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Detection of alkali metal ions in DNA crystals using state-of-the-art X-ray diffraction experiments.

The observation of light metal ions in nucleic acids crystals is generally a fortuitous event. Sodium ions in particular are notoriously difficult to detect because their X-ray scattering contributions are virtually identical to those of water and Na(+.)O distances are only slightly shorter than strong hydrogen bonds between well-ordered water molecules. We demonstrate here that replacement of Na(+) by K(+), Rb(+) or Cs(+) and precise measurements of anomalous differences in intensities provide a particularly sensitive method for detecting alkali metal ion-binding sites in nucleic acid crystals. Not only can alkali metal ions be readily located in such structures, but the presence of Rb(+) or Cs(+) also allows structure determination by the single wavelength anomalous diffraction technique. Besides allowing identification of high occupancy binding sites, the combination of high resolution and anomalous diffraction data established here can also pinpoint binding sites that feature only partial occupancy. Conversely, high resolution of the data alone does not necessarily allow differentiation between water and partially ordered metal ions, as demonstrated with the crystal structure of a DNA duplex determined to a resolution of 0.6 A.

Barium↗

Effects of selected water toxicants on the in vitro activity of fish carbonic anhydrase.

Carbonic anhydrase (CA, carbonate hydro-lyase EC 4.2.1.1) from lysed red blood cells of the channel catfish (Ictalurus punctatus) was studied to determine physico-chemical kinetic properties and relative sensitivity to 56 chemicals of significance in water quality research. In general, enzyme activity was strongly reduced by heavy metal inorganic cations; less strongly by organometallic cations, some anions, and certain pesticides; and weakly inhibited by light metal cations and organometallic and organic compounds. Dose--response curves were qualitatively similar in most cases.

Animals↗

[Spectral control of metal admixtures in tetracycline].

Analysis of circular dichroism spectra made it possible to offer a method for estimation of tetracycline solutions contamination with metal ions. By its sensitivity the method is much superior to the spectrophotometric one used at present for determination of the antibiotic purity. In the latter method formation of complexes with metals is traced by batochromic displacement of the absorption spectra. The new method is rapid, relatively selective and requires comparatively small quantities of the substance for the analysis, which provides its use under both laboratory and manufacture conditions. The method is based on identification of the circular dichroism spectra of tetracycline complexes with metals in the long wavelength region. The presence of the circular dichroism concervative bands with strictly defined extremums in the spectra of tetracycline low acid solutions contaminated by multiply charged metal ions allowed vs. the circular dichroism spectra of pure tetracycline sample to conclude that the solution contained admixtures and to suggest their nature. It was shown that the charge, ion radius and tetracycline:metal relation were the factors defining the mark and location of the dichroism band extremums. At lambda(extr)-410-415 nm the tetracycline complexes with light metal ions such as Mg2+, Al3+ and Ca2+ were detected by the circular dichroism negative band in the spectra, while the complexes with heavy metal ions such as Sc3+, Sr3+, Cu3+, Cd3+, Ba2+, Y3+ and the cerium subgroup lanthanides were detected by the circular dichroism positive band. The tetracycline complexes with the lanthanides of the second half of the yttrium subgroup (Ho(3+)-Lu3+) were characterized by the presence of the circular dichroism minimum at lambda(min)-425 nm. When the tetracycline concentration was above 1.5 x 10(-3) M, multiligand complexes with circular dichroism negative extremum at lambda(min)-400 nm formed.

Circular Dichroism↗

[The evaluation of wear resistance of hybrid denture teeth].

Wear characteristics of hybrid denture teeth, plastic denture teeth which were partially reinforced with metal, was evaluated. The plane specimens were made up with resin and metal. Light curing veneering resin, new metacolor, heat curing veneering resin, Mitel-OM and PMMA (Poly methyl methacrylate) were used for resin parts, while gallium containing filling alloy, silver alloy, palladium alloy and titanium containing chromium cobalt alloy were used for metal parts. The specimens were abraded by the rod specimens of palladium alloy with abrasion test machine. The wear depth and width were measured at 1, 5, 10 and 20 x 10(4) times of abrasion which stroke was 10 mm each. The specimens of heat cured veneering resin reinforced with chromium cobalt alloy showed the least wear loss while the specimens of PMMA reinforced with silver alloy did the most. The difference of wear ratio between light cured and heat cured veneering resin was not statistically significant.

Dental Alloys↗

Modelling of proton and metal exchange in the alginate biopolymer.

