Bio-fabrication of porous magnetic Chitosan/Fe3O4 nanocomposite using Azolla pinnata for removal of chromium - Parametric effects, surface characterization and kinetics.

In this research, a novel porous nanocomposite, namely Chitosan-iron-oxide @ Azolla pinnata nanocomposite, has been synthesized by co-precipitation and hydrothermal method. The effect of process parameter on adsorption process was investigated. Batch removal of chromium (Cr) was optimized with respect to solution pH, batch stirring time, sorbent dose, initial chromium concentration and temperature. The maximum removal efficiency was found to be 98.58%. The Fourier transform infrared (FTIR) spectroscopy and scanning electron microscope (SEM) analysis of the nano composite confirmed the presence of characteristic functional groups and porous structure of synthesized nanocomposite. The adsorption data fitted well with Langmuir adsorption isotherm (R2 = 0.996) confirming mono layer sorption and the maximum uptake was found to be 294.12 mg/g. The adsorption was found to follow pseudo second order model (R2 = 0.997). Thermodynamic studies revealed that adsorption is endothermic and spontaneous. Reusability studies have confirmed that removal efficiency attained was 85% after completion of five adsorption-desorption cycles. Electrostatic attraction, ion exchange, coordination bonding and reduction are the major mechanisms responsible for removal of chromium. Surface modification of Azolla pinnata with chitosan and iron oxide improved the ability of Azolla in the adsorption of chromium from aqueous media. The combined effects of facile synthesis, improved adsorption features and easier magnetic separation promotes Chitosan-iron-oxide @ Azolla pinnata nanocomposite as a novel adsorbent.

Potential risks and approaches to reduce the toxicity of disinfection by-product - A review.

Water contamination through anthropogenic and industrial activities has led to the emergence and necessity of disinfection methods. Chlorine and bromine gases, often used to disinfect water, resulted in the by-product formation by reacting with organic matter. The Disinfectant by-products (DBP) led to the formation of Trihaloaceticacid (TAA), Trihalomethane (THM), and other minor components. The release of chemicals has also led to the outbreak of diseases like infertility, asthma, stillbirth, and types of cancer. There are new approaches that are found to be useful to compensate for the generation of toxic by-products and involve membrane technologies, namely reverse osmosis, ultrafiltration, and nanofiltration. This review mainly focuses on the toxicology effects of DBPs and various approaches to mitigate the same. The health hazards caused by different DBPs and the various treatment techniques available for the removal are discussed. In addition, a critical comparison of the different removal techniques was discussed.

Performance evaluation of polymer-marine biomass based bionanocomposite for the adsorptive removal of malachite green from synthetic wastewater.

In this experimental investigation, feasibility and performance of a polymer hybrid bio-nano composite were evaluated to remove malachite green (MG) under controlled environment conditions. The polymer hybrid bio-nanocomposite was characterized using FTIR, SEM and EDS. The influence of operating variables, namely effect of pH (2-11), nanocomposite dosage (20-100 mg), initial MG concentration (10- 200 mg/L), contact time (10-120 min) and temperature (298-318 K) were explored. The maximum removal efficiency (RE) of 99.79% was achieved at neutral pH at the dosage level of 50 mg with the initial MG concentration of 150 mg/L in 40 min. The equilibrium results revealed that the adsorption of MG data fitted to Langmuir isotherm (R2 > 0.970) indicating monolayer adsorption. The maximum adsorption capacity of polymer hybrid nanocomposite was found to be 384.615 mg/g. Kinetic studies were performed using five kinetic models and results showed the pseudo second order model fitted very well with the MG adsorption data (R2 > 0.990). The thermodynamic results confirmed that MG adsorption onto polymer hybrid nanocomposite is feasible and (ΔS ͦ = 0.2893 kJ/mol K), spontaneous (ΔH ͦ = 81.103 kJ/mol K) and exothermic (ΔG ͦ < 0). A mechanism is also proposed for the removal of MG using the polymer nanocomposite and identified that electrostatic attraction and hydrogen bonding as the major mechanism for removal of MG. FTIR results confirmed the presence of carboxyl (-COO) and hydroxyl (-OH) groups which helped in effective binding of cationic dye. The overall results revealed that polymer nanocomposite could be used as a potential adsorbent for removing MG from aqueous solution.

