STRUCTURAL ELUCIDATION OF THE O-ANTIGEN LIPOPOLYSACCHARIDE FROM 2 STRAINS OF PLESIOMONAS-SHIGELLOIDES THAT SHARE A TYPE-SPECIFIC ANTIGEN WITH SHIGELLA-FLEXNERI-6, AND THE COMMON GROUP-1 ANTIGEN WITH SHIGELLA-FLEXNERI SPP AND SHIGELLA-DYSENTERIAE-1

被引：1

作者：

LINNERBORG, M

WIDMALM, G

WEINTRAUB, A

ALBERT, MJ

机构：

[1] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT ORGAN CHEM,S-10691 STOCKHOLM,SWEDEN

[2] HUDDINGE UNIV HOSP,KAROLINSKA INST,DEPT IMMUNOL MICROBIOL PATHOL & INFECT DIS,S-14186 HUDDINGE,SWEDEN

[3] INT CTR DIARRHOEAL DIS RES,DHAKA 1000,BANGLADESH

来源：

EUROPEAN JOURNAL OF BIOCHEMISTRY | 1995年 / 231卷 / 03期

关键词：

PLESIOMONAS; LIPOPOLYSACCHARIDE; STRUCTURAL; NMR;

D O I：

10.1111/j.1432-1033.1995.tb20769.x

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Sugar and methylation analyses of native polysaccharides together with one-dimensional H-1- and C-13- NMR spectroscopy revealed that the two polysaccharides from strains 22074 and 12254 of Plesiomonas shigelloides are identical. The structure of the polysaccharide from strain 22074 was deduced from a uronic acid degradation and by NMR spectroscopy where heteronuclear multiple bond connectivity and tyro-dimensional nuclear Overhauser effect spectroscopy experiments established the pentasaccharide repeating unit: as -->4)-alpha-D-GalpA-(1-->3)-alpha-D-GlcpNAc-(1-->3)-alpha-L-(Rhap-(1-->2)-alpha-L-Rhap-(1-->2)-alpha-L- Rhap-(1-->.

引用

页码：839 / 844

页数：6

共 26 条

[21] SYNTHESIS OF LIGANDS RELATED TO THE O-SPECIFIC ANTIGEN OF SHIGELLA-DYSENTERIAE TYPE-1 .2. STEREOSELECTIVE SYNTHESES OF A DISACCHARIDE, TRISACCHARIDE, AND TETRASACCHARIDE FRAGMENT OF SHIGELLA-DYSENTERIAE TYPE-1 O-ANTIGEN USING 3,4,6-TRI-O-ACETYL-2-AZIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL CHLORIDE AS A GLYCOSYL DONOR
PAVLIAK, V
KOVAC, P
GLAUDEMANS, CPJ
CARBOHYDRATE RESEARCH, 1992, 229 (01) : 103 - 116
[22] SYNTHESIS OF LIGANDS RELATED TO THE O-SPECIFIC ANTIGEN OF SHIGELLA-DYSENTERIAE TYPE-1 .7. FLUORINATION AT POSITION-6 OF DERIVATIVES OF METHYL ALPHA-D-GALACTOPYRANOSIDE
MULARD, LA
KOVAC, P
GLAUDEMANS, CPJ
CARBOHYDRATE RESEARCH, 1994, 259 (01) : 117 - 129
[23] SYNTHESIS OF LIGANDS RELATED TO THE O-SPECIFIC ANTIGEN OF SHIGELLA-DYSENTERIAE TYPE-1 .6. SYNTHESIS OF METHYL O-ALPHA-L-RHAMNOPYRANOSYL-(1 -] 2)-ALPHA-D-GALACTOPYRANOSIDES SPECIFICALLY DEOXYGENATED AT POSITION-3, POSITION-4, OR POSITION-6 OF THE GALACTOSE RESIDUE
MULARD, LA
KOVAC, P
GLAUDEMANS, CPJ
CARBOHYDRATE RESEARCH, 1994, 251 : 213 - 232
[24] SYNTHESIS OF LIGANDS RELATED TO THE O-SPECIFIC ANTIGEN OF SHIGELLA-DYSENTERIAE TYPE .1. A SHORT SYNTHESIS OF 1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-BETA-D-GLUCOPYRANOSE AND THE CORRESPONDING ALPHA-GLUCOSYL CHLORIDE FROM D-MANNOSE
PAVLIAK, V
KOVAC, P
CARBOHYDRATE RESEARCH, 1991, 210 : 333 - 337
[25] SYNTHESIS OF LIGANDS RELATED TO THE O-SPECIFIC ANTIGEN OF TYPE-1 SHIGELLA-DYSENTERIAE .3. GLYCOSYLATION OF 4,6-O-SUBSTITUTED DERIVATIVES OF METHYL 2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE WITH GLYCOSYL DONORS DERIVED FROM MONOSACCHARIDES AND OLIGOSACCHARIDES
KOVAC, P
EDGAR, KJ
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (08): : 2455 - 2467
[26] SYNTHESIS OF LIGANDS RELATED TO THE O-SPECIFIC ANTIGEN OF SHIGELLA-DYSENTERIAE TYPE-1 .4. ENHANCED STEREOSELECTIVITY OF ALPHA-D-GALACTOSYLATION IN THE SYNTHESIS OF THE SEQUENCE ALPHA-D-GALP-(1-]3)-ALPHA-D-GLCPNAC, ALLOWING FURTHER EXTENSION OF THE CHAIN AT C-2'
KOVAC, P
JOURNAL OF CARBOHYDRATE CHEMISTRY, 1992, 11 (08) : 999 - 1014

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