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    785 research outputs found

    Structure and Function Predictions of Hypothetical Proteins in Vibriophages

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    The Vibriophages are the potential agents for the transfer of the virulence factor to their host through lateral gene transfer. The complete genome sequencing of various known vibriophages has been done which deciphered the presence of various gene sequences for hypothetical proteins whose function is not yet understood. We analyzed complete genome of 21such Vibriophages for hypothetical proteins from which 13 phages were sorted for our studies. Our attempt is to predict the structure and function of these hypothetical proteins by the application of computational methods and Bioinformatics. The probable function prediction of the hypothetical protein was done by using Bioinformatics web tools like CDD-BLAST, INTERPROSCAN, PFAM and COGs by searching sequence databases for the presence of orthologous enzymatic conserved domains in the hypothetical sequences. While tertiary structures were constructed using PS2 Server (Protein Structure Prediction server). These study revealed presences of enzymatic functional domain in 92 uncharacterized proteins; their roles are yet to be discovered in Vibriophages. These deciphered enzymatic data for hypothetical proteins can be used for the understanding of functional, structural, evolutionary and metabolic development of Vibriophages and its life cycle along with their role in host evolution and pathogenicity

    Solidification and stabilization of chromium laden wastes in cementitious binders

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    Solidification/stabilization (S/S) technology was applied to a simulated sludge containing chromium. Leaching tests such as toxicity characteristic leaching procedure (TCLP), ANS 16.1 and multiple TCLP tests conducted on stabilized blocks showed that chromium was immobilized by the binder studied. A linear relationship was obtained between the cumulative fraction of chromium leached and time1/2 in the stabilized samples proving that chromium is leached by diffusion. The leachability indices obtained for the solidified materials satisfy the guidance value as per US Nuclear Regulatory Commission. Chromium concentrations in the TCLP leachates were well within the regulatory levels of the United States Environmental Protection Agency. Microchemistry and morphology of the stabilized samples were studied using Fourier transformation infrared (FTIR) technique and scanning electron microscopy (SEM). FTIR confirms the presence of ν2 CO3 band and O–H stretching of Ca(OH)2 and SEM shows uniform dense crystalline morphologies in all the samples. X-ray diffraction indicates the presence of bentorite, which proves that Cr replaces Al in the ettringit

    Chemical Composition of Precipitation in the Coastal Environment of India

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    The present study investigated the chemical composition of precipitation at Comba, Madgaon, South Goa during southwest monsoon. The rainwater samples were collected on event basis during June–September 2008 and were analyzed for pH, major anions F, Cl, NO3, SO4) and cations (Ca, Mg, Na, K,NH4). The pHvalue varied from 5.36 to 6.91 (6.25 ± 0.28) indicating alkaline nature of rainwater and dominance of Cl and Na in precipitation. The Neutralization factors (NF) was found to be NFCa = 1.22, NFMg = 0.42, NFNH4 = 0.37 and NFK = 0.14 indicating below cloud process in which crustal components are responsible for neutralization of anions

    DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells

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    Human chromosomal fragile sites are regions of the genome that are prone to DNA breakage, and are classified as common or rare, depending on their frequency in the population. Common fragile sites frequently coincide with the location of genes involved in carcinogenic chromosomal translocations, suggesting their role in cancer formation. However, there has been no direct evidence linking breakage at fragile sites to the formation of a cancer-specific translocation. Here, we studied the involvement of fragile sites in the formation of RET/PTC rearrangements, which are frequently found in papillary thyroid carcinoma (PTC). These rearrangements are commonly associated with radiation exposure; however, most of the tumors found in adults are not linked to radiation. In this study, we provide structural and biochemical evidence that the RET, CCDC6 and NCOA4 genes participating in two major types of RET/PTC rearrangements, are located in common fragile sites FRA10C and FRA10G, and undergo DNA breakage after exposure to fragile site-inducing chemicals. Moreover, exposure of human thyroid cells to these chemicals results in the formation of cancer-specific RET/PTC rearrangements. These results provide the direct evidence for the involvement of chromosomal fragile sites in the generation of cancer-specific rearrangements in human cell

    Pure phase LaFeO3 perovskite with improved surface area synthesized using different routes and its characterization

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    Three different wet chemistry routes, namely co-precipitation, combustion and sol–gel methods were used to synthesize LaFeO3 perovskite with improved surface area. The synthesized perovskite was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometer (EDS), Brunauer–Emmett–Teller (BET) nitrogen adsorption, ultraviolet diffused reflectance spectroscopy (UVDRS) and Fourier transform infrared (FTIR) spectroscopy techniques. Improved surface area was observed for all three methods as compared to the previously reported values. The perovskite synthesized using sol–gel method yields comparatively pure, crystalline phase of LaFeO3 and relatively higher surface area of 16.5m2 g−1 and porosity. The material synthesized using co-precipitation method yielded other phases in addition to the targeted phase. The morphology of perovskite synthesized using co-precipitation method was uniform agglomerates. Combustion method yields flakes type morphology and that of sol–gel method was open pore type morphology. The selection of method for perovskite synthesis largely depends on the targeted application and the desired properties of perovskites. The results reported in this study are useful for establishing a simple scalable method for preparation of high surface area LaFeO3 as compared to solid-oxide method. Further, the typical heating cycle followed for calcinations resulted in relatively high surface area in the case of all three methods

