[Chemical and biological characterization of lipopolysaccharides from the Pseudomonas syringae pv. maculicola IMV 381 collection culture and its dissociants].

Lipopolysaccharides (LPS) were isolated from the crude bacterial mass of the Pseudomonas syringae pv. maculicola IMV 381 collection culture and its virulent and avirulent subcultures isolated earlier from the heterogeneous collection culture due to its natural variability during long-term storage. The composition, immunochemical properties, and certain parameters of the biological activity of the LPS preparations obtained were studied.

[Isolation and characterization of Rahnella aquatilis lipopolysaccharides].

Lipopolysaccharides (LPS) of six strains of Rahnella aquatilis isolated from freshwater reservoirs, plant rhizosphere, and from patient have been investigated. It was shown, that LPS of type strain was characterized by the presence of rhamnose and mannose as predominant monosaccharides, while LPS of the rest strains contained galactose and fucose. The glucosamine content was insignificant (0.

[The study of bacterial glycopolymers using laser spectroscopy].

A possibility has been demonstrated to use laser spectroscopy of bacterial glycopolymers by means of measurement of their water solutions fluorescence. Comparative investigations of native lipopolysaccharide (LPS) Ralstonia solanacearum and its structure components permits a supposition to be made that the LPS total spectrum is a result of superposition of the spectrum of O-specific polysaccharide and core oligosaccharide as well as core oligosaccharide and lipid A. The LPS spectrum maximum shift is determined by core oligosaccharide and lipid A luminescence contribution.

[Chemical characterisation and serological activity of lipopolysaccharides of Ralstonia solanacearum].

Lipopolysaccharides (LPS) of 8 strains of Ralstonia solanacearum (767, 4157, 5712, 7944, 7945, 7955, 8089 and 8110) characterized by different types of the structures of O-specific polysaccharide chains have been investigated. The ELISA and ELISA-inhibition methods were used to investigate the extent of antigenic activity of the presented LPS with respect to the obtained polyclonal O-antisera to the above strains. When analyzing the results obtained the strains were divided into five serogroups as the result of biochemical and serological investigations.

[Isolation and characterization of Cytophaga lytica lipopolysaccharide].

Lipopolysaccharide (LPS) and its structural components: lipid A, O-specific polysaccharide (O-PS) and oligosaccharide core (OG-core) have been isolated from Cytophaga lytica. 3-Oxytetradecanoic (40.8%) and dodecanoic (28.