Application of a polymer-magnetic-algae based nano-composite for the removal of methylene blue - Characterization, parametric and kinetic studies.

The potential ability of synthesized PPy-Fe3O4-SW nano-composite to remove Methylene Blue (MB) from synthetic textile dye solution was investigated under batch conditions. Through parametric studies, the influence of process parameters namely solution pH, on the effective performance of nano-composite was studied. PPy - Fe3O4- SW nano-composite removed 99.14% of MB at the optimized conditions of pH-10, temperature - 25 °C, initial MB concentration - 50 mg/L, nano-composite dosage - 20 mg and contact time - 20 min. PPy - Fe3O4- SW nano-composite has a maximum sorption capacity of 666.66 mg/g. The kinetics and isotherm study revealed that the chromium adsorption obeys pseudo second order (PSO) model (R2 = 0.9941) and Freundlich isotherm (R2 = 0.9910) respectively. The PSO kinetic constant (K2) was found to be 0.000442 (g/mg) min. The thermodynamic feasibility was confirmed through negative values of standard free energy at all tested conditions. The characteristics of adsorption study were analyzed and the results of FTIR, SEM and EDS confirmed the uptake of MB by PPy-Fe3O4-SW nano-composite.

Surface modified polymer-magnetic-algae nanocomposite for the removal of chromium- equilibrium and mechanism studies.

The present work explains the sorption ability of a novel nano-composite, Polypyrrole -iron oxide-seaweed (PPy - Fe3O4 - SW), for Cr(VI) removal. The influence of operating parameters, namely pH, contact time, nanocomposite dosage, initial Chromium concentration and operating temperature, on the hexavalent chromium removal was studied. The novel nano-composite was analyzed using FTIR, SEM and EDS to confirm the sorption of Cr(VI) and to understand the mechanism of sorption. PPy - Fe3O4- SW nano-composite removed 96.36% of Cr(VI) at the optimized conditions of pH = 2, temperature = 30 °C, initial Cr(VI) concentration = 50 mg/L, nanocomposite dosage = 100 mg and contact time = 30min. PPy-Fe3O4-SW nanocomposite has a maximum sorption capacity of 144.93 mg/g. The kinetic studies revealed that the metal adsorption obeys pseudo second order (PSO) model and the sorption was found to be monolayer in nature as confirmed by Langmuir isotherm (R2 > 0.9985). Electrostatic interaction and ion-exchange are identified as the fundamental mechanisms for Cr(VI) sorption on PPy-Fe3O4-SW composite.

Mineral content of water and food in fluorotic villages and prevalence of dental fluorosis.

The fluoride (F), calcium (Ca), magnesium (Mg), zinc (Zn), copper (Cu), and phosphorus (P) content in potable water and food samples from endemic and nonendemic villages for fluorosis were analyzed. It was found that the F content in water was significantly higher (p<0.01) in endemic villages (4.20+/-1.6 ppm) than control villages (0.63+/-0.15 ppm), whereas the Ca, Cu, and Mg contents were found to be significantly lower (p<0.05) in endemic villages compared to control villages. However, there was no significant difference in Zn and P contents between the villages. Foods grown in endemic villages contained significantly higher (p<0.01) fluoride content as compared to control villages. There was no significant difference in Ca, Mg, P, and Zn contents in food grown in endemic and control villages. Copper content in cereals (p<0.05), pulses (p<0.01), and vegetables (p<0.01) in endemic villages was found significantly higher as compared to control villages. The overall prevalence of dental fluorosis in six endemic villages was 97.4% in boys and 96% in girls, which was significantly higher (p<0.01) than that of control villages, where it was 10.5% in boys and 8.3% in girls. The prevalence of dental fluorosis was positively correlated (r=0.125, p<0.01) to fluoride and negatively correlated to Ca and Cu content in drinking water in endemic villages.

