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      Mechanismen des radialen Volumenflusses und der radialen Permeation von Osmolyten in verzweigten Wurzeln junger Maispflanzen (Zea mays L.) und halmbürtigen Adventivwurzeln des Schilfes (Phragmites australis Trin. ex Steudel)

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          Abstract

          Der radiale Wasserfluss durch die feinen Seitenwurzeln von Schilf- und Mais ist vom radialen Teilchenfluss entkoppelt. Der radiale Wasserfluss wird bereits im Kortex der Wurzel durch den Protoplasten kontrolliert, da die Strömung auf dem apoplastischen Zellwandweg um die Protoplasten herum gegenüber der Strömung durch die Protoplasten nicht signifikant ist. Der radiale Reflexionskoeffizient der Wurzeln wird durch den Reflexionskoeffizient der Plasmamembran bestimmt. Die Feinwurzeln von Schilf- und Mais besitzen einen Reflexionskoeffizienten für Salze, Zucker, Zuckeralkohole und Polymere der sich nicht signifikant von eins unterscheidet. An intakten Wurzeln wurde dies durch die Abwesenheit von solvent drag für NaCl und Mannitol bei der Steigerung des Wasserflusses und der gleich großen hydraulischen Wirkung von osmotischen und hydrostatischen Kräften auf die Exsudation nachgewiesen. Die radialen Wände der Endodermis von Schilf- und Maiswurzeln sind keine perfekte Diffusionsbarriere. Liegen die genannten Stoffe in einer signifikanten Konzentration in der Zellwand vor permeieren sie passiv unter Umgehung der Protoplasten durch die Endodermis in die Xylemgefäße. Auch die Epidermis/Hypodermis der untersuchten Wurzeln hat die Eigenschaft einer semipermeablen Membran in der osmotische Druckgradienten einen Volumenfluss erzeugen. Es wurden zwei Methoden etabliert, mit denen sich der osmotische Druck des Xylemsaftes in isolierten Feinwurzeln bestimmen lässt. Die Feinwurzeln unterschieden sich hinsichtlich des osmotischen Druckes ihres Xylemsaftes und ihrer radialen hydraulischen Leitfähigkeit stark. Die bekannte Fähigkeit der Schilfpflanzen Natriumionen an der Sprossbasis aus dem Xylem zu eliminieren muss um Chloridionen erweitert werden. Die hohe Permeabilität der Endodermis für NaCl verringert die osmotische Wirkung des Brackwassers auf die Wasseraufnahme. Die Entkopplung der Salzaufnahme vom Wasserfluss vermeidet eine exzessive Salzbelastung des Sprosses.

          Abstract

          Radial Water fluxes are not coupled to the radial solute fluxes in fine lateral roots of mays and reed. The radial water flow is already controlled by the protoplast in the cortical parenchyma as the hydraulic conductivity of the cell wall path circumventing the protoplasts is negligible compared to hydraulic conductivity of the pathway through the protoplast. The radial reflection coefficient of the root is defined by the reflection coefficient of the plasma membrane. Therefore fine laterals of the common reed (Phragmites australis) and maize (Zea mays) therefore exhibit a reflection coefficient for salts, sugars, alditols and polymers that is not significantly different from unity. This conclusion was drawn from the absence of solvent drag for NaCl and mannitol with increasing water flux and by the observation of equality of the hydraulic effect of both osmotic and hydrostatic forces on the exudation flow in intact roots of both plants. The radial walls of the endodermis are no absolute barrier for diffusion of small osmolytes. In the presence of high cell wall concentrations, the abovementioned osmolytes passively permeated into the xylem vessels at high rates circumventing the protoplast. The epidermis/hypodermis exhibits a semipermeable barrier as well wherein osmotic forces can create a radial volume flux. Two methods were established that allow for the determination of the flow direction and the osmotic pressure of the xylem sap in isolated fine laterals. Laterals differed strongly regarding their hydraulic conductivity and the osmotic pressure of their xylem sap. The known ability of the reed plant to remove sodium ions from the ascending sap has to be expanded for chloride. The high permeability of the endodermis for NaCl reduces the osmotic force of the brackish medium on water uptake. Uncoupling of radial water from the solute fluxes avoids the excessive permeation of NaCl and its accumulation in the assimilating leaves at high rates of transpiration.

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          Most cited references30

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          The role of aquaporins in root water uptake.

