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PubMed2005

Bioaccumulation of waterborne selenium in the Asiatic clam Corbicula fluminea: influence of feeding-induced ventilatory activity and selenium species.

A set of experiments was performed to investigate the bioavailability and the effect of Se on the ventilatory activity of the bivalve Corbicula fluminea, under different conditions of both algal cell densities and dissolved Se chemical forms and concentrations. A first set of experiments was conducted without selenium to investigate the changes in the ventilatory flow rate as a function of the concentration of the unicellular alga Chlamydomonas reinhardtii (10(5)-10(6) cells mL(-1)). For algal concentrations below 2-3x10(5) cells mL(-1), ventilatory activity was highly stimulated whereas it was independent of algal densities for higher values (up to 10(6) cells mL(-1)). To investigate the influence of this first ventilatory drive on selenium contamination process, bivalves were exposed to waterborne selenium at two different algal concentrations, selected to provide contrasting reference ventilatory activities. Three different selenium forms were studied [selenite Se(+IV), selenate Se(+VI) and selenomethionine SeMet] and were added into the water at concentrations of 50 and/or 500 microg L(-1). Each selenium form induced a specific behavioural response, an increase, a decrease or no change of ventilation being observed for Se(+IV), SeMet and Se(+VI), respectively. Selenium accumulation by the organisms was investigated at the organ level for the different exposure conditions. Selenomethionine was the most bioaccumulated form, followed by selenate and selenite, respectively. Despite the bivalves displaying different ventilatory behaviours at low or high algal density, there was no evidence showing reduction or enhancement of Se uptake in the chemical domain investigated.

Analysis of Variance↗
PubMed2005

Selenium binding to human hemoglobin via selenotrisulfide.

Selenotrisulfide (e.g., glutathione selenotrisulfide (GSSeSG)) is an important intermediate in the metabolism of selenite. However, its reactivity with biological substances such as peptides and proteins in the subsequent metabolism is still far from clearly understood, because of its chemical instability under physiological conditions. Penicillamine (Pen) is capable of generating a chemically stable and isolatable selenotrisulfide, PenSSeSPen. To explore the metabolic fate of selenite in red blood cells (RBC), we investigated the reaction of selenotrisulfide with human hemoglobin (Hb) using PenSSeSPen as a model. PenSSeSPen rapidly reacted with Hb under physiological conditions. From the analysis of selenium binding using the Langmuir type binding equation, the apparent binding number of selenium per Hb tetramer almost corresponded to the number of reactive thiol groups of Hb. The thiol group blockade of Hb by iodoacetamide treatment completely inhibited the reaction of PenSSeSPen with Hb. In addition, MALDI-TOF mass spectrometric analysis of the selenium-bound Hb revealed that PenSSe moiety binds to the beta subunits of Hb. Overall, the reaction of PenSSeSPen with Hb appears to involve the thiol exchange between Pen and the cysteine residues on the beta subunit of Hb.

Glutathione↗
PubMed2005

Characterization of sediment bacteria involved in selenium reduction.

Bacterial reduction of selenium (Se) oxyanions (Se[VI] and Se[IV]) to elemental Se (Se[0]) is one of the major biogeochemical processes removing Se from agricultural drainage water and depositing Se in the sediment. This study was conducted to characterize Se-reducing bacterial populations in Lost Hills evaporation pond sediment and to observe their response to Se(VI) and organic C amendments. Se(VI) was removed from the dissolved phase in the sediment slurries amended with organic C with a decrease in redox potential (Eh). Se(VI) concentrations decreased from 2137 to 79 microg L-1 after 9 days of incubation in a 5% soil slurry. Upon our screening process, 9 Se(VI)- and 14 Se(IV)-reducing bacteria were isolated from sediment slurries and identified by amplification and sequencing of 16S rDNA. Bacillus strains appeared to be dominant in the bacterial assemblages active in Se(VI) and Se(IV) reduction in the sediment. Halomonas pacifica and Staphylococcus warneri were also identified as Se(IV)-reducers. Indigenous bacteria have a significant role in the biogeochemical cycling of Se and may be stimulated by addition of a suitable organic source for Se reduction. The bacterial strains isolated from salt-affected and Se-contaminated Lost Hills evaporation pond sediment may have potential application in removing Se from high salt drainage water.

Bacillaceae↗
PubMed2004

The effects of ebselen on [3H]glutamate uptake by synaptic vesicles from rat brain.

