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Aerobic chromate reduction by chromium-resistant bacteria isolated from serpentine soil.

A group of 34 chromium-resistant bacteria were isolated from naturally occurring chromium percolated serpentine soil of Andaman (India). These isolates displayed different degrees of chromate reduction under aerobic conditions. One of the 34 isolates identified as Bacillus sphaericus was tolerant to 800 mgl(-1) Cr(VI) and reduced > 80% Cr(VI) during growth. In Vogel Bonner broth, B. sphaericus cells (10(10) cells ml(-1)) reduced 62% of 20mg l(-1) of Cr(VI) in 48h with concomitant discoloring of yellow medium to white one. Reduction of chromate was pronounced by the addition of glucose and yeast extract as electron donors. In the presence of 4.0 g l(-1) of glucose, 20mg l(-1) of Cr(VI) was reduced to 2.45mg l(-1) after 96h of incubation. Optimum pH and temperature for reduction were 6.0 and 25 degrees C, respectively. Increase in cell density and initial Cr(VI) concentration increased chromate reduction but was inhibited by metal ions like, Ni2+, Co2+, Cd2+ and Pb2+. Experiments with cell-free extracts indicated that the soluble fraction of the cell was responsible for aerobic reduction of Cr(VI) by this organism.

Aerobiosis↗

Chromium is the proximate clastogenic species for lead chromate-induced clastogenicity in human bronchial cells.

Hexavalent chromium (Cr(VI)) is a well-established human lung carcinogen with potentially widespread exposure. Solubility is a key factor in the carcinogenicity of Cr(VI), with the water-insoluble or 'particulate' compounds being the more potent carcinogens. Studies have indicated that the component ions are responsible for their clastogenicity, but it is uncertain whether chromium (Cr), lead (Pb) or some combination of the two is responsible for the clastogenic effects. Accordingly, we compared the clastogenicity of lead chromate (LC) with soluble sodium chromate (SC) and lead glutamate (LG) in WTHBF-6 human lung cells. We found that 1436microM was the maximal intracellular level of Pb after exposure to clastogenic concentrations of LC. However, clastogenesis was not observed after exposure to LG, even when intracellular Pb concentrations reached 13,347microM, indicating that intracellular Pb levels did not reach clastogenic levels in WTHBF-6 cells after LC treatment. By contrast, SC was clastogenic damaging 16 and 44% of metaphase cells at intracellular Cr doses of 312 and 1262microM respectively, which was comparable to the clastogenesis observed after LC treatment. LC damaged 10, 27 and 37% of metaphases at intracellular Cr doses of 288, 926 and 1644microM, respectively. These data indicate that with respect to LC-induced clastogenicity, Cr and not Pb is the proximate clastogenic species in human lung cells.

Bronchi↗

Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells.

Particulate hexavalent chromium (Cr(VI)) is a well-established human lung carcinogen. It is currently a major public health concern, there is widespread exposure to it in occupational settings and to the general public. However, despite the potential widespread exposure and the fact that the lung is its target organ, few studies have considered the toxic effects of particulate Cr(VI) in human lung cells. Accordingly, we used lead chromate as a model particulate Cr(VI) compound and determined its cytotoxicity and genotoxicity in cultured human bronchial epithelial cells, using BEP2D cells as a model cell line. We found that lead chromate induced concentration-dependent cytotoxicity in BEP2D cells after a 24h exposure. Specifically, the relative survival was 78, 59, 53, 46 and 0% after exposure to 0.5, 1, 5, 10 and 50 microg/cm(2) lead chromate, respectively. Similarly, the amount of chromosome damage increased with concentration after 24h exposure to lead chromate. Specifically, 0.5, 1, 5 and 10 microg/cm(2) damaged 10, 13, 20 and 28% of metaphase cells with the total amount of damage reaching 11, 15, 24 and 36 aberrations per 100 metaphases, respectively. Lead chromate (50 microg/cm(2) lead chromate) induced profound cell cycle delay and no metaphases were found. In addition we investigated the effects of soluble hexavalent chromium, sodium chromate, in this cell line. We found that 1, 2.5, 5 and 10 microM sodium chromate induced 66, 35, 0 and 0% relative survival, respectively. The amount of chromosome damage increased with concentration after 24h exposure to sodium chromate. Specifically, 1, 2.5 and 5 microM damaged 25, 34 and 41% of metaphase cells with the total amount of damage reaching 33, 59 and 70 aberrations per 100 metaphases, respectively. Ten micromolar sodium chromate induced profound cell cycle delay and no metaphases were found. Overall the data clearly indicate that hexavalent Cr(VI) is cytotoxic and genotoxic to human lung epithelial cells.

