aN. D. Zelinsky Institute of Organic
Chemistry, Russian Academy of Sciences, Moscow, Russia
bResearch Center Borstel, Center for Medicine and Biosciences,
Germany
cInstitute of Microbiology and Immunology, University of Lodz,
Poland
KEYWORDS: Proteus penneri; Lipopolysaccharide; O-specific polysaccharide; 2,3 Diacetamido-2,3,6-trideoxy-L-mannose, 6-Deoxy-L-talose
European J. Biochem., 1999, v. 261, pp. 392-397
DOI: 10.1046/j.1432-1327.1999.00250.x (free full text)
Bacteria of the genus Proteus are a common cause of urinary tract
infections which may result in severe complications, such as pyelonephritis
and formation of kidney stones. Proteus penneri is a new species
proposed for strains formerly described as Proteus vulgaris biogroup
I. Unlike strains of P. mirabilis and P. vulgaris, those
of P. penneri are not serologically classified. In our chemical
and immunochemical studies of Proteus O-antigens, we determined
the structure of the O-specific polysaccharide chain of P. penneri
strain 2 lipopolysaccharide.
Sugar analysis revealed D-glucose, 2-acetamido-2-deoxy-D-glucose, 6-deoxy-L-talose
(L-6dTal) and 2,3-diacetamido-2,3,6-trideoxy-L-mannose (L-RhaNAc3NAc).
The last-named sugar was isolated in the pure state and characterised by
the specific optical rotation and 1H- and 13C-NMR
spectroscopic data. Methylation analysis showed that the polysaccharide
is branched with the lateral RhaNAc3NAc residue and the Glc
residue at the branching point. In addition to monosaccharides, a partially
methylated Glc-6dTal disaccharide was detected by GLC-MS. Partial
acid hydrolysis of the polysaccharide resulted in a branched trisaccharide
containing GlcNAc and RhaNAc3NAc at the non-reducing
ends and Glc at the reducing end. These data and data of NMR spectroscopic
analysis, including two-dimensional rotating-frame NOE spectroscopy (ROESY)
and H-detected 1H,13C heteronuclear multiple-quantum
coherence (HMQC) experiments, suggested that the polysaccharide has a non-stoichiometrically
O-acetylated tetrasaccharide repeating unit having the following structure:
bLRhap2NAc3NAc |3 -4)aDGlcp(1-3)[45%AcO(1-2)]aL6dTalp(1-3)bDGlcpNAc(1- |
The O-antigen studied has the unique composition and structure and, therefore, P. penneri strain 2 may be considered as a representative of a new Proteus O-serogroup.