Acid-base behaviour of a commercial sodium alginate extracted from brown seaweed (Macrocystis pyrifera) has been investigated at different ionic strengths (0.1<or=I/mol l(-1)<or=1.0) and in different supporting electrolytes (Et4NI, NaCl, KCl, LiCl, NaCl+MgCl2), with the aim of examining the influence of ionic medium on the proton-binding capacity and of quantifying the strength of interaction with light metal ions in the perspective of speciation studies in natural aqueous systems. Potentiometric ([H+]-glass electrode) and titration calorimetric data were expressed as a function of the dissociation degree (alpha) using different models (Henderson-Hasselbalch modified, Högfeldt three parameters and linear equations). The dependence on ionic strength of the protonation constants was taken into account by a modified specific interaction theory model. Differences among different media were explained in terms of the interaction between polyanion and metal cations of the supporting electrolytes. Quantitative information on the proton-binding capacity, together with the stabilities of different species formed, is reported. Protonation thermodynamic parameters, at alpha=0.5, are log K H=3.686+/-0.005, DeltaG 0=-21.04+/-0.03 kJ mol(-1), DeltaH 0=4.8+/-0.2 kJ mol(-1) and TDeltaS 0=35.7+/-0.3 kJ mol(-1), at infinite dilution. Protonation enthalpies indicate that the main contribution to proton binding arises from the entropy term. A strict correlation between DeltaG and TDeltaS was found, TDeltaS=-9.5-1.73 DeltaG. Results are reported in light of building up a chemical complexation model of general validity to explain the binding ability of naturally occurring polycarboxylate polymers and biopolymers. Speciation profiles of alginate in the presence of sodium and magnesium ions, naturally occurring cations in natural waters, are also reported.

Alginates↗

Migration of metal and polyethylene particles from articular prostheses may generate lymphadenopathy with histiocytosis.

Wear particles released from hip or knee prostheses are known to be involved in the fibrohistiocytic membrane interposed between bone and implant. During surgical treatment for pelvic carcinoma (5 cases) and for isolated pseudomalignant lymphadenopathy (4 cases) lymph nodes in 9 patients who had had lower limb articular replacement were harvested. Light microscopy and image analysis of the nodes showed florid endosinusal histiocytosis, predominant in the cortical area. Using Oil Red O staining and polarized light, metal particles and polyethylene particles were detected in the large histiocytes. Scanning electron microscopy with electron backscattering allowed us to localize metal particles and perform elemental microanalysis. Iron, cobalt, chromium, nickel, zirconium, and barium, known to be used in prosthetic and cementing materials, were identified as component of these particles. Large amounts of polyethylene particles appeared in all cases while metal particles were found to be abundant in only 2 cases. Thus, migration of polyethylene debris from the prosthetic site seems to be the major factor in development of the histiocytes induced in satellite lymph nodes.

Aged↗

Aluminum corrolin, a novel chlorophyll analogue.

A corrole-based chlorophyll analogue has been prepared, based on the notation that the major differences between the prosthetic groups of chlorophylls and hemes are the presence of a non-transition metal (Mg vs. Fe) and one reduced double bond in the porphyrin ligand. As corroles act as tri- rather than dianionic ligands, the analogy requires the insertion of aluminum into the macrocycle and the reduction of one of its double bonds, two reactions that have not been previously reported with any corrole. The aluminum complexes of both the corrole and the corrolin (the dihydrocorrole) display fluorescence quantum yield that are much larger than of chlorophyll and of all other previously reported synthetic analogues. The results suggest that the light metal atom ion is responsible for low intersystem crossing probability to the triplet excited state and the structural rigidity of the hexa-coordinated complexes for reducing the probability of internal conversion.

Aluminum↗

Detection of inorganic species by chemical reaction laser desorption ionization mass spectrometry.

The oxidation numbers of metals in inorganic compounds were identified by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) by using their acetylacetonates, which are soluble in acetone. For the MALDI analysis of inorganic species insoluble in common solvents used for matrices, such as acetone, methanol, water, etc., a suspension method of sample preparation was developed. Turbid suspensions of inorganic species in the solvent were spotted on the sample holder with chelating reagents, as in the conventional sample preparation for MALDI-MS. Chemical reaction between the inorganic species and the chelating reagents occurred in the plume after irradiation by laser light. Metal oxides were also analyzed by this method, and samples with different oxidation numbers gave different mass spectra. These results suggest that many other metal oxides with different oxidation numbers could be identified if suitable chelating reagents are chosen for sample preparation for MALDI-MS.

