Effect of Industrial Effluent on the Growth of Marine Diatom, Chaetoceros simplex (Ostenfeld, 1901)

The marine centric diatom,Chaetoceros simplex (Ostenfeld, 1901) was exposed to five different concentrations of industrial effluent for 96 hrs to investigate the effect on growth. The physico-chemical parameters viz. colour, odour, temperature, salinity, dissolved oxygen, turbidity, pH, alkalinity, hardness, ammonia, nitrite, nitrate, inorganic phosphate, total phosphorous, reactive  silicate, calcium and magnesium were estimated in the effluent. The Ammonia  (326 μg. L-1), Nitrite (19.53 μg. L-1) and Nitrate (471.4 μg. L-1) were observed at higher levels. About 50% of the cell density of C. simplex reached a lesser dilutions of effluent viz. 1:625 and 1:1250 than the control. The highest cell density (14.3 × 104 cell ml-1) was recorded in 1:10000 diluted effluent followed by control and the lowest cell density was observed in 1:625 diluted effluents. From the results, it is evidenced that the lower volume of effluent discharge into higher volume of water could not affect the growth rate of phytoplankton. It is more important that to reduce the effect of pollution and environmental sustainability. @JASEMJ. Appl. Sci. Environ. Manage. December, 2010, Vol. 14 (4) 35 - 3

Heterogeneous polymer supported and soluble tantalum metal complex catalysts for acylation reaction: A kinetic study

495-505New soluble and insoluble Tantalum pentachloride complex catalysts are prepared by simple procedures using pyridine and polymer-supported cross-linked (poly-4-vinyl pyridine) beads (PSCPVP) respectively as supports and Tantalum pentachloride as a catalytic moiety (TaCl5). The prepared soluble Py-TaCl5 and insoluble bead-shaped PSCPVP-TaCl5 catalysts have been characterized with FT-IR, UV-Vis, SEM, TGA and elemental analysis techniques. The catalytic efficiency of these catalysts has been examined through acylation of ethanol as a model reaction under identical pseudo first order reaction condition. From the calculated kobs values, it has been noticed that both the catalysts are active and however, Py-TaCl5shown 1.65 fold has increased activity (kobs =11.42x103 min-1) than insoluble PSCPVP-TaCl5 catalyst (kobs= 6.98x103, min-1). Although, PSCPVP-TaCl5 has shown lesser activity than soluble due to its lower cost, recyclability and reusable nature up to third cycle, it has received greater recognition. Hence, in order to utilize this insoluble bead-shaped PSCPVP-TaCl5 catalyst to pack in column reactor and to carry out the same reaction for continuous mode operation at industrial level, detailed kinetics study for acylation of ethanol has been conducted under pseudo first order condition by varying the different experimental parameters and has observed that each parameter has influenced the reaction. The obtained kobs value reveals that reaction rates increase with the increase in the stirring speed, [substrate], [catalyst] and temperature. The thermodynamic parameters viz., activation energy (Ea), entropy (∆S), enthalpy (∆H) and free energy (∆G#) for the reaction are also calculated for the first time and their observed values are 35.2 kJmol-1, -64.6 kJ-1mol-1, 37.7 kJmol-1and 57.3 kJmol-1 respectively. The prepared insoluble catalyst is stable even after its use for three times in acylation without losing its efficiency, thus it is better suited for industrial applications

Outgassing Behavior and Heat Treatment Optimization of JSC-1A Lunar Regolith Simulant

As NASA Strives towards a Long Duration Presence on the Moon, It Has Become Increasingly Important to Learn How to Better Utilize Resources from the Lunar Surface for Everything from Habitats, Vehicle Infrastructure, and Chemical Extraction. to that End, a Variety of Lunar Simulants Have Been Sourced from Terrestrially Available Volcanic Minerals and Glass as Apollo Regolith is Unavailable for Experimentation Needing Large Masses. However, While Mineralogy and Chemical Composition Can Approach that of Lunar Material in These Simulants, There Are Still Distinct Non-Lunar Phases Such as Hydrates, Carbonates, Sulfates, and Clays that Can Cause Simulants to Behave Distinctly Non-Lunar in a Variety of Processing Conditions that Maybe Applied In-Situ to Lunar Material. Notably, Severe Glassy Bubbling Has Been Documented in a Variety of Vacuum Sintering Experiments on JSC-1A Lunar Mare Simulant Heated Via Microwaves. the Origins of This Outgassing Have Not Been Well Understood But Are Normally Attributed to the Decomposition of Non-Lunar Contaminates Intrinsic to Virtually All Terrestrially Sourced Simulants. as Such, a Series of Controlled Environmental Tests Were Performed to Ascertain the Origins of the High Temperature Outgassing and to Develop Heat Treatments that Can Drive JSC-1A Closer to Lunar Composition and Behavior. It Was Found that in JSC-1A at Elevated Temperatures Distinct Gas Evolutions of Water, Carbon Dioxide, and Sulfur Dioxide Occur in Both Inert Gas and Vacuum. Additionally, the Presence of Hydrogen during Heat Treatments Was Shown to Dramatically Change Gas Evolutions, Leading to Distinctly More Lunar-Like Composition and Behavior from JSC-1A Simulant

