Highly Efficient Method Towards In Situ Immobilization of Invertase Using Cryogelation

A novel method was developed for the immobilization of Saccharomyces cerevisiae invertase within supermacroporous polyacrylamide cryogel and was used to produce invert sugar. First, the cross-linking of invertase with soluble polyglutaraldehyde (PGA) was carried out prior to immobilization in order to increase the bulkiness of invertase and thus preventing the leakage of the cross-linked enzyme after immobilization by entrapment. And then, in situ immobilization of PGA cross-linked invertase within cryogel synthesis was achieved by free radical polymerization in semi-frozen state. The method resulted in 100 % immobilization and 74 % activity yields. The immobilized invertase retained all the initial activity for 30 days and 30 batch reactions. Immobilization had no effect on optimum temperature and it was 60 °C for both free and immobilized enzyme. However, optimum pH was affected upon immobilization. Optimum pH values for free and immobilized enzyme were 4.5 and 5.0, respectively. The immobilized enzyme was more stable than the free enzyme at high pH and temperatures. The kinetic parameters for free and immobilized invertase were also determined. The newly developed method is simple yet effective and could be used for the immobilization of some other enzymes and microorganisms.     

The star function for meromorphic functions of several complex variables

We define an analogue of the Baernstein star function for a meromorphic function f in several complex variables. This function is subharmonic on the upper half-plane and encodes some of the main functionals attached to f. We then characterize meromorphic functions admitting a harmonic star function.     

Generalized Alexandroff Duplicates and CD 0(K) spaces

We define and investigateCD _Σ,Γ(K, E)-type spaces, which generalizeCD ₀-type Banach lattices introduced in [1]. We state that the space CD _Σ,Γ(K, E) can be represented as the space of E-valued continuous functions on the generalized Alexandroff Duplicate of K. As a corollary we obtain the main result of [6, 8].     

Non-Stationary Ordering Policies for Multi-Item Inventory Systems Subject to a Single Resource Constraint

This paper studies the multi-item inventory problem with a single constraint. Two well-known approaches to this problem are the Lagrangian method and the fixed-cycle approach. Both of these methods generate stationary ordering policies. A competing approach is presented here that generates non-stationary ordering policies, with order quantities that vary over time. These non-stationary policies are, in all cases, preferred to those generated by the Lagrangian approach, and in some cases preferred to those generated by the fixed-cycle approach. Computational results comparing the three methods are also given.     

Composition and origin of trace elements in fog water studied by INAA

Characterization of dilute solution of gamma-irradiated polymethyl methacrylate (PMMA) in acetone has been carried out. The polymer sample in form of natural beads was administered a gamma-ray dose of 30 kGy by a cobalt-60 radiationsource. Various types of viscosities, viscosity average molecular weight, shape and size of irradiated PMMA and its two fractions were calculated. The results were compared with those for unirradiated PMMA. Degradation of PMMA as a result of irradiation has been observed.     

The level structure of 184W FROM THE β− decay of 184Ta

Levels of ¹⁸⁴W populated in the decay of 8.7 h ¹⁸⁴Ta have been studied by a variety of experimental techniques. As a result of β and γ-ray energy and intensity determinations and extensive β-γ and γ-γ coincidence measurements, a detailed ¹⁸⁴Ta decay scheme accommodating more than 99.5% of the decay intensity has been established. Intense β-ray groups of end-point energies 1165±26 and 1123±26 keV populate levels in ¹⁸⁴W at 1699 and 1746 keV, which de-excite predominantly to the 8.3 μs isomeric level at 1285 keV, recently identified as the $\text{1}\text{2}{}^{\mathrm{?}}\text{[510]ν?}\text{11}\text{2}{}^{\mathrm{+}}\text{[615]ν K}{}^{\mathrm{\pi }}\text{= 5}{}^{\mathrm{?}}$ band origin. The 1699 keV level also de-excites to members of a $\text{1}\text{2}{}^{\mathrm{?}}\text{[510]ν?}\text{7}\text{2}\text{[503]ν K}{}^{\mathrm{\pi }}\text{= 3}{}^{\mathrm{+}}$ band based at 1425 keV. New information about the properties of the γ-vibrational and K = 2 octupole bands in ¹⁸⁴W is presented and the possible configurations of the levels directly populated in the β^? decay are discussed. The configuration $\text{7}\text{2}{}^{\mathrm{+}}\text{[404]π ?}\text{3}\text{2}{}^{\mathrm{?}}\text{[512]ν K}{}^{\mathrm{\pi }}\text{= 5}{}^{\mathrm{?}}$ is indicated for the ¹⁸⁴Ta ground state.     

