Conversion of shrimp heads to α-glucosidase inhibitors via co-culture of <Emphasis Type="Italic">Bacillus mycoides</Emphasis> TKU040 and <Emphasis Type="Italic">Rhizobium</Emphasis> sp. TKU041

Alpha-glucosidase inhibitors (aGIs) have potential use as antidiabetic drugs for the treatment of type II diabetes. Most aGIs place a burden on the liver and cause gastrointestinal distress, therefore the development of new aGIs has become very important. In this study, we investigated the production of aGIs by the co-culture of Bacillus mycoides TKU040 and Rhizobium sp. TKU041 using shrimp head powder (SHP) as the sole source of carbon and nitrogen. After fermentation in 50 mL of 1% SHP-containing medium (0.1% K₂HPO₄ and 0.05% MgSO₄·7H₂O, pH 9.2) at 37 °C for 4 days, the maximum productivity of aGIs (143 U/mL) was reached. The IC₅₀ of the aGIs produced in the culture supernatant was 3 mg/mL. The aGI activity was only 60% after treatment at pH 3 for 30 min; this increased to 140% after treatment at pH 11 for 30 min. The aGI activity remained at 60% after treatment at 60 °C for 30 min.     

Chemical constituents from the fruiting bodies of Phellinus igniarius

A new tirucallane-type triterpenoid igniarine (1), and four known compounds meshimakobnol A (2), meshimakobnol B (3), ergosterol (4) and ergosterol peroxide (5), were purified from the methanol extracts of the fruiting bodies of Phellinus igniarius (DC. ex Fr.) Quél. The structure of 1 was elucidated using a combination of 1D and 2D NMR techniques and HR-ESI-MS analyses. In addition, the isolated compounds were examined for their cytotoxicity against several tumour cell lines and part of the tested compounds demonstrated weak cytotoxicity.     

IR Spectrum and Structure of Protonated Monosilanol: Dative Bonding between Water and the Silylium Ion

We report the spectroscopic characterization of protonated monosilanol (SiH₃OH₂⁺) isolated in the gas phase, thus providing the first experimental determination of the structure and bonding of a member of the elusive silanol family. The SiH₃OH₂⁺ ion is generated in a silane/water plasma expansion, and its structure is derived from the IR photodissociation (IRPD) spectrum of its Ar cluster measured in a tandem mass spectrometer. The chemical bonding in SiH₃OH₂⁺ is analyzed by density functional theory (DFT) calculations, providing detailed insight into the nature of the dative H₃Si⁺‐OH₂ bond. Comparison with protonated methanol illustrates the differences in bonding between carbon and silicon, which are mainly related to their different electronegativity and the different energy of the vacant valence p_z orbital of SiH₃⁺ and CH₃⁺.     

Effect of Armoring Composition on the Yield of Nanodiamonds and Content of Impurities

Efficiency of using detonation nanodiamonds is strongly affected by the amount and elemental composition of impurities. The study considers the possibility of affecting the yield of detonation nanodiamonds and diamond-containing stock and the content and composition of incombustible impurities in the stock and diamonds by varying the composition of the water armor (shell) of the classical TNT–hexogen (50/50) charge. As compounds affecting the above parameters were used hydrazine, urotropin, ammonia, urea, Trilon B (disodium salt of ethylene diamine tetraacetic acid), aminotetrazole, and boric acid. It was found that using urotropin was the optimal as regards a whole set of parameters. In this case, the maximum yield of detonation nanodiamonds (6.9%) and diamond-containing stock (13.4%) was obtained. A close yield of the diamond-containing stock and detonation nanodiamonds was provided by using hydrazine and urea in the armor. Use of boric acid in the armor can substantially diminish the variety of impurity elements in the diamond-containing stock and detonation nanodiamonds at an acceptable yield of the diamond-containing stock (11.1%) and detonation nanodiamonds (6.13%). Use of pure water as the armor is inefficient.     

