Response of Predatory Insect Scolothrips takahashii Toward Herbivore-Induced Plant Volatiles Under Laboratory and Field Conditions

We studied the response of a predatory thrips, Scolothrips takahashii, towards herbivore-induced plant volatiles emitted by Lima bean plants infested by two-spotted spider mites Tetranychus urticae (green form). Tests were conducted with a Y-tube olfactometer in the laboratory and with traps under field conditions. The odor of artificially damaged and uninfested Lima bean leaves was not more attractive than clean air in the Y-tube olfactometer. The predatory insects showed a greater preference for Lima bean leaves infested by the two-spotted spider mites than for either clean air or uninfested bean leaves. They showed the same preference towards infested leaves from which all spider mites and their visible products had been removed. Neither the spider mites themselves nor their products attracted the predators. In a satsuma mandarin grove, two traps with infested Lima bean plants as an odor source attracted 42 adult S. takahashii in 55 days, whereas no S. takahashii were trapped in two control traps with uninfested Lima bean plants during the same period. No S. takahashii were found during this period in the vicinity of either the sample traps or the control traps (5-m radius of each trap). These data showed that S. takahashii use herbivore-induced plant volatiles in their foraging behavior in natural ecosystems.     

Synthesis of proton conductive membranes based on inorganic–organic hybrid structure bound with phosphonic acid

Proton conductive inorganic–organic hybrid membranes were synthesized from styrene derivatives of alkoxysilane and ethyl 2-[3-(dihydroxyphosphonyl)-2-oxopropyl] acrylate (EPA) through copolymerization followed by sol–gel reaction. Self-standing, homogeneous and transparent hybrid membranes with chemically bound phosphonic acid groups were synthesized. FT-IR analysis exhibited the hybrid membranes included phosphonic acid groups. ¹³C and ²⁹Si NMR studies indicated that alkoxysilyl functionalized styrene derivatives were not only copolymerized with EPA but also condensed yielding Si–O–Si linkages by sol–gel reaction. TG–DTA analysis revealed that these membranes were thermally stable up to 200 °C in dry O₂. The proton conductivities of the hybrid membranes increased with phosphonic acid content and temperature. The P/Si ratio of the membrane was dependent on the number of alkoxy group in the starting alkoxysilane. The hybrid membrane from (dimethylmethoxysilylmethyl)styrene (DMMSMS(M))/EPA = 1/6 revealed proton conductivities of 6.3 × 10⁻³ and 2.4 × 10⁻⁴ S cm⁻¹ at 68.0% relative humidity and 18.8% relative humidity, respectively, at 140 °C.     

Freezing step controls the mannitol phase composition heterogeneity

Freeze-dried samples were prepared from D-mannitol solution by selected freezing conditions. Crystalline structures of prepared samples were determined by XRD analysis, and distributions of the various crystal structures of mannitol were obtained for each sample. It was found that the amount of each polymorph was quite well correlated to the freezing conditions, namely the ice crystal nucleation temperature and the cooling rate. In case of samples prepared at fast cooling rates, the samples where the ice crystals nucleated at higher temperature contained much more stable form than the samples nucleated at lower temperature. Besides, the samples prepared at slow cooling rates predominantly contained stable crystalline forms despite of the variation of nucleation temperatures. Moreover, the experimental results also indicated that the various polymorphs were also distributed vertically through the sample along the direction of the heat flux during freezing. The tendency of the polymorph distribution through the freeze-dried cake was also elucidated by using the simulated temperature profiles during freezing. Thus, the profiles of mannitol polymorphs after the freezing derived from the temperature distributions could predict the global tendency of polymorphism behaviour, and, consequently, would be useful to achieve quality control of freeze-dried formulations.     