Ebselen is a selenium organic compound, which has been shown to be a neuroprotective agent in brain disorders involving glutamate receptors. However, the effects of ebselen on the functionality of the glutamatergic system are still poorly investigated. In this study, by using synaptic vesicle preparation, we investigated the effects of ebselen (0.3 to 10 microM) on (i) vesicular glutamate uptake, (ii) bafilomycin-sensitive H+ -ATPase activity, and (iii) proton gradient formation (DeltapH). Ebselen presented a dual effect on glutamate uptake: the 1 microM concentration resulted in a 60% increase of the uptake, while the 10 microM concentration resulted in 60% inhibition. We also observed that ebselen (10 microM) inhibited the H+ -ATPase activity and dissipated the DeltapH. The inhibitory effects of ebselen were prevented by dithiothreitol (DTT). These findings suggest that high concentrations of ebselen may oxidize the essential thiol groups of the H+ -ATPase, which in turn affect its activity and compromise the vesicular glutamate uptake, and consequently lead to an impairment of the neural homeostasis.

Animals↗
PubMed2004

The thio-Mitsunobu reaction: a useful tool for the preparation of 2,5-anhydro-2-thio- and 3,5-anhydro-3-thiopentofuranosides.

The unprotected methyl L-arabinofuranosides, D-ribofuranosides and D-xylofuranosides are transformed into the corresponding S-acetyl-5-thio derivatives by the thio-Mitsunobu reaction. Mesylation and subsequent reaction with sodium hydrogen carbonate led, depending on the configuration of the intermediate, to 2,5-anhydro-2-thio- or 3,5-anhydro-3-thiopentofuranosides. Due to inversion at C-3 or C-2 during the intramolecular nucleophilic displacement the products exhibit L-lyxo-, D-arabino- or D-lyxo-configuration. Analogously, the methyl 2,3-anhydro-D-ribofuranosides yielded 5-thio-S-acetates with intact 2,3-oxirane groups, which were cyclised with sodium hydrogen carbonate by epoxide ring opening and concomitant ring closure to form exclusively 3,5-anhydro-3-thio-D-xylofuranosides. A related 3,5-anhydro-3-seleno-D-lyxofuranoside was obtained by reaction of a 3,5-di-O-mesyl-D-arabinofuranoside with sodium hydrogen selenide. Several X-ray diffraction analyses proved the structures of the products.

Acetates↗
PubMed2005

Influence of organic selenium on hsp70 response of heat-stressed and enteropathogenic Escherichia coli-challenged broiler chickens (Gallus gallus).

The effect of dietary selenium yeast, a source of organic selenium, on heat shock protein 70 (hsp70) responses, redox status, growth and feed utilization were evaluated either in enteropathogenic Escherichia coli-challenged (EPEC) or in heat-stressed (HS) male broiler chickens grown to 42 days of age. One day-old chicks in experiment 1 were challenged orally with EPEC (10(6) cfu/chicken on day 1 and boosted by water application on days 2, 3, and 4) and fed diets with or without selenium yeast. Body weight (BW), feed conversion ratio (FCR), and total mortality were determined at 42 days of age, and this was followed by collection of ileal tissue for the quantification of total glutathione (TGSH), reduced glutathione (GSH), oxidized glutathione (GSSG), and hsp70 in randomly selected chickens from each treatment. In experiment 2, male broiler chickens were fed diets with or without selenium yeast under a thermoneutral rearing condition. At four weeks of age, blood and hepatic tissue were collected from chickens maintained in the thermoneutral environment and from chickens subjected to HS (40 degrees C for 1 h) and analyzed for TGSH, GSH, GSSG, and hsp70. Selenium yeast improved BW, FCR, and decreased mortality in both control and EPEC-challenged chicks. Selenium yeast significantly attenuated hsp70 expression in EPEC-challenged chickens and in those subjected to HS. The EPEC challenge increased TGSH and GSSG levels and decreased GSH/GSSG ratio. However, GSSG level accumulated in chickens fed diets without selenium supplementation resulting in a lower GSH/GSSG ratio in the selenium yeast-fed group. Heat stress increased GSSG level and decreased GSH/GSSG ratio. Selenium yeast-fed groups maintained higher levels of GSSG before and after HS with a resultant lower GSH/GSSG ratio. The hsp70 response was significantly less in those chickens fed selenium yeast and challenged with either EPEC or HS than in those chickens given no supplemental selenium. The results of this study suggest that selenium yeast supplementation had imparted resistance to oxidative stress associated with enteric bacteria infection and to high temperature exposure. It is believed that the resistance to the stressors was due to an improved redox status of the selenium yeast-fed chickens.