Carcinogens, Environmental↗

Functional characteristics of NaS2, a placenta-specific Na+-coupled transporter for sulfate and oxyanions of the micronutrients selenium and chromium.

NaS2 is a Na+-coupled transporter for sulfate that belongs to the SLC13 gene family. This transporter was originally cloned from high endothelial venule endothelial cells, but nothing is known about the functional characteristics of this transporter except that it transports sulfate in a Na+-coupled manner. Northern blot analysis indicates that NaS2 is expressed most robustly in placenta. In the present study, we cloned NaS2 from rat placenta and characterized its transport function in detail using the Xenopus laevis oocyte expression system. Rat NaS2 consists of 629 amino acids and is highly similar to human NaS2. In situ hybridization studies with mouse placental sections show that NaS2 transcripts are expressed primarily in trophoblasts of the labyrinth zone. The expression of the transporter is confirmed in primary cultures of trophoblasts isolated from human placenta. When expressed in X. laevis oocytes, rat NaS2 mediates Na+-coupled transport of sulfate. The transport of sulfate is inhibited by oxyanions of selenium, chromium, arsenic, molybdenum, and phosphorous, suggesting that the transporter may mediate the transport of these oxyanions in addition to sulfate. The Kt for sulfate is 153+/-30 microM and the Na+:sulfate stoichiometry is 3:1. The transport process is electrogenic as evidenced from the inhibition of the uptake process by K+-induced depolarization. We conclude that NaS2 is a placenta-specific Na+-coupled, electrogenic, transporter for sulfate expressed in trophoblasts and that it is also responsible for the transport of oxyanions of the micronutrients selenium and chromium.

Amino Acid Sequence↗

New route to the synthesis of bis[N-(2-aminoethyl) salicylaldiminato] chromium(III) chloride monohydrate Spectroscopic characterization, crystal structure and interaction with DNA.

The reaction of [Cr(urea)(6)]Cl(3).3H(2)O with H(2)salen (H(2)salen=N,N(')-ethylenebis(salicylaldimine) in water-methanol mixture (40:60v/v) under reflux yielded the complex bis[N-(2-aminoethyl)salicylaldiminato]chromium(III) chloride monohydrate, [Cr(aesaldmn)(2)]Cl.H(2)O. The complex was characterized by elemental analysis, molar conductance, magnetic susceptibility, spectroscopic (UV-vis and IR) data and X-ray diffraction studies. The new ligand, N-(2-aminoethyl)salicylaldimine, Haesaldmn, possibly resulted from the hydrolytic cleavage of one end of the H(2)salen ligand during reflux. Binding of this chromium(III) complex to CT DNA has been studied using UV-vis spectroscopy with an apparent binding constant of 2.68 x 10(3)M(-1). It shows that the binding mode is electrostatic while the emission of ethidium bromide to CT DNA in the absence and in the presence of the complex show that it binds DNA with partial intercalation.

Chromium Compounds↗

Synthesis and spectroscopic studies on chromium(III) complex containing mixed-valence chrysenesemiquinone-chrysenecatecholate ligands and 2,2'-bipyridine coligand.

