STRUCTURAL-ANALYSIS OF THE LIPID-A COMPONENT OF CAMPYLOBACTER-JEJUNI CCUG 10936 (SEROTYPE O-2) LIPOPOLYSACCHARIDE - DESCRIPTION OF A LIPID-A CONTAINING A HYBRID BACKBONE OF 2-AMINO-2-DEOXY-D-GLUCOSE AND 2,3-DIAMINO-2,3-DIDEOXY-D-GLUCOSE

被引:76
作者
MORAN, AP
ZAHRINGER, U
SEYDEL, U
SCHOLZ, D
STUTZ, P
RIETSCHEL, ET
机构
[1] FORSCHUNGSINST BORSTEL,INST EXPTL BIOL & MED,PK ALLEE 22,W-2061 BORSTEL,GERMANY
[2] UNIV HELSINKI,DEPT BACTERIOL & IMMUNOL,SF-00100 HELSINKI 10,FINLAND
[3] SANDOZ GMBH,A-1235 VIENNA,AUSTRIA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1991年 / 198卷 / 02期
关键词
D O I
10.1111/j.1432-1033.1991.tb16036.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
The chemical structure of Campylobacter jejuni CCUG 10936 lipid A was elucidated. The hydrophilic backbone of the lipid A was shown to consist of three (1 --> 6)-linked bisphosphorylated hexosamine disaccharides. Neglecting the phosphorylation pattern, a D-glucosamine (2-amino-2-deoxy-D-glucose) disaccharide [beta-D-glucosaminyl-(1 --> 6)-D-glucosamine], a hybrid disaccharide of 2,3-diamino-2,3-dideoxy-D-glucose and D-glucosamine [2,3-diamino-2,3-dideoxy-beta-D-glucopyranosyl-(1 --> 6)-D-glucosamine], and a 2,3-diamino-2,3-dideoxy-D-glucose disaccharide were present in a molar ratio of 1:6:1.2. Although the backbones are bisphosphorylated, heterogeneity exists in the substitution of the polar head groups. Phosphorylethanolamine is alpha-glycosidically bound to the reducing sugar residue of the backbone, though C-1 is also non-stoichiometrically substituted by diphosphorylethanolamine. Position 4' of the non-reducing sugar residue carries an ester-bound phosphate group or is non-stoichiometrically substituted by diphosphorylethanolamine. By methylation analysis it was shown that position 6' is the attachment site for the polysaccharide moiety in lipopolysaccharide. These backbone species carry up to six molecules of ester- and amide-bound fatty acids. Four molecules of (R)-3-hydroxytetradecanoic acid are linked directly to the lipid A backbone (at positions 2, 3, 2', and 3'). Laser desorption mass spectrometry showed that both (R)-3-hydroxytetradecanoic acids linked to the non-reducing sugar unit carry, at their 3-hydroxyl group, either two molecules of hexadecanoic acid or one molecule of tetradecanoic and one of hexadecanoic acid. It also suggested that the (R)-3-(tetradecanoyloxy)-tetradecanoic acid was attached at position 2', whereas (R)-3-(hexadecanoyloxy)-tetradecanoic acid was attached at position 3', or at positions 2' and 3'. Therefore, the occurrence of three backbone disaccharides differing in amino sugar composition and presence of a hybrid disaccharide differentiate the lipid A of this C. jejuni strain from enterobacterial and other lipids A described previously.
引用
收藏
页码:459 / 469
页数:11
相关论文
共 55 条
[1]   ANALYTICAL STUDIES OF LIPOPOLYSACCHARIDE AND ITS DERIVATIVES FROM SALMONELLA-MINNESOTA R595 .1. PHOSPHORUS MAGNETIC-RESONANCE SPECTRA [J].
BATLEY, M ;
PACKER, NH ;
REDMOND, JW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 821 (02) :179-194
[2]   MONOSACCHARIDE COMPOSITION OF LIPOPOLYSACCHARIDES FROM CAMPYLOBACTER-JEJUNI AND CAMPYLOBACTER-COLI [J].
BEER, W ;
ADAM, M ;
SELTMANN, G .
JOURNAL OF BASIC MICROBIOLOGY, 1986, 26 (04) :201-204
[3]   A MODIFIED URONIC ACID CARBAZOLE REACTION [J].
BITTER, T ;
MUIR, HM .
ANALYTICAL BIOCHEMISTRY, 1962, 4 (04) :330-&
[4]   ISOLATION, PURIFICATION, AND CHEMICAL-ANALYSIS OF THE LIPOPOLYSACCHARIDE AND LIPID-A OF ACINETOBACTER-CALCOACETICUS NCTC-10305 [J].
BRADE, H ;
GALANOS, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1982, 122 (02) :233-237
[5]  
BRADE H, 1988, ZBL BAKT-INT J MED M, V268, P151
[6]  
BRANQUINHO MR, 1983, REV MICROBIOL, V14, P90
[7]   DETERGENT-ACCELERATED HYDROLYSIS OF BACTERIAL-ENDOTOXINS AND DETERMINATION OF THE ANOMERIC CONFIGURATION OF THE GLYCOSYL PHOSPHATE PRESENT IN THE ISOLATED LIPID-A FRAGMENT OF THE BORDETELLA-PERTUSSIS ENDOTOXIN [J].
CAROFF, M ;
TACKEN, A ;
SZABO, L .
CARBOHYDRATE RESEARCH, 1988, 175 (02) :273-282
[8]   O-DEMETHYLATION OF PER-O-METHYL DERIVATIVES OF 2-AMINO-2-DEOXYHEXITOLS DURING ACID-HYDROLYSIS AND ACETOLYSIS [J].
CAROFF, M ;
SZABO, L .
CARBOHYDRATE RESEARCH, 1980, 84 (01) :43-52
[9]   A SIMPLE AND RAPID METHOD FOR THE PERMETHYLATION OF CARBOHYDRATES [J].
CIUCANU, I ;
KEREK, F .
CARBOHYDRATE RESEARCH, 1984, 131 (02) :209-217
[10]  
COTTER RJ, 1987, ANAL CHIM ACTA, V195, P45