    A roadmap for development of sustainable E-waste management system in India

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    The problem of E-waste has forced Environmental agencies of many countries to innovate, develop and adopt environmentally sound options and strategies for E-waste management, with a view to mitigate and control the ever growing threat of E-waste to the environment and human health. E-waste management is given the top priority in many developed countries, but in rapid developing countries like India, it is difficult to completely adopt or replicate the E-waste management system in developed countries due to many country specific issues viz. socio-economic conditions, lack of infrastructure, absence of appropriate legislations for Ewaste, approach and commitments of the concerned, etc. This paper presents a review and assessment of the E-waste management system of developed as well as developing countries with a special emphasis on Switzerland, which is the first country in the world to have established and implemented a formal E-waste management system and has recycled 11 kg/capita of WEEE against the target of 4 kg/capita set by EU. And based on the discussions of various approaches, laws, legislations, practices of different countries, a road map for the development of sustainable and effective E-waste management system in India for ensuring environment, as well as, occupational safety and health, is proposed

    Emissions of SO2, NOx and particulates from a pipe manufacturing plant and prediction of impact on air quality

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    Integrated pipe manufacturing industry is operation intensive and has significant air pollution potential especially when it is equipped with a captive power production facility. Emissions of SO2, NOx, and particulate matter (PM) were estimated from the stationary sources in a state-of-the-art pipe manufacturing plant in India. Major air polluting units like blast furnace, ductile iron spun pipe facility, and captive power production facility were selected for stack gas monitoring. Subsequently, ambient air quality modeling was undertaken to predict ground-level concentrations of the selected air pollutants using Industrial Source Complex (ISC 3) model. Emissions of SO2, NOx, and particulate matter from the stationary sources in selected facilities ranged from 0.02 to 16.5, 0.03 to 93.3, and 0.09 to 48.3 kg h−1, respectively. Concentration of SO2 and NOx in stack gas of 1,180-kVA (1 KW =1.25 kVA) diesel generator exceeded the upper safe limits prescribed by the State Pollution Control Board, while concentrations of the same from all other units were within the prescribed limits

    Copper oxide incorporated mesoporous alumina for defluoridation of drinking water

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    In the present study mesoporous alumina was modified by coating copper oxide to enhance the defluoridation of water. The copper oxide coated alumina (COCA) was synthesised by impregnating alumina with copper sulphate solution followed by calcination at 450 �C in presence of air. The COCA was thoroughly characterised using powder XRD, SEM and BET surface area analysis. It was observed that coating of copper oxide improves the adsorption capacity of unmodified alumina from 2.232 to 7.770 mg g�1. Various adsorption isotherm and kinetic parameters were computed using batch adsorption studies to determine the adsorption capacity and to understand the mechanism of adsorption. The results revealed that the adsorption follows Langmuir isotherm and pseudo-second-order kinetic models. The adsorption capacity obtained from Langmuir isotherm plots were 3.155 mg g�1. Assessment of the water quality before and after treatment with COCA also confirmed that the there is no leaching of copper and other parameters were also within permissible limits of Indian drinking water standard indicating that the COCA can be used for treatment of fluoride contaminated drinking water

    In situ nitrogen enriched carbon for carbon dioxide capture

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    In situ nitrogen enriched carbon was synthesized from locally available low cost soybean as the proteinaceous source. The material was synthesized by chemical activation using zinc chloride followed by physical activation using CO2. The surface area of synthesized nitrogen enriched carbon was found to be 811m2/g which is comparable with commercially available activated carbon. The nitrogen enriched carbon was having a breakthrough adsorption capacity of 23 mg/g at 120 �C which was almost three times higher in comparison with the commercially available activated carbon for a gas mixture comprising 15% CO2 balanced with helium. This high adsorption capacity was attributed to the presence of nitrogen group within the carbon matrix, which was estimated to be about 0.64% as determined using the Kjeldahl’s method. The presence of different nitrogen containing groups assisting the adsorption of CO2 in the synthesized sample was also confirmed by infrared analysis. For checking the consistent performance of the synthesized carbon, multi-cycle adsorption–desorption studies were carried out at 30 and 75 �C in binary mixture of CO2/N2

    La0.9Ba0.1CoO3 perovskite type catalysts for the control of CO and PM emissions

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    Perovskite type catalysts with LaCoO3 and La0.9Ba0.1CoO3 compositions have been prepared by sol–gel method and their catalytic activity was studied for CO oxidation in presence of CO2, water and also for particulate matter (PM)/carbon oxidation. The catalysts were characterized using XRD, BET-SA, SEM, TPD, XPS and their catalytic activity was evaluated using a steady state gas evaluation assembly, as well as thermo gravimetric analysis. La0.8Ba0.1CoO3 catalyst shows enhanced catalytic activity as compared to LaCoO3 for CO and PM oxidation. Barium substitution appears to be responsible for low temperature activity of the catalyst by influencing redox and oxygen desorption properties as also suggested by TPD studies

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