The changes in endopeptidase activity in different parts of germinating triticale cv. Malno were investigated. Haemoglobin, gliadin, azocasein and azoalbumin were used as substrates. During the first day of germination the activity of haemoglobin hydrolyzing endopeptidases predominated while after the second day, mainly in the endosperm, a rapid increase in endopeptidases activity preferring gliadin hydrolysis was observed. In all the investigated tissues azocaseinolytic activities increased with the successive days of germination. Similar changes were observed using azoalbumin with one exception: in the embryo axis this activity decreased with the progression of germination. Separation of endopeptidases on the DEAE Sepharose CL-6B reveals three activity peaks in extract from dry seeds and four peaks in extract from 3 d germinated seeds. The obtained peaks differed in substrate specificity and in sensitivities to class-specific inhibitors.

Two soybean (Glycine max (L.) Merr.) cultivars, Tachiyutaka and Dare, were grown in pots at 30 and 70 % relative humidity (RH) and treated with 0 (control), 40 (moderate), 80 and 120 (severe) mM NaCl for 3 weeks. Increasing RH enhanced growth of salt sensitive cultivar, Tachiyutaka, but had no effect on salt tolerant cultivar, Dare, under control and moderate saline conditions. Both cultivars benefited from elevated humidity under severe saline conditions. Cultivar Tachiyutaka had poorer ability for controlling translocation of Na⁺ to the leaves, lower Na⁺ exclusion ability in the roots, and lower root activity under NaCl treatment, compared with cv. Dare. The increased growth of cv. Tachiyutaka at high RH was consistent with decreased Na⁺ accumulation in the leaves, increased stomatal conductance and root activity, while the unchanged growth of cv. Dare was consistent with similar Na⁺ accumulation in the leaves, and the decreased root activity.

Gas exchange in Gossypium hirsutum L. cv. H-777 as affected by water deficit and growth regulators (IAA, GA₃, BAP, ABA, ethrel) was examined. Sixty days after sowing, growth regulators in concentration 50 µM were applied as foliar spray and irrigation was withheld to get desired (moderate and severe) water deficit. All the parameters were measured on the third leaf from the top between 10:00 and 11:00. Net photosynthetic rate (P_N), transpiration rate (E), stomatal conductance (g_s), carboxylation efficiency (CE), and water potential (ψ_w) decreased significantly with the increasing water stress, however, water use efficiency (WUE) was unaffected. Foliar spray with IAA, GA₃ and BAP partially counteracted the effect of water deficit on the above parameters except ψ_w, which became more negative. ABA and up to some extent ethrel increased WUE and maintained higher ψ_w, however, caused further decrease in P_N, E, and g_s.

Leaf discs from vegetative plants greatly increase their phenolic content when cultivated in vitro. Under long days the values remained constant, and were higher when compared with short days cultures. Under short days total phenolics decreased after 10 d, corresponding to the induction and expression of in vitro flowering. The effect of photoperiod and chlorogenic acid (0.01 mM) on leaf discs cultured from induced and non-induced plants, were analyzed regarding the neo-formation of roots, as well as vegetative and flower buds. Chlorogenic acid enhances the regeneration of roots in all treatments tested, with the highest stimulation on induced leaf discs cultivated in short days. The flowering was not affected by chlorogenic acid, but an inhibitory effect was observed on the neo-formation of vegetative buds in non-induced explants maintained in short days. Vegetative buds were reduced by 50% in flower-induced leaf discs cultivated under short days.

The root cell walls of the resistant cultivars of the date palm were more resistant to the action of the cell wall-degrading enzymes (CWDE) of Fusarium oxysporum f. sp. albedinis than those of the susceptible cultivars. Date palm roots contain four cell wall-bound phenolics identified as p-hydroxybenzoic acid, p-coumaric acid, ferulic acid and sinapic acid. The contents of p-coumaric acid and ferulic acid in the resistant cultivars (IKL, SLY, BSTN) were about 2 times higher than those in the susceptible cultivars (BFG, JHL, BSK). The contents of p-hydroxybenzoic acid and sinapic acid in the resistant cultivars were 8.4 and 4.5 times, respectively, higher than those in the susceptible cultivars. The lignin contents in roots of the resistant cultivars were 1.8 times higher than those of the susceptible cultivars. The cell wall-bound phenols accumulated particularly in resistant cultivars reduced strongly the mycelial growth and the CWDE production in vitro.