Journal Article↗

Effects of iron-, manganese-, or magnesium-deficiency on the growth and morphology of Euglena gracilis.

Iron-, manganese-, or magnesium-deficiency has been induced in Euglena gracilis. Each arrests cell proliferation, decreases the intracellular content of the deficient metal, and increases that of several other metals. Light and electron microscopy of stationary phase cells reveal that Fe-deficient (-Fe) cells are similar in size and shape to control organisms. Magnesium-deficient (-Mg) cells, however, are larger, and approximately 14% are multilobed, containing 2 to 12 lobes of equal size emanating from a central region. Individual (-Mg) cells and each lobe of multilobed cells contain a single nucleus. Manganese-deficient (-Mn) organisms are morphologically more heterogeneous than (-Fe) or (-Mg) cells. Most are spherical and larger than controls. Approximately 15% are multilobed but, unlike (-Mg) cells, contain lobes of unequal size with either zero, one, or several nuclei present in each. Nuclei of (-Mn) cells differ in size and shape from those of control, (-Fe), or (-Mg) cells. All three deficient cell types accumulate large quantities of paramylon. Other cytoplasmic structures, however, appear normal. Addition of Fe, Mn, or Mg to the respective deficient stationary phase cultures reverses growth arrest and restores normal morphology. The results suggest that Fe-, Mn-, and Mg-deficiencies affect different stages of the E. gracilis cell cycle.

Cell Nucleus↗

A single nocturnal exposure to 2-7 millitesla static magnetic fields does not inhibit the excretion of 6-sulfatoxymelatonin in healthy young men.

The present study sought to evaluate possible acute effects on 6-sulfatoxymelatonin (aMT6s) excretion, a surrogate for melatonin levels in blood, in volunteers exposed to static magnetic fields with flux densities representative for workers in light metal reduction plants and operators of medical MRI in hospitals. Eleven healthy male volunteers (23-43 years) participated. Urine samples were collected for two consecutive 24 h periods from 22:00 hours day 1 (exposure day) through day 2 (day after exposure) and then for 24 h from 07:00 hours on day 7 (control day). On the day of exposure the subjects slept in the MRI room from 22:00 hours until 07:00 hours next morning, thus receiving a 9 h exposure to the magnetic field (2-7 mT). On the day after exposure and on the control day, they slept at home and otherwise performed their ordinary daily activities. Total daily urine production was collected in four parts: 22:00-07:00 hours, 07:00-11:00 hours, 11:00-18:00 hours, 18:00-22:00 hours, and the volume for each interval was measured and recorded. Samples were transferred to coded bottles and frozen for later RIA analysis of aMT6s. Pairs of values of mean hourly aMT6s excretion, both diurnal and for the four daily intervals, were compared using two-sided Wilcoxon signed ranks test. The day of exposure and the day after exposure were not significantly different from the control day, either for the total diurnal secretion or the interval data. In summary, the study shows no association between a single nocturnal exposure to a static magnetic field of strength 2-7 mT and excretion of aMT6s in urine.

Adult↗

Transmission line probes for scanning photon-tunneling microscopy.

Because metalized light probes for scanning photon-tunneling microscopy are tapered waveguides beyond cut-off, tapered coaxial transmission lines have been tried instead. It is shown here that insertion losses in such a line can be reduced by asymmetrically phase-apodizing the illuminating lens. Alternatively, a strip rather than a coaxial line can be used.

Electric Conductivity↗

Characterization of Pb2+ biosorption from aqueous solution by Rhodotorula glutinis.

The yeast Rhodotorula glutinis was examined for its ability to remove Pb(2+) from aqueous solution. Within 10 min of contact, Pb(2+) sorption reached nearly 80% of the total Pb(2+) sorption. The optimum initial pH value for removal of Pb(2+ )was 4.5-5.0. The percentage sorption increased steeply with the biomass concentration up to 2 g/l and thereafter remained more or less constant. Temperature in the range 15-45 degrees C did not show any significant difference in Pb(2+ )sorption by R. glutinis. The light metal ions such as Na(+), K(+), Ca(2+), and Mg(2+) did not significantly interfere with the binding. The Langmuir sorption model provided a good fit throughout the concentration range. The maximum Pb(2+ )sorption capacity q(max) and Langmuir constant b were 73.5 mg/g of biomass and 0.02 l/mg, respectively. The mechanism of Pb(2+) removal by R. glutinis involved biosorption by direct biosorptive interaction with the biomass through ion exchange and precipitation by phosphate released from the biomass.

