Abstract Calcium ions (Ca 2+ ) are absorbed from the soil by the root cells before being distributed throughout the plant. The transport of Ca 2+ to aboveground parts relies on the movement of xylem, which is influenced by the transpiration rate of individual organs. The final distribution of Ca 2+ in tissues and cells depends on the effective function of channels and transporters that facilitate Ca 2+ movement through plasma and specific intracellular membranes. Local fluctuations in free Ca 2+ concentrations serve as a mechanism to elicit cellular responses, characterized by distinct calcium signatures, or to enable long-distance signaling in a cell-to-cell network. The specificity of individual Ca 2+ transport proteins is primarily determined through studies in plants with induced changes in the expression of these proteins. Concurrently, it is recognized that plant cells contain significant reserves of Ca 2+ both in the labile and in the permanently bound states, which influences various aspects such as biomechanical properties or the defensive capabilities of the cells. The diverse roles of Ca 2+ in plant cells highlight the importance of a thorough understanding of Ca 2+ metabolism.
The role of the cell wall in the life of the plant. The molecular components of the wall. Cell wall architecture and the skeletal functions of the wall. Cell-wall formation. The cell wall and control of cell growth. The cell wall and intracellular transport. The cell wall and interactions with other organisms. The cell wall and reproduction. Cell-wall degradation and biotechnological applications. Cell walls in diet and health. Outstanding problems for future research.
The extensibility of synthetic polymers is routinely modulated by the addition of lower molecular weight spacing molecules known as plasticizers, and there is some evidence that water may have similar effects on plant cell walls. Furthermore, it appears that changes in wall hydration could affect wall behavior to a degree that seems likely to have physiological consequences at water potentials that many plants would experience under field conditions. Osmotica large enough to be excluded from plant cell walls and bacterial cellulose composites with other cell wall polysaccharides were used to alter their water content and to demonstrate that the relationship between water potential and degree of hydration of these materials is affected by their composition. Additionally, it was found that expansins facilitate rehydration of bacterial cellulose and cellulose composites and cause swelling of plant cell wall fragments in suspension and that these responses are also affected by polysaccharide composition. Given these observations, it seems probable that plant environmental responses include measures to regulate cell wall water content or mitigate the consequences of changes in wall hydration and that it may be possible to exploit such mechanisms to improve crop resilience.
L.). Rice plants at the tillering stage were exposed to gamma rays for 8 h (acute irradiation) or 10 days (chronic irradiation), with a total irradiation dose of 100, 200, or 300 Gy. Plants exposed to gamma irradiation were then analyzed for DNA damage, oxidative stress indicators including free radical content and lipid peroxidation, radical scavenging, and antioxidant activity. The results showed that all stress indices increased immediately after exposure to both acute and chronic irradiation in a dose-dependent manner, and acute irradiation had a greater effect on plants than chronic irradiation. The photosynthetic efficiency and growth of plants measured at 10, 20, and 30 days post-irradiation decreased in irradiated plants, i.e., these two parameters were more severely affected by acute irradiation than by chronic irradiation. In contrast, acutely irradiated plants produced seeds with dramatically decreased fertility rate, and chronically irradiated plants failed to produce fertile seeds, i.e., reproduction was more severely affected by chronic irradiation than by acute irradiation. Overall, our findings suggest that acute gamma irradiation causes instantaneous and greater damage to plant physiology, whereas chronic gamma irradiation causes long-term damage, leading to reproductive failure.
This review discusses how the pressure probe has evolved from an instrument for measuring cell turgor and other water relations parameters into a device for sampling the contents of individual higher plant cells in situ in the living plant. Together with a suite of microanalytical techniques it has permitted the mapping of water and solute relations at the resolution of single cells and has the potential to link quantitatively the traditionally separate areas of water relations and metabolism. The development of the probe is outlined and its modification to measure root pressure and xylem tension described. The deployment of the pressure probe to determine and map turgor, hydraulic conductivity, reflection coefficient, cell rheological properties, solute concentrations and enzyme activities at the resolution of single cells is discussed. The controversy surrounding the interpretation of results obtained with the xylem-pressure probe is included. Possible further developments of the probe and applications of single cell sampling are suggested.