Trichloroacetic acid (TCA) belongs to secondary atmospheric pollutants affecting the forest health. Distribution of [1,2-¹⁴C]TCA-residues and TCA biodegradation were investigated in 4-year-old nursery-grown trees of Norway spruce [Picea abies (L.) Karst.] in the whole plant/soil system. Radioactivity was monitored in needles, wood, roots and soil as well as in the air. During two weeks of exposure TCA was continuously degraded, especially in the soil. Estimates of radioactivity balance showed loss of radioactivity into the atmosphere in the form of ¹⁴CO₂; unincorporated [1,2-¹⁴C]TCA, chloroform, carbon monoxide and methane were not detected at all. TCA degradation to CO₂ was indicated also in the spruce needles. Moreover, it was found that soil litter contained [1,2-¹⁴C]TCA unavailable to microorganisms.

Natural genetic variation present in two populations of the critically endangered legume C. longipes was revealed by random amplified polymorphic DNA (RAPD) analysis. Out of the 30 primers used to test the intra-specific genetic polymorphism (between individuals from isolated populations) only 21 gave amplification. Eight primers produced monomorphic bands and 13 primers produced polymorphism. But the range of percent polymorphism was only 0 to 33 %. There was close similarity between individuals within and between populations. Cluster analysis based on Nei's indices did not reveal any population differentiation and individuals of both populations clustered with each other. These results point to a very low genetic polymorphism in C. longipes populations.

Wheat leaves contain two charge/mass-separable isoforms of glutathione reductase (GR, EC 1.6.4.2), one chloroplastic and the other probably cytosolic. The chloroplastic GR was purified to homogeneity, and its biochemical and molecular characterisation showed features very similar to the other plant GRs. In its native conformation the enzyme is composed by two subunits of 56 kDa and an associated polypeptide of 32 kDa, with an overall molecular mass of approximately 150 kDa. Optimum activity was observed at pH 8.00 and with an ionic strength between 60 to 100 mM. GR activity is highly sensitive to temperature changes, exhibiting an exponential increase up to 45 °C. It showed a high affinity for oxidised glutathione and an intermediate affinity for NADPH at pH 8.0. Inhibition tests with thiol and histidine modifiers demonstrated that -SH groups and histidine residues are essential for the catalytic properties of the enzyme. T study the origin of GR isoforms, the number of GR gene copies and the number and size of GR transcripts were determined. Southern analyses showed that wheat GR isoforms are encoded by multiple gene copies. However, a single size transcript of approximately 1.4 kb was observed, suggesting that different GR isoforms could be generated by post-transcriptional and/or post-translational modifications.

The induction of sister chromatid exchanges (SCE) by chloride and nitrate salts of nickel, cobalt, cadmium and zinc were studied in meristematic root cells of Vicia faba. Salts of nickel, cobalt and cadmium significantly increased the frequency of SCE, whereas chloride and nitrate salts of zinc did not increase the frequency of SCE significantly above the spontaneous level. The reported data demonstrate that the induction of SCE in Vicia faba may represent a valuable bioindicator for detecting the cytogenetic damage of heavy metals.

The effects of different concentrations (10^-5 - 10^-2 M) of copper sulfate on root growth, cell division and nucleoli in root tip cells of Zea mays L. were investigated. 10^-5 M Cu stimulated root growth, but at higher concentrations (10^-4 - 10^-2 M) inhibited it. Cu had toxic effects on chromosomal morphology: c-mitosis, anaphase bridges, and chromosome stickiness were induced. Some nuclei had irregular shape and particles extruded from nucleoli to nuclei and finally from the nuclei into the cytoplasm.

Cultural conditions affecting the induction of rhizogenesis in vitro were evaluated in cashew (Anacardium occidentale L.) shoot-node-derived microshoots. The application of auxins was essential for the formation of adventitious roots. A 5-d indole-3-butyric acid (IBA) induction period was more suitable than continuous IBA treatment or a shorter induction period. N⁶-[2-Isopentenyl]adenine in low concentrations (0.3 - 1 µM) in the root induction medium supported root formation. Precultivation of microshoots with gibberellic acid (GA₃) suppressed the subsequent rhizogenesis. Activated charcoal did not affect rooting. No significant differences in rooting abilities of cashew shoots were observed between 25, 29 and 35 °C and roots did not develop at 19 °C. Salts of low osmotic composition were more suitable than richer media. Microshoots originated from cotyledonary nodes showed higher rooting when compared to standard microshoots.

