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For source identification, a field campaign involving simultaneous sampling of particulate matter (PM 10 ) was conducted at eight sampling sites in the Indian mainland during winter 2014. The sampling sites include Delhi (upper IGP), Lucknow (middle IGP), and Kolkata (lower IGP) in the Indo-Gangetic Plains (IGP); Mohal-Kullu and Darjeeling in the Indo-Himalayan Range (IHR). In addition, Ajmer, located upwind of the IGP in NW-India and Giridih and Bhubaneswar, in the downwind to the IGP has also been chosen. To characterize the sources of the ambient PM 10 , stable isotope ratios of carbon (δ 13 C TC ) and nitrogen (δ 15 N TN ) for the total carbon (TC) and total nitrogen (TN) fractions have been considered. Ancillary chemical parameters, such as organic carbon (OC), elemental carbon (EC), and water-soluble ionic components (WSIC) mass concentrations are also presented in this paper. There was very small variation in the daily average δ 13 C TC ratios (- 24.8 to - 25.9‰) among the sites. Comparison with end-member stable C isotopic signatures of major typical sources suggests that the PM 10 at the sites was mainly from fossil fuel and biofuel and biomass combustion. Daily average δ 15 N TN ratios were not observed to vary much between sites either (8.3 to 11.0‰), and the low δ 15 N TN levels also indicate substantial contributions from biofuel and biomass burning of primarily C3 andC4 plant matter. Graphical abstract Scatter plot of the average (± 1 standard deviation (SD)) δ 13 C TC (‰) compared to δ 15 N TN (‰) at the sampling sites.

A sequence-independent single-primer amplification method and a modified enterovirus VP1 gene typing primer were used for identification of echovirus 19 and enterovirus 101, which remained undiagnosed by standard enterovirus molecular typing methods. Six different serotypes were identified during this study, with the predominance of ECV 19 (n = 20) followed by echovirus 21 (n = 3), EV 69 and EV 101 (n = 2 each), coxsackievirus B5 and ECV 27 (n = 1 each). To our knowledge, this is the first report of enteroviruses 69 and 101 in encephalitis cases in India.

An investigation was carried out to ascertain the effect of arsenic in the blocks of Ballia district in Uttar Pradesh in the upper and middle Ganga plain, India. Analysis of 100 drinking water samples revealed that arsenic concentration was below 10 μg l⁻¹ in 60% samples, 10-50 μg l⁻¹ in 6%, 100 μg l⁻¹ in 24% and 200 μg l⁻¹ in 10% samples, respectively. The arsenic concentration in drinking water ranged from 12.8 to 132.2 μg l⁻¹. The depth of source of drinking water (10-60 m) was also found with a mean of 36.12 ± 13.61 μg l⁻¹ arsenic concentration. Observations revealed that at depth ranging from 10 to 20 m, the mean level of arsenic concentration was 17.398 ± 21.796 μg l⁻¹, while at 21 to 40 m depth As level was 39.685 ± 40.832 μg l⁻¹ and at 41 to 60 m As level was 46.89 ± 52.80 μg l⁻¹, respectively. These observations revealed a significant positive correlation (r = 0.716, t = 4.215, P < 0.05) between depth and arsenic concentration in drinking water. The age of water sources were ranged from zero to 30 years. The study indicates that the older sources of drinking water showed higher chance of contamination. Results showed that group 21-30 years having maximum arsenic concentration with mean value of 52.57 ± 53.79 μg l⁻¹. Correlation analysis also showed a significant positive correlation (r = 0.801, t = 5.66, P < 0.05) between age of drinking water sources and their respective arsenic concentration (μg l⁻¹). Arsenic concentration in blood with mean value 0.226 ± 0.177 μg dl⁻¹ significantly increased as compared to control. The blood arsenic content correlated significantly (r = 0.6823, t = 3.93, P < 0.05) with drinking water arsenic level and exposure time (r = 0.545, t = 3.101 & *P < 0.05) for populations residing in Ballia districts. Observations and correlation analysis revealed that individuals having depth of drinking water sources 20-30 m were less affected with arsenic exposure.