Plant leaves are optically complex, which makes them difficult to image by light microscopy. Careful sample preparation is therefore required to enable researchers to maximize the information gained from advances in fluorescent protein labeling, cell dyes and innovations in microscope technologies and techniques. We have previously shown that mounting leaves in the non-toxic, non-fluorescent perfluorocarbon (PFC), perfluorodecalin (PFD) enhances the optical properties of the leaf with minimal impact on physiology. Here, we assess the use of the PFCs, PFD, and perfluoroperhydrophenanthrene (PP11) for in vivo plant leaf imaging using four advanced modes of microscopy: laser scanning confocal microscopy (LSCM), two-photon fluorescence microscopy, second harmonic generation microscopy, and stimulated Raman scattering (SRS) microscopy. For every mode of imaging tested, we observed an improved signal when leaves were mounted in PFD or in PP11, compared to mounting the samples in water. Using an image analysis technique based on autocorrelation to quantitatively assess LSCM image deterioration with depth, we show that PP11 outperformed PFD as a mounting medium by enabling the acquisition of clearer images deeper into the tissue. In addition, we show that SRS microscopy can be used to image PFCs directly in the mesophyll and thereby easily delimit the "negative space" within a leaf, which may have important implications for studies of leaf development. Direct comparison of on and off resonance SRS micrographs show that PFCs do not to form intracellular aggregates in live plants. We conclude that the application of PFCs as mounting media substantially increases advanced microscopy image quality of living mesophyll and leaf vascular bundle cells.
concentrations between tissues and within individual cell types, such as root hairs. Progression of hypoxia reveals substantial plasticity of ATP homeostasis in seedlings, demonstrating that ATP dynamics can be monitored in the living plant.
Global Analysis of Gene Networks to Solve complex Abiotic Stress responses, K Shinozaki, RIKEN Tsukuba Institute, Japan and K Yamaguchi-Shinozaki, Japan International Research Center for Agricultural Sciences, Japan The CBF Cold Response Pathways of Arabidopsis and Tomato, J T Vogel, Michigan State University, USA, D Cook, Mississippi State University, USA, S G Fowler and M F Thomashow, Michigan State University, USA Barley Contains a Large CBF Gene Family Associated with Quantitative Cold Tolerance Traits, J S Skinner, J von Zitzewitz, L Marquez-Cedillo, T Filichkin, Oregon State University, USA, P Szucs, Agricultural Research Institute of the Hungarian Academy of Sciences, Hungary, K Amundsen, Michigan State University, USA, E Stockinger, Ohio State University, USA, M F Thomashow, Michigan State University, USA, T H H Chen, and P M Hayes, Oregon State University, USA Structural Organization of Barley CBF Genes Coincident with QTLs for Cold Hardiness, E J Stockinger, H Cheng, Chinese Academy of Agricultural Sciences, China and J Skinner The genetic basis of vernalization response in barley, L L D Cooper, Oregon State University, USA, J von Zitzewitz, J S Skinner, P Szucs, I Karsai, Agriculturtal Research Institute of the Hungarian Academy of Sciences, Hungary, E Francia, A M Stanca, Experimental Institute for Cereal Resources, Italy, N Pecchioni, Universita di Modena e Reggio Emilia, Italy, D A Laurie, John Innes Research Centre, UK T H H Chen, and P M Hayes Vernalization Genes in Winter Cereals, N A Kane, J Danyluk, and F Sarhan, Universite du Quebec a Montreal, Canada A Bulk Segregant Approach to Identify Genetic Polymorphisms Associated with Cold Tolerance in Alfalfa, Y Castonguay, J Cloutier, S Laberge, A Bertrand and R Michaud, Agriculture and Agri-Food Canada, Canada Ectopic Over-expression of AtCBFI in Potato Enhances Freezing Tolerance, M T Pino, J S Skinner, Z Jeknic, E J Park, Oregon State University, USA, P M Hayes, and T H H Chen Over-expression of a Heat-inducible apx Gene Confers Chilling Tolerance to Rice Plants, Y Sato, National Agricultural Research Center for Hokkaido Region, Japan, and H Saruyama, Hokkaido Green-Bio Institute, Japan Physiological and Morphological Alterations Associated with Development of Freezing Tolerance in The Moss Physcomitrella patens, A Minami, M Nagao, Iwate University, Japan, K Arakawa, S Fujikawa, Hokkaido University and D Takezawa, Saitama University, Japan Control of Growth and Cold Acclimation in Silver Birch, M K Aalto and E T