Glutathione-S-transferase polymorphism, metallothionein expression, and mercury levels among students in Austria

BACKGROUND: Detoxification is an essential process in all living organisms. Humans accumulate heavy metals primarily as a result of lifestyle and environmental contamination. However, not all humans experience the estimated individual exposure. This suggests the presence of genetic regulatory mechanisms. OBJECTIVE: In order to identify genetic factors underlying the inter-individual variance in detoxification capacity for the heavy metal mercury, 192 students were investigated. We focused on the relationship between polymorphisms in glutathione-S-transferase (GST) genes and mercury concentrations in blood, urine, and hair. The correlation between blood mercury levels, GSTT1 and GSTM1 polymorphism, and gene expression of certain metallothionein subgroups (MT1, MT3) was evaluated in a further group of students (N=30). METHODS: Mercury levels in acid digested samples were measured by cold vapor AAS. Genotyping of the GSTT1 and GSTM1-gene deletion polymorphism was performed by means of PCR. Gene expression of several MT genes was analyzed in lymphocytes from fresh peripheral blood by semiquantitative RT-PCR. RESULTS: The following was noted: a) hair mercury concentrations are significantly increased in persons with the double deleted genotype (GSTT1-/- and GSTM1-/-) as compared to persons with the intact genotype, and b) MT1X expression is higher in persons with the intact genotype (GSTT1+/+ and GSTM1+/+). CONCLUSIONS: We conclude that the epistatic effect of the GSTT1 and the GSTM1 deletion polymorphism is a risk factor for increased susceptibility to mercury exposure. The relationship between MT gene expression and GST gene polymorphisms needs further investigation. If MT expression depends on GST polymorphisms it would have important implications on the overall metal detoxification capability of the human organism.     

Evaluation of UV irradiation for photolytic and oxidative degradation of pharmaceutical compounds in water

A medium-pressure (MP) ultraviolet (UV) system was used to investigate the UV photolysis and UV/H(2)O(2) oxidation of pharmaceutically active compounds (PhACs) that belong to different therapeutic classes and were found to occur in the aquatic environment. The results obtained in laboratory-grade water (LGW) and surface water (SW) were compared with low-pressure (LP) results reported previously. Overall, MP lamps proved to be more efficient to maximize the bench-scale degradation of the selected group of compounds (ketoprofen, naproxen, carbamazepine, ciprofloxacin, clofibric acid, and iohexol) by both UV photolysis and UV/H(2)O(2) oxidation. Fundamental direct and indirect photolysis parameters obtained in LGW are reported and used to model the MP-UV photolysis and MP-UV/H(2)O(2) oxidation of the pharmaceuticals in SW, predicting the experimental results very well.     

Comparative studies of pyruvate kinase from PSE and normal pig muscles

A fast breakdown of glycogen is observed in muscles of stress-susceptible pigs leading to pale, soft and exudative (PSE) meat. We report a comparative study of pyruvate kinase from muscles of normal and PSE-prone pigs. Compared with the enzyme from normal muscle, pyruvate kinase isolated from PSE muscle shows a five times lower Michaelis constant,K _m, for phosphoenol pyruvate and a more than ten times higherk _cat/K _m value. The pH dependency of the enzymatic activity is shifted to more acidic values for pyruvate kinase from PSE muscles. According to isoelectric focusing, pyruvate kinase from PSE muscle consists of three isoforms, while only two isoforms are detectable in pyruvate kinase preparations from normal pigs. The various isoforms were isolated by preparative isoelectric focusing and their steady-state properties were compared. Isoform 3, which is found only in PSE muscle, shows a 10-fold higher specific activity, a 30-fold lowerK _m value and a 100-fold increasedk _cat/K _m value for phosphoenol pyruvate as compared to isoform 1. The presence of isoform 3 in PSE muscle appears to be responsible for the high activity of this enzyme under the more acidic conditions prevailing in PSE muscle. In vitro phosphorylation and dephosphorylation experiments using total enzyme and purified isoenzyme 1 suggest that isoforms 2 and 3 arise from isoform 1 by phosphorylation. Thus protein phosphorylation seems to be responsible for the shift in activity of pyruvate kinase, a key enzyme of glycolysis, under the acidic conditions of PSE muscles.     

New potato fibre for improvement of texture and colour of wheat bread

The aim of this project was to compare the functional properties of five fibre fractions by baking of wheat bread by substitution 0, 4, 8 and 12 w/w% of wheat flour using dry potato pulp (Fibre 1), a commercial potato fibre (Fibre 2), two fibre prepared from potato pulp by enzymatic hydrolysis (Fibre 3 and 4), and one solubilised fibre (Fibre 5). The effect of chemical composition of fibre on texture, colour, specific weight and volume of wheat bread was studied using objective methods for measurement of texture characteristics, colour (L, a, b) and sensory analysis. Dry potato pulp, Potex (Fibre 2) and two enzymatically prepared fibre powders (Fibre 3 and 4) with a high concentration of lignin and insoluble non-starch polysaccharides (INCP) had a detrimental effect on bread quality by substitution of more than 8% of the wheat flour by fibre. The detrimental effect was mainly due to increased hardness, deformation energy, modulus and gumminess. Multiple linear regression analysis with forward selection was used for determination of the relationship between quality characteristics and of soluble non-starch polysaccharides (SNSP), insoluble non-starch polysaccharides (INCP), cellulose and lignin. The enzymatic solubilised fibre (Fibre 5) with a high concentration of soluble fibre and a low concentration of cellulose and lignin could be used for substitution of at least 12% wheat flour for baking of bread with an attractive colour, delicious texture and flavour.     

