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Proton Release (proton + release)

Distribution by Scientific Domains

Chemistry	50%

Selected Abstracts

Proton release by N2 -fixing plant roots: A possible contribution to phytoremediation of calcareous sodic soils

JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 1 2003
Manzoor Qadir Prof. Dr.
Abstract With a world-wide occurrence on about 560 million hectares, sodic soils are characterized by the occurrence of excess sodium (Na+) to levels that can adversely affect crop growth and yield. Amelioration of such soils needs a source of calcium (Ca2+) to replace excess Na+ from the cation exchange sites. In addition, adequate levels of Ca2+ in ameliorated soils play a vital role in improving the structural and functional integrity of plant cell walls and membranes. As a low-cost and environmentally feasible strategy, phytoremediation of sodic soils , a plant-based amelioration , has gained increasing interest among scientists and farmers in recent years. Enhanced CO2 partial pressure (PCO2) in the root zone is considered as the principal mechanism contributing to phytoremediation of sodic soils. Aqueous CO2 produces protons (H+) and bicarbonate (HCO3 - ). In a subsequent reaction, H+ reacts with native soil calcite (CaCO3) to provide Ca2+ for Na+ Ca2+ exchange at the cation exchange sites. Another source of H+ may occur in such soils if cropped with N2 -fixing plant species because plants capable of fixing N2 release H+ in the root zone. In a lysimeter experiment on a calcareous sodic soil (pHs = 7.4, electrical conductivity of soil saturated paste extract (ECe) = 3.1 dS m -1, sodium adsorption ratio (SAR) = 28.4, exchangeable sodium percentage (ESP) = 27.6, CaCO3 = 50 g kg -1), we investigated the phytoremediation ability of alfalfa (Medicago sativa L.). There were two cropped treatments: Alfalfa relying on N2 fixation and alfalfa receiving NH4NO3 as mineral N source, respectively. Other treatments were non-cropped, including a control (without an amendment or crop), and soil application of gypsum or sulfuric acid. After two months of cropping, all lysimeters were leached by maintaining a water content at 130% waterholding capacity of the soil after every 24±1 h. The treatment efficiency for Na+ removal in drainage water was in the order: sulfuric acid > gypsum = N2 -fixing alfalfa > NH4NO3-fed alfalfa > control. Both the alfalfa treatments produced statistically similar root and shoot biomass. We attribute better Na+ removal by the N2 -fixing alfalfa treatment to an additional source of H+ in the rhizosphere, which helped to dissolve additional CaCO3 and soil sodicity amelioration. Protonenabgabe durch N2 -fixierende Pflanzenwurzeln: ein möglicher Beitrag zur Phytomelioration von kalkreichen Natriumböden Bei einem weltweiten Vorkommen auf etwa 560 Millionen Hektar sind Natriumböden durch einen Überschuss an Natrium (Na+) gekennzeichnet, der das Wachstum und den Ertrag von Kulturpflanzenbeständen nachteilig beeinflussen kann. Die Melioration solcher Böden erfordert Calcium (Ca2+), um überschüssiges Na+ von Kationen-Austauscherplätzen zu verdrängen. Außerdem spielt Ca2+ eine wichtige Rolle bei der Verbesserung der strukturellen und funktionellen Integrität pflanzlicher Zellwände und Membranen. Als kostengünstige und umweltfreundliche Strategie hat die Phytomelioration von Natriumböden , eine auf Pflanzen beruhende Melioration , in den letzten Jahren zunehmendes Interesse bei Wissenschaftlern und Landwirten gefunden. Ein erhöhter CO2 -Partialdruck (PCO2) in der Rhizosphäre wird als hauptsächlicher Mechanismus angesehen, der zur Phytomelioration von Natriumböden beiträgt. In Wasser gelöst, erzeugt CO2 Protonen (H+) und Bikarbonate (HCO3 - ). Anschließend reagiert H+ mit nativem Calcit (CaCO3), wobei sich Ca2+ löst und Na+ von Austauscherplätzen verdrängt. Eine weitere H+ -Quelle könnte die H+ -Abgabe von Wurzeln N2 -fixierender Pflanzen sein, da diese in der Lage sind, H+ in die Rhizosphäre abzugeben. In einem Lysimeterversuch mit einem kalkreichen Natriumboden (pHs = 7, 4; ECe = 3, 1 dS m -1; SAR = 28, 4; ESP = 27, 6; CaCO3 = 50 g kg -1) wurde die Möglichkeit einer Phytomelioration mit N2 -fixierender Luzerne (Medicago sativa L.) im Vergleich zu einer mit mineralischem N ernährten Luzerne (NH4NO3) untersucht. In weiteren Varianten (Applikation von Gips bzw. Schwefelsäure) wurde die chemische Melioration einer nicht behandelten Kontrolle gegenübergestellt. Beide Ernährungsformen führten zu statistisch ähnlicher Wurzelund Sprossmasse der Luzerne. Nach zweimonatigem Pflanzenwachstum erfolgte alle 24±1 h eine Dränung der Lysimeter durch Zugabe einer Wassermenge von 130% der maximalen Wasserkapazität zum Boden. Hinsichtlich der Effizienz, Na+ über Auswaschung aus dem Boden zu entfernen, zeigte sich folgende Reihenfolge: Schwefelsäure > Gips = N2 -fixierende Luzerne > NH4NO3 -ernährte Luzerne > Kontrolle. Wir führen das bessere Meliorationsergebnis in der Variante der N2 -fixierenden Luzerne auf eine zusätzliche H+ -Quelle in der Rhizosphäre zurück, die zur Lösung von zusätzlichem CaCO3 beitrug. [source]