Introduction of red palm oil into the 'ready to eat' used supplementary feeding programme through ICDS.

Children attending the anganwadi centres were fed with Ready to eat (RTE) food containing 2g of Red Palm Oil (RPO). Daily children's attendance, their participation in the feeding programme, quantity of food supplement consumed were recorded. Heights, weights, clinical signs of vitamin A deficiency and morbidity pattern of the beneficiary children were assessed. There was increase in attendance of the children in the feeding programme after introduction of RPO. Quantity of the food supplement consumed by the children also increased. An improvement in the nutritional grades of children was observed. Signs of vitamin A deficiency were absent. Anganwadi teachers, helpers and parents accepted the inclusion of RPO in the supplementary feeding programme.

Glycemic index of grain amaranth, wheat and rice in NIDDM subjects.

Glycemic index of grain amaranth, wheat and rice preparations was studied in non-insulin dependent diabetic subjects. Diets containing 50 g carbohydrate equivalent were given and post-prandial blood glucose estimated at different intervals. Glycemic index calculated for different experimental diets showed that GI of amaranth-wheat composite flour diet (25:75) was the least (65.6%) followed by wheat diet (65.7%), rice diet (69.2%), amaranth-wheat flour 50:50 (75.5%), and popped amaranth in milk (97.3%). Therefore 25:75 combination of amaranth and wheat, wheat and rice can be considered low GI food, 50:50 grain amaranth and wheat medium GI food and popped amaranth and milk combination high GI food.

Hypocholesterolemic effect of amaranth seeds (Amaranthus esculantus).

Hypocholesterolemic effect of amaranth seeds was studied in male wistar strain albino rats as against Bengal gram. The results showed that liver weights were significantly higher in animals with hypercholesterolemia inducing diet. Contrarily, weights of other organs like brain, kidney, testes and spleen showed higher weights with amaranth and bengal gram diets. Serum lipid and TG (triglyceride) contents were lower and HDL-cholesterol fraction was higher and comparable with amaranth seed diet. Feeding with amaranth seed showed a definite hypocholesterolemic effect.

Interaction, functional relations and evolution of large and small subunits in Rubisco from prokaryota and eukaryota.

In early biological evolution anoxygenic photosynthetic bacteria may have been established through the acquisition of ribulose bisphosphate carboxylase-oxygenase (Rubisco). The establishment of cyanobacteria may have followed and led to the production of atmospheric oxygen. It has been postulated that a unicellular cyanobacterium evolved to cyanelles which were evolutionary precursors of chloroplasts of both green and non-green algae. The latter probably diverged from ancestors of green algae as evidenced by the occurrence of large (L) and small (S) subunit genes for Rubisco in the chloroplast genome of the chromophytic algae Olisthodiscus luteus. In contrast, the gene for the S subunit was integrated into the nucleus in the evolution of green algae and higher plants. The evolutionary advantages of this integration are uncertain because the function of S subunits is unknown. Recently, two forms of Rubisco (L8 and L8S8) of almost equivalent carboxylase and oxygenase activity have been isolated from the photosynthetic bacterium Chromatium vinosum. This observation perpetuates the enigma of S subunit function. Current breakthroughs are imminent, however, in our understanding of the function of catalytic L subunits because of the application of deoxyoligonucleotide-directed mutagenesis. Especially interesting mutated Rubisco molecules may have either enhanced carboxylase activity or higher carboxylase:oxygenase ratios. Tests of expression, however, must await the insertion of modified genes into the nucleus and chloroplasts. Methodology to accomplish chloroplast transformation is as yet unavailable. Recently, we have obtained the first transformation of cyanobacteria by a colE1 plasmid. We regard this transformation as an appropriate model for chloroplast transformation.

Transformation of the cyanobacterium Anacystis nidulans 6301 with the Escherichia coli plasmid pBR322.