Occurrence of Oratosquilla oratoria (De Haan, 1844) and Oratosquillina gravieri (Manning, 1978) from the trawl bycatches of Nagapattinam region, Tamil Nadu

1029-1036Six species of mantis shrimps were recorded in the trawl catches of Nagapattinam region during January – December, 2018. The occurrence of two species namely Oratosquilla oratoria (De Haan, 1844) and Oratosquillina gravieri (Manning, 1978) were reported for the first time in the trawl bycatches of Nagapattinam region. The morphometrics of these two species is reported in this paper. Presence of inferodistal spine in the merus of the raptorial claw, rostral plate short and trapezoid to square in shape, 5th abdominal segment without submedian patch, 4th abdominal segment submedian carinae unarmed in Oratosquilla oratoria and rostral plate elongate and rectangle, lateral process of 6th thoracic somite with slender, triangular anterior lobe and dactylus of the raptorial claw with 6 teeth in Oratosquillina gravieri are chief characters to differentiate from other species

αA-Crystallin Peptide 66SDRDKFVIFLDVKHF80 Accumulating in Aging Lens Impairs the Function of α-Crystallin and Induces Lens Protein Aggregation

The eye lens is composed of fiber cells that are filled with α-, β- and γ-crystallins. The primary function of crystallins is to maintain the clarity of the lens through ordered interactions as well as through the chaperone-like function of α-crystallin. With aging, the chaperone function of α-crystallin decreases, with the concomitant accumulation of water-insoluble, light-scattering oligomers and crystallin-derived peptides. The role of crystallin-derived peptides in age-related lens protein aggregation and insolubilization is not understood.We found that αA-crystallin-derived peptide, (66)SDRDKFVIFLDVKHF(80), which accumulates in the aging lens, can inhibit the chaperone activity of α-crystallin and cause aggregation and precipitation of lens crystallins. Age-related change in the concentration of αA-(66-80) peptide was estimated by mass spectrometry. The interaction of the peptide with native crystallin was studied by multi-angle light scattering and fluorescence methods. High molar ratios of peptide-to-crystallin were favourable for aggregation and precipitation. Time-lapse recordings showed that, in the presence of αA-(66-80) peptide, α-crystallin aggregates and functions as a nucleus for protein aggregation, attracting aggregation of additional α-, β- and γ-crystallins. Additionally, the αA-(66-80) peptide shares the principal properties of amyloid peptides, such as β-sheet structure and fibril formation.These results suggest that crystallin-derived peptides such as αA-(66-80), generated in vivo, can induce age-related lens changes by disrupting the structure and organization of crystallins, leading to their insolubilization. The accumulation of such peptides in aging lenses may explain a novel mechanism for age-related crystallin aggregation and cataractogenesis

Chitosan complements entrapment of silicon inside nitrogen doped carbon to improve and stabilize the capacity of Li-ion batteries

Abstract A facile strategy to entrap milled silicon (m-Si) particles using nitrogen-doped-carbon (N-C@m-Si) to overcome the dramatic volume changes in Si during intercalation of lithium ions and to improve its electronic conductivity is reported here. The only natural nitrogen containing biomaterial alkaline polysaccharide, i.e., chitosan, is used as the carbon source. Simple hydrothermal technique followed by a subsequent carbonization process is used to synthesize N-C and N-C@m-Si particles. N-C@m-Si exhibited significantly improved electrochemical performance as compared to bare m-Si, which is confirmed by the obtained discharge capacity of 942.4 mAh g−1 and columbic efficiency of 97% after 50 cycles at 0.1C rate. With regard to the N-C electrodes, the obtained discharge capacity of 485.34 mAh g−1 and columbic efficiency of 99.78%, after 50 cycles at 0.1C rate is superior to the commercial graphite electrodes. The solid electrolyte interphase (SEI) layer that formed over m-Si and N-C@m-Si electrodes is characterized using X-ray photoelectron spectroscopy. Compared to the SEI layer that formed over m-Si electrode after 10 charge-discharge cycles, the N-C@m-Si electrode had a stable lithium fluoride and carbonate species. Brief reaction mechanisms, representing the formation of different species in the SEI layer, is derived to explain its behavior during the electrochemical processes