Encountering a foreign body (FB) in the kidney is uncommon. Most of the time a FB is introduced externally (violence or accident) or through endourological interventions. An ingested FB reaching the kidneys is extremely rare. This article includes an interesting case of FB, which apparently reached the kidney through the gastrointestinal tract as well as a brief review of the relevant literature. The case was successfully managed laparoscopically.

A preliminary investigation was conducted to assess lignocellulolytic efficiency of crude extracts from three white-rot fungi, Pleurotus florida PF05 (PF), Pleurotus sajor-caju PS07 (PS) and Pleurotus eryngii PE08 (PE). The activities of CMC-ase, xylanase, beta-glucosidase, beta-xylosidase, laccase and Mn peroxidase in extracts were evaluated. PF produced its highest CMC-ase (317 UL(-1)'), beta-glucosidase (62 UL(-1)), beta-xylosidase (37 UL(-1)) and laccase (347 UL(-1)) activities while, PS produced highest xylanase (269 UL-(1)) and Mn peroxidase (69 UL(-1)) activities. In addition, crude extracts extracted were employed for their in vitro degradability assessment; and were evaluated with mono and mixed extracts separately to corn cob substrate. The losses in cell wall components and dry matter during 5 and 10 days incubations were analyzed after treatments of extracts. Maximum 8.2, 4.4 and 2.8% loss were found respectivelyin hemicellulose (HC), cellulose (C) and lignin (L) with mono extract of PF within 10 days. The influence of mono extract of each strain (PF PS and PE) and their mixed extracts (PF+PS, PF+PE, PS+PE and PF+PS+PE) on degradation of cell wall constituents were remarkably differed. The mixed extract treatment proved maximum 13.6% HC loss by PF+PS+PE extract, 9.2% loss in C by PF+PS extract and 5.2% loss of L by the PF+PS+PE extract treatment. The highest dry matter loss (8.2%) was recorded with PF+PS+PE mixed extract combination.

The various dilution levels of treated tannery effluent (T.E.) (10, 25, 50 and 100%) and Cr6+ (0.5, 2.0, 5.0 and 10 ppm) were used in experiment to know their effect on seed germination, seedling growth, pigments and enzymes content in Black gram (Phaseolus mungo Roxb.). Chromium is known as the main toxic component of tannery effluent so its various concentration were given to know their effects. For the recovery of plant damage, protective value of 10 and 25 ppm of zinc, potassium and iron sulphate were also given with 50% treated tannery effluent and 10 ppm Cr6+ levels in separate petridishes. The different concentrations of tannery effluent and Cr6+ showed significant reduction in germination percentage, seedling growth (plumule and radicle length, number of lateral roots, fresh and dry weight, and moisture %) and pigments (chlorophyll, pheophytin and carotenoids) with increase in concentrations. The lower doses of tannery effluent (10%) and Cr6+ (0.5, 2 and 5 ppm) slightly increases the pigments concentration. The amylase activity and total sugar contents were also significantly decreased while catalase and peroxidase activity showed significant increase with rise in concentrations of treatments. The lower concentrations of tannery effluent (dilution 10 and 25%) and Cr6+ (0.5 and 2 ppm) showed significant increase in total protein contents while decrease at higher concentrations. The zinc, potassium and iron treatments led to recover the damage caused by chromium and tannery effluent in all parameters. In recovery treatments zinc showed highest and significant recovery in maximum parameters. Iron also showed almost similar effect to the zinc while potassium showed minimum recovery.

