Crystallization and preliminary X-ray diffraction studies of the soluble 14 kDa beta-galactoside-binding lectin from bovine heart

The soluble 14 kDa beta-galactoside-binding lectin from bovine heart, a member of the S-type lectin family, has been crystallized in a form suitable for X-ray diffraction analysis. The crystals, in the absence of a saccharide ligand, diffract beyond 2.5 A resolution. They are obtained from polyethylene glycol 6000 at pH 6.0. Crystals grow as monoclinic plates, space group P2(1), with cell dimensions: a = 35.47 A, b = 64.33 A, c = 58.78 A and beta = 91.7 degrees. The asymmetric unit contains two molecules related by a 2-fold non-crystallographic axis. Two lectin monomers in the asymmetric unit give a Vm of 2.4 A3/Da, i.e. a solvent content of approximately 50%. The complex of lectin with the saccharide ligand, N-acetyllactosamine, crystallizes in the space group P2(1)2(1)2 with cell dimensions: a = 63.55 A, b = 82.13 A and c = 62.39 A. Crystals of this complex diffract beyond 2.0 A resolution. Two complexes in the asymmetric unit lead to a Vm value of 2.8 A3/Da (57% solvent).     

Solving the stochastic support vector regression with probabilistic constraints by a high-performance neural network model

This paper offers a recurrent neural network to support vector machine (SVM) learning in stochastic support vector regression with probabilistic constraints. The SVM is first converted into an equivalent quadratic programming (QP) formulation in linear and nonlinear cases. An artificial neural network for SVM learning is then proposed. The presented neural network framework guarantees obtaining the optimal solution of the SVM problem. The existence and convergence of the trajectories of the network are studied. The Lyapunov stability for the considered neural network is also shown. The efficiency of the proposed method is shown by three illustrative examples.

     

State-of-the-art technology: Recent investigations on laser-mediated synthesis of nanocomposites for environmental remediation

In both developing and industrialized/developed countries, various hazardous/toxic environmental pollutants are entering water bodies from organic and inorganic compounds (heavy metals and specifically dyes). The global population is growing whereas the accessibility of clean, potable and safe drinking water is decreasing, leading to world deterioration in human health and limitation of agricultural and/or economic development. Treatment of water/wastewater (mainly industrial water) via catalytic reduction/degradation of environmental pollutants is extremely critical and is a major concern/issue for public health. Light and/or laser ablation induced photocatalytic processes have attracted much attention during recent years for water treatment due to their good (photo)catalytic efficiencies in the reduction/degradation of organic/inorganic pollutants. Pulsed laser ablation (PLA) is a rather novel catalyst fabrication approach for the generation of nanostructures with special morphologies (nanoparticles (NPs), nanocrystals, nanocomposites, nanowires, etc.) and different compositions (metals, alloys, oxides, core-shell, etc.). Laser ablation in liquid (LAL) is generally considered a quickly growing approach for the synthesis and modification of nanomaterials for practical applications in diverse fields. LAL-synthesized nanomaterials have been identified as attractive nanocatalysts or valuable photocatalysts in (photo)catalytic reduction/degradation reactions. In this review, the laser ablation/irradiation strategies based on LAL are systematically described and the applications of LAL synthesized metal/metal oxide nanocatalysts with highly controlled nanostructures in the degradation/reduction of organic/inorganic water pollutants are highlighted along with their degradation/reduction mechanisms.     

Investigation of photo-electrochemical response of iron oxide/mixed-phase titanium oxide heterojunction toward possible solar energy conversion