The effect of the methyl ester of jasmonic acid (MeJA) in 10 μM concentration was studied on the development of the bacterial contaminants and on the content of some metabolites in Scenedesmus incrassulatus cultivated at temperatures 15, 20, 25, 30, and 36 °C. The number of bacteria on algae cells increased with the rise in temperature. Application of MeJA into nutrient medium inhibited the development of bacterial pathogens more than 3 times at 20 °C, 2.3 times at 30 °C, and 2.6 times at 36 °C without changing the species composition. MeJA caused an increase of the protein content in algae cells. The contents of palmitic and linoleic acids increased with the rise of temperature from 15 to 36 °C. At the same time the contents of linolenic and oleic acid decreased. At low temperatures, cultivation with MeJA induced more significant changes in the composition of C18 acids while at high temperature the changes were more pronounced in C16 acids. Treatment with MeJA decreased the activity of glutamate dehydrogenase at optimal and suboptimal temperatures and increased it at superoptimal temperature. Hence MeJA jasmonate had a positive effect on the tolerance of S. incrassulatus to stress temperatures, which was also demonstrated by better growth.

Water transport was assessed in seedlings of the mangrove Avicennia germinans L. grown at 171 and 684 mol m^-3 NaCl. Leaf specific conductivity declined by 25 % at high salinity. This was related to low specific conductivity, because Huber values remained similar. Leaves of A. germinans featured low internal conductance to water transport. This was lowered further under high salinity. Water transport constrains imposed by whole shoot and leaf blade at high salinity were balanced by stomatal regulation of water loss, which possibly maintain stem water potentials above embolisms levels.

A cell culture system has been developed to examine a multicomponent defense response induced in grapevine (Vitis vinifera L. cv. Limberger) tissues by both biotic and abiotic elicitors. H₂O₂ from the oxidative burst, cell death, extracellular alkalinization, and defense responses such as the accumulation of defense-related proteins and expression of corresponding genes were analyzed in grapevine suspension cultures. Cultured cells responded differentially to a set of 14 elicitors. The most effective group of elicitors was represented by salicylic acid, chitosan, methyl jasmonate, and elicitor released from cell walls of phytopathogen Botrytis cinerea. These four representative elicitors highly stimulated accumulation of pathogenesis-related proteins and key enzymes of the phenylpropanoid pathway. Further, fungal elicitor caused rapid transcriptional activation of genes encoding diverse defense-related products. The expression kinetics of four defense-related genes (PR-1, PR-9, PAL, and CHI) were different and strongly dependent on the nature of elicitor used.

In pigeonpea (Cajanus cajan L.) shoot buds were induced when cotyledonary node explants were supplemented with benzylaminopurine (BAP; 2 mg dm^-3). When 0.1 mg dm^-3 BAP and 0.01 mg dm^-3 naphtahalene acetic acid were supplemented to the medium, the 34 - 35 % of induced buds developed to microshoots. By supplementing amino acids like proline, glutamine, asparagine and L-cysteine, shoot bud development to microshoots was enhanced at least by two fold. Amongst the amino acids proline gave maximum number of microshoots per explant. With increase in concentration of amino acids, fresh mass increased but microshoot number decreased. Also methane evolution was increased by addition of amino acids, and also in medium containing more of its nitrogen in the form of ammonia. Increased evolution of methane was accompanied by reduction in evolution of ethylene, and enhancement of efficiency of microshoot development.

The relationships between photosynthesis, leaf nitrogen content and water stress were studied in ten genotypes of wheat differing in the presence of dwarfing genes. Net photosynthetic rate (P_N) was mostly higher at ear emergence stage than at anthesis stage. P_N decreased with water stress (leaf water potential from -2.0 to -2.5 MPa), and with reduced leaf N content in all genotypes studied. Among the various genotypes, single dwarf and wild types showed higher P_N rate and maintained higher leaf N content under different N doses and water supply as compared to the other types studied.

The structure and ultrastructure of the second leaves of 10-d-old barley plants (Hordeum vulgare L. cv. Alfa) was investigated after long-term treatment with salicylic acid (SA) in concentrations of 0.1, 0.5 and 1.0 mM. The treatment induced: 1) suppressed bulliform cells formation in the adaxial epidermis (1.0 mM SA); 2) reduction of apoplast in the mesophyll (0.5 and 1.0 mM SA); 3) formation of invaginations (0.1 and 0.5 mM SA) and proliferations (0.5 mM SA); and 4) thylakoid destruction and coagulation of the stroma (1.0 mM SA).

Effects of water stress at pre-flowering stage were studied in three genotypes (RMO-40, Maru moth and CZM-32 E) of moth bean [Vigna aconitifolia (Jacq.) Marechal]. Increasing water stress progressively decreased plant water potential, leaf area, net photosynthetic rate, starch and soluble protein contents and nitrate reductase activity while contents of reducing sugars, total soluble sugar, free amino acids and free proline progressively increased. Significant genotypic differences were observed and genotype CZM-32-E displayed a better drought tolerance than other genotypes.