Whereas ribosomal proteins (r-proteins) are known primarily as components of the translational machinery, certain of these r-proteins have been found to also have extraribosomal functions. Here we report the novel ability of an r-protein, L4, to regulate RNA degradation in Escherichia coli. We show by affinity purification, immunoprecipitation analysis, and E. coli two-hybrid screening that L4 interacts with a site outside of the catalytic domain of RNase E to regulate the endoribonucleolytic functions of the enzyme, thus inhibiting RNase E-specific cleavage in vitro, stabilizing mRNAs targeted by RNase E in vivo, and controlling plasmid DNA replication by stabilizing an antisense regulatory RNA normally attacked by RNase E. Broader effects of the L4-RNase E interaction on E. coli transcripts were shown by DNA microarray analysis, which revealed changes in the abundance of 65 mRNAs encoding the stress response proteins HslO, Lon, CstA, YjiY, and YaeL, as well as proteins involved in carbohydrate and amino acid metabolism and transport, transcription/translation, and DNA/RNA synthesis. Analysis of mRNA stability showed that the half lives of stress-responsive transcripts were increased by ectopic expression of L4, which normally increases along with other r-proteins in E. coli under stress conditions, and also by inactivation of RNase E. Our finding that L4 can inhibit RNase E-dependent decay may account at least in part for the elevated production of stress-induced proteins during bacterial adaptation to adverse environments.

The present study was to evaluate heavy metal toxicity stress symptoms in fish blood during long-term exposure of sublethal concentration of copper sulphate (CuSO4). The effects of copper on various heamatological parameters were evaluated exposing Indian fresh water fish, Channa punctatus to a sub-lethal concentration of copper sulphate (0.36 mg l(-1)) for different periods. Exposure of fish to copper showed a significant decrease in the haemoglobin (Hb) content from 10.73 to 6.60%, red blood cells (RBC) from 2.86 to 1.84 x 10(6)/mm3 and packed cell volume (PCV) from 31.00 to 23.33% at the end of 45th day as compared to control. Whereas the white blood cells (WBC) increased from 60.00 to 92.48 x10(3)/mm3, clotting time (CT) from 27.66 to 43.00 second, erythrocyte sedimentation rate from 5.0 to 13.66 mm/hr and mean corpuscular volume from 108.11 to 126.85 cmu, significantly, with increase in exposure periods. Although mean corpuscular haemoglobin concentration (MCHC) and mean corpuscular haemoglobin (MCH) values showed significant increase during 15 and 30 days exposures, both the values were found significantly increased at the end of the experimental period. The differential leucocytes count (DLC) showed a significant increase in the populations of lymphocytes and eosinophils, whereas neutrophils, monocytes and basophiles were found decreased after exposure to copper.

The decay of mRNA plays an important role in the regulation of gene expression. Although relatively ignored for many years and regarded as a simple ribonucleotide salvage pathway, mRNA decay has been established in recent years as a well-defined cellular process that plays an integral role in determining gene expression. The recent application of microarray methods to the study of diverse organisms will help us to better understand these gene regulatory circuits and the influence of transcript stability on gene expression. DNA microarray technology is the method of choice to study individual mRNA half-lives on a global scale. It is important to standardize these methods to generate reproducible and reliable results. In this chapter, we describe experimental designs for the analysis of mRNA decay on a genome-wide scale and provide detailed protocols for each experimental step. We also present an analysis of the decay of chromosomally encoded mRNAs in E. coli.