The synthesis and spectroscopic properties of Cr(bpy)(chrySQ)(chryCat), a complex containing chromium(III) metal ion and chrysenequinone ligand in its partially reduced (chrySQ) and fully reduced (chryCat) forms, are described. The complex has been prepared by two different routes from Cr(CO)6 and Cr(chrySQ)3. Variable temperature magnetic susceptibility measurements indicated a strong antiferromagnetic coupling between Cr(III) (S=3/2) and chrysenesemiquinone radical (S=1/2), giving a magnetic coupling constant J=-342 cm(-1). Ligand-based redox couples were observed in the electrochemical studies that consist of quasi-reversible chrySQ/chryCat and bpy/bpy*- reductions and chryCat/chrySQ oxidation at negative potentials and irreversible chrySQ/chryBQ oxidation at positive potential. However, the metal was inert in the studied potential range. The electronic spectra of the complex revealed interesting properties. In addition to interaligand pi-pi* and n-pi* transitions, other bands corresponding to Cr(t(2g))-->chrySQ(pi*) and Cr(t(2g))-->bpy(pi*) metal-to-ligand charge-transfer MLCT transitions were observed. The infrared spectral analysis was informative in assigning the vibrations due to SQ and Cat ligands. Also, it was a useful tool in confirming the coordination of bpy ligand to chromium metal ion.

2,2'-Dipyridyl↗

Leaching of copper, chromium and arsenic from treated vineyard posts in Marlborough, New Zealand.

There have been conflicting reports as to the extent that copper-chromium-arsenic (CCA) treatments leach from timber. In New Zealand, vineyards utilise CCA-treated posts at a rate of 579 posts per hectare. This represents a potential CCA burden on the soil of 12, 21, and 17 kg/ha, respectively, for the three elements. Given a replacement rate of 4% per year, the use of CCA-treated posts may result in an accumulation of these elements in the soil, possibly leading to groundwater contamination. We undertook a general survey to determine the extent of CCA leaching from treated vineyard posts. Treated Pinus radiata posts were sampled at six sites around the Marlborough region of New Zealand to represent a range of post ages and soil types. For each post, above- and belowground wood samples were taken. As well, the soil adjacent to the post was sampled at a 50 mm horizontal and 100 mm vertical distances from the post. The belowground wood samples of the posts had significantly lower CCA concentrations than the aboveground portions, which were not significantly different from new posts. This indicates leaching. Soils surrounding the posts had significantly higher CCA concentrations than control soils. Higher CCA concentrations were measured under the posts than laterally. Some 25% of the samples exceeded 100 mg/kg As, the Australian National Environment Protection Council (ANEPC) guideline level for As in agricultural soil, and 10% exceeded 100 mg/kg Cr, the ANEPC limit for chromium. At one site, we found a significant positive correlation between post age and CCA-leaching. The CCA issue could be eliminated by using alternative posts, such as steel, concrete, or untreated woods such as Eucalyptus or beech. Alternatively, CCA-treated posts could, for example, be lacquered or otherwise protected, to reduce the rate of CCA leaching.

Agriculture↗

Activation of MAP kinases by hexavalent chromium, manganese and nickel in human lung epithelial cells.

