonium compounds increased with increasing NaCl concentration, but under addition of CaCl₂ or CaSO₄, contents of these compounds were decreased. Low concentrations of NaCl stimulated soluble proteins, production, but higher concentrations decreased the content of soluble proteins. Addition of Ca²⁺ in the media did not improve the soluble protein production. Insoluble proteins content was increased with the rise of salinity level, but these effects were more pronounced with NaCl and CaCl₂ or CaSO₄ than with NaCl only.

The slot-immunobinding assay (SIBA) was adapted for detection of plum pox virus (PPV) and compared with DAS-ELISA. SIBA was easy to perform and as sensitive as DAS-ELISA in detection of various PPV isolates in herbaceous and woody plants, but not in aphids (Myzus persicae).

Between 1986 and 1989 we studied the influence of γ-irradiation (2.5-80 Gy) on growth processes and the content of arbutin glycoside. Bearberry [Arctostaphylos uva-ursi (L.) Sprengel] shows polycyclic characteristics of growth; the vegetation period is divided by summer dormancy (June) into periods of spring and summer growth. As plants age the summer dormancy gets longer and the period of summer growth is shorter. Irradiation with a dose of 80 Gy was lethal and a dose of 60 Gy damaged plants so much that they were not able to grow in the first spring after irradiation. Significant growth stimulation (both in the height of plants and in branching) was shown only in the second year after irradiation (2.5-60 Gy). In the fourth year the growth in all irradiated variants was weaker than in the control. Doses of 2.5 and 5 Gy did not influence the content of arbutin significantly; higher doses of irradiation changed the dynamics of production and decomposition which is connected with growth changes.

Eleven genotypes of sunflower were used to screen their regeneration potential in a meristem regeneration test. The inbred line HNK-81 showed the best regeneration of shoots directly from apical meristems and meristem derived calli, and rarely also the formation of adventious shoots from leaves of regenerated shoots.

Floret pieces prepared from the methanol-treated and air-dried flowers of safflower (Carthamus tinctorius L.) were subjected to an enzymatic hydrolysis in a buffered solution and the rate of precarthamine solubilization was assessed spectrophotometrically. The amount of precarthamine was risen by treating the floral pieces with a β-glucosidase (EC 3.2.1.21), supporting a previous assumption that precarthamine is in the floral tissues associated with cellular components. The enzyme activity was reduced by various inhibitors. On the basis of the experimental data, it is proposed that the precarthamine may be bound through 0-β-glucosyl linkage(s).

For clonal propagation ofAsparagus cooperi, shoot tips and node explants of 7, 20 and 35 d old spear from the region within 10 cm and below 25 cm from the apex were cultured in modified Murashige and Skoog's (1962) medium containing 6-benzylaminopurine (BAP). The required concentration of BAP varied in explants of different ages and types. In shoot tip culture, the rate of shoot multiplication was higher after 40 d than 60 d of culture. The maximum mumber (62-65) of shoots were obtained from shoot tip explants of 20 d old spear in the medium containing 2.0 mg dm^-3 of BAP, 80 mg dm^-3 of adenine and 0.02 mg dm^-3 of α-naphthalene acetic acid after 60 d of culture. From node cultures, high number of shoots were obtained after 30 d. Pretreatment with BAP in liquid medium for 48 h was effective for semirejuvenescence. The individual shoots produced roots in presence of indole-3-butyric acid and also in potassium salt of indole-3-butyric acid, the later being more effective. All regeneratns were cytologically stable.

The intracellular enzyme activities ofChlorophyllum molybditis (Mayerex. Fr.) Massee andCortinarius melliolens Fries were determined at different stages of sporophore maturity. In both mushroom species, total amylase, α-amylase, proteinase, lipase, peroxidase, catalase and polyphenol oxidase activities were increased with sporophore maturity. In contrast, glucose-6-phosphatase activity was higher in the young sporophore than in very young and mature ones. All the enzymes assayed except cellulase and β-amylase showed greater activity in the pilei than in the stipes.C. molybditis showed greater total amylase, α-amylase, cellulase, proteinase, catalase and glucose-6-phosphatase activities thanC. melliolens.