An Electroanalytical Investigation on the Redox Properties of Calcium Antagonist Dihydropyridines

ELECTROANALYSIS, Issue 10 2003
Rosanna Toniolo
Abstract The antioxidant capacity of some calcium antagonists and one calcium agonist 1,4-dihydropyridines (DHPs) was evaluated by a competitive kinetic procedure. With the exception of Amlodipine, all the calcium antagonist DHPs display an unambiguous antioxidant capacity, while for the calcium agonist DHP (Bay K 8644) no measurable reactivity towards peroxyl radicals could be detected. The finding was corroborated by an electroanalytical investigation of the redox properties of DHPs compounds to get an insight about both the thermodynamic constraints of their oxidation process and reaction pattern. The oxidation potentials decrease with both antioxidant capacity and increasing basic character, thus suggesting the relevance of the electron density on the DHP ring. For all the compounds investigated, the overall oxidation process takes place through a primary one-electron step accompanied by a fast proton release and the formation of a neutral radical undergoing a second much easier one-electron step. The protonated form of the parent pyridine derivative is thus generated as the final product. This pattern is relevant for the antioxidant effect, since the radical intermediate is much more prone to be oxidized than to be reduced, thus fully preventing the propagation of the oxidative chain reaction. In the case of calcium antagonist DHPs, the above release of protons complicates the overall oxidation process by introducing a parasitic side reaction where a coupling between protons and the starting species takes place. This DHP self-protonation subtracts part of the original species from the electrode process because the parent cationic species is no longer electroactive. Conversely, the calcium agonist DHP, which is more difficult to be oxidized, turned out to be such a weak base as to be unable to undergo the self-protonation reaction. The combined effect of oxidation potentials and proton binding capacity of DHPs is a key element for the redox transition, which could support their antioxidant effect and should be considered to some extent in accounting for the calcium antagonist vs calcium agonist effect. [source]

The evolution of coenzyme Q

BIOFACTORS, Issue 1-4 2008
Frederick L. Crane
In the 50 years since the identification of coenzyme Q as an electron carrier in mitochondria, it has been identified with diverse and unexpected functions in cells. Its discovery came as a result of a search for electron carriers in mitochondria following the identification of flavin and cytochromes by Warburg, Keilin, Chance and others. As a result of investigation of membrane lipids at D.E. Green's laboratory at University of Wisconsin coenzyme Q was identified as the electron carrier between primary flavoprotein dehydrogenases and the cytochromes. Then Peter Mitchell identified the role of transmembrane proton transfer as a basis for ATP synthesis. The general distribution of coenzyme Q in all cell membranes then led to the recognition of a role as a primary antioxidant. The protonophoric function was extended to acidification of Golgi and lysosomal vericles. A further role in proton release through the plasma membrane and its relation to cell proliferation has not been fully developed. A role in generation of H2 O2 as a messenger for hormone and cytokine action is indicated as well as prevention of apoptosis by inhibition of ceramide release. Identification of the genes and proteins required for coenzyme Q synthesis has led to a basis for defining deficiency. For 50 years Karl Folkers has led the search for deficiency and therapeutic application. The development of large scale production, better formulation for uptake, and better methods for analysis have furthered this search. The story isn't over yet. Questions remain about effects on membrane structure, breakdown and control of cellular synthesis and uptake and the basis for therapeutic action. [source]

How Does a Membrane Protein Achieve a Vectorial Proton Transfer Via Water Molecules?

CHEMPHYSCHEM, Issue 18 2008
Steffen Wolf
Abstract We present a detailed mechanism for the proton transfer from a protein-bound protonated water cluster to the bulk water directed by protein side chains in the membrane protein bacteriorhodopsin. We use a combined approach of time-resolved Fourier transform infrared spectroscopy, molecular dynamics simulations, and X-ray structure analysis to elucidate the functional role of a hydrogen bond between Ser193 and Glu204. These two residues seal the internal protonated water cluster from the bulk water and the protein surface. During the photocycle of bacteriorhodopsin, a transient protonation of Glu204 leads to a breaking of this hydrogen bond. This breaking opens the gate to the extracellular bulk water, leading to a subsequent proton release from the protonated water cluster. We show in detail how the protein achieves vectorial proton transfer via protonated water clusters in contrast to random proton transfer in liquid water. [source]