ChemInform Abstract: Structural Elucidation of the Capsular Polysaccharide of Bacteroides fragilis Strain 23745M1.

ChemInform ◽  
2010 ◽  
Vol 27 (5) ◽  
pp. no-no
Author(s):  
V. PAVLIAK ◽  
D. UHRIN ◽  
J.-R. BRISSON ◽  
A. O. TZIANABOS ◽  
D. L. KASPER ◽  
...  
1995 ◽  
Vol 275 (2) ◽  
pp. 333-341 ◽  
Author(s):  
Viliam Pavliak ◽  
Dušan Uhrín ◽  
Jean-Robert Brisson ◽  
Arthur O. Tzianabos ◽  
Dennis L. Kasper ◽  
...  

1992 ◽  
Vol 267 (25) ◽  
pp. 18230-18235
Author(s):  
A.O. Tzianabos ◽  
A Pantosti ◽  
H Baumann ◽  
J.R. Brisson ◽  
H.J. Jennings ◽  
...  

Microbiology ◽  
2009 ◽  
Vol 155 (4) ◽  
pp. 1039-1049 ◽  
Author(s):  
Sheila Patrick ◽  
Simon Houston ◽  
Zubin Thacker ◽  
Garry W. Blakely

The obligate anaerobe Bacteroides fragilis is a normal resident of the human gastrointestinal tract. The clinically derived B. fragilis strain NCTC 9343 produces an extensive array of extracellular polysaccharides (EPS), including antigenically distinct large, small and micro- capsules. The genome of NCTC 9343 encodes multiple gene clusters potentially involved in the biosynthesis of EPS, eight of which are implicated in production of the antigenically variable micro-capsule. We have developed a rapid and robust method for generating marked and markerless deletions, together with efficient electroporation using unmodified plasmid DNA to enable complementation of mutations. We show that deletion of a putative wzz homologue prevents production of high-molecular-mass polysaccharides (HMMPS), which form the micro-capsule. This observation suggests that micro-capsule HMMPS constitute the distal component of LPS in B. fragilis. The long chain length of this polysaccharide is strikingly different from classical enteric O-antigen, which consists of short-chain polysaccharides. We also demonstrate that deletion of a putative wbaP homologue prevents expression of the phase-variable large capsule and that expression can be restored by complementation. This suggests that synthesis of the large capsule is mechanistically equivalent to production of Escherichia coli group 1 and 4 capsules.


1996 ◽  
Vol 241 (2) ◽  
pp. 602-610 ◽  
Author(s):  
Olivier Adam ◽  
Michel Riviere ◽  
Alain Vercellone ◽  
Pierre F. Monsan ◽  
Germain Puzo

2010 ◽  
Vol 192 (21) ◽  
pp. 5832-5836 ◽  
Author(s):  
Erin B. Troy ◽  
Vincent J. Carey ◽  
Dennis L. Kasper ◽  
Laurie E. Comstock

ABSTRACT Orientations of the seven invertible polysaccharide biosynthesis locus promoters of B acteroides fragilis were determined from bacteria grown in vitro, from feces of monoassociated and complex colonized mice, and from B. fragilis-induced murine abscesses. Bacteria grown in vivo have greater variability in orientation of polysaccharide locus promoters than culture-grown organisms.


1984 ◽  
Vol 62 (8) ◽  
pp. 1519-1524 ◽  
Author(s):  
Francis Michon ◽  
René Roy ◽  
Harold J. Jennings ◽  
Fraser E. Ashton

The capsular polysaccharide from newly isolated Neisseriameningitidis group H elaborates a structurally unique polysaccharide which is the group specific antigen. The polysaccharide contains D-galactose, glycerol, and phosphate in the molar ratio of 1:1:1 and is composed of the following basic repeating unit:[Formula: see text]The polysaccharide contains O-acetyl groups, in the molar ratio of 0.8:1.0 with D-galactose, which are essential to the formation of the major group specific determinant based on serological experiments described. Although all the O-acetyl groups are located on D-galactopyranosyl residues, the substitution pattern is complex, 60% of the residues being substituted at O-3 and 20% at O-2.


2000 ◽  
Vol 68 (11) ◽  
pp. 6176-6181 ◽  
Author(s):  
Michael J. Coyne ◽  
Wiltrud Kalka-Moll ◽  
Arthur O. Tzianabos ◽  
Dennis L. Kasper ◽  
Laurie E. Comstock

ABSTRACT Bacteroides fragilis produces a capsular polysaccharide complex (CPC) that is directly involved in its ability to induce abscesses. Two distinct capsular polysaccharides, polysaccharide A (PS A) and PS B, have been shown to be synthesized by the prototype strain for the study of abscesses, NCTC9343. Both of these polysaccharides in purified form induce abscesses in animal models. In this study, we demonstrate that the CPC of NCTC9343 is composed of at least three distinct capsular polysaccharides: PS A, PS B, and PS C. A previously described locus contains genes whose products are involved in the biosynthesis of PS C rather than PS B as was originally suggested. The actual PS B biosynthesis locus was cloned, sequenced, and found to contain 22 genes in an operon-type structure. A mutant with a large chromosomal deletion of the PS B biosynthesis locus was created so that the contribution of PS B to the formation of abscesses could be assessed in a rodent model. Although purified PS B can induce abscesses, removal of this polysaccharide does not attenuate the organism's ability to induce abscesses.


1995 ◽  
Vol 277 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Grigorij Kogan ◽  
Jean-Robert Brisson ◽  
Dennis L. Kasper ◽  
Christina von Hunolstein ◽  
Graziella Orefici ◽  
...  

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