Structure of type 3Gn coaggregation receptor polysaccharide from Streptococcus cristatus LS4

The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s antigenic and coaggregation properties. Examination of RPS isolated from strain LS4 by a combination of 2-dimensional and pseudo 3-dimensional s...

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Published inCarbohydrate research Vol. 346; no. 11; pp. 1342 - 1346
Main Authors Yang, Jinghua, Cisar, John O., Bush, C. Allen
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 16.08.2011
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Abstract The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s antigenic and coaggregation properties. Examination of RPS isolated from strain LS4 by a combination of 2-dimensional and pseudo 3-dimensional single quantum heteronuclear NMR methods that included detection of 13C chemical shifts at high resolution revealed the following repeat unit structure: →6)-β- d-Gal f-(1→6)-β- d-Gal pNAc-(1→3)-α- d-Gal p-(1→P→6)-α- d-Gal p-(1→3)-β-L-Rha p-(1→4)-β- d-Glc p-(1→. The identification of this polysaccharide as RPS3Gn, a new structural type, was established by the α- d-Gal p-containing epitope of RPS serotype 3 and Gn recognition motif (i.e., β- d-Gal pNAc (1→3)-α- d-Gal p) for coaggregation with other bacteria.
AbstractList The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s antigenic and coaggregation properties. Examination of RPS isolated from strain LS4 by a combination of 2-dimensional and pseudo 3-dimensional single quantum heteronuclear NMR methods that included detection of 13C chemical shifts at high resolution revealed the following repeat unit structure: →6)-β- d-Gal f-(1→6)-β- d-Gal pNAc-(1→3)-α- d-Gal p-(1→P→6)-α- d-Gal p-(1→3)-β-L-Rha p-(1→4)-β- d-Glc p-(1→. The identification of this polysaccharide as RPS3Gn, a new structural type, was established by the α- d-Gal p-containing epitope of RPS serotype 3 and Gn recognition motif (i.e., β- d-Gal pNAc (1→3)-α- d-Gal p) for coaggregation with other bacteria.
The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s antigenic and coaggregation properties. Examination of RPS isolated from strain LS4 by a combination of 2-dimensional and pseudo 3-dimensional single quantum heteronuclear NMR methods that included detection of 13 C chemical shifts at high resolution revealed the following repeat unit structure: →6)-β- d -Gal f -(1→6)-β- d -Gal p NAc-(1→3)-α- d -Gal p -(1→P→6)-α- d -Gal p -(1→3)-β- l -Rha p -(1→4)-β- d -Glc p -(1→ The identification of this polysaccharide as RPS3Gn, a new structural type, was established by the α-D-Gal p -containing epitope of RPS serotype 3 and Gn recognition motif (i.e. β-D-Gal p NAc (1→3)-α-D-Gal p ) for coaggregation with other bacteria.
The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain's antigenic and coaggregation properties. Examination of RPS isolated from strain LS4 by a combination of 2-dimensional and pseudo 3-dimensional single quantum heteronuclear NMR methods that included detection of (13)C chemical shifts at high resolution revealed the following repeat unit structure: →6)-β-d-Galf-(1→6)-β-d-GalpNAc-(1→3)-α-d-Galp-(1→P→6)-α-d-Galp-(1→3)-β-L-Rhap-(1→4)-β-d-Glcp-(1→. The identification of this polysaccharide as RPS3Gn, a new structural type, was established by the α-d-Galp-containing epitope of RPS serotype 3 and Gn recognition motif (i.e., β-d-GalpNAc (1→3)-α-d-Galp) for coaggregation with other bacteria.
The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s antigenic and coaggregation properties. Examination of RPS isolated from strain LS4 by a combination of 2-dimensional and pseudo 3-dimensional single quantum heteronuclear NMR methods that included detection of ¹³C chemical shifts at high resolution revealed the following repeat unit structure: →6)-β-d-Galf-(1→6)-β-d-GalpNAc-(1→3)-α-d-Galp-(1→P→6)-α-d-Galp-(1→3)-β-L-Rhap-(1→4)-β-d-Glcp-(1→. The identification of this polysaccharide as RPS3Gn, a new structural type, was established by the α-d-Galp-containing epitope of RPS serotype 3 and Gn recognition motif (i.e., β-d-GalpNAc (1→3)-α-d-Galp) for coaggregation with other bacteria.
Author Yang, Jinghua
Cisar, John O.
Bush, C. Allen
AuthorAffiliation a Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland 20892
b Department of Chemistry and Biochemistry, University of Maryland Baltimore County, Baltimore, Maryland 21250
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Issue 11
Keywords Polysaccharides
Oral bacteria
Structure
NMR spectroscopy
Language English
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Snippet The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s...
The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s...
The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain's...
The presence of a novel coaggregation receptor polysaccharide (RPS) on the dental plaque isolate Streptococcus cristatus LS4 was suggested by this strain’s...
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SubjectTerms bacteria
Carbohydrate Sequence
carbon
epitopes
Magnetic Resonance Spectroscopy
NMR spectroscopy
nuclear magnetic resonance spectroscopy
Oral bacteria
Polysaccharides
Polysaccharides - chemistry
serotypes
stable isotopes
Streptococcus - chemistry
Streptococcus cristatus
Structure
Title Structure of type 3Gn coaggregation receptor polysaccharide from Streptococcus cristatus LS4
URI https://dx.doi.org/10.1016/j.carres.2011.04.035
https://www.ncbi.nlm.nih.gov/pubmed/21601178
https://search.proquest.com/docview/871382668
https://pubmed.ncbi.nlm.nih.gov/PMC3534726
Volume 346
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