Under the reutilization and recycling strategy of industrial effluents, treated distillery and sugar factory mixed effluent was used in petridish culture experiments to investigate its effect on seed germination and seedling growth in wheat, garden pea, black gram and mustard. The seed germination and seedling growth were significantly reduced with increase in concentration of the effluent. The fresh matter was found significantly increased in barley (1.16 g per seedling in 25% dilution level of effluents in comparison to 0.93 in control), while other higher dilution levels reduce it. Wheat, garden pea, black gram, mustard invariably showed inhibition in fresh weight. Dry weight was found consistently reduced or unchanged in different treatments. Total chlorophyll contents in barley were significantly increased in different treatments (2.351 and 2.721 mg/g fresh weight of tissue at 25, 50% dilution levels in comparison to 1.781 of control) while in other crop it was reduced alloverthe treatments. Amylase activity in wheat, garden pea, black gram and mustard was reduced in all the treatments. Only in barley its level was enhanced from 0.76 to 0.85, 0.96, 0.81 in 25, 50, 75% dilution levels of the effluent mixture respectively Based on the data of different crops barley was found to be highly tolerant as the 25 and 50% dilution levels of combined effluents. It showed no change in germination %, while seedling growth was increased in lower dilution levels of combined effluent as compared to control Barley>garden pea>wheat>black gram>mustard gradually showed increased level of sensitivity respectively Most detrimental effects were seen in mustard. This toxicity might be due to excess of nutrients, beyond the limits of tolerance. Therefore, the higher concentration of mixed effluent was not advisable for irrigation purpose, however it could be used for irrigation purpose after proper treatment and dilution (one part treated effluent and five parts of available irrigation water), as this dilution level was found growth and yield promotory

The experiment was performed to study the seed germination and seedling growth in wheat under the influence of different concentrations of copper. The germination %, plumule and radicle length, and number of lateral roots decreased with increase in copper concentration (5, 25, 50 and 100 mgl(-1)). Total chlorophyll contents declined on 14th day from 1.605 of control to 1.581, 1.242, 1.275 and 1.107 mg g(-1) fresh weight in respective treatments. Similarly, on 21st day the decline in total chlorophyll contents was 1.288, 1.123, 1.077 and 0.985 mg g(-1) fresh weight in respective treatments against 1.724 of control. Likewise the pheophytin contents also declined showing the same pattern. However, carotenoid contents increased in different treatments, ranging between 0.366 to 0.464 mg g(-1) fresh weight in comparison to control (0.328) on 14th day, but showed adverse effects on 21st day as the carotenoid contents decreased in different copper treatments. The activity of amylase was found to be gradually reduced 14th day from 29.73 of control to 27.80, 27.33, 21.86 and 20.00 mg g(-1) and at 21st day from 14.40 of control to 11.46, 11.01, 9.86 and 5.60 mg g(-1) fresh weight with increase in concentrations of copper The catalase activity increased 14th day from 97.33 of control to 134.66, 161.33, 216.00 and 232.00 and on 21st day from 140.00 of control to 245.33, 274.66, 278.66 and 300.66 ml H2O2 hydrolyzed/g fresh weight in different increased concentrations of copper Similarly the peroxidase activity was also increased with increase in copper concentration. Likewise fresh weight and moisture contents decreased with increase in copper concentration. The dry weight was increased with increase in concentration of copper treatment. Total protein contents were initially decreased on 14th day from 80.69 of control to 66.75, 60.41, 56.41 and 48.48 microg/mg and on 21st day 81.37 of control to 67.06, 62.31, 54.92 and 46.47 microg/mg fresh weight in different copper concentrations respectively Sugar contents were significantly decreased in all the doses of copper on both 14th and 21st days i.e. (5.53 of control to 4.76, 3.69, 3.68 and 2.86 microg/mg in different copper treatments on 14th day and 4.81 of control to 4.49, 3.40, 2.79 and 2.15 microg/mg on 21st day respectively.

Variability in the organization of repeats of 5S rDNA is useful for phylogenetic studies in various crops. We found variable repeats of 5S rDNA gene in the genome of tea (Camellia sinensis (L.) O. Kuntze) during Southern hybridization. Variability in the repeats of 5S rDNA with specific restriction endonucleases (Sau3AI, BamHI, and ApoI) was analyzed in 28 different tea clones representing 3 types of tea. Our results clearly show that the 5S rDNA gene in tea could be used as a molecular marker to distinguish C. sinensis Chinary tea from the other important types of tea, namely Assamica and Cambod. Upon analysis with restriction endonucleases, the 5S rDNA gene in the tea genome was found to be heavily methylated.