Effects of carrier-induced modal intermodulation on dynamic spectral characteristics of multimode Fabry-Pérot lasers

The physical mechanism attributed to producing rabbit-ears on the chirped multimode optical spectra of gain-switched Fabry-Pérot semiconductor lasers is investigated thoroughly. It has been observed experimentally that the short-wavelength rabbit-ears are dominant in the short-wavelength longitudinal modes. However, the long-wavelength rabbit-ears are dominant in the modes near the lasing wavelength, while the short-wavelength rabbit-ears are again dominant in the longest-wavelength modes. In this paper, the unequal rabbit-ears of each mode and the asymmetric chirped spectrum are shown to be a result of the dynamic power transfer between the modes during the gain-switched optical pulse due to carrier-induced modal intermodulation. Such an understanding, and the ability to model accurately this characteristic, is also shown to be essential for designing Fabry-Pérot laser systems, for short-haul applications such as fibre-to-the-home.     

High-efficiency fused-silica transmission gratings

We describe the design, fabrication, and performance of high-efficiency transmission gratings fabricated in bulk fused silica for use in high-power ultraviolet laser systems. The gratings exhibit a diffraction efficiency of 94% in order m=-1 and a damage threshold greater than 13>J/cm( 2) for 3-ns pulses at 351 nm. Model calculations and experimental measurements are in good agreement.     

Adenine radicals in the gas phase: an experimental and computational study of hydrogen atom adducts to adenine

The elusive hydrogen atom adduct to the N-1 position in adenine, which is thought to be the initial intermediate of chemical damage, was specifically generated in the gas phase and characterized by neutralization-reionization mass spectrometry. The N-1 adduct, 1,2-dihydroaden-2-yl radical (1), was generated by femtosecond electron transfer to N-1-protonated adenine that was selectively produced by electrospray ionization of adenine in aqueous-methanol solution. Radical 1 is an intrinsically stable species in the gas phase that undergoes specific loss of the N-1-hydrogen atom to form adenine, but does not isomerize to the more stable C-2 adduct, 1,2-dihydroaden-1-yl radical (5). Radicals 1 that are formed in the fifth and higher electronically excited states of DeltaE > or = 2.5 eV can also undergo ring-cleavage dissociations resulting in expulsion of HCN. The relative stabilities, dissociation, and transition state energies for several hydrogen atom adducts to adenine have been established computationally at highly correlated levels of theory. Transition state theory calculations of 298 K rate constants in the gas phase, including quantum tunnel corrections, indicate the branching ratios for H-atom additions to C-8, C-2, N-3, N-1, and N-7 positions in adenine as 0.68, 0.20, 0.08, 0.03, and 0.01, respectively. The relative free energies of adenine radicals in aqueous solution point to the C-8 adduct as the most stable tautomer, which is predicted to be the predominating (>99.9%) product at thermal equilibrium in solution at 298 K.     

Synthesis,assembly, and thin film transistors of dihydrodiazapentacene: an isostructural motif for pentacene

The study below details the synthesis, assembly, and thin film transistors from dihydrodiazapentacenes. These molecules have the same molecular shape as pentacene but are much easier to prepare and have much greater environmental stability. Thin films made from the dihydrodiazapentacene behave as field effect transistors with mobilities and on/off ratios high enough to be useful in certain applications. X-ray diffraction and AFM experiments on these films show that the molecules stack in layers with their long axis upright from the surface. Some of the derivatives synthesized for this study have unexpectedly high solubility in polar solvents such as DMF and DMSO. The crystal structure from DMF reveals self-assembled channels with each of the aniline functionalities forming a hydrogen bond with solvent. In more nonpolar solvents, the solid-state assembly switches to a herringbone motif characteristic of the linear acenes.     

Synthesis and antitubercular activity of tricyclic analogs of puupehenone

Tricyclic analogs 2a and 8 were prepared by four-step routes. The key step was an intermolecular hetero Diels-Alder reaction involving a quinone methide.