Interaction of L-glutamic acid with human T-lymphocytes

A specific interaction of [3H]Glu with T lymphocytes from the blood of healthy donors (Kd = 0.236 microM) was revealed and described. It was found that unlabeled quisqualate, a structural analogue of L-glutamic acid, and unlabeled dipeptides Ala-Glu, Glu-Ala, and Glu-Glu competitively inhibit the specific binding of [3H]Glu to T lymphocytes (with Ki 0.19, 2.4, 3.4, and 1.2 microM, respectively). Binding experiments with conjugates of labeled and unlabeled glutamic acid with dextran showed that the receptors of [3H]Glu are localized on the outer surface of the plasma membrane of T lymphocytes.     

Carbon nanofibres and activated carbon nanofibres as electrodes in supercapacitors

Carbon nanofibres have been prepared by a floating catalyst procedure at industrial scale in a metallic furnace. The nanofibres (50-500 nm diameter and 5-200 μm length) are grown from the Fe particles used as catalyst. Soot appears together with the carbon nanofibres. The sample has been chemically activated using KOH as activating agent. Scanning electron microscopy has shown a smooth surface for the as-prepared carbon nanofibres but a rough surface for the activated ones. The specific surface area increases from 13 to 212 m²/g due to the activation. The volume of the micropores (in the 1-2 nm range) and the mesopores (2-5 nm range), as deduced by density functional theory methods, also increases after the activation. Electrochemical behaviour of the as-prepared and activated carbon nanofibres has been tested in a supercapacitor at laboratory scale using 6 M KOH aqueous solution as electrolyte. The specific capacitance, which is less than 1 F/g for the as-prepared sample, increase up to ≈60 F/g for the activated sample. Only a slight decrease in capacitance has been observed as the current density increases. Specific power of ≈100 W/kg at specific energy of 1 Wh/kg has been found in some particular cases. We have compared the electrochemical parameters of our activated carbon nanofibres with those of activated carbon nanofibres coming from a commercial sample; the latter was activated by the same way as our sample.     

Trace elements in soils and plants in temperate forest plantations subjected to single and multiple applications of mixed wood ash

Wood ash, a by-product generated in power plants, can be used to fertilize forest plantations to replenish nutrients lost during harvesting. Although wood ash generally contains low levels of trace metals, release of some of these may occur soon after ash application in acid soils. The risk of heavy metal contamination associated with application of mixed wood ash was assessed in six Pinus radiata D. Don plantations, on two types of mineral soil differing in texture, drainage and CECe. Four of the stands received a single application of 4500 kg ha(-1) (March 2003), and in the other two stands the same treatment was applied over three consecutive years (2003-2005). Trace metal (Cd, Cr, Cu, Mn, Ni, Pb, Zn) concentrations were monitored throughout the 3 years in different components of the forest ecosystem--soil solid fraction, soil solution, tree needles, ground vegetation and different mushroom species. Repeated applications of wood ash led to moderate increases in soil extractable Mn and Zn, and Mn in all mushrooms species. However, the maximum concentrations did not reach levels potentially harmful to organisms. Concentrations of Zn, Cu and Cd decreased in some mushroom species, probably because of increased soil pH caused by the treatment. Heavy metal concentrations in tree needles and ground vegetation were not altered. Although the risk of heavy metal contamination appears to be low, the long-term effects of wood ash application must be assessed.     

Carbon nanofibers enhance the fracture toughness and fatigue performance of a structural epoxy system

This study investigates the monotonic and dynamic fracture characteristics of a discontinuous fiber reinforced polymer matrix. Specifically, small amounts (0-1 wt.%) of a helical-ribbon carbon nanofiber (CNF) were added to an amine cured epoxy system. The resulting nanocomposites were tested to failure in two modes of testing; Mode I fracture toughness and constant amplitude of stress tension-tension fatigue. Fracture toughness testing revealed that adding 0.5 and 1.0 wt.% CNFs to the epoxy matrix enhanced the resistance to fracture by 66% and 78%, respectively. Fatigue testing at 20 MPa peak stress showed a median increase in fatigue life of 180% and 365% over the control by the addition of 0.5 and 1.0 wt.% CNF, respectively. These results clearly demonstrate the addition of small weight fractions of CNFs to significantly enhance the monotonic fracture behavior and long-term fatigue performance of this polymer. A discussion is presented linking the two behaviors indicating their interdependence and reliance upon the stress intensity factor, K.     

