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It has long been recognized that diffusive boundary layers affect the determination of active transport parameters, but this has been largely overlooked in plant physiological research. We studied the short-term uptake of cadmium (Cd), zinc (Zn), and nickel (Ni) by spinach (Spinacia oleracea) and tomato (Lycopersicon esculentum) in solutions with or without metal complexes. At same free ion concentration, the presence of complexes, which enhance the diffusion flux, increased the uptake of Cd and Zn, whereas Ni uptake was unaffected. Competition effects of protons on Cd and Zn uptake were observed only at a very large degree of buffering, while competition of magnesium ions on Ni uptake was observed even in unbuffered solutions. These results strongly suggest that uptake of Cd and Zn is limited by diffusion of the free ion to the roots, except at very high degree of solution buffering, whereas Ni uptake is generally internalization limited. All results could be well described by a model that combined a diffusion equation with a competitive Michaelis-Menten equation. Direct uptake of the complex was estimated to be a major contribution only at millimolar concentrations of the complex or at very large ratios of complex to free ion concentration. The true K(m) for uptake of Cd(2+) and Zn(2+) was estimated at <5 nm, three orders of magnitude smaller than the K(m) measured in unbuffered solutions. Published Michaelis constants for plant uptake of Cd and Zn likely strongly overestimate physiological ones and should not be interpreted as an indicator of transporter affinity.
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http://dx.doi.org/10.1104/pp.112.202200 | DOI Listing |
Nanoscale Adv
August 2025
Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum DresdenRossendorf 01328 Dresden Germany
Ion irradiation has routinely been used to create defects or even pattern two-dimensional (2D) materials. For efficient defect engineering, that is, choosing the proper ion fluence to achieve the desired concentration of defects, it is of paramount importance to know the probability of creating defects as a function of ion energy. Atomistic simulations of ion impacts on 2D targets can provide such information, especially for free-standing systems, but in the case of supported 2D materials, the substrate can strongly affect defect production.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
University of the Free State, Chemistry Department, Bloemfontein, South Africa.
The crystal structure of a nitrate anion caged in spherical vanadium and oxygen structure surrounded by sodium hy-droxy and water solvent mol-ecules, systematic name poly[[hepta-deca-aqua-tetra-deca-oxidonona-sodium][penta-cosa-aqua-nitratoundeca-oxido-penta-deca-vanadium]], HNNaOV is reported. The complex crystallizes in the non-centrosymmetric space group and exhibits many inter- and intra-molecular hydrogen-bonding inter-actions. The complex contains V and V centres, which are six-coordinate or octa-hedrally coordinated.
View Article and Find Full Text PDFRSC Adv
September 2025
State Key Laboratory of Disaster Prevention & Reduction for Power Grid Changsha China
Positive temperature coefficient (PTC) materials are pivotal for safeguarding lithium iron phosphate batteries, yet their industrial application is hindered by critical drawbacks: excessive film thickness, high internal resistance, and poor solvent sustainability. Addressing these challenges, this study innovatively develops a solvent-free thermal rolling process to fabricate an asymmetric expansion polymer film, specifically thermoplastic polyurethane (TPU) reinforced polyethylene (PE)/carbon composites, which significantly enhances the PTC effect. The core mechanism lies in the asymmetric thermal expansion of TPU and PE: this unique behavior disrupts the conductive carbon network, triggering a sharp PTC transition at around 120 °C.
View Article and Find Full Text PDFAnalyst
September 2025
Functional Nanomaterial-based Chemical and Biological Sensing Technology Innovation Team of Department of Education of Yunnan Province, Yunnan Minzu University, Kunming 650504, P. R. China.
Copper ions are essential elements in the human body and participate in various physiological activities in the bodies of organisms. Herein, an ultrasensitive electrochemical biosensor was developed for detection of copper ions (Cu) based on FeO@Au magnetic nanoparticles (FeO@Au MNPs) and a Cu-dependent DNAzyme assisted nicking endonuclease signal amplification (NESA) strategy. dsDNA is formed by a hybridization reaction between DNA S2 and S1 immobilized on the surface of FeO@Au MNPs.
View Article and Find Full Text PDFNanoscale Horiz
September 2025
Departamento de Ciencias del Ambiente, Facultad de Química y Biología, Universidad de Santiago de Chile (USACH), Av. Libertador Bernardo O'Higgins 3363, Estación Central, Santiago, 9170022, Chile.
The functional electronic and spectro-electrochemical properties of two structural pyridinium isomers, Py_Down-BF and Py_Up-BF, were studied at the single-molecule level using the STM-BJ technique. These isomers differ in the position of the redox-active pyridinium core. The aim was to identify the role of core's position in promoting reversible switching between electromers (redox isomers) in solution and at the gold-pyridinium-gold junction circuit.
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