Photocatalysts are part of key strategies to enable green fuel. Photocatalysis and water splitting could be a promising solution to challenges associated with the intermittent nature of sunlight as a huge energy source on Earth. In this study, photo-electrochemical performance and behavior of mixed-phase titanium oxide and iron oxide heterojunction (Ti-TiO_x (High-voltage)-FeO_x electrode) are compared to the photo-electrochemical performance and behavior of titanium oxide nanotubes with the rutile phase and iron oxide heterojunction (TiO_x-nanotubes (H₂SO₄/KF)-FeO_x electrode). The results of photo-electrochemical experiments show that the application of stabilization potential and the presence/absence of dissolved oxygen could not be considered as significant factors affecting the photo-electrochemical properties of the Ti-TiO_x (High-voltage)-FeO_x and TiO_x-nanotubes (H₂SO₄/KF)-FeO_x electrodes. The Ti-TiO_x (High-voltage)-FeO_x electrode shows an anodic photo-electrochemical response in wavelengths shorter than 530 nm and cathodic photo-electrochemical response in wavelengths longer than 530 nm. However, the Ti-nanotubes (H₂SO₄/KF)-FeO_x electrode consistently exhibits the anodic photo-electrochemical response. Both of the prepared heterojunctions are further characterized through Scanning Electron Microscopy, Energy-dispersive X-ray Spectroscopy, Diffuse Reflectance UV–Vis Spectroscopy, X-ray Diffraction, and Attenuated Total Reflectance Spectroscopy methods. These experiments show that despite different morphologies observed in SEM imaging data, the deposited iron oxide layers on both mixed-phase titanium oxide and titanium oxide nanotubes share the same hematite phase structure. However, only iron oxide electro-deposited on the surface of the mixed-phase titanium oxide, which contains both anatase and rutile phases, with vacant sites of oxygen, exhibits un-expected anodic and cathodic photo-electrochemical responses. Furthermore, according to the results of the characterization and photo-electrochemical investigations, the different chemical environment of mixed-phase titanium oxide, and the possible formation of different types of heterojunction structures in mixed-phase titanium oxide and iron oxide, in contrast to the titanium oxide nanotubes and iron oxide, might be considered the possible discernible reasons for the observed different photo-electrochemical responses. This paper sheds new light on photo-electrochemistry of iron oxide/mixed-phase titanium oxide heterojunction for possible solar energy conversion.     

Vibrational spectroscopic studies on crystallisation of sol–gel derived thin films of calcia–alumina binary compound

An optimized sol–gel process has been developed to produce homogeneous thin films of calcium aluminate binary (12CaO·7Al₂O₃) compound, on magnesium oxide substrates via spin coating. Fourier transform infrared and Raman spectroscopies have been employed to investigate the effect of annealing temperature and duration on the phase transformations in the films. Heat treatment at 1,300 °C under air atmosphere for 2 h produced single-phase 12CaO·7Al₂O₃ films. However, annealing at a lower temperature of 1,100 °C in air for a period of 4 h in total resulted in the crystallization of 5CaO·3Al₂O₃ rather than 12CaO·7Al₂O₃. The X-ray photoelectron spectrum of the thin film annealed at 1,300 °C corresponds to the binding energies of C12A7 compound. The annealing temperature of 1,300 °C for 2 h is found to be sufficient for formulating single phase calcia–alumina binary films in correct stoichiometric ratio of 12:7.     

Robust Audio Data Hiding Using Correlated Quantization With Histogram-Based Detector

In this paper, two blind audio watermarking methods using correlated quantization for data embedding with histogram-based detector have been proposed. First, a novel mapping called the point-to-point graph (PPG) is introduced. In this mapping, the value of samples is important as well as the correlation among them. As this mapping increases the dimension of the signal, the data embedding procedure (quantization) will be diversified more securely than that of the 1-D domains such as the time or frequency domains. Hence, two watermarking techniques coined as hard and soft quantization methods based on the quantization of the PPG point radii are suggested. The performance of both techniques is analyzed by obtaining the radii distribution of PPG points after watermarking. Experimental results against AWGN attack confirm the validity of theoretical analysis. Moreover, the robustness of the proposed methods against other common attacks such as echo, low pass, resampling, and MP3 are investigated through extensive simulations.     