Application and development of synthetic polymer membranes. VI. Pervaporation of aqueous ethanol solution through quaternized poly[3-(N′,N′-dimethyl) aminopropylacrylamide-co-acrylonitrile] membranes

Membranes obtained from polymers, quaternized poly[3-(N′,N′-dimethyl) aminopropylacrylamide-co-acrylonitrile]s, showed selective separation of water from aqueous ethanol solution by pervaporation. The separation factor toward water reached over 15,000. Membrane performance showed a good correlation to membrane polarity. Differential scanning calorimetric melting endotherms of the water-swollen membranes were studied to clarify the state of water in the membranes. The results suggested that there are two states of water in the membrane: bound and free. The higher the fraction of bound water in the membrane, clearly, the more preferentially was water permeated.     

Selective oxidation of alcohols using novel crystalline Mo-V-O oxide as heterogeneous catalyst in liquid phase with molecular oxygen

Catalytic selective oxidation of benzyl alcohol with molecular oxygen under mild conditions was carried out over novel crystalline Mo-V-O oxide. The present research is focused on investigation of recycling, reusability and stability of the crystalline oxide in the liquid-phase reaction. The Mo-V-O oxide catalyst was used at least four times with comparable activities to that of fresh catalyst. The separation of the catalyst from reaction medium can stop the conversion of benzyl alcohol, and the addition of the catalyst to the reaction medium can trigger the reaction immediately. The catalytic oxidation of 2,3,6-trimethylphenol as a reference reaction suggested that there were no leached active species in the reaction mixture. The results of the ICP–MS analysis, XRD, and SEM characterization confirmed that the structure and composition of the catalyst were stable. Besides, the Mo-V-O oxide can catalyze the oxidation of a series of alcohols with high selectivities for corresponding carbonyl compounds.     

Phylogenetic analysis of Rhodococcus erythropolis based on the variation of ribosomal proteins as observed by matrix-assisted laser desorption ionization-mass spectrometry without using genome information

Rhodococcus erythropolis strains characterized as antibiotic producers can be classified into three groups according to their antibiotic spectrum and growth compatibility. Due to their high genotypic similarity, the taxonomic relationship of these strains has not been elucidated. In this study, ribosomal protein profiling using matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS) was employed to classify twenty-one strains of R. erythropolis (15 antibiotic producers and 6 non-antibiotic producers). In the first step in this method, a total of 30 intense peaks observed for purified ribosomal subunit proteins of the type strain (R. erythropolis JCM 3201^T) were selected as the reference peaks. The mass spectra observed for the cell lysates of each sample strain were then checked as to whether peaks were observed at the same masses of the reference peaks. The results of peak matching were processed by cluster analysis, generating a dendrogram. Four major clusters of the R. erythropolis strains corresponded to three antibiotic groups and the non-antibiotic group. Furthermore, the topology of the dendrogram was highly comparable with the phylogenetic tree based on DNA gyrase subunit B gene (gyrB) sequencing. These results indicate that our proposed ribosomal protein profiling method using MALDI-MS is a potentially reliable and sufficiently high-throughput technique for the taxonomic analysis of closely related bacterial strains without using DNA sequence information.     

Catalytic behavior of AMoOx (A = Ba, Sr) in oxidation of 2-propanol

Perovskite-type oxides, BaMoO₃ and SrMoO₃, were prepared by reduction of scheelite-type oxides, BaMoO₄ and SrMoO₄, in H₂ flow at 873 K and characterized by XRD, TG, SEM, TPR, NH₃-TPD, UV-vis DRS and BET measurement. The catalytic activity of these alkaline-earth molybdenum oxide catalysts was tested for oxidation of 2-propanol with gaseous oxygen under atmospheric pressure. Dehydration to propylene was mainly promoted over the scheelite-type with Mo⁶⁺, while oxidative dehydrogenation to acetone was mainly promoted over the perovskite-type with Mo⁴⁺, and selectivity to acetone was much higher over BaMoO₃ than over SrMoO₃. Both perovskite-type oxide catalysts underwent oxidation to some degree during the catalytic reaction, so that they also contained some Mo⁶⁺. We concluded that the high selectivity to acetone resulting from oxidative dehydrogenation during 2-propanol conversion is related to the constantly changing oxidation state of the catalyst, resulting in coexistence of Mo⁶⁺ octahedra and Mo⁴⁺ octahedra on the AMoO₃ oxides.