Frontiers in research on cystic fibrosis: understanding its molecular and chemical basis and relationship to the pathogenesis of the disease

In recent years a new family of transport proteins called ABC transporters has emerged. One member of this novel family, called CFTR (cystic fibrosis transmembrane conductance regulator), has received special attention because of its association with the disease cystic fibrosis (CF). This is an inherited disorder affecting about 1 in 2000 Caucasians by impairing epithelial ion transport, particularly that of chloride. Death may occur in severe cases because of chronic lung infections, especially by Pseudomonas aeruginosa, which cause a slow decline in pulmonary function. The prospects of ameliorating the symptoms of CF and even curing the disease were greatly heightened in 1989 following the cloning of the CFTR gene and the discovery that the mutation (deltaF508), which causes most cases of CF, is localized within a putative ATP binding/ATP hydrolysis domain. The purpose of this introductory review in this minireview series is to summarize what we and others have learned during the past eight years about the structure and function of the first nucleotide binding domain (NBF1 or NBD1) of the CFTR protein and the effect thereon of disease-causing mutations. The relationship of these new findings to the pathogenesis of CF is also discussed.     

ACAT inhibitors derived from hetero-Diels-Alder cycloadducts of thioaldehydes

Acyl-CoA:cholesterol acyltransferase (ACAT) is the enzyme largely responsible for intracellular cholesterol esterification. A systemic inhibitor of ACAT is believed to be able to slow or even reverse the atherosclerotic process. Towards that goal, a series of cyclic sulfides, derived from the hetero-Diels-Alder reaction of thioaldehydes with 1,3-dienes, and bearing carboxamide substituents, were prepared and evaluated for in vitro (in several tissues and species) and ex vivo ACAT inhibition. Minor changes in subsequent structure were found to have a significant effect in optimization of the biological activity of this series of compounds.     

Condensation polymerization of pyrogallol and benzaldehyde

Novolac-type polycondensation of benzaldehyde (B) and pyrogallol (P) has been carried out at 60°C, 75°C and 90°C and at B/P mole ratios of 1.5 and 3.0 using phosphoric acid as catalyst. The reaction follows a 2nd order rate law. By using GC consumption data of benzaldehyde and pyrogallol, kinetic parameters such as the overall rate constants, activation energies (E_a) and logA values are investigated. The activation energies for 1.5 and 3.0 B/P mole ratios are found as 62.3 kJ mol^?1 and 56.4 kJ mol^?1, respectively. The molecular weights of the resins determined by measuring intrinsic viscosities (25°C, THF) are in the range of 0.03 to 0.07 dL g^?1 at various temperatures and B/P mole ratios.     

Applying real options in investment decisions relating to environmental pollution

This study focuses on how to assess the optimal environmental investment decisions under economic and ecological uncertainty, and establishes the continuous time model using the real option approach to optimize environmental pollution policy. Unlike traditional cost benefit analysis, this work extends the model of [Pindyck, R.S., 2002. Optimal timing problems in environmental economics. Journal of Economic Dynamics and Control 26(9–10), 1677–1697], and attempts to identify the storage threshold of pollution stocks and the optimal timing for implementing environmental pollution decisions.     

以不同PAN系炭纤维布制备燃料电池气体扩散层之研究

采用石墨化PAN系炭纤维布制备了高分子电解质燃料电池气体扩散层。通过电学实验、X-ray绕射与元素分析考察了所制气体扩散层的性能。结果表明：随热处理温度的升高，气体扩散层的电阻率降低，L2增加，d（x）2减小。高温处理后的炭纤维布作为高分子电解质燃料电池气体扩散层显示了较高的电池效能。     

Residual fracture energy of high-performance and normal concrete subject to high temperatures

Test data on the residual fracture energy of two significantly different concrete types are presented. About 80 beams of high performance basalt concrete and ordinary gravel concrete have been tested in accordance with the RILEM work of fracture method. The beams are heated at 1°C per minute up to a certain maximum temperature and kept at this temperature for 8 hours before cooling them back to room temperature and testing in three-point bending. The tests show that the two concretes behave almost identifical when the fracture energyG _F is considered as a function of maximum temperature. It is found that the damage introduced by a maximum temperature of 300 to 400°C increases the fracture energy by 50% compared with the reference tests at room temperature. A more tortuous crack surface is one plausible explanation for the significant increase inG _F. The article also presents temperature and weight loss recordings from the heating scenarios and finally, the characteristic length and the cohesive tensile softening curve are shown to depend on the maximum temperature. Basically it is demonstrated that the temperature exposure makes the concrete significantly more ductile.

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Résumé Des données sur l'énergie résiduelle de rupture de deux bétons différents sont présentées. Environ 80 poutres de béton à base de basalte de très haute performance et de béton à base de gravier ordinaire ont été examinées conformément au travaux de la RILEM sur l'énergie de rupture. Les poutres sont chauffées à 1°C par minute jusqu'à une température maximale, puis maintenues à cette température pendant 8 heures avant d'être refroidies de nouveau à la température ambiante. Les poutres sont ensuite testées en flexion (système de flexion en trois points). Les essais prouvent que les deux bétons se comportent d'une manière presque identique quandG _F est considéré comme une fonction de la température maximale. On peut aussi constater que le dommage occasionné par une température maximale de 300 à 400°C augmente l'énergie de rupture de 50% par comparaison aux essais de référence réalisés à la température ambiante. Une surface de rupture plus tortueuse semble être une explication plausible pour l'augmentation significative deG _F. L'article présente également les évolutions de la température et de la perte de poids pour les scénarios de chauffage utilisés. En conclusion, cette étude montre que la longueur caractéristique et la courbe de post pic dépendent de la température maximale. Fondamentalement cela démontre que l'exposition à la température rend le béton sensiblement plus ductile.

     

Changes in polymer foils used in food packaging tested by using differential scanning calorimetry

This work is an experimental study of the differential scanning calorimetry characterisation of polymer materials used in food packaging materials, such as polypropylene (0.03 mm), polyethylene (0.1 and 0.03 mm), poly(D-(-)-Β-hydroxybutyrate) (powder), two-layered polypropylene (0.064 mm), and two-layered polypropylene with poly-vinylidene-chloride (0.012/0.021). The polymer stability was checked by simulation of conditions during food preparation in microwave ovens, sterilisation or rapid freezing. The materials were tested in the temperature range from 40 to 200‡C at different scan rates from 2 to 30°C min⁻¹ during heating or cooling. The enthalpies show a high correlation coefficient (0.964) with scan rate. All samples undergo phase change in the temperature range from 107 to 173°C during heating and enthalpies are in the range from 31.8 to 71.1Jg⁻¹. Upon subsequent cooling from 200°C, the temperature range of phase changes is shifted to lower temperatures from 86 to 102°C with enthalpies ranging from 30.4 to 57.8 J g⁻¹. Experiments with exposure of polymers to microwave radiation and freezing prove that the phase change considering the temperature range is very similar in all experiments.     

Polarity control of GaN epilayers grown on ZnO templates

We report the successful growth of Ga-polar GaN epilayers on O-polar ZnO templates pre-deposited on c-sapphire. Prior to GaN growth, NH₃ is exposed onto the ZnO template. The polarity of the GaN layers is confirmed by etching of the surface and by conversion beam electron diffraction (CBED), while the O-polar ZnO is confirmed by CBED. It is suggested that the NH₃ pre-exposure helps form a Zn₃N₂ layer, which possesses inversion symmetry and inverts the crystal from anion polar to cation polar.