Hypocotyls of seedling plants of the sunflower inbred line HNK-81 were used as a source of protoplasts. Optimal conditions of isolation and culture of protoplasts were established. Using the method of individual culture in microdrops, a 77% final plating efficiency was achieved. Cytokinins, especially zeatin, showed a significant influence on the formation of globular embryo-like structures, but these failed to develop into mature embryos. Calli obtained in liquid media containing auxins and cytokinins grew on agar solidified media without growth regulators.

The enzyme activities of the proline metabolic pathways were determined in control and satt-treated (140 M NaCl) calli derived from cotyledons of the domestic saltsensitive tomatoLycopersicon esculentum and the wild salt-tolerantL. pennellii. Glutamate, glutamine, asparagine, and aspartate levels increased in both genotypes under salt stress, while proline accumulation increased markedly only in the salt sensitive tomato. Activity of glutamine synthetase (GS) decreased in the salt-treated calli of the domestic species, whereas both NADH- and NADPH-glutamate synthase (GOGAT) activities increased; GS and NADPH-GOGAT decreased together in the salinized calli of the wild species. Decreasing ornithine levels were found due to NaCl in both tomato populations, while ornithine transaminase (OT) decreased in the wild type only. Increasing NADPH-Δ-pyrroline-5-carboxylate reductase (P5CR) and decreasing proline oxidase (Pro oxi) occurred in the salinized calli of the wild type. Conversely, Pro oxi and proline dehydrogenase (Pro dH) decreased highly in the salinized calli of the domestic population, while no significant changes in P5CR were found.

The fatty acids composition of the polar and non-polar lipid fractions of wheat leaves was affected due to progressive brown rust infection during early stages of pathogenesis,i.e. 0, 12, 24, 36, 48 and 72 h after inoculation. The three races ofPuccinia recondita differentially affected the composition of saturated and unsaturated fatty acids and their relative occurrence in wheat leaves. The infection of wheat by race 77 resulted in a relative decrease in fatty acid chain length as measured through C₁₆∶C₁₈ fatty acid ratio. An increase in the relative degree of unsaturation (18∶2/18∶3 acids ratio) was recorded in both lipid fractions. Such changes may be taken as one of the earliest characteristics of disease development.

Forward streptomycin-resistant mutations and reverse mutations at the ARG7 locus after UV irradiation were studied in two photoreactivation-deficient mutants ofChlamydomonas reinhardtii, Phrl and Phr2. The mutant Phrl was more mutable than Phr2. Caffeine increased survival and reduced mutation rate of streptomycin-resistant mutations induced in both photoreactivation-deficient strains. Two different alleles of ARG7 locus (arg2 and arg7) were introduced into photoreactivation-deficient mutants. It was found that in the presence of both alleles, the frequency of mutants resistant to streptomycin was reduced. The reduction was more remarkable in the presence of arg2. But also under these conditions Phr1 was more mutable than Phr2.

A fast and efficient method for the isolation of major late heat-shock protein (HSP89) from the seedlings of spring barley (Hordeum vulgare L. cv. Fatran) incubated at 40°C for 15 h was described.

In comparison with the parental cv. Finale the 'RisfixC' supernodulator exhibited higher, continuously increasing nodule number and fresh mass accumulation, but substantially lower individual nodule fresh mass, leghemoglobin concentration, and specific acetylene reduction activity of nodule tissue. There were no substantial differences between Finale and 'RisfixC' in total acetylene reduction, nodule leghemoglobin accumulation per nodulated root, total and specific CO₂ evolution from nodulated roots and gross CO₂ respiratory costs of acetylene reduction. The 'RisfixC' also exhibited a substantially lower plant dry mass production (by 30%), but nitrogen concentration in shoots and carotenoid concentration in leaf tissue were significantly higher by 33 and 14%, and the chlorophylla+b content insignficantly higher than in the parental cultivar. In contrast, the nodulation mutant 'Risnod29', exhibited a somewhat higher nodule fresh mass accumulation (by 21%) and individual nodule fresh mass (by 23%), total and specific acetylene reduction (by 49 and 19%) and a somewhat more rapid plant dry mass accumulation compared with the cv. Finale.