Animals↗
PubMed2005

Trace elements and butyltins in a Dall's porpoise (Phocoenoides dalli) from the Sanriku coast of Japan.

Concentrations and body burdens of 14 trace elements (Hg, Cr, Mn, Co, Cu, Zn, Sr, Ag, Cd, V, Se, Pb, Mo, and Fe) and butyltins (BTs) (tributyltin TBT, dibutyltin DBT, and monobutyltin MBT) were determined in various tissues of a mature male Dall's porpoise (Phocoenoides dalli) collected off the Sanriku coast of Japan. Selective accumulation in this porpoise was observed for Hg, Mn, Cu, Ag, Mo, Fe, and total BTs (TBT, DBT, and MBT) in the liver, Cd in the kidney, Zn, Sr, V, Pb, and Co in the bone, and Se in the skin. In contrast, Cr concentrations in all tissues were similar. This distribution pattern in this mature porpoise was in general agreement with the accumulation characteristics of trace elements and butyltins reported for other marine mammals. The whole body of the porpoise contained approximately 62 g Fe, 8.8 g Zn, 4.0 g Sr, 0.6g Se, 0.41 g Cu, 0.19 g Hg, 0.17 g Cd, 0.16 g Mn, 0.05 g Cr, 0.009 g Ag, 0.008 g Mo, 0.005 g Pb, 0.004 g Co, and 0.7 mg of BTs (0.4 mg TBT, 0.2 mg DBT, and 0.1 mg MBT). Metabolism of TBT to its breakdown products of this porpoise seems to be limited, since TBT still accounted for about half of the total burden of BTs. As in the cases of Hg, Mn, Cu, Se, and Fe, the muscle was the most important reservoir (43%) for the whole body burden of total BTs, 80% of which was TBT, and thus muscle played a crucial role in the higher body composition of TBT in this Dall's porpoise.

Animals↗
PubMed2004

Interpretation of alkyl diselenide and selenosulfenate mass spectra.

The mass spectral fragmentation of aliphatic diselenides and selenosulfenates is analyzed to gain a better understanding of the behavior of these species. The main fragmentation pathways of these species include the fragmentation along the Se?C bond, fragmentation along the Se?Se or Se?S bonds and intra-molecular rearrangements. In general, negative ionization favors the fragmentation along the Se?Se or Se?S bonds while positive ionization leads to stable molecular ions. Density functional theory calculations of bond dissociation energies and molecular orbital analysis was undertaken to explain the observed trends in molecular fragmentation. Besides the analysis of molecular fragmentation, a phenomenon of molecular association in negative electron impact and positive chemical ionization conditions was observed and investigated using a high resolution time-of-flight mass spectrometer. Molecular association that occurs during the ionization of species includes the formation of symmetrical diselenides from asymmetrical selenosulfenates and formation of alkylseleno adducts from the corresponding diselenides. For species which is hard to resolve by mass analysis, such as isobars of CHSe, CH(2)Se, and CH(3)Se, the isotope pattern superimposition procedure was applied to define the overlapping clusters.

Ions↗
PubMed2006

Mass spectrometric separation and quantitation of overlapping isotopologues. H2O/HOD/D2O and H2Se/HDSe/D2Se mixtures.

Three conceptually different mathematical methods are presented for accurate mass spectrometric determination of H2O/HOD/D2O and H2Se/HDSe/D2Se concentrations from mixtures. These are alternating least-squares, weighted two-band target entropy minimization, and a statistical mass balance model. The otherwise nonmeasurable mass spectra of partially deuterated isotopologues (HOD and HDSe) are mathematically constructed. Any recorded isotopologue mixture mass spectra are then deconvoluted by least-squares into their components. This approach is used to study the H2O/D2O exchange reaction, and is externally validated gravimetrically. The H2O/D2O exchange equilibrium constant is also measured from the deconvoluted 70 eV electron impact GC/MS data (K = 3.85 +/- 0.03).

Algorithms↗
PubMed2006

Adsorption mechanisms of selenium oxyanions at the aluminum oxide/water interface.