          The capacity of roots to take up water is determined in part by the resistance of living tissues to radial water flow. Both the apoplastic and cell-to-cell paths mediate water transport in these tissues but the contribution of cell membranes to the latter path has long been difficult to estimate. Aquaporins are water channel proteins that are expressed in various membrane compartments of plant cells, including the plasma and vacuolar membranes. Plant aquaporins are encoded by a large multigene family, with 35 members in Arabidopsis thaliana, and many of these aquaporins show a cell-specific expression pattern in the root. Mercury acts as an efficient blocker of most aquaporins and has been used to demonstrate the significant contribution of water channels to overall root water transport. Aquaporin-rich membranes may be needed to facilitate intense water flow across root tissues and may represent critical points where an efficient and spatially restricted control of water uptake can be exerted. Roots, in particular, show a remarkable capacity to alter their water permeability over the short term (i.e. in a few hours to less than 2-3 d) in response to many stimuli, such as day/night cycles, nutrient deficiency or stress. Recent data suggest that these rapid changes can be mostly accounted for by changes in cell membrane permeability and are mediated by aquaporins. Although the processes that allow perception of environmental changes by root cells and subsequent aquaporin regulation are nearly unknown, the study of root aquaporins provides an interesting model to understand the regulation of water transport in plants and sheds light on the basic mechanisms of water uptake by roots.
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            The regulation of nitrate and ammonium transport systems in plants.

            Inorganic nitrogen concentrations in soil solutions vary across several orders of magnitude among different soils and as a result of seasonal changes. In order to respond to this heterogeneity, plants have evolved mechanisms to regulate and influx. In addition, efflux analysis using (13)N has revealed that there is a co-ordinated regulation of all component fluxes within the root, including biochemical fluxes. Physiological studies have demonstrated the presence of two high-affinity transporter systems (HATS) for and one HATS for in roots of higher plants. By contrast, in Arabidopsis thaliana there exist seven members of the NRT2 family encoding putative HATS for and five members of the AMT1 family encoding putative HATS for. The induction of high-affinity transport and Nrt2.1 and Nrt2.2 expression occur in response to the provision of, while down-regulation of these genes appear to be due to the effects of glutamine. High-affinity transport and AMT1.1 expression also appear to be subject to down-regulation by glutamine. In addition, there is evidence that accumulated and may act post-transcriptionally on transporter function. The present challenge is to resolve the functions of all of these genes. In Aspergillus nidulans and Chlamydomonas reinhardtii there are but two high-affinity transporters and these appear to have undergone kinetic differentiation that permits a greater efficiency of absorption over the wide range of concentration normally found in nature. Such kinetic differentiation may also have occurred among higher plant transporters. The characterization of transporter function in higher plants is currently being inferred from patterns of gene expression in roots and shoots, as well as through studies of heterologous expression systems and knockout mutants.
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              The exodermis: a variable apoplastic barrier.

              The exodermis (hypodermis with Casparian bands) of plant roots represents a barrier of variable resistance to the radial flow of both water and solutes and may contribute substantially to the overall resistance. The variability is a result largely of changes in structure and anatomy of developing roots. The extent and rate at which apoplastic exodermal barriers (Casparian bands and suberin lamellae) are laid down in radial transverse and tangential walls depends on the response to conditions in a given habitat such as drought, anoxia, salinity, heavy metal or nutrient stresses. As Casparian bands and suberin lamellae form in the exodermis, the permeability to water and solutes is differentially reduced. Apoplastic barriers do not function in an all-or-none fashion. Rather, they exhibit a selectivity pattern which is useful for the plant and provides an adaptive mechanism under given circumstances. This is demonstrated for the apoplastic passage of water which appears to have an unusually high mobility, ions, the apoplastic tracer PTS, and the stress hormone ABA. Results of permeation properties of apoplastic barriers are related to their chemical composition. Depending on the growth regime (e.g. stresses applied) barriers contain aliphatic and aromatic suberin and lignin in different amounts and proportion. It is concluded that, by regulating the extent of apoplastic barriers and their chemical composition, plants can effectively regulate the uptake or loss of water and solutes. Compared with the uptake by root membranes (symplastic and transcellular pathways), which is under metabolic control, this appears to be an additional or compensatory strategy of plants to acquire water and solutes.
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                Author and article information

                Journal
                Mathematisch-Naturwissenschaftliche Fakultät I, Humboldt-Universität (kvv )
                4 June 2012
                Article
                oai:HUBerlin.de:39391
                235d61cf-ad9b-47d7-8f6a-52455e93a963
                History

                Biologie,Biowissenschaften, Biologie,WE 5360,Salztoleranz,salt tolerance,Apoplast,Wassertransport in Seitenwurzeln,Wurzel-Reflexionskoeffizient,Xylem,apoplast,root reflection coefficient,water transport in lateral roots,xylem,WN 1500

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