Journal Article↗

A novel enzyme-linked immunosorbent assay (ELISA) for the detection of beryllium antibodies.

A novel immunological method has been developed for detecting antibodies (IgG molecules) specific to beryllium, a light metal used in industry and capable of causing chronic beryllium disease. Beryllium metal was vacuum deposited onto commercially available immunological microsticks, which were then exposed to test plasma containing the putative antibodies. Antigen-antibody complexes were located using a biotin-avidin amplification method. One employee diagnosed with chronic beryllium disease and one diagnosed as "sensitized" (lymphocyte transformation positive) exhibited antibody titers graphically and statistically different and higher than a pooled baseline control population. Plasma from these two employees (former beryllium workers) was used in four different approaches to validate the presence of beryllium antibodies. The assay proved to be reproducible.

Antibodies↗

A novel technique for the evaluation of mechanical pain and hyperalgesia.

We describe a new technique which is useful for the evaluation of mechanically induced pain and hyperalgesia. Light metal cylinders are guided and accelerated in a barrel. On impact against the skin they elicit a brief sensation of pain. This method allows the application of a wide range of controllable innocuous and noxious impact velocities of the cylinder at variable stimulus repetition rates. The system is sufficiently flexible to stimulate perpendicularly any skin area and to move rapidly to adjacent target regions if desired. Psychophysical testing using magnitude estimation techniques revealed that pain thresholds were normally distributed. Over a wide range of stimulation intensities monotonically increasing stimulus response functions were obtained. Repeated testing showed a good intra-individual reproducibility of both threshold and supramaximal pain ratings. The method was also useful in determining the time course of pain and mechanical hyperalgesia following a brief painful stimulus. We conclude that the new technique is useful for evaluating psychophysical stimulus response functions of mechanically induced pain and its changes following tissue injury. This technique may also hold some promise in quantifying altered pain sensitivity in patients.

Adult↗

Effect of pH on nickel biosorption by aerobic granular sludge.

The Ni2+ biosorption by aerobic granular sludge was studied at various initial pH values of 2-7. Results showed that the initial pH would play an important role in the Ni2+ removal by aerobic granules and affected the zeta potential of aerobic granules. A thermodynamic equilibrium isotherm previously developed can fit the experimental data very well at all studied pH values. The close relationship between the zeta potential and Ni2+ biosorption capacity of aerobic granules showed the electrostatic attraction between the aerobic granules and Ni2+ ions. It was also found that some light metals, such as K+, Mg2+ and Ca2+ would be released into the bulk solution during the Ni2+ uptake onto the aerobic granules, which in turn indicated that ion-exchange was one of the Ni2+ biosorption mechanisms.

Adsorption↗

Crab shell-based biosorption technology for the treatment of nickel-bearing electroplating industrial effluents.

This paper discusses the possible application of a biosorption system with acid-washed crab shells in a packed bed up-flow column for the removal of nickel from electroplating industrial effluents. Between two nickel-bearing effluents, effluent-1 is characterized by considerable amount of light metals along with trace amounts of lead and copper. Effluent-2 is characterized by relatively low conductivity, total dissolved solids and total hardness compared to effluent-1. Crab shells exhibited uptakes of 15.08 and 20.04 mg Ni/g from effluent-1 and effluent-2, respectively. The crab shell bed was regenerated using 0.01 M EDTA (pH 9.8, aq. NH3) and reused for seven sorption-desorption cycles. The EDTA elution provided elution efficiencies up to 99% in all the seven cycles. This, together with the data from regeneration efficiencies for seven cycles, provided evidence that the reusability of crab shell in the treatment of nickel-bearing electroplating industrial effluents is viable.

Adsorption↗

A selective role for potassium in the phytotoxicity of thallium.

The presence of K-ion prevents inhibition of Plantago maritima seed germination and Asperigillus flavus mycelial growth by Tl-ion. The effect of potassium could not be replaced by Na-ion in either system. Aspergillus was cultured in a medium low in light metal ions (Na+ and K+), and its growth was enhanced quantitatively by addition of Kminus but not Na-ions. Growth without added potassium was inhibited severely by Tl-ions, whereas K-enhanced growth was not. It is suggested that the thallium-potassium interaction is specific involving competition between ions of quite similar charge and radius.

Aspergillus↗