Showing papers on "Plant physiology published in 1994"

Effects of cobalt on plants

Abstract: Cobalt, a transition element, is an essential component of several enzymes and co-enzymes. It has been shown to affect growth and metabolism of plants, in different degrees, depending on the concentration and status of cobalt in rhizosphere and soil. Cobalt interacts with other elements to form complexes. The cytotoxic and phytotoxic activities of cobalt and its compounds depend on the physico-chemical properties of these complexes, including their electronic structure, ion parameters (charge-size relations) and coordination. Thus, the competitive absorption and mutual activation of associated metals influence the action of cobalt on various phytochemical reactions. The distribution of cobalt in plants is entirely species-dependent. The uptake is controlled by different mechanisms in different species. Biosorption involves ion-exchange mechanism in algae, but in fungi both metabolism-independent and -dependent processes are operative. Physical conditions like salinity, temperature, pH of the medium, and presence of other metals influence the process of uptake and accumulation in algae, fungi, and mosses. Toxic concentrations inhibit active ion transport. In higher plants, absorption of Co2+ by roots involves active transport. Transport through the cortical cells is operated by both passive diffusion and active process. In the xylem, the metal is mainly transported by the transpirational flow. Distribution through the sieve tubes is acropetal by complexing with organic compounds. The lower mobility of Co2+ in plants restricts its transport to leaves from stems. Cobalt is not found at the active site of any respiratory chain enzymes. Two sites of action of Co2+ are found in mitochondrial respiration since it induces different responses toward different substrates like α-keto glutarate and succinate. In lower organisms, Co2+ inhibits tetraphyrrole biosynthesis, but in higher plants it probably participates in chlorophyll b formation. Exogenously added metal causes morphological damage in plastids and changes in the chlorophyll contents. It also inhibits starch grain differentiation and alters the structure and number of chloroplasts per unit area of leaf. The role of cobalt in photosynthesis is controversial. Its toxic effect takes place by inhibition of PS2 activity and hence Hill reaction. It inhibits either the reaction centre or component of PS2 acceptor by modifying secondary quinone electron acceptor Qb site. Co2+ reduces the export of photoassimilates and dark fixation of CO2. In C4 and CAM plants, it hinders fixation of CO2 by inhibiting the activity of enzymes involved. Cobalt acts as a preprophase poison and thus retards the process of karyokinesis and cytokinesis. The action of cobalt on plant cells is mainly turbagenic. Cobalt compounds act on the mitotic spindle, leading to the formation of chromatin bridges, fragmentation, and sticky bridges at anaphase and binucleate cells. High concentrations of cobalt hamper RNA synthesis, and decrease the amounts of the DNA and RNA probably by modifying the activity of a large number of endo- and exonucleases. The mutagenic action of cobalt salts results in mitochondrial respiratory deficiency in yeasts. In cytokinesis-deficient mutant of Chlamydomonas it increases the amount of sulfhydryl compounds. Cobalt has been shown to alter the sex of plants like Cannabis sativa, Lemna acquinoclatis, and melon cultivars. It decreases the photoreversible absorbance of phytochrome in pea epicotyl and interferes with heme biosynthesis in fungi. Low concentration of Co2+ in medium stimulates growth from simple algae to complex higher plants. Relatively higher concentrations are toxic. A similar relationship is seen with crop yield when the metal is used in the form of fertilizer, pre-seeding, and pre-sowing chemicals. Toxic effect of cobalt on morphology include leaf fall, inhibition of greening, discolored veins, premature leaf closure, and reduced shoot weight. Being a component of vitamin B12 and cobamide coenzyme, Co2+ helps in the fixation of molecular nitrogen in root nodules of leguminous plants. But in cyanobacteria, CoCl2 inhibits the formation of heterocyst, ammonia uptake, and nitrate reductase activity. The interaction of cobalt with other metals mainly depends on the concentration of the metals used. For example, high levels of Co2+ induce iron deficiency in plants and suppress uptake of Cd by roots. It also interacts synergistically with Zn, Cr, and Sn. Ni overcomes the inhibitory effect of cobalt on protonemal growth of moss, thus indicating an antagonistic relationship. The beneficial effects of cobalt include retardation of senescence of leaf, increase in drought resistance in seeds, regulation of alkaloid accumulation in medicinal plants, and inhibition of ethylene biosynthesis. In lower plants, cobalt tolerance involves a cotolerance mechanism. The mechanism of resistance to toxic concentration of cobalt may be due to intracellular detoxification rather than defective transport. In higher plants, only a few advanced copper-tolerant families showed cotolerance to Co2+. Tolerance toward Co2+ may sometimes determine the taxonomic shifting of several members of Nyssaceae. Due to the high cobalt content in serpentine soil, essential element uptake by plants is reduced, a phenomenon known as “serpentine problem,” for New Caledonian families like Flacourtiaceae. Large amounts of calcium in soil may compensate for the toxic effects of heavy metals in adaptable genera grown in this type of soil. The biomagnification of potentially toxic elements, such as cobalt from coal ash or water into food webs, needs additional study for effective biological filtering.