Magnetocaloric effect of Pr2Fe17−x Mn x alloys

Polycrystalline Pr2Fe17-xMnx（x = 0, 1, and 2）alloys were studied by X-ray diffraction（XRD）, heat capacity, ac susceptibility, and isothermal magnetization measurements. All the alloys adopt the rhombohedral Th2Zn17-type structure. The Curie temperature increases from 283 K at x = 0 to 294 K at x = 1, and then decreases to 285 K at x = 2. The magnetic phase transition at the Curie temperature is a typical second-order paramagnetic–ferromagnetic transition. For an applied field change from0 to 5 T, the maximum-△SM for Pr2Fe17-xMnxalloys with x = 0, 1, and 2 are 5.66, 5.07, and 4.31 J·kg^-1·K^-1,respectively. The refrigerant capacity（RC） values range from 458 to 364 J·kg^-1, which is about 70 %–89 % that of Gd. The large, near room temperature △SM and RC values,chemical stability, and a high performance-to-cost ratio make Pr2Fe17-xMnxalloys be selectable materials for room temperature magnetic refrigeration applications.     

Sintered silicon nitride/nano-silicon carbide materials based on preceramic polymers and ceramic powder

A flexible method is presented, which enables the fabrication of porous as well as dense Si₃N₄/nano-SiC components by using Si₃N₄ powder and a preceramic polymer (polycarbosilazane) as alternative ceramic forming binder. The SiCN polymer benefits consolidation as well as shaping of the green body and partially fills the interstices between the Si₃N₄ particles. Cross-linking of the precursor at 300 °C increases the mechanical stability of the green bodies and facilitates near net shape machining. At first, pyrolysis leads to porous ceramic bodies. Finally, subsequent gas pressure sintering results in dense Si₃N₄/nano-SiC ceramics. Due to the high ceramic yield of the polycarbosilazane binder, the shrinkage during sintering is significantly reduced from 20 to 15 lin.%. Investigations of the sintered ceramics reveal, that the microstructure of the Si₃N₄ ceramic contains approx. 6 vol.% nano-scaled SiC segregations, which are located both at the grain boundaries and as inclusions in the Si₃N₄ grains.     

Supply chain coordination and setup cost reduction in case of asymmetric information

Previous research shows that asymmetric information triggers a decrease of lot sizes compared to the supply chain optimum. Thus, the setup costs per period are suboptimally high. To analyse, whether setup cost reduction can mitigate this effect, we extend the standard framework of lotsizing decisions under asymmetric information by allowing investments in setup cost reduction. We find that asymmetric information tends to lead to an overinvestment in setup cost reduction. The overall effect of setup cost reduction on supply chain performance is therefore ambiguous. We show that these results hold for a wide variety of investment functions.     

Kinetics and dynamics of thermally-induced shape-memory behavior of crosslinked short-chain branched polyethylenes

Systematic investigation of the relation between shape-memory (SM) behavior and characteristics of the covalent network and the crystalline domains of a crosslinked polymer, i.e., crosslink density and crystallinity, respectively, was performed using homogeneous ethylene-1-octenecopolymers (EOC) as model polymers. The EOCs have been crosslinked by 2,5-dimethyl-2,5-di(t-butylperoxy)hexane (DHBP) decomposition. Two EOCs with a degree of branching of 30 and 60 hexyl side chains per 1000C atoms with each four different crosslink densities were employed. The investigated EOCs differ significantly in crystallinity, melting temperature (T_m) and crosslink density. The crosslinked EOC undergone the programming at a strain of 100% showed high strain fixity ratio (R_f) and strain recovery ratio (R_r). The R_f and R_r values increase with increasing crystallinity and crosslink density, respectively, and decline only slightly in a subsequent SM cycle. The switching temperature (T_sw) is strictly related to T_m and decreases with increasing degree of branching as well as crosslink density in the temperature range of 101–63 °C. T_sw remains nearly unchanged when the programming temperature (T_pr) or the load during SM recovery is varied. The kinetics of SM recovery as characterized by the temperature dependence of recovery rate is controlled by the melting behavior. The specific work generated by the programmed specimen during thermally-induced recovery under constant load, gains with increasing crosslink density, and is proposed as dynamical characteristic of practical relevance. The opportunity of tailoring T_sw by variation of the degree of branching and crosslink density makes such polymers attractive candidates for applications requiring T_sw temperatures in the range from 60 to 100 °C.