Regioselective intramolecular [3+2] annulation of allene-nitrones

The regioselective intramolecular 1,3-dipolar cycloaddition of the phenylsulfonylallene-nitrone derivatives has been developed. This reaction showed that the distal double bond of the allene exclusively reacted with the nitrone group to produce the bicyclic isoxazolidine derivatives regardless of the substitution pattern on the allenyl moiety.     

Quantitative SNP genotyping by affinity capillary electrophoresis using PEG-oligodeoxyribonucleotide block copolymers with electroosmotic flow

Quantitative SNP detection was demonstrated with an ACE using a PEG-oligodeoxyribonucleotide block copolymer (PEG-b-ODN) as a probe in the presence of an EOF. The probe's PEG segment with large molecular weight and small polydispersity yielded a high resolution in the separation of a chemically synthesized 60-base ssDNA (WT) and its single-base-substituted mutant (MT). A mixture of WT and MT was clearly separated within 10 min by simultaneously using two types of PEG-b-ODN probes whose ODN segments were complementary to WT and MT and whose PEG segments were of different lengths. The peak area ratio between WT and MT was in good agreement with the feed ratio. The averaged difference between the feed and observed ratio of MT was determined to be 0.23%, which is lower than that of any other methods. The ACE using the PEG-b-ODN probes in the presence of EOF could be utilized as a facile method for estimating SNP allele frequency in various research fields.     

Calorimetric study on the electronic structure in UP-US system

The heat capacity of UP_1?xS_x (x = 0.0, 0.1, 0.2, 0.4, 0.6, 0.8, 1.0) has been measured from 80 to 670 K by laser-flash calorimetry. All samples exhibit an anomaly corresponding to the magnetic transition. The magnetic transition temperatures determined are in good agreement with literature values. UP_0.4S_0.6 shows an additional small peak at 86 K below T_c. It has been derived that the US-rich ferromagnetically ordered state should be divided into two phases in terms of the direction of the moments. Above 250 K, the heat capacities of all samples increase monotonically with temperature and are well represented in the form of C_p= 6R + AT ? BT^?2. The conduction band structure has been derived from the high-temperature linear term and has been compared with that in literature. It has been suggested that the magnetically ordering behavior such as the direction of the moments would be closely correlated with the band structure.     

The Riemann problem for thermoelastic materials with phase change

We consider the Riemann problem for a system of conservation laws related to a phase transition problem. The system is nonisentropic and we treat the case where the latent heat is not zero. We study the cases where the initial data are given in the same phase and in the different phases. The role of the entropy condition is studied as well as the kinetic relation and the entropy rate admissibility criterion. We confine our attention to the case where the speeds of phase boundaries are close to zero. This is one interesting case in physics. We discuss the number of phase boundaries consistent with the above criteria and the uniqueness and nonuniqueness issue of the solution to the Riemann problem.     

In situ spatial-profile monitoring of beam flux of neutral free radicals produced by photo-deionization of negative ion beams

Ion-current difference measurement by light intensity modulation (ICD) is introduced as a convenient method to characterize a purified beam of momentum-controlled neutral free radicals produced by photo-deionization of a negative ion beam for the purpose of surface-reaction-selective device processing. The ICD setup developed in this study to estimate the number flux of the photo-deionized neutral particles exhibited the high precision, sensitivity, and spatial resolution.     

Two-Staged Temperature and Agitation Strategy for the Production of Transglutaminase from a Streptomyces sp. Isolated from Brazilian Soils

Transglutaminase catalyzes the cross-linking reaction between a glutamine residue and a free amine residue of proteins leading to the formation of protein aggregates. In this research, the effects of temperature, agitation, and aeration on the production of transglutaminase in a bench reactor by a newly isolated Streptomyces sp. from Brazilian soils were investigated using a factorial experimental design. The parameters evaluated influenced the enzyme production, and the data showed that the best conditions to enhance cell growth were different from those leading to enhanced transglutaminase production. Thus, a temperature and agitation shift strategy was adopted to increase transglutaminase productivity. The temperature and agitation were first set at 34 °C and 350 rpm, respectively, and after 24 h decreasing to 26 °C and 150 rpm until the end of fermentation. The transglutaminase activity obtained was 2.18 U/mL after 42 h of fermentation, which was twice than that obtained using a constant temperature and agitation fermentation strategy.     

