Topological transformation of phase diagrams in KBr–оxyethylated surfactant–water pseudo-ternary systems

A scheme was developed to explain the transformation of phase diagrams for KBr–oxyethylated surfactant–water systems in response to varying temperature. This scheme was shown to correspond with the respective scheme for salt–binary solvent systems. The surfactant structure was shown to have an effect on the temperature ranges of existence of a liquid–liquid two-phase equilibrium field and the positions of critical points. The elucidated trends serve as the basis for selecting components and optimizing parameters of surfactant- involving extraction processes.     

Temperature distribution in a triangular laser rod

Variational methods are applied to give approximate solutions for the temperature distribution in a right equilateral triangular prism.     

Regulation of acid phosphatase in reverse micellar system by lipids additives: structural aspects

Reverse micelles system is suggested as a direct tool to study the influence of membrane matrix composition on the activity and structure of membrane-associated enzymes with the use of acid phosphatase (AP) as an example. In reverse micelles the functioning of the monomeric and dimeric forms of AP could be separately observed by variation of the size of the micelles. We found that including the lipids into the micellar system can dramatically affect the enzyme functioning even at low lipid content (2% w/w), and this effect depends on the lipid nature. Structural studies using CD spectroscopy and DLS methods have shown that the influence of lipid composition on the enzyme properties might be caused by the interaction of lipids with the enzyme as well as by the influence of lipids on structure and properties of the micellar matrix.     

Synthesis of (2S, 5S)-2,5-dimethoxyadipic acid

Conclusions (2S,5S)-Dimethoxyadipic acid was synthesized from the D-mannitol derivative.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2151–2153, September, 1974.     

Investigation of intermolecular interactions in solutions by means of millimeter-wave spectroscopy 4. Negative and positive hydration in aqueous solutions of urea

Measurements have been made of the absorption of EHF radiation ( 5 cm^–1) by aqueous solutions of urea at 20–70°C, over the entire interval of urea solubility. Excess absorption has been found in comparison with the additive magnitude, and this has been attributed to an increase in the fraction of water molecules in the solution with rotational degrees of freedom. A model has been proposed for the hydration of urea, based on the concept of inhomogeneity of the hydrate shell of urea: stabilization of the structure of water under the influence of carbonyl oxygen and H_cis atoms (positive hydration) and a simultaneous breakdown of the structure of water in the region of two H_trans atoms that have approached to a distance of 2.14 » (negative hydration).For Previous Communication, See [1].Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 314–320, February, 1990.     

Lytic enzymes of staphylococcal phages: Correlation between secondary structure and stability

Lytic enzymes of bacteriophages K, phi11, and phi80α can lyse (destroy) cells of antibiotic-resistant strains of Staphylococcus aureus, which makes these enzymes promising antimicrobial agents. The stability of recombinant lysins of phages K, phi11, and phi80α was investigated under the conditions of storage and functioning, and the correlation between the stability and the secondary structure of the enzymes was found. It has been shown that the lower the content of disordered structures in the enzyme molecules, the greater the stability (half-inactivation time) of the lysins. At the storage temperature, the beta-structural lysin of phage phi11 shows the highest stability, while the phage K lysin with an alpha-helical structure and the phi80α lysin with a disordered secondary structure are less stable.     

Effect of the salting-out agent anion nature on the phase separation of a potassium salt–potassium bis(alkyl polyoxyethylene)phosphate–water systems

The effect the salting-out agent anion nature has on the temperature and concentration intervals of the existence of the separation area is established by analyzing the phase diagrams of pseudoternary KCl (KBr, KI, KNO₃, K₂SO₄, K₄P₂O₇)–potassium bis(alkyl polyoxyethylene)phosphate (oxyphos B)–water systems. It is concluded that the anionic salting-out capability is reduced in the order P₂O₇^4-> SO₄^2-> Cl^? > Br^?> NO₇^4-> SO₃^-> I^?. The thermodynamic parameters of phase separation used to interpret the results are calculated. The observed pattern of a change in the salting-out ability of the investigated salts relative to aqueous solutions of the surfactants is in good agreement with the lyotropic (Hofmeister) series.