Epidemiological studies indicate that workers who perform welding operations are at increased risk for bronchitis, siderosis, occupational asthma and lung cancer due to fume exposure. Welding fumes are a complex chemical mixture, and the metal composition is hypothesized to be an etiological factor in respiratory disease due to this exposure. In the present study, human lung epithelial cells in vitro responded to hexavalent chromium, manganese and nickel over a concentration range of 0.2-200 microM with a significant increase in intracellular phosphoprotein (a measure of stress response pathway activation). The mitogen-activated protein kinases ERK1/2, SAPK/JNK and p38 were activated via phosphorylation following 1-h exposures. Hexavalent chromium up-regulated p-38 phosphorylation 23-fold and SAPK/JNK phosphorylation 17-fold, with a comparatively modest 4-fold increase in ERK1/2 phosphorylation. Manganese caused a two- to four-fold increase in SAPK/JNK and ERK 1/2 phosphorylation, with no observed effects on p38 kinase. Nickel caused increased (two-fold) phosphorylation of ERK 1/2 only, and was not cytotoxic over the tested concentration range. The observed effects of welding fume metals on cellular signaling in lung epithelium demonstrate a potentially significant interplay between stress-response signaling (p38 and SAPK/JNK) and anti-apototic signaling (ERK 1/2) that is dependant on the specific metal or combination of metals involved.

Air Pollutants, Occupational↗

Determination of total chromium in environmental water samples.

It is often desirable to quantify both dissolved Cr(VI) and total Cr in samples accurately. Various protocols are now being utilized to quantify the amount of total chromium in natural waters and each of these has possible interferences. This study describes the shortcomings of each method when particulate iron is present in a water sample, and a more rigorous digestion protocol is tested. Data from bench studies as well as a field survey of 21 water utilities are presented. Additionally, field data from several hundred water utility samples are presented to illustrate the potential for incomplete recovery of total chromium using accepted protocols.

Carcinogens, Environmental↗

Sorptive removal of trivalent and hexavalent chromium from binary aqueous solutions by composite alginate-goethite beads.

In this study, the removal of hexavalent and trivalent chromium ions from binary aqueous solutions by composite alginate-goethite beads was investigated in a batch mode. Equilibrium sorption experiments were carried out at different temperatures and pH values. The data were correlated with Langmuir and Freundlich equations. The thermodynamic parameters calculated were: change in free energy, in enthalpy, in entropy and the heat of adsorption. The influence of mixing rate, sorbent concentration and sorbent particle size was studied at kinetic runs. The effective diffusion coefficients were evaluated by employing the homogeneous diffusion model and the shrinking core model for hexavalent and trivalent chromium, respectively. Desorption experiments were conducted by employing various eluants showed that the loaded material could be regenerated satisfactorily.

Absorption↗

Speciation of chromium dyes by high-performance liquid chromatography with inductively coupled plasma mass spectrometric detection.

High-performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP-MS) was employed for the separation and detection of chromium species in azo dyes, Acid blue 158 and Acid Blue 193; mainly Cr(III) and Cr(VI). The dyes were first analyzed for total metal content using ICP-MS and their stability in solution was studied by measuring their absorbance through a range of pH values. Then an isocratic chromatographic method employing reversed-phase liquid chromatography with mass spectrometric detection was developed. Applying this method to the separation of these dyes, the absolute detection limits of Acid Blue 158 and 193 were 1 and 5 ng respectively. Additionally, Acid Blue 158 did not contain any chromium species. On the other hand, Acid Blue 193 contained uncomplexed and potentially bioavailable Cr(III). Acid Blue 193 did not have any toxic Cr(VI) present in the samples.

Anions↗

On-line preconcentration and determination of chromium(VI) in waters by high-performance liquid chromatography using precolumn complexation with 1,5-diphenylcarbazide.

A method for on-line chromatographic preconcentration and determination of chromium(VI) traces has been developed. Chromate was preconcentrated on a C18 column (50 x 6 mm I.D.) after complexation with diphenylcarbazide (DPC). Following the preconcentration step, analysis of the sample was performed using a C18 column (100 x 6 mm I.D.) with an eluent containing 6.10(-3) mol/l sulphuric acid and 20% (v/v) acetonitrile. Direct spectrophotometric detection at 546 nm was used. Experimental parameters such as mobile phase pH, DPC concentration, preconcentration flow-rate, sample volume were optimized for preconcentration and detection of Cr(VI)-DPC complex. Under the optimum conditions, most metal ions [Cr(III), Fe(III), Cu(II), Hg(II), Mo(VI), V(V)] and inorganic anions did not interfere. A detection limit of 0.02 ng/ml Cr(VI) can be attained when a sample volume of 100 ml is used. The technique has been applied successfully to the determination of Cr(VI) traces in drinking, surface and groundwater samples and the recoveries of added chromium were in the range 94-104%.