Palva, Viikki Biocenter, Finland The Role of the CBF-Dependent Signalling Pathway in Woody Perennials, C Benedict, Umea University, Sweden, J S Skinner, R Meng, Y Chang, Oregon State University, USA, R Bhalerao, Swedish University of Agricultural Sciences, Sweden, C Finn, USDA-ARS, USA, T H H Chen, V Hurry, Umea University, Sweden Functional Role of Winter-accumulating Proteins from Mulberry Tree in adaptation to Winter-induced Stresses, S Fujikawa, N Ukaji, Hokkaido University, Japan, M Nagao, K Yamane, Hokkaido University, Japan, D Takezawa, and K Arakawa The Role of Compatible Solutes in Plant Freezing Tolerance: A Case Study on Raffinose, D K Hincha, E Zuther, M Hundertmark, A G Heyer, Max-Planck-Institut fur Molekulare Pflanzenphysiologie, Germany Dehydration in model membranes and protoplasts: contrasting effects at low, intermediate and high hydrations, K L Koster, University of South Dakota, USA, and G Bryant, RMIT University, Australia Effect of Plasma Membrane-associated Proteins on Acquisition of Freezing Tolerance in Arabidopsis thaliana, Y Tominaga, Universite du Quebec a Montreal, Canada, C Nakagawara, Y Kawamura and M Uemura, Iwate University, Japan.
Could a disjoint group of enzymes synchronize their activities and execute a complex multi-step, measurable, and reproducible response? Here, I surmise that the alpha-ketoglutarate dependent superfamily of non-haem iron (II) dioxygenases could influence cell physiology as a cohesive unit, and that the broad spectra of substrates transformed is an absolute necessity to this portrayal. This eclectic group comprises members from all major taxa, and participates in pesticide breakdown, hypoxia signaling, and osmotic stress neutralization. The oxidative decarboxylation of 2-oxoglutarate to succinate is coupled with a concomitant substrate hydroxylation and, in most cases, is followed by an additional specialized conversion. The domain profile of a protein sequence was used as an index of miscellaneous reaction chemistry and interpreted alongside existent kinetic data in a linear model of integrated function. Statistical parameters were inferred by the creation of a novel, empirically motivated flat-file database of over 3800 sequences (DB2OG) with putative 2-oxoglutarate dependent activity. The collated information was categorized on the basis of existing annotation schema. The data suggests that 2OG-dependent enzymes incorporate several desirable features of a systems level player. DB2OG, is free, accessible without a login to all users, and available at the following URL (http://comp-biol.theacms.in/DB2OG.html).
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Expression and stability of immunoglobulins in transgenic plants have been investigated and optimized by accumulation in different cellular compartments as cytosol, apoplastic space and endoplasmic reticulum (ER) as will be discussed in this review. In several cases described the highest accumulation of complete active antibodies was achieved by targeting into the apoplastic space. High-level expression of active recombinant single-chain Fv antibodies (scFv's) was obtained by retention of these proteins in the lumen of the endoplasmic reticulum. This has been shown for leaves and seeds of transgenic tobacco as well as for potato tubers. Transgenic tobacco seeds, potato tubers and tobacco leaves can facilitate stable storage of scFv's accumulated in the ER over an extended (seeds, tubers) or a short (leaves) period of time. The expression of specific scFv's in different plant species, plant organs and cellular compartments offers the possibility of blocking regulatory factors or pathogens specifically. Examples are scFv's expressed in the cytosol and the apoplastic space of transgenic plant cells modulating the infection process of plant viruses and a cytosolically expressed scFv that influenced the activity of phytochrome A protein. The immunomodulation approach has been shown to be also applicable for investigating the action of the phyto-hormone abscisic acid (ABA). High-level accumulation of specific anti-ABA scFv's in the ER of all leaf cells has been used to block the influence of ABA on the stomatal functions. Seed-specific expression of high amounts of anti-ABA-scFv's at a defined time of seed-development induced a developmental switch from seed ripening to vegetative growth. It has been demonstrated that ER retention is essential for the accumulation of sufficient scFv to bind high concentrations of ABA in the transgenic seeds.