Template-Assisted Synthesis and Characterization of Passivated Nickel Nanoparticles

Potential applications of nickel nanoparticles demand the synthesis of self-protected nickel nanoparticles by different synthesis techniques. A novel and simple technique for the synthesis of self-protected nickel nanoparticles is realized by the inter-matrix synthesis of nickel nanoparticles by cation exchange reduction in two types of resins. Two different polymer templates namely strongly acidic cation exchange resins and weakly acidic cation exchange resins provided with cation exchange sites which can anchor metal cations by the ion exchange process are used. The nickel ions which are held at the cation exchange sites by ion fixation can be subsequently reduced to metal nanoparticles by using sodium borohydride as the reducing agent. The composites are cycled repeating the loading reduction cycle involved in the synthesis procedure. X-Ray Diffraction, Scanning Electron Microscopy, Transmission Electron microscopy, Energy Dispersive Spectrum, and Inductively Coupled Plasma Analysis are effectively utilized to investigate the different structural characteristics of the nanocomposites. The hysteresis loop parameters namely saturation magnetization and coercivity are measured using Vibrating Sample Magnetometer. The thermomagnetization study is also conducted to evaluate the Curie temperature values of the composites. The effect of cycling on the structural and magnetic characteristics of the two composites are dealt in detail. A comparison between the different characteristics of the two nanocomposites is also provided

Identification of the Rheumatoid Arthritis Shared Epitope Binding Site on Calreticulin

Background: The rheumatoid arthritis (RA) shared epitope (SE), a major risk factor for severe disease, is a five amino acid motif in the third allelic hypervariable region of the HLA-DRb chain. The molecular mechanisms by which the SE affects susceptibility to – and severity of- RA are unknown. We have recently demonstrated that the SE acts as a ligand that interacts with cell surface calreticulin (CRT) and activates innate immune signaling. In order to better understand the molecular basis of SE-RA association, here we have undertaken to map the SE binding site on CRT. Principal Findings: Surface plasmon resonance (SPR) experiments with domain deletion mutants suggested that the SE binding site is located in the P-domain of CRT. The role of this domain as a SE-binding region was further confirmed by a sulfosuccinimidyl-2-[6-(biotinamido)-2-(p-azido-benzamido) hexanoamido] ethyl-1,3-dithiopropionate (sulfo-SBED) photoactive cross-linking method. In silico analysis of docking interactions between a conformationally intact SE ligand and the CRT P-domain predicted the region within amino acid residues 217–224 as a potential SE binding site. Site-directed mutagenesis demonstrated involvement of residues Glu 217 and Glu 223- and to a lesser extent residue Asp 220- in cell-free SPR-based binding and signal transduction assays. Significance: We have characterized here the molecular basis of a novel ligand-receptor interaction between the SE and CRT. The interaction represents a structurally and functionally well-defined example of cross talk between the adaptive an

High Throughput Ratio Imaging to Profile Caspase Activity: Potential Application in Multiparameter High Content Apoptosis Analysis and Drug Screening

Recent advancement in the area of green fluorescent protein techniques coupled with microscopic imaging has significantly contributed in defining and dissecting subcellular changes of apoptosis with high spatio-temporal resolution. Although single cell based studies using EGFP and associated techniques have provided valuable information of initiation and hierarchical changes of apoptosis, they are yet to be exploited for multiparameter cell based real time analysis for possible drug screening or pathway defining in a high throughput manner. Here we have developed multiple cancer cell lines expressing FRET sensors for active caspases and adapted them for high throughput live cell ratio imaging, enabling high content image based multiparameter analysis. Sensitivity of the system to detect live cell caspase activation was substantiated by confocal acceptor bleaching as well as wide field FRET imaging. Multiple caspase-specific activities of DEVDase, IETDase and LEHDase were analysed simultaneously with other decisive events of cell death. Through simultaneous analysis of caspase activation by FRET ratio change coupled with detection of mitochondrial membrane potential loss or superoxide generation, we identified several antitumor agents that induced caspase activation with or without membrane potential loss or superoxide generation. Also, cells that escaped the initial drug-induced caspase activation could be easily followed up for defining long term fate. Employing such a revisit imaging strategy of the same area, we have tracked the caspase surviving fractions with multiple drugs and its subsequent response to retreatment, revealing drug-dependent diverging fate of surviving cells. This thereby indicates towards a complex control of drug induced tumor resistance. The technique described here has wider application in both screening of compound libraries as well as in defining apoptotic pathways by linking multiple signaling to identify non-classical apoptosis inducing agents, the greatest advantage being that the high content information obtained are from individual cells rather than being population based