Plasma membrane H⁺ATPase extracted from leaves of spinach plants induced to flower by gibberellic acid treatments or by a transfer to a photoperiod of 24 h had a lower Km_app than that from vegetative plants grown in short days. The Km_app obtained after inhibition by vanadate was decreased in vegetative plants and increased in induced ones showing a differential effect of this inhibitor on the kinetic properties of the enzyme between vegetative and induced plants. The phospholipid fatty acid analysis of the purified plasma membrane showed an increase of C18:1/C18:2 fatty acid ratio upon induction by light or by gibberellic acid treatments, whereas the saturated to unsaturated fatty acid ratio was kept constant. The decrease in the Km_app observed after induction may be thus interpreted in terms of the observed changes in lipid environment.

Paclobutrazol, the gibberellin biosynthesis inhibitor, acceleratedin vitro tuber initiation of potato cv. Rema and increased the uniformity of tuberization period. However, the high concentrations (10-1000 mg l^-1) of this retardant, strongly decreased mass and/or number of microtubers. The microtubers were harvested and stored in darkness (22±2°C) for 250 d. After this period both sprouting and growth of sprouts were affected by previous paclobutrazol treatment.

Twenty-five visnagin sulfonamide derivatives were testedin vitro against sclerotial germination, growth and cellulolytic activity ofSclerotium cepivorum Berk. The effectiveness of the derivatives depends on the concentration and the substituent introduced to the title compounds. The introduction of SO₂Cl₂ to C₉ of visnagin induced high toxicity than introducing SO₂NH₂. Compounds with sulfonyl piperidine or sulfonyl morpholine gave small toxicity only at 30 and 75 μg cm^-3. Addition of N-aryl ring to visnagin-9-sulfonamide rendered the title compound to be more toxic. The substitution of the N-aryl ring bym-CH₃,m-Cl orp-Cl enhanced the toxicity, while its substitution witho-CH₃,p-CH₃,p-Br,o-OCH₃ orm-OCH₃ caused a drop in the toxicity as compared to compounds with unsubstituted aryl ring. Visnagin sulfonamide derivatives having azole rings were strongly inhibitory for sclerotial germination, growth, sclerotial formation and cellulolytic activity, even when applied at 4 μg cm^-3. The most toxic one was that having dimethyl isoxazole. The cleavage of γ-pyrone ring led to a decline in the toxicity as compared with the other sulfonamide derivatives.

Paraquat (methylviologen) at concentrations above 0.05 mM inhibited the growth of photoautotrophic cyanobacteriumGleeocapsa sp. in axenic cultures. The growth rate was not affected by concentrations of 0.01 mM or less. This concentration resulted after a lag period in a moderate increase in superoxide dismutase level. After removal of paraquat, the cyanobacterium continued to generate higher levels of superoxide dismutase. There was a lag period of one hour before resumption of normal enzyme activity. Addition of puromycin at concentration of 0.5 mg cm^-3 had no effect on cell survival, but greatly enhanced the sensitivity of the culture to the toxicity of paraquat. The data showed an increase of SOD activity by temperatures above the normal growth temperature level. However, this increase was suppressed by chloramphenicol which revealed that the induction of superoxide dismutase by high temperatures was associated withde novo protein synthesis.

C. rubrum plants of different age were treated with methyl jasmonate (JA-Me), in some cases in combination with photoperiodic flower induction. Plants treated with JA-Me (3×10^-4, 3×10^-5 and 5×10^-7M) showed inhibition of growth and flowering. No effect of JA-Me application on ethylene formation was observed.

The isoperoxidase and isopolyphenol oxidase patterns were studied in undifferentiated calli and regenerated shoots and roots of two cultivars ofActinidia deliciosa: one female cv. Hayward and one male cv. Matua. One characteristic, very stable isoperoxidase band (0.85<Rf<0.90) was found only in the male callus, shoots and roots cultured on media supplemented with zeatin (ZEA) or indole-3-butyric acid (IBA). In contrary, one isopolyphenol oxidase band (0.35<Rf<0.40) was typical for male callus and shoots cultured on the medium enriched with ZEA and another one (0.85<Rf<0.90) for male shoots and roots cultured on the medium with IBA. These specific bands had never been found in female cultivar.