A turgid leaf exposed to bright sunshine can transpire an amount of water several times its own weight during a summer day. Rapid evaporation is sustained by a supply of heat from the atmosphere and by a movement of water within the plant preventing the desiccation of leaf tissue. In analysis, the need for energy and the need for water have often been disassociated. Meteorologists investigating the energetics of transpiration have assumed that leaves behave like pieces of wet, green blotting paper, and plant physiologists have demonstrated mechanisms for the conduction of water at arbitrary rates unrelated to the physics of the environment. This paper describes progress towards a reconciliation of parallel concepts in meteorology and physiology. The path for the diffusion of water vapour from leaf cells to the free atmosphere is divided into two parts, one determined primarily by the size and distribution of stomata, and the other by wind speed and the aerodynamic properties of the plant surface. Diffusive resistances for single leaves and for plant communities are established from measurements in the laboratory and in the field and are then used: (i) to predict relative rates of evaporation from leaves with wet and dry surfaces; (ii) to investigate the dependence of transpiration rate on wind speed and surface roughness; (iii) to demonstrate that the relation between transpiration rate and lead area is governed by stomatal closure in leaves well shaded from sunlight; (iv) to calculate maximum rates of transpiration for different crops and climates. A final section on the convection of dry air stresses the importance of physiological restraint on the rate of transpiration from an irrigated field surrounded by dry land.
The xerophytic, but salt-sensitive Sorghum cultivar ‘Sweet Sioux’ is known as an ion excluder with a high K/Na selectivity at the plasmalemma and tonoplast of epidermal root cells. The aim of this study is the correlation of salt-effected changes in physiological parameters with structural and ultrastructural changes in root cells. The investigation was carried out with root cells because these cells are most directly exposed to the growth medium. Sorghum bicolor × S. sudanensis cv. Sweet Sioux plants were grown under steady-state conditions on nutrient solutions with or without 40 mol m−3 NaCl. Sorghum sustained this treatment but showed several salt-induced structural and physiological changes which were studied in various cell types of the root tip. (1) NaCl salinity led to a shorter growth region and to salt-induced alterations in the chemical and physical properties of the cell walls in the root tips. (2) Salt treatment also increased the membrane surface in root cells: root cells showed an increase in the quantity of vesicles in the epidermis and in the middle cortex cells. Additionally, some of the epidermis cells of salt-treated plants revealed a characteristic build-up of transfer cells, suggesting an increase in membrane surfaces to increase the uptake and storage of substances. (3) The number of mitochondria increased in the epidermal and in the cortex cells after salt stress thus indicating an additional supply of energy for osmotic adaptation and for selective uptake and transport processes. (4) In the epidermal cytoplasm NaCl stress led to a significant decrease of the P, K, Ca, and S concentrations accompanied by an increase of Na concentration. Electron micrographs show an increase in electron optical contrast within the cytosol and in the matrix of the mitochondria. These results are discussed with regard to the possibility of influence on the part of metabolic functions. (5) The NaCl concentrations were seen to increase and the K concentrations to decrease during salt stress in the vacuoles of the epidermis and cortex cells. The salt-induced increase in vacuolar NaCl concentrations of epidermis and cortex cells are in the region 2 cm behind the root tip, which is sufficient for an osmotic balance towards the growth medium. Additional solutes are necessary 0.5 mm behind the root tip to facilitate osmotic adaptation. The results show ultrastructural changes caused by an Na-avoiding mechanism characterized by a high level of energy consumption. The exclusion of Na from the symplast seems to lead additionally to a decrease in cytoplasmic concentrations of such essential elements as Mg, P, S, and Ca and is thus responsible directly (via energy supply in mitochondria, homeostasis, selectivity of K over Na) or indirectly (via enzyme conformation, cytoplasmic hydration) for the ultra-structural degradation indicated. The salinity-induced multiplicity of structural and functional changes within cell compartments constitutes a group of indicators for the limited NaCl tolerance of Sorghum.