Monoclonal antibody 91.9H raised against sulfated mucins is specific for the 3'-sulfated Lewisa tetrasaccharide sequence

The IgG1hybridoma antibody, 91.9H, was originally raised against sulfated mucins isolated from normal human colonic mucosa. Previous studies have shown that the 91.9H antigen is expressed on normal colonic epithelial cells and the sulfomucins that they produce, but not in the normal small intestine and stomach. Tissue-specific changes occur in 91.9H antigen expression in disease: the antigen diminishes in colonic carcinomas, whereas in regions of gastric mucosa showing intestinal metaplasia and in gastric carcinomas, the antigen is expressed as a "neo-antigen." This report is concerned with elucidation, by the neoglycolipid technology, of the determinant recognized by antibody 91.9H using sulfated and sialyl oligosaccharides of Lewisa(Lea) and Lextypes, and analogs that lack sulfate, sialic acid, or fucose. Binding experiments with the lipid-linked oligosaccharides immobilized on chromatograms or on microwells, and inhibition of binding experiments with free oligosaccharides based on di-, tri- and tetrasaccharide backbones, show that the 91.9H antigenic determinant is based on a trisaccharide backbone, and consists of the 3'-sulfated Leatetrasaccharide sequence, which is a potent ligand for the E- and L-selectins. The antibody gives a relatively low signal with the 3'-sulfated non-fucosylated backbone, and has no detectable cross-reaction with the 3'-sulfated Lexisomer, nor with sialyl-Leaand -Lexanalogues. Antibody 91.9H is a valuable addition, therefore, to the repertoire of reagents for mapping details of the distribution, and determining the relative importance of sulfated and sialyl oligosaccharides as ligands for the selectins, in normal and pathological epithelia and endothelia.     

On Seismic Response of Substation Equipment and Application of Base Isolation to Transformers

This paper presents seismic performance of electric substation transformers, and discusses advantages and considerations in the use of base isolation as a viable hazard mitigation option. Substation transformers and bushings are the most critical elements within the power delivery system and their performances during past earthquakes in the U.S. and abroad have not been satisfactory. Finite-element analyses indicate that the interaction between these two critical elements has a significant effect on seismic vulnerability of substations. In light of dynamic characteristics of this equipment, base isolation can be very effective in mitigating this adverse interaction. Furthermore, due to high-inertia reduction, base isolation can also have beneficial effects on the long-term longevity of transformers and on foundation performance during seismic events. Larger displacement demand and uplift, however, are issues that must be considered in the application of base isolation. Through an actual case study (433.3-MVA transformer in a high-voltage substation), a simplified model of the transformer bushing will be developed and the results of fixed base case and base isolated case are compared. Moreover, design concepts will be investigated that will demonstrate larger displacement can be accommodated; and that considering transformer geometry, peak ground acceleration, amount of inertia reduction, and isolator's friction coefficient for this transformer uplift is not an issue.     

Synthesis of new sulfonated copolyimides in organic and ionic liquid media for fuel cell application

New sulfonated copolyimides containing ether, carbonyl, and bulky naphthyl group in backbone were synthesized in two reaction media: organic solvent and ionic liquid media. For this purpose a new sulfonated diamine (BANBPDS) and an unsulfonated diamine (BANBP) was prepared through reactions of 4,4′‐dichlorobenzophenone‐3,3′‐disulfonic acid, and also 4,4′‐dichlorobenzophenone with 5‐amino‐1‐sodium naphthoxide, respectively. Three series of sulfonated copolyimide with different sulfonation contents (40–80%) were prepared by reaction of the sulfonated diamine (BANBPDS) in companion with three unsulfonated diamines including BANBP, 4,4′‐oxydianiline (ODA), and 1,8‐diamino‐3,6‐dioxaoctane (DADO) with 1,4,5,8‐naphthalene tetracarboxylic dianhydride (NTDA). Two media were selected for preparation of copolyimides. Copolyimides synthesized in ionic liquid had higher inherent viscosity and higher molecular weight in comparison with similar copolyimides that were synthesized via common organic solvent method. Incorporation of flexible groups in polyimide structures increased solubility and processability of the copolyimides. After characterization of polymers with common methods, their water uptake, water stability, ion exchange capacity (IEC), thermal behavior and stability, crystallinity, and morphology were studied. The polymers showed suitable properties including high thermal stability and ion exchange capacity, which were the basic requirements for application as fuel cell membranes. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012