Sorption processes at the mineral/water interface typically control the mobility and bioaccessibility of many inorganic contaminants such as oxyanions. Selenium is an important micronutrient for human and animal health, but at elevated concentrations selenium toxicity is a concern. The objective of this study was to determine the bonding mechanisms of selenate (SeO4(2-) and selenite (SeO3(2-) on hydrous aluminum oxide (HAO) over a wide range of reaction pH using extended X-ray absorption fine structure (EXAFS) spectroscopy. Additionally, selenate adsorption on corundum (alpha-Al2O3) was studied to determine if adsorption mechanisms change as the aluminum oxide surface structure changes. The overall findings were that selenite forms a mixture of outer-sphere and inner-sphere bidentate-binuclear (corner-sharing) surface complexes on HAO, selenate forms primarily outer-sphere surface complexes on HAO, and on corundum selenate forms outer-sphere surface complexes at pH 3.5 but inner-sphere monodentate surface complexes at pH 4.5 and above. It is possible that the lack of inner-sphere complex formation at pH 3.5 is caused by changes in the corundum surface at low pH or secondary precipitate formation. The results are consistent with a structure-based reactivity for metal oxides, wherein hydrous metal oxides form outer-sphere complexes with sulfate and selenate, but inner-sphere monodentate surface complexes are formed between sulfate and selenate and alpha-Me2O3.

Adsorption↗
PubMed2005

Quaternized agricultural by-products as anion exchange resins.

The objectives of this study were the chemical modification of readily available, low-cost agricultural by-products to anion exchange resins and the selection of the best modified by-product for further use in anion removal. Resins were prepared through the quaternization of a series of 12 agricultural by-products with N-(3-chloro-2-hydroxypropyl) trimethylammonium chloride (CHMAC). Phosphate ion adsorption assays were conducted at pH 7 in order to compare adsorption properties among the by-products. Quaternized corn stover showed the highest phosphorus adsorption at 0.66 mmole/g. Since corn stover exhibited the best uptake of phosphate ion, it was compared to a commercially available, cellulose-based anion exchange resin. Additionally, adsorption capacities of quaternized corn stover for arsenate, chromate, and selenate were evaluated and adsorption efficiencies were determined in simulated wastewater samples. Our results indicate that modified corn stover demonstrates good adsorption uptake for arsenate and selenate and especially for chromate.

Adsorption↗
PubMed2004

Crystal structure, differential scanning calorimetry and vibrational low temperature investigation of C(NH2)3 x HSeO4.

The first X-ray and vibrational spectroscopic analysis of a new molecular complex between guanidinium and selenic acid is reported. The crystal of guanidinium hydrogenselenate at room temperature belongs to P2(1)/n space group of the monoclinic system with Z=4, a=8.330A, b=5.109A, c=14.855A and beta=92.65 degrees . Room temperature powder infrared and Raman spectra for the titled complex (1:1) were measured. The observed IR and Raman spectra are in accordance with this crystallographic structure. The differential scanning calorimetric (DSC) experiment on powder samples indicates on continuous phase transition at ca. 160K. To explain in detail the behavior of the crystal during the phase transition the infrared and Raman powder spectra in low temperature range (10-300K) were measured. The temperature dependencies of bands position and intensities for obtained spectra are analysed.

Calorimetry, Differential Scanning↗
PubMed2006

Structural and polarized vibrational studies of pentacaesium trihydrogentetraselenate monohydrate.

Polarized IR and Raman spectra of single crystal were measured at room and at low temperature. The polarized IR spectra were measured by transmission and specular reflection method. The IR-microscope was used for vibrational measurement of small monocrystals. Assignment of the bands is proposed on the basis of oriented gas model approximation. The polarized vibrational spectra are discussed in relation to the crystal structure and possible proton conductivity and phase transition.

Calorimetry, Differential Scanning↗
PubMed2006

Vibrational spectra of the trifluoromethylsulfinate anion and scaled quantum mechanical force fields for CF3SO2- and CF3SeO2-.

The infrared and Raman spectra of KCF(3)SO(2) were obtained and the observed spectral features assigned to the expected normal modes of vibration. Besides, the vibrational properties of the CF(3)SO(2)(-) and CF(3)SeO(2)(-) related anions were studied by means of density functional theory (DFT) techniques. After obtaining the optimized geometrical parameters and conformations, the vibrational wavenumbers and the associated force constants were calculated. The original force fields in cartesian coordinates were transformed to local symmetry coordinates and subsequently scaled to reproduce the experimental wavenumbers. Some trends observed in the force constants of the studied species and of the related CF(3)SO(3)(-) anion could be explained by the differences in geometrical parameters.

Anions↗
PubMed2006

Effect of PVA surrounding medium on ZnSe nanoparticles: size, optical, and electrical properties.