Physiological and ecological constraints play key roles in the evolution of plant growth patterns, especially in relation to defenses against herbivores. Phenotypic and life history theories are unified within the growth-differentiation balance (GDB) framework, forming an integrated system of theories explaining and predicting patterns of plant defense and competitive interactions in ecological and evolutionary time. Plant activity at the cellular level can be classified as growth (cell division and enlargement) of differentiation (chemical and morphological changes leading to cell maturation and specialization). The GDB hypothesis of plant defense is premised upon a physiological trade-off between growth and differentiation processes. The trade-off between growth and defense exists because secondary metabolism and structural reinforcement are physiologically constrained in dividing and enlarging cells, and because they divert resources from the production of new leaf area. Hence the dilemma of plants: They must grow fast enough to complete, yet maintain the defenses necessary to survive in the presence of pathogens and hervivores. The physiological trade-off between growth and differentiation processes interacts with herbivory and plant-plant competition to manifest itself as a genetic trade-off between growth and defense in the evolution of plant life history strategies. Evolutionary theories of plant defense are reviewed. We also extend a standard growth rate model by separating its ecological and evolutionary components,and formalizing the role of competition in the evolution of plant defense. We conclude with a conceptual model of the evolution of plant defense in which plant physioligical trade-offs interact with the abiotic environment, competition and herbivory.
The relationships of guard cell ABA content to eight stress-related physiological parameters were determined on intact Vicia faba L. plants that were grown hydroponically with split-root systems. Continuous stress was imposed by the addition of PEG to part of the root system. The water potentials of roots sampled after the addition of PEG were 0.25 MPa lower than the water potentials of other roots of the same plant, which were similar to the roots of untreated plants. The leaflet water potentials of plants sampled within 2 h of stress imposition were similar to those of control plants. However, leaf conductance was lower in plants sampled after only 20 min of stress imposition, and the root- and leaflet apoplastic ABA concentrations of these plants were higher than those of untreated plants. As the essence of this report, there was a linear relationship between guard cell ABA content and leaf conductance. Leaflet apoplastic ABA concentrations <150 nM were also linearly related to leaf conductance, but higher leaflet apoplastic ABA concentration did not cause equally large further declines in leaf conductance. It is suggested that evaporation from guard cell walls caused ABA to accumulate in the guard cell apoplast and this pool was saturated at high leaflet apoplastic ABA concentrations.
Browning phenomena are ubiquitous in plant cell cultures that severely hamper scientific research and widespread application of plant cell cultures. Up to now, this problem still has not been well controlled due to the unclear browning mechanisms in plant cell cultures. In this paper, the mechanisms were investigated using two typical materials with severe browning phenomena, Taxus chinensis and Glycyrrhiza inflata cells. Our results illustrated that the browning is attributed to a physiological enzymatic reaction, and phenolic biosynthesis regulated by sugar plays a decisive role in the browning. Furthermore, to confirm the specific compounds which participate in the enzymatic browning reaction, transcriptional profile and metabolites of T. chinensis cells, and UV scanning and high-performance liquid chromatography-mass spectrometry (HPLC-MS) profile of the browning compounds extracted from the brown-turned medium were analyzed, flavonoids derived from phenylpropanoid pathway were found to be the main compounds, and myricetin and quercetin were deduced to be the main substrates of the browning reaction. Inhibition of flavonoid biosynthesis can prevent the browning occurrence, and the browning is effectively controlled via blocking flavonoid biosynthesis by gibberellic acid (GA3 ) as an inhibitor, which further confirms that flavonoids mainly contribute to the browning. On the basis above, a model elucidating enzymatic browning mechanisms in plant cell cultures was put forward, and effective control approaches were presented.