Cations↗

Bonding of a cobalt-chromium alloy with acidic primers and tri-n-butylborane-initiated luting agents.

Limited information is available about chemical bonding of cobalt-chromium alloys for resin-retained fixed partial dentures. This study evaluated the effect of acidic primers on the bonding of luting agents joined to a cobalt-chromium alloy. Disk alloy specimens were bonded with eight combinations of five primers and two luting agents. Shear bond strengths were determined before and after thermocycling. The effect of priming on bond strength varied among the combinations of primer and luting agent. In particular, after thermocycling three groups demonstrated greater bond strengths than the other groups did. These were (1) specimens treated with a phosphate-methacrylate primer (Cesead Opaque Primer), (2) specimens bonded with an adhesive resin (Super-Bond Opaque), or (3) a combination of both.

Acrylic Resins↗

Effect of beryllium on the castability and resistance of ceramometal bonds in nickel-chromium alloys.

STATEMENT OF PROBLEM: Castability and ceramometal bond resistance play an important role in accepting nickel-chromium alloys as a substitute for gold alloys in dentistry. PURPOSE: This study was developed to verify the effect of beryllium on these factors in several compositions of nickel-based alloys by submitting them to castability and ceramometal bonding resistance tests. MATERIAL AND METHODS: Three experimental compositions of Ni-Cr alloys with different amounts of beryllium were used. One beryllium-free alloy was used as the control. RESULTS: Analysis of variance and Tukey's test showed significant differences (alpha = .001) for the castability test results and significant differences (alpha = .05) for ceramometal bond resistance between alloys. CONCLUSIONS: Although the amounts of chromium, manganese, and niobium were maintained, the variations in the amounts of beryllium allowed the estimation that Be-containing alloys presented better castability than Be-free alloys. The 0.9% Be-containing alloy demonstrated higher resistance of the ceramometal bond than the Be-free alloy.

Analysis of Variance↗

Laser welding of a cobalt-chromium removable partial denture alloy.

STATEMENT OF PROBLEM: The electric alloy brazed joints of removable partial denture alloys have failed frequently after routine usage. PURPOSE: A technique providing higher joint strengths was investigated. This investigation compared the tensile strengths of electric-brazed and laser-welded joints for a cobalt-chromium removable partial denture alloy. MATERIAL AND METHODS: Twenty-four cobalt-chromium standard tensile testing rods were prepared and divided into three groups of eight. All specimens in the control group (group 1) were left in the as-cast condition. Groups 2 and 3 were the test specimens, which were sectioned at the center of the rod. Eight specimens were joined by using electric brazing, and the remaining specimens were joined by using laser welding. After joining, each joint was ground to a uniform diameter, then tested to tensile failure on an Instron universal testing machine. Failure loads were recorded and fracture stress calculated. Statistical analysis was applied. RESULTS: The student-Newman-Keuls test showed a highly significant difference between the joint strengths of the as-cast control specimens, the electric-brazed and laser-welded joints. CONCLUSIONS: The tensile strengths of the as-cast joints were higher than those for the laser-welded joints, and both were higher than the electric-brazed joint strengths.

Analysis of Variance↗

[Metal serum levels in 48 patients bearing a chromium-cobalt total hip arthroplasty with a metal-on-polyethylene combination].