The Physiology and Molecular Biology of Plant 1,3-β-D-Glucanases and 1,3;1,4-β-D-Glucanases

Abstract: This review covers the physiology and molecular biology of the plant β-glucanases possessing either endo-1,3-β-D-glucanase (EC 3.2.1.39) or endo-1,3;1,4-β-D-glucanase (EC 3.2.1.73) activity. These β-glucanases are structurally related enzymes that are believed to be involved in many important aspects of plant physiology and development, such as germination, growth, defense against pathogens, flowering, cellular and tissue development and differentiation, and probably other roles. They also are regulated by numerous plant hormones, biotic and abiotic elicitors and stresses, and they exhibit complex tissue- and developmental-specific gene expression.

Effects of nitrogen supply on the acclimation of photosynthesis to elevated CO2.

Abstract: A common observation in plants grown in elevated CO2 concentration is that the rate of photosynthesis is lower than expected from the dependence of photosynthesis upon CO2 concentration in single leaves of plants grown at present CO2 concentration. Furthermore, it has been suggested that this apparent down regulation of photosynthesis may be larger in leaves of plants at low nitrogen supply than at higher nitrogen supply. However, the available data are rather limited and contradictory. In this paper, particular attention is drawn to the way in which whole plant growth response to N supply constitutes a variable sink strength for carbohydrate usage and how this may affect photosynthesis. The need for further studies of the acclimation of photosynthesis at elevated CO2 in leaves of plants whose N supply has resulted in well-defined growth rate and sink activity is emphasised, and brief consideration is made of how this might be achieved.

Different characteristics of roots in the cadmium-tolerance and Cd-binding complex formation between mono- and dicotyledonous plants

Abstract: Effects of Cd2+ on growth and Cd-binding complex formation in roots were examined with various seedlings of mono- and dicotyledonous plants. Maize, oat, barley and rice exhibited the greater tolerance to Cd2+ (100 μM) than did azuki bean, cucumber, lettuce, pea, radish, sesame and tomato (10–30 μM). Azuki bean was the most sensitive to Cd2+ (<10 μM). Under these Cd-treatments, cereal roots accumulated Cd2+ in the cytoplasmic fractions and transported Cd2+ into the same fractions of shoot tissues, to larger extents than did dicotyledonous roots. Cereal roots synthesized a Cd-binding complex containing phytochelatins in the cytoplasmic fractions, depending upon Cd2+ concentrations applied (30–100 μM). Such a complex was not detected from the same fractions of dicotyledonous roots treated with Cd2+. These results suggest that the Cd-binding complex formation has an important role in the tolerance of cereal roots against Cd2+.

Biochemistry of C3-photosynthesis in high CO2

Abstract: The short-term responses of C3 photosynthesis to high CO2 are described first. Regulation of photosynthesis in the short term is determined by interaction among the capacities of light harvesting, electron transport, ribulose-1, 5-bisphosphate carboxylase (Rubisco) and orthophosphate (Pi) regeneration during starch and sucrose synthesis. Photosynthesis under high CO2 conditions is limited by either electron transport or Pi regeneration capacities, and Rubisco is deactivated to maintain a balance between each step in the photosynthetic pathway. Subsequently, the long-term effects on, photosynthesis are discussed. Long-term CO2 enhancement leads to carbohydrate accumulation. Accumulation of carbohydrates is not associated with a Pi-regeneration limitation on photosynthesis, and this limitation is apparently removed during long-term exposure to high CO2. Enhanced CO2 does not affect Rubisco content and electron transport capacity for a given leaf-nitrogen content. In addition, the deactivated Rubisco immediately after exposure to high CO2 does not recover during the subsequent prolonged exposure. Such evidence may indicate that plants do not necessarily have an ideal acclimation response to high CO2 at the biochemical level.

Phytochrome-Mediated Phototropism in Adiantum cuneatum Young Leaves

Abstract: Phototropism of youngAdiantum fern leaves is induced by red light as well as blue light The red light response is mediated by phytochrome This is the first evidence of phytochrome action in diploid fern tissue The blue light response is mainly mediated not by phytochrome, but probably by a blue light-absorbing pigment as in the case of almost all plants and fungi The red light-induced phototropism becomes detectable within 2 hr after the onset of unilateral light The highest bending rate is about 10 degrees/hr, which occurs between 3–5 hr after the induction of the tropic response The bending region is about 6–8 mm from the highest point of the coiled crozier where the growth rate becomes slow

Effects of Sulfur Dioxide and Ozone on Intact Leaves and Isolated Mesophyll Cells of Groundnut Plants (Arachis hypogaea L.)

Abstract: Difference between effects of sulfur dioxide (SO2) and ozone (O3) on groundnut plants (Arachis hypogaea L.) was studied by use of an exposure system of enzymatically-isolated mesophyll cells. SO2 inhibited photosynthesis of intact groundnut leaves but induced no visible injury on leaves. SO2 also inhibited photosynthesis of isolated mesophyll cells but did not kill the cells, suggesting that SO2 inhibits photosynthesis by attacking rather specifically the photosynthetic apparatus in chloroplasts. O3 inhibited photosynthesis of intact leaves and at the same time induced visible injury corresponding to the extent of photosynthesis inhibition. O3 also inhibited photosynthesis of isolated mesophyll cells and killed the cells to the extent corresponding to photosynthesis inhibition, suggesting that O3 inhibits photosynthesis not directly by attacking the photosynthetic apparatus but indirectly by killing cells. Since the response of intact leaves to each pollutant resembled that of isolated mesophyll cells, the difference between responses of intact leaves to both pollutants may considerably reflect that of mesophyll cells.