BACKGROUND: Plants are often subjected to periods of soil and atmospheric water deficits during their life cycle as well as, in many areas of the globe, to high soil salinity. Understanding how plants respond to drought, salt and co-occurring stresses can play a major role in stabilizing crop performance under drought and saline conditions and in the protection of natural vegetation. Photosynthesis, together with cell growth, is among the primary processes to be affected by water or salt stress. SCOPE: The effects of drought and salt stresses on photosynthesis are either direct (as the diffusion limitations through the stomata and the mesophyll and the alterations in photosynthetic metabolism) or secondary, such as the oxidative stress arising from the superimposition of multiple stresses. The carbon balance of a plant during a period of salt/water stress and recovery may depend as much on the velocity and degree of photosynthetic recovery, as it depends on the degree and velocity of photosynthesis decline during water depletion. Current knowledge about physiological limitations to photosynthetic recovery after different intensities of water and salt stress is still scarce. From the large amount of data available on transcript-profiling studies in plants subjected to drought and salt it is becoming apparent that plants perceive and respond to these stresses by quickly altering gene expression in parallel with physiological and biochemical alterations; this occurs even under mild to moderate stress conditions. From a recent comprehensive study that compared salt and drought stress it is apparent that both stresses led to down-regulation of some photosynthetic genes, with most of the changes being small (ratio threshold lower than 1) possibly reflecting the mild stress imposed. When compared with drought, salt stress affected more genes and more intensely, possibly reflecting the combined effects of dehydration and osmotic stress in salt-stressed plants.
The plant cell-wall matrix is equipped with more than 20 glycosylhydrolase activities, including both glycosidases and glycanases (exo- and endo-hydrolases, respectively), which between them are in principle capable of hydrolysing most of the major glycosidic bonds in wall polysaccharides. Some of these enzymes also participate in the 'cutting and pasting' (transglycosylation) of sugar residues-enzyme activities known as transglycosidases and transglycanases. Their action and biological functions differ from those of the UDP-dependent glycosyltransferases (polysaccharide synthases) that catalyse irreversible glycosyl transfer. Based on the nature of the substrates, two types of reaction can be distinguished: homo-transglycosylation (occurring between chemically similar polymers) and hetero-transglycosylation (between chemically different polymers). This review focuses on plant cell-wall-localized glycosylhydrolases and the transglycosylase activities exhibited by some of these enzymes and considers the physiological need for wall polysaccharide modification in vivo. It describes the mechanism of transglycosylase action and the classification and phylogenetic variation of the enzymes. It discusses the modulation of their expression in plants at the transcriptional and translational levels, and methods for their detection. It also critically evaluates the evidence that the enzyme proteins under consideration exhibit their predicted activity in vitro and their predicted action in vivo. Finally, this review suggests that wall-localized glycosylhydrolases with transglycosidase and transglycanase abilities are widespread in plants and play important roles in the mechanism and control of plant cell expansion, differentiation, maturation, and wall repair.
Reactive oxygen species (ROS) were initially recognized as toxic by-products of aerobic metabolism. In recent years, it has become apparent that ROS plays an important signaling role in plants, controlling processes such as growth, development and especially response to biotic and abiotic environmental stimuli. The major members of the ROS family include free radicals like O - 2 , OH and non-radicals like H 2 O 2 and 1 O 2 . The ROS production in plants is mainly localized in the chloroplast, mitochondria and peroxisomes. There are secondary sites as well like the endoplasmic reticulum, cell membrane, cell wall and the apoplast. The role of the ROS family is that of a double edged sword; while they act as secondary messengers in various key physiological phenomena, they also induce oxidative damages under several environmental stress conditions like salinity, drought, cold, heavy metals, UV irradiation etc., when the delicate balance between ROS production and elimination, necessary for normal cellular homeostasis, is disturbed. The cellular damages are manifested in the form of degradation of biomolecules like pigments, proteins, lipids, carbohydrates, and DNA, which ultimately amalgamate in plant cellular death. To ensure survival, plants have developed efficient antioxidant machinery having two arms, (i) enzymatic components like superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), guaiacol peroxidase (GPX), glutathione reductase (GR), monodehydroascorbate reductase (MDHAR), and dehydroascorbate reductase (DHAR); (ii) non-enzymatic antioxidants like ascorbic acid (AA), reduced glutathione (GSH), -tocopherol, carotenoids, flavonoids, and the osmolyte proline. These two components work hand in hand to scavenge ROS. In this review, we emphasize on the different types of ROS, their cellular production sites, their targets, and their scavenging mechanism mediated by both the branches of the antioxidant systems, highlighting the potential role of antioxidants in abiotic stress tolerance and cellular survival. Such a comprehensive knowledge of ROS action and their regulation on antioxidants will enable us to develop strategies to genetically engineer stress-tolerant plants.