Bimetallic complexes of Schiff base bis-[4-hydroxycuomarin-3-yl]-1N,5N-thiocarbohydrazone as a potentially dibasic pentadentate ligand. Synthesis, spectral, and antimicrobial properties

The Schiff base bis-[4-hydroxycuomarin-3-yl]-¹N,⁵N-thiocarbohydrazone, H²L, was prepared by the reaction of 4-hydroxycoumarine-3-carbaldehyde with thiocabohydrazide in 2:1 molar ratio. The ligand and its binuclear complexes with Cu(II), Ni(II), Zn(II), Co(II), Mn(II), Fe(III) and Cr(III) ions were characterized via elemental analysis, ¹H NMR, mass spectrometry, infrared, and electronic spectra, as well as room temperature magnetic susceptibilities. Furthermore, the thermal stabilities of two representative complexes were also investigated. The Schiff base and its metal complexes were screened for their antifungal and antibacterial activities against different species of pathogenic fungi and bacteria and their biopotency have been discussed.     

Interfacial Behavior of Cysteine between Mild Steel and Sulfuric Acid as Corrosion Inhibitor

Interfacial behavior of cysteine (Cys) between mild steel and sulfuric acid solution as a corrosion inhibitor has been studied with electrochemical AC (alternating current) and DC (direct current) techniques at (25.0±0.1) °C. The AC impedance results were evaluated using equivalent circuits in which a constant phase element (CPE) has been replaced with double layer capacitance (C_dl) to represent the frequency distribution of experimental data. Changes in impedance parameters (charge transfer resistance and double layer capacitance) indicated that cysteine molecules acted by accumulating at the metal/solution interface. The fractional coverage of the metal surface () was determined using AC impedance results and it was found that the adsorption of cysteine on the mild steel surface followed a Langmuir isotherm model with a standard free energy of adsorption (ΔG⁰_ads) of −35.1 kJ·mol⁻¹.To clarify the type of interaction between mild steel surface and cysteine molecules with a molecular orbital approach, electronic properties, such as, the highest occupied molecular orbital (HOMO) energy, the lowest unoccupied molecular orbital (LUMO) energy, and the frontier molecular orbital coefficients have been calculated. Energy gaps for the interaction of mild steel surface and cysteine molecules (E_{LUMO Fe}−E_{HOMO Cys} and E_{LUMO Cys}−E_{HOMO Fe}) were used to determine whether cysteine molecules acted as electron donors or electron acceptors when they interacted with the mild steel surface. The local reactivity was evaluated through the condensed Fukui indices. Theoretical calculations were carried out using the density functional theory (DFT) at B3LYP level with the 6-311++G(d,p) basis set for all atoms by Gaussian 03W program.     

Mass‐Selected Circular Dichroism of Supersonic‐Beam‐Cooled [D4]‐(R)‐(+)‐3‐Methylcyclopentanone

UV spectroscopy and electronic circular dichroism (ECD) experiments on supersonic‐beam‐cooled deuterated (R)‐(+)‐3‐methylcyclopentanone ([D₄]‐(R)‐(+)‐3‐MCP) have been performed by using a laser mass spectrometer. The spectral resolution not only allowed excitation and CD measurements for single vibronic transitions but also for the rotational P, Q, and R branches of these transitions. The investigated transition showed the largest anisotropy factor ever observed for chiral molecules in the gas phase, which, due to residual saturation of the excited transition, represents only a lower limit for the real anisotropy factor. Furthermore, one‐color (1+1+1) and two‐color (1+1′) resonance‐enhanced multiphoton ionization (REMPI) measurements were performed and the effusive‐beam (room temperature) and supersonic‐beam results for [D₄]‐(R)‐(+)‐3‐MCP were compared. These results allowed a differentiation between single‐step ECD (comparable to conventional ECD) and cumulative ECD (only possible in multiphoton excitation) under supersonic‐beam conditions.