Temporal variation of atmospheric polycyclic aromatic hydrocarbon concentrations in PM10 from the Kathmandu Valley and their gas-particle concentrations in winter

The concentrations of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM) with a diameter <10 µm (PM₁₀, 50% cut off) were investigated in the Kathmandu Valley, Nepal, during 2003. In order to understand the dynamics of atmospheric PAHs in winter, the PAH concentrations in total PM and in the gaseous phase were investigated in the valley in December 2005. Total of 45 PAH compounds (∑45PAHs) were analysed by high-resolution gas chromatography/high-resolution mass spectrometry (HRGC/HRMS). In 2003, the ∑45PAH concentrations in PM₁₀ ranged between 4.3 and 89 ng m^?3 (annual average; 27 ± 24 ng m^?3). The average concentrations of ∑45PAHs in December 2005 were 210 ± 33 ng m^?3 in total PM and 430 ± 90 ng m^?3 in the gaseous phase. The ∑45PAH concentration in PM accounted for more than 30% of the sum of their particulate and gaseous forms. Phenanthrene (Ph) was the most predominant compound in the gaseous phase, whereas four- to seven-ring PAHs were predominant in total PM. The highest values of ∑45PAHs occurred in the winter and spring. Estimates of emission sources based on diagnostic molecular ratios showed that atmospheric PAHs in the Kathmandu Valley mainly originated from the exhaust gas of diesel engine. In the winter and spring, PAH pollution would be accelerated by the operations of brick kilns and the frequent formation of an atmospherically stable layer in the valley.     

Lupin Protein Isolate Structure Diversity in Frozen-Cast Foams: Effects of Transglutaminases and Edible Fats

This study addresses an innovative approach to generate aerated foods with appealing texture through the utilization of lupin protein isolate (LPI) in combination with edible fats. We show the impact of transglutaminases (TGs; SB6 and commercial), glycerol (Gly), soy lecithin (Lec) and linoleic acid (LA) on the micro- and nanostructure of health promoting solid foods created from LPI and fats blends. 3-D tomographic images of LPI with TG revealed that SB6 contributed to an exceptional bubble spatial organization. The inclusion of Gly and Lec decreased protein polymerization and also induced the formation of a porous layered material. LA promoted protein polymerization and formation of homogeneous thick layers in the LPI matrix. Thus, the LPI is a promising protein resource which when in blend with additives is able to create diverse food structures. Much focus has been placed on the great foamability of LPI and here we show the resulting microstructure of LPI foams, and how these were improved with addition of TGs. New food applications for LPI can arise with the addition of food grade dispersant Lec and essential fatty-acid LA, by improved puffiness, and their contributing as replacer of chemical leavening additives in gluten-free products.     

Size-Selective Encapsulation Property of Unimolecular Reverse Micelle Consisting of Hyperbranched D-Glucan Core and L-Leucine Ethyl Ether Shell

The synthesis of a unimolecular reverse micelle ( 3 ) consisting of hyperbranched D -glucan as the core and L -leucine ethyl ester as the shell was accomplished through the carbamation reaction of the hyperbranched D -glucan ( 1 ) with the N-carbonyl L -leucine ethyl ester ( 2 ) in pyridine at 100 °C. The polymer 3 was soluble in a large variety of organic solvents, such as methanol, acetone, chloroform, and ethyl acetate, and insoluble in water, which remarkably differed from the solubility of 1 . The solubilities of 3 were also changed by the substitution degrees of the L -leucine moiety. The encapsulation ability of 3 toward water-soluble dyes has been investigated. These results indicated that 3 was a unimolecular reverse micelle with an encapsulation ability toward hydrophilic dye molecules. In addition, 3 showed an molecular size-selective encapsulation ability.     

Shrinkage dynamics of a vesicle in surfactant solutions

We develop a theory for shrinkage dynamics of a vesicle interacting with surfactant molecules. A stepwise shrinkage is formulated in such a way that it consists of two processes. One is a nucleation process of a pore under increasing of the membrane tension. The other is a closure process of the pore due to the line tension of the pore edge after leakage of the inner fluid. We carry out numerical simulations and show that the results agree with experiments semi-quantitatively. An analytical study is also carried out to understand the periodic shrinkage.