Polyvinyl alcohol (PVA) matrix was used to confine the particle size of ZnSe nanocrystallites as well as the variation of zinc (Zn) to selenium (Se) ion ratio which showed a remarkable decrease on the particle size as this ratio increased. The particle size decrease was monitored from the UV-vis absorption measurement as well as photoluminescence which suffered a blue shift with particle size decrease. The particle size was characterized with the aid of X-ray diffraction (XRD). The Raman spectra showed that, as the particle size increases, the peak position of the line centers (LO) mode were found to be red shifted from 239 to 234 cm(-1), accompanied by an increase in the full-width at half-maximum (FWHM). The electrical measurements and FT-IR spectra (overtone and normal) band vibration were used to study the effect of ZnSe NPs size on the PVA matrix.

Adsorption↗
PubMed2006

ESR and optical study of Mn2+ doped ammonium selenate single crystals.

ESR and optical absorption studies of manganese doped ammonium selenate single crystals are performed at X-band and room temperature to ascertain the site symmetry and location of impurity ions in the lattice. Manganese ions are expected to enter the lattice interstitially. Various spin Hamiltonian parameters are determined. Optical absorption study is also done and associated distortion in the crystal lattice is estimated.

Cations, Divalent↗
PubMed2005

Effect of arsenate and molybdate on removal of selenate from an aqueous solution by zero-valent iron.

Zero-valent iron (ZVI) is an inexpensive agent that can remove many common environmental contaminants. We investigated the effects of arsenate [As(V)] and molybdate [Mo(VI)] on the removal of selenate [Se(VI)] (1000 microg/L) in a 5 mM Cl- and SO4(2-) solution by ZVI. Analysis of selenium (Se) species in a control experiment revealed that there was no detectable selenite [Se(IV)] in the solution and Se(IV) was the only dominant form of Se in the PO(4)3- extract, revealing that the removal of Se(VI) by ZVI appeared to be partly attributed to the reduction of Se(VI) to Se(IV) by Fe(II) oxidized from ZVI, followed by rapid adsorption of Se(IV) to Fe oxyhydroxes (Fe(OH)). Addition of As(V) in a range of 5 to 25 mg/L in the solution did not affect Se(VI) removal. As(V) was removed at much faster rates than Se(VI). It took 16 h for ZVI to completely remove As(V) from the solutions, whereas it needed 31 h to remove 99% of the added Se(VI). Addition of Mo(VI) to the solution significantly affects the removal of Se. After 16 h, 99%, 98%, and 73% of the added Mo(VI) was removed from the solutions with 10, 50, and 200 mg/L Mo(VI) added, respectively. Whereas about 18%, 38%, and 78% of the added Se(VI) still remained in the solutions, respectively. This study suggests that a sequence for rapid element removal by ZVI is As(V)>Mo(VI)>Se(VI) and that ZVI can be used to effectively remove a high concentration level of As(V), Mo(VI), and Se(VI) from water.

Arsenates↗
PubMed2006

Supplementing Bacillus sp. RS1 with Dechloromonas sp. HZ for enhancing selenate reduction in agricultural drainage water.

Cost and efficiency are two important factors considered in the remediation of Se-contaminated agricultural drainage water through bacterial reduction of soluble Se(VI) to insoluble Se(0). Bacillus sp. RS1 isolated from rice straw was assessed for its ability to use inexpensive molasses to reduce Se(VI) in agricultural drainage water containing NO3- levels of 0, 50, 100, 250, and 500 mg/L. The results showed that Se(VI) (1000 microg/L) was almost entirely reduced to Se(IV) (62.7%) and Se(0) (36.4%) by Bacillus sp. RS1 in synthetic agricultural drainage (SAD) water without the presence of NO3-. The reduction Se(VI) to Se(0) was limited in the SAD water with NO3- levels of 100, 250, and 500 mg/L. The addition of Dechloromonas sp., a NO3- reducer, to the SAD water not only increased NO3- removal, but also enhanced Se(VI) reduction by Bacillus sp. RS1. During an 8-day experiment, 98-99% of the added Se(VI) was reduced to Se(0) with small amounts of Se(IV) and Se(-II) in the SAD water containing 100 and 250 mg/L NO3-. The addition of Dechloromonas sp. HZ to the natural agricultural drainage water also significantly increased the reduction of Se(VI) (748 microg/L) by Bacillus sp. RS1, with a production of Se(0) (65%) and Se(-II) (32%). These results suggest that a combination of Bacillus sp. RS1 with Dechloromonas sp. HZ has great potential with the use of inexpensive molasses to remediate Se-contaminated agricultural drainage water containing relatively high NO3- levels.

Agriculture↗