Characterisation of gold kiwifruit pectin isolated by enzymatic treatment

Pectin was extracted from gold kiwifruit by four commercial enzyme preparations (Celluclast 1.5 L, Cytolase CL, Cellulyve TR 400 and NS33048). The chosen enzymes were used either in single or in combination, with and without protease addition. The recovered pectin was characterised and compared for the yield, total nonstarch polysaccharide and neutral sugar composition, protein and ash, pectin, molecular weight distribution and the viscosity. Results indicated that enzyme‐extracted gold kiwifruit pectin was rich in galacturonic acid. Purified pectin yield, and their physicochemical composition and rheological property (viscosity), was significantly affected by the type of enzyme used. The pectin extracted by Celluclast 1.5 L demonstrated to be the most viscous and recorded the highest in molecular weight (M_w) (1.65 × 10⁶ g mol^–1) compared with the other extracts. The extract M_w and their distribution were discussed and related to their viscosity behaviour.     

Sequence analysis of small cryptic plasmids isolated from Selenomonas ruminantium S20

The degradation kinetics of five glutamine dipeptides in aqueous solution, i.e. glycyl-L-glutamine (Gly-Gln), L-alanyl-L-glutamine (Ala-Gln), L-valyl-L-glutamine (Val-Gln), L-leucyl-L-glutamine (Leu-Gln) and L-isoleucyl-L-glutamine (Ile-Gln), were studied. Stability tests were performed using a stability-indicating high-performance liquid chromatographic assay. Two different Ala-Gln degradation routes, i.e. the cleavage of a peptide bond and the deamination of an amide group, were observed. The degradation was adequately described by pseudo-first-order kinetics. The maximum stability of Ala-Gln was obtained at an approximate pH of 6.0. The pH-rate profile described by specific acid-base catalysis and hydrolysis by water molecules agreed with the experimental results. The activation energy of Ala-Gln at pH 6.0 was determined to be 27. 1kcal mol-1, and the shelf-life (90% remaining) at 25 and 40 degrees C was predicted to be 5.3 years and 7.1 months, respectively. The rate constants of the glutamine dipeptides were influenced by the N-terminal amino acid residue and decreased in the order: Gly-Gln, Ala-Gln, Leu-Gln, Val-Gln and Ile-Gln.     

Comparison of methods to enumerate bacteria in dental unit water lines

Millipore HPC samplers are simple, self-contained test devices that can be used by personnel in dental offices who do not have microbiologic training to easily and economically monitor dental unit water quality without laboratory support. This study evaluated the correlation of HPC samplers to R2A agar for enumerating planktonic bacteria in dental unit treatment water. Eight different dental units were sampled. Five replicates were performed for each media at each dilution. The Pearson correlation coefficient between the R2A agar and HPC sampler is 0.89. These data suggest HPC samplers correlate with conventional laboratory-based R2A culture techniques for determining dental unit water line contamination.     

Optical absorption and selective thermal emission in directionally solidified Al2O3-Er3Al5O12 and Al2O3-Er3Al5O12-ZrO2 eutectics

Al₂O₃-Er₃Al₅O₁₂ and Al₂O₃-Er₃Al₅O₁₂-ZrO₂ eutectic ceramic rods were directionally solidified using the laser floating zone technique at several growth rates. Binary eutectic microstructure consisted in a three-dimensional interpenetrated network of the eutectic phases whereas the ternary eutectic showed a geometrical microstructure at low growth rates and a nanofibrillar pattern at high rates. The microstructure size was strongly dependent on the growth rate, decreasing when the processing rate increased. The optical absorption was measured in the samples at room temperature and Judd–Ofelt analysis was used to model the optical absorption of the Er³⁺ ions. Thermal emission of the eutectic rods was studied at temperatures up to 1600 °C. An intense narrow emission band at 1.55 μm matching with the sensitive region of the GaSb photoconverter was obtained. The intensity of the selective emission band is larger for the binary eutectic than for the ternary compound and increases as the microstructural size decreases.