Anacystis nidulans 6301 has been transformed in the light to ampicillin resistance with the plasmid pBR322. Permeaplasts prepared by 2-hr treatment of cells with lysozyme and EDTA are transformed with a 50-fold higher efficiency than that observed for cells. beta-Lactamase is present in A. nidulans transformed either with pBR322 or the plasmid pCH1 as evidenced by hydrolysis of the beta-lactam ring of Nitrocefin in extracts of transformants. beta-Lactamase also can be immunoprecipitated from extracts of [35S]methionine-labeled pBR322 transformants and coprecipitates with ribulose-bisphosphate carboxylase. Expression of the carboxylase is apparently amplified in pBR322 transformants as is that for several soluble proteins in pCH1 transformants. Chromosomal DNA per cell is increased about 6-fold after transformation of A. nidulans 6301 with either pBR322 or pCH1. A 4.3-kilobase-pair plasmid can be isolated from pBR322 transformants in addition to the endogenous plasmids pUH24 and pUH25.

Inhibition of glycine oxidation by carboxymethoxylamine, methoxylamine, and acethydrazide.

Carboxymethoxylamine (amino-oxyacetate), methoxylamine, and acethydrazide are shown to be effective, although not completely specific, inhibitors of glycine oxidation by the isolated glycine decarboxylase multienzyme complex, mitochondria, protoplasts, and leaf discs from peas. The inhibition probably results from a reaction between these compounds and the pyridoxal 5-phosphate cofactor of the enzyme.

Extraction and partial characterization of the glycine decarboxylase multienzyme complex from pea leaf mitochondria.

Glycine decarboxylase has been successfully solubilized from pea (Pisum sativum) leaf mitochondria as an acetone powder. The enzyme was dependent on added dithiothreitol and pyridoxal phosphate for maximal activity. The enzyme preparation could catalyze the exchange of CO(2) into the carboxyl carbon of glycine, the reverse of the glycine decarboxylase reaction by converting serine, NH(4) (+), and CO(2) into glycine, and (14)CO(2) release from [1-(14)C]glycine. The half-maximal concentrations for the glycine-bicarbonate exchange reaction were 1.7 millimolar glycine, 16 millimolar NaH(14)CO(2), and 0.006 millimolar pyridoxal phosphate. The enzyme (glycine-bicarbonate exchange reaction) was active in the assay conditions for 1 hour and could be stored for over 1 month. The enzymic mechanism appeared similar to that reported for the enzyme from animals and bacteria but some quantitative differences were noted. These included the tenacity of binding to the mitochondrial membrane, the concentration of pyridoxal phosphate needed for maximum activity, the requirement for dithiothreitol for maximum activity, and the total amount of activity present. Now that this enzyme has been solubilized, a more detailed understanding of this important step in photorespiration should be possible.

Simultaneous oxidation of glycine and malate by pea leaf mitochondria.

Mitochondria isolated from pea leaves (Pisum sativum L.) readily oxidized malate and glycine as substrates. The addition of glycine to mitochondria oxidizing malate in state 3 diminished the rate of malate oxidation. When glycine was added to mitochondria oxidizing malate in state 4, however, the rate of malate oxidation was either unaffected or stimulated. The reason both glycine and malate can be metabolized in state 4 appears to be that malate only used part of the electron transport capacity available in these mitochondria in this state. The remaining electron transport capacity was used by glycine, thus allowing both substrates to be oxidized simultaneously. This can be explained by differential use of two NADH dehydrogenases by glycine and malate and an increase in alternate oxidase activity upon glycine addition. These results help explain why photorespiratory glycine oxidation and its associated demand for NAD do not inhibit citric acid cycle function in leaves.

On the active species in bicarbonate stimulation of Hill reaction in thylakoid membranes.

At 5 degree C addition of CO2 or HCO3- to CO (HCO3-)-depleted thylakoids (containing 100 mM formate) initiates, within 10 s, the activation of the Hill reaction in light. In contrast to HCO3- addition, where there is a lag of 6-8 s, the activation by CO2 addition is almost instantaneous. With CO2, prior addition of carbonic anhydrase produces a lag of about 6 s that approaches the lag observed by the HCO3- addition. These data suggest that CO2 is an active species involved in stimulating the Hill reaction. Binding of CO2 (HCO3-) to a component on the external side of the thylakoid membranes is supported by the present study.