179 research outputs found

    Effect of phosphorus limiting on phytase activity, proton efflux and oxygen consumption by nodulatedroots of common bean (Phaseolus vulgaris)

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    This work intended to measure the nodulated-roots oxygen consumption, proton efflux and phytase activity in 2 lines of common bean (Phaseolus vulgaris) (115, 147) at 2 levels of P supply. Rooted seedlings were inoculated with Rhizobium tropici CIAT 899 in hydroaeroponic cultivation under glasshouse. Phosphorus was supplied as KH2PO4 at 15 and 250 ìmol pl-1 week-1 (15P and 250P, respectively). Our results showed that plant growth nodulation and symbiotic nitrogen fixation were significantly affected by P limiting (15P) for the both lines, but this adverse effect was more pronounced in 147 than in 115. For the both lines, the phytase activity, higher in roots than in nodules, was significantly increased by P limiting, but 115 maintained higher values as compared to 147 line. Incotyledons, the phytase activity was higher in 115 than in 147. Phosphorus shortage increased the cumulated proton release only in 115, whereas it was lowered for 147. In this line, the proton release was linked to symbiotic nitrogen fixation. Under 15P, the proton efflux per unit of nodulated-root biomass was 25% greater for 115 than 147, suggesting that under P limitation, proton efflux may constitute an efficient way to increase P uptake in the tolerant line (115). 15P increased significantlynodulated-root O2 consumption per g nodule DW and nodule conductance, but to a higher extent in 147. As a whole, bean plants at P-deficient conditions increased the activity of phytases and proton efflux, thus maintaining the oxygen diffusion in nodules. This may represent an adaptive mechanism for N2- fixing legumes to respond to P deficiency, by increasing the utilisation and the uptake of phosphorus for symbiotic nitrogen fixation

    High-resolution characterization of the diffusion of light chemical elements in metallic components by scanning microwave microscopy

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    International audienceAn original sub-surface, high spatial resolution tomographic technique based on scanning microwave microscopy (SMM) is used to visualize in-depth materials with different chemical compositions. A significant phase difference in SMM between aluminum and chromium buried patterns has been observed. Moreover this technique was used to characterize a solid solution of a light chemical element (oxygen) in a metal lattice (zirconium). The large solubility of the oxygen in zirconium leads to modifications of the properties of the solid solution that can be measured by the phase shift signal in the SMM technique. The signal obtained in cross-section of an oxidized Zr sample shows the excellent agreement between phase shift profiles measured at different depths. Such a profile can reveal the length of diffusion of the oxygen in zirconium under the surface. The comparison with the oxygen concentration measured by nuclear reaction analysis shows excellent agreement in terms of length of diffusion and spatial distribution of the oxygen. A rapid calibration shows a linear dependence between the phase shift and the oxygen concentration. The SMM method opens up new possibilities for indirect measurements of the oxygen concentration dissolved in the metal lattic

    Advances in quantitative nanoscale subsurface imaging by mode-synthesizing atomic force microscopy

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    This paper reports on advances toward quantitative non-destructive nanoscale subsurface investigation of a nanofabricated sample based on mode synthesizing atomic force microscopy with heterodyne detection, addressing the need to correlate the role of actuation frequencies of the probe f(p) and the sample f(s) with depth resolution for 3D tomography reconstruction. Here, by developing a simple model and validating the approach experimentally through the study of the nanofabricated calibration depth samples consisting of buried metallic patterns, we demonstrate avenues for quantitative nanoscale subsurface imaging. Our findings enable the reconstruction of the sample depth profile and allow high fidelity resolution of the buried nanostructures. Non-destructive quantitative nanoscale subsurface imaging offers great promise in the study of the structures and properties of complex systems at the nanoscale

    Full-wave modeling of broadband near field scanning microwave microscopy

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    The authors would like to thank professor Dr. Gabriel Gomila from Institut de Bioenginyeria de Catalunya (IBEC) and Universitat de Barcelona for the fruitful discussion and support, as well as to Dr. Georg Gramse from Johannes Kepler University Linz for the experimental data. B.W. thanks the funding from the China Scholarship Council (CSC) for the support of his research at Queen Mary University of London, UK. Y.H. would like to thank EU-FP7 Nanomicrowave project for the financial support

    The Compact Linear Collider (CLIC) - 2018 Summary Report

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    Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

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    Familial Adult Myoclonic Epilepsy (FAME) is a genetically heterogeneous disorder characterized by cortical tremor and seizures. Intronic TTTTA/TTTCA repeat expansions in SAMD12 (FAME1) are the main cause of FAME in Asia. Using genome sequencing and repeat-primed PCR, we identify another site of this repeat expansion, in MARCH6 (FAME3) in four European families. Analysis of single DNA molecules with nanopore sequencing and molecular combing show that expansions range from 3.3 to 14 kb on average. However, we observe considerable variability in expansion length and structure, supporting the existence of multiple expansion configurations in blood cells and fibroblasts of the same individual. Moreover, the largest expansions are associated with micro-rearrangements occurring near the expansion in 20% of cells. This study provides further evidence that FAME is caused by intronic TTTTA/TTTCA expansions in distinct genes and reveals that expansions exhibit an unexpectedly high somatic instability that can ultimately result in genomic rearrangements
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