Optimization of Capsular Polysaccharide Production by Streptococcus pneumoniae Type 3

Author(s):  
Sheng-De Jin
1986 ◽  
Vol 17 (6) ◽  
Author(s):  
A. YA. CHERNYAK ◽  
K. V. ANTONOV ◽  
N. K. KOCHETKOV ◽  
L. N. PADYUKOV ◽  
N. V. TSVETKOVA

2002 ◽  
Vol 80 (1) ◽  
pp. 76-81 ◽  
Author(s):  
Dirk J Lefeber ◽  
Eneko Aldaba Arévalo ◽  
Johannis P Kamerling ◽  
Johannes FG Vliegenthart

In the framework of the development of a new generation of neoglycoconjugate vaccines against Streptococcus pneumoniae, the synthesis is described of a spacer-containing hexasaccharide fragment related to the capsular polysaccharide of S. pneumoniae type 3. Hexasaccharide β-D-GlcpA-(1[Formula: see text]4)-β-D-Glcp-(1[Formula: see text]3)-β-D-GlcpA-(1[Formula: see text]4)-β-D- Glcp-(1[Formula: see text]3)-β-D-GlcpA-(1[Formula: see text]4)-β-D-Glcp-(1[Formula: see text]O-(CH2)3NH2) (1), comprised of three repeating units, was synthesized via a blockwise strategy employing suitably protected disaccharide building blocks. Carboxylic groups were introduced by selective oxidation with TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) in the last reaction steps. Deprotection afforded target hexasaccharide 1.Key words: oligosaccharide synthesis, Streptococcus pneumoniae type 3, TEMPO oxidation.


PLoS ONE ◽  
2018 ◽  
Vol 13 (1) ◽  
pp. e0190402 ◽  
Author(s):  
Zuleeza Ahmad ◽  
Richard M. Harvey ◽  
James C. Paton ◽  
Alistair J. Standish ◽  
Renato Morona

2017 ◽  
Vol 66 (1) ◽  
pp. 111-122 ◽  
Author(s):  
Yu. E. Tsvetkov ◽  
D. V. Yashunsky ◽  
E. V. Sukhova ◽  
E. A. Kurbatova ◽  
N. E. Nifantiev

1988 ◽  
Vol 106 (1) ◽  
pp. 101-107 ◽  
Author(s):  
Guy J.W.J. Zigterman ◽  
AndréF.M. Verheul ◽  
Erna B.H.W. Ernste ◽  
Ronald F.M. Rombouts ◽  
Marinus J. De Reuver ◽  
...  

1984 ◽  
Vol 160 (2) ◽  
pp. 386-397 ◽  
Author(s):  
L S McDaniel ◽  
G Scott ◽  
J F Kearney ◽  
D E Briles

Monoclonal antibodies were raised against surface determinants of Streptococcus pneumoniae by hyperimmunizing X-linked immunodeficient (xid) CBA/N mice with the heat-killed rough strain R36A. 17 hybridomas produced antibody that bound intact R36A and did not cross-react with phosphocholine, an antigen common in the cell wall of all S. pneumoniae. The antibody produced by at least two of these hybridomas, Xi64 (IgM) and Xi126 (IgG2b), could protect mice from a lethal intravenous challenge of type 3 S. pneumoniae strains WU2 and A66 and of the type 2 strain D39. The minimum amount of antibody required to protect xid mice from 100 WU2 was 4.5 micrograms/mouse for Xi64 and 2.6 micrograms/mouse for Xi126,. Free phosphocholine, C-polysaccharide, and type 3 capsular polysaccharide all failed to inhibit the binding of Xi64 or Xi126 to R36A. These antibodies appeared to bind surface polypeptides, since treatment of R36A with either pepsin or trypsin, or of R36A lysate with trypsin, effectively eliminated the ability of Xi64 and Xi126 to bind antigens in these preparations. Binding studies indicated that these two antibodies recognized different epitopes that were expressed on several but not all serotypes of pneumococci.


1999 ◽  
Vol 181 (19) ◽  
pp. 6214-6219 ◽  
Author(s):  
Rosario Muñoz ◽  
Marta Mollerach ◽  
Rubens López ◽  
Ernesto García

ABSTRACT The complete nucleotide sequence of the capsular gene cluster (cap8) responsible for the biosynthesis of the capsular polysaccharide of Streptococcus pneumoniae type 8 has been determined. The cap8 gene cluster, located between the genes dexB and aliA, is composed of 12 open reading frames. A 14.7-kb DNA fragment embracing the cap8genes was sufficient to transform an unencapsulated type 3 S. pneumoniae strain to a strain with the type 8 capsule. A possible scenario for the evolution of pneumococcal types 2 and 8 is outlined.


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