PURPOSE OF THE STUDY: Component wear and dissemination of wear debris, particularly with metal-on-metal combinations, is the predominant long-term complication of total hip arthroplasty. The purpose of our work was to search for metal pArticles released when using the metal-on-polyethylene combination by analyzing serum levels of chromium (Cr), cobalt (Co), nickel (Ni), and molybdium (Mo) in patients with a metal-on-polyethylene chromium-cobalt total hip arthroplasty. We compared the observed levels with those observed in a control population and studied changes as a function of signs of loosening. MATERIAL AND METHODS: During a thirty-Month period, 53 patients with degenerative hip disease underwent total hip arthroplasty. The same implant, PVL, being used for all hips. Forty-eight patients were available for analysis at a minimum follow-up of 32 Months. Results of the clinical and radiological examination of the operated hip were recorded. Serum metal levels were assayed by mass spectrometry on total blood samples. Patient activity was determined with the Devane classification and hip function with the Postel-Merle-d'Aubligné score; walking distance was recorded in kilometers. Signs of prosthetic loosening were identified on plain radiograms (AP and lateral views) searching for femoral and/or acetabular lucent lines, cement fracture, granuloma. The control group included 56 patients scheduled for total hip arthroplasty. Non-parametric statistical analysis was used to search for correlations between the clinical, radiological, and biological parameters. RESULTS: At mean 44 Months follow-up, 17% of the patients had a fair or mediocre function score and 37% had radiological signs of femoral component loosening. Serum cobalt increased significantly in the implanted group (serum cobalt >or=0.60 microg/L in 50% of patients) compared with the control group (serum cobalt >or=0.60 microg/L in 9%) (P<0.001, Mann-Whittney test). Increased serum cobalt was highest in patients with radiographic signs of loosening. This significant difference was not found for other metals. Patient activity, hip function, and follow-up were not correlated with serum levels. DISCUSSION: Serum cobalt appears to be a good biological marker of prosthetic function although intra- and inter-individual variations are influenced by assay technique, metal ion solubility, and metal dissemination in the organism. The metal-on-metal combination does not appear to be the only friction couple which increases the serum level of metal ions. Our results do not allow defining a time of latency between onset of radiographic signs and increased serum levels.

Aged↗

Process development for the removal of lead and chromium from aqueous solutions using red mud--an aluminium industry waste.

Red mud, an aluminium industry waste, has been converted into an inexpensive and efficient adsorbent and used for the removal of lead and chromium from aqueous solutions. Effect of various factors on the removal of these metal ions from water (e.g. pH, adsorbent dose, adsorbate concentration, temperature, particle size, etc.) has been studied and discussed. The effect of presence of other metal ions/surfactants on the removal of Pb2+ and Cr6+ has also been studied. The material exhibits good adsorption capacity and the data follow both Freundlich and Langmuir models. Thermodynamic parameters indicate the feasibility of the process. Kinetic studies have been performed to understand the mechanism of adsorption. Dynamic modelling of lead and chromium removal on red mud has been undertaken and found to follow first-order kinetics. The rate constant and mass transfer coefficient have also been evaluated under optimum conditions of removal in order to understand the mechanism. Column studies have been carried out to compare these with batch capacities. The recovery of Pb2+ and Cr6+ and chemical regeneration of the spent column have also been tried.

Aluminum↗

Removal of chromium from aqueous solutions by diatomite treated with microemulsion.

In order to evaluate the sorption of heavy metals, a crude diatomite was impregnated with a microemulsion which showed remarkable increase in chromium sorption capacity as compared to untreated diatomite. Samples with two different granulometries were investigated, both yielding practically complete adsorption. The adsorption process is pH dependent and the best results for the initial Cr (III) concentration of 1.5 g/L were obtained at pH 2.95. The effect of the concentration of the chromium synthetic solution was also investigated. The adsorption isotherms were obtained (30. 40 and 50 degrees C) and the Freundlich and Langmuir models were used to determine the adsorption capacity of the adsorbent. Following the adsorption step, a desorption process was carried out using several eluant solutions. The best results were obtained using hydrochloric acid (100%) as eluant.

Adsorption↗