Relative reactivity of substituted acetophenones in enantioselective biocatalytic reduction catalyzed by plant cells of Daucus carota and Petroselinum crispum

We have examined enantioselective bioreduction of acetophenone and its substituted derivatives into corresponding S-alcohols catalyzed by Daucus carota and Petroselinum crispum plant cells in water and isooctane. We found that the nature of the substituent has a profound effect on the relative reactivity of substituted acetophenones and enantioselectivity of biocatalytic reduction. Electron-withdrawing substituents –Br and –NO₂ enhance the initial rate of reaction and yields of products, while electron-donating substituent –OCH₃ decreases them. The reduction rates and yields of products in water were noticeably higher in comparison with similar reductions conducted in isooctane. Correlations between the initial reaction rate and the substituent constant (σ⁺) in the aromatic ring characterizing its nature were established. Comparison of ρ constants of bioreduction catalyzed by D. carota and P. crispum shows that the sensitivity of the reduction to the nature of the substituents is more significant in the case of D. carota biocatalyst. Comparison of ρ constants for D. сarota and P. crispum in water and isooctane indicates that the sensitivity of bioreduction to the nature of the substituent tends to increase from water to isooctane.     

A state space formalism for anisotropic elasticity. Part I: Rectilinear anisotropy

A state space formalism for anisotropic elasticity including the thermal effect is developed. A salient feature of the formalism is that it bridges the compliance-based and stiffness-based formalisms in a natural way. The displacement and stress components and the thermoelastic constants of a general anisotropic elastic material appear explicitly in the formulation, yet it is simple and clear. This is achieved by using the matrix notation to express the basic equations and grouping the stress in such a way that it enables us to cast neatly the three-dimensional equations of anisotropic elasticity into a compact state equation and an output equation. The homogeneous solution to the state equation for the generalized plane problem leads naturally to the eigen relation and the sextic equation of Stroh. Extension, twisting, bending, temperature change and body forces are accounted for through the particular solution. Based on the formalism the general solution for generalized plane strain and generalized torsion of an anisotropic elastic body are determined in an elegant manner.     

Ultrasonic waves in diluted and densified suspensions

A theory of propagation of stress waves in diluted and densified suspensions is developed to make the theoretical basis for analysis of ultrasonic waves through these media. The formulae for the phase velocity and the attenuation coefficient are determined as the function of wave frequency and the suspension structure parameter, which is the volume or mass fraction of the solid phase. These formulae can be use, after suitable calibration, for determination of the solid volume fraction in diluted suspensions, and the solid mass fraction or the water content in densified suspensions, that is, parameters that characterize the structure of a suspension. These structure parameters can be determined by measuring the transition time of ultrasonic wave through a given distance of suspension. The phase velocity dispersion curves and the attenuation coefficients determined theoretically and experimentally are plotted as a function of the volume fraction of the solid phase for dilute suspension, or the solid mass fraction for densified suspension.     

Vestibular responses to loud dance music: a physiological basis of the "rock and roll threshold"?

In this paper new evidence is provided to indicate that vestibular responses may be obtained from loud dance music for intensities above 90 dB(A) SPL (Impulse-weighted). In a sample of ten subjects acoustically evoked EMG were obtained from the sternocleidomastoid muscle in response to a sample of techno music typical of that which may be experienced in a dance club. Previous research has shown that this response is vestibularly mediated since it can be obtained in subjects with loss of cochlear function, but is absent in subjects with loss of vestibular function (Colebatch et al. [J. Neurol. Neurosurg. Psychiatr. 57, 190-197 (1994)]. Given that pleasurable sensations of self-motion are widely sought after by more normal means of vestibular stimulation, it is suggested that acoustically evoked sensations of self-motion may account for the compulsion to exposure to loud music. Given further the similarity between the thresholds found, and the intensities and frequency distributions that are typical in rock concerts and dance clubs, it is also suggested that this response may be a physiological basis for the minimum loudness necessary for rock and dance music to work-the "rock and roll threshold".     

Livsic Regularity Theorems for Twisted Cocycle Equations Over Hyperbolic Systems

Let be a hyperbolic map. Cocycle equations of the form f =u·g·u^–1 are considered, with f, g, u takingvalues in a compact connected Lie group G, being an automorphismof G and f, g being Hölder continuous. When the eigenvaluesof the derivative of have modulus 1, it is proved that anymeasurable solution u has a Hölder continuous version.This condition on is optimal. When f, g are C^k then u may betaken to be C^k–1+ for any (0, 1).     

Crystal structure of a μ-oxo-bridged dimeric iron(III) complex

A dimeric [{Fe(5-ClL1)}₂(μ-O)], [H₂-5-ClL1 = N,N′-bis(5-chloro-2-hydroxybenzylidene)-2-methylpropane-1,2-diamine] tetradentate Schiff-base complex, 1, has been synthesized and its crystal structure has been determined by single crystal X-ray diffraction analysis. Structural analysis of complex 1 shows that the complex is a centrosymmetric dimer. Each of the Fe(III) ions has a five-coordinate geometry and one oxygen atom bridges two Fe(III) ions to form a μ-oxo structure. The geometry around iron atom can be described as a square based pyramid with the FeN₂O₂ coordination plane and oxo ligand.     

Bismuth Nanoparticles Incorporated Centri‐voltammetry for Phenol Detection

A novel approach has been developed for phenol detection by combining centri‐voltammetry with bismuth nanoparticles that are used as carrier reagent. The interaction between bismuth and phenol and also the application of centrifugation provide the effective deposition of phenol onto the electrode surface. Direct voltammetric scan without applying any filtration or decantation prevents the analyte loss. As a result, very sensitive results were obtained with linear ranges of 2–75 μM and 100–500 μM and LOD values of 40 nM and 395 nM, respectively. Developed system was also applied for phenol detection in river sample and recovery value was calculated as 115 %.     

A novel Salvialactomine from the callus culture of Salvia santolinifolia Boiss

A novel compound Salvialactomine (1) along with two other unusual occurring natural products Pentatriacontanoic acid 1, 3-dihydroxypropyl ester (2) and 5-Methylflavone (3) were isolated from the callus of Salvia santolinifolia Boiss. Callus was initiated on MS medium containing NAA (0.5 mg/L) and further sub-cultured on MS medium supplemented with NAA with BA (0.5 + 1.5 mg/L). The structures of isolated compounds were determined by using mass spectrometry, 1D, and 2D–NMR techniques. Compounds 1, and 3 were tested for two different cancer cell lines, i.e. Hela (Cervical cancer cell) and PC-3 (Prostate cancer cells). IC₅₀ was found as > 30 using Doxorobicin (0.912 ± 0.12 μmol L^?1) as a standard.     

Comparative investigation of LiNbO3 crystals Raman spectra in the temperature range 100–400 K

We have investigated Raman spectra of congruent and stoichiometric LiNbO₃ crystals in the temperature range 100–450 K. Slope gradient is greater for the temperature dependence of band width associated with Nb⁵⁺ ions vibrations than that associated with Li⁺ ions vibrations in a lithium niobate crystal structure. This fact indicates that the anharmonicity of Nb⁵⁺ ions vibrations along the polar axis is greater compared to Li⁺ ions vibrations. It is likely that O^2– ions contribute to this anharmonicity. The O^2– ions vibrations are characterized by an anharmonic potential in the LiNbO₃ crystal structure. The O^2– ions vibrations according to ab initio calculations strongly interact with vibrations of Nb⁵⁺ ions. We have found that the temperature dependence of the fundamental bands intensity is nonmonotonic and the “extra bands” intensity is strictly linear.