OmpF porin from Yersinia ruckeri as pathogenic factor: Surface antigenic sites and biological properties.

Bacterium Yersinia ruckeri as a pathogen induces causative agent of intestinal fish disease called enteric redmouth disease (ERM) is known. In this study, outer membrane OmpF porin from the Y. ruckeri (YrOmpF) has been identified as a pathogenic factor which affects host macrophage activation and life cycle of eukaryotic cells.

[Characterisation of circulating microRNA-21 levels in patients with hypertrophic cardiomyopathy].

Aim: To study the levels of circulating microRNA-21 in patients with hypertrophic cardiomyopathy (HCM) of different ages.

Materials And Methods: The study included 49 patients with HCM. The proportion of females was 55.

Estimation of Hydration Degree of Blended Cements with the Help of k-Values.

The growing utilization of various mineral additives in the building industry has caused concern worldwide to reduce the emissions of carbon dioxide from Portland cement (OPC) production. The present paper is focused on the determination of the degree of hydration of blended binding systems based on Portland cement. Blast furnace slag, fly ash, and ceramic powder are used in the study; they are applied by 12.

Interaction of chitosans and their N-acylated derivatives with lipopolysaccharide of gram-negative bacteria.

The interactions of lipopolysaccharide (LPS) with the natural polycation chitosan and its derivatives--high molecular weight chitosans (80 kD) with different degree of acetylation, low molecular weight chitosan (15 kD), acylated oligochitosan (5.5 kD) and chitooligosaccharides (biose, triose, and tetraose)--were studied using ligand-enzyme solid-phase assay. The LPS-binding activity of chitosans (80 kD) decreased with increase in acetylation degree.

Determination of binding constants of lipopolysaccharides of different structure with chitosan.

The interaction of endotoxins--lipopolysaccharides (LPS) different in degree of the O-specific chain polymerization--with 20- and 130-kD chitosan was studied using the competitive binding of LPS with the complex of chitosan-anionic dye (tropaeolin 000-2) and the direct binding of (125)I-labeled LPS with chitosan immobilized on Sepharose 4B. The interaction of 20-kD chitosan with LPS was non-cooperative, and immobilization of the polycation on Sepharose resulted in its binding to (125)I-labeled LPS with a positive cooperativity. The interaction of LPS possessing a long O-specific chain with 130-kD chitosan was characterized by negative cooperativity.