Comparative structural analyses of the α-glucan and glycogen from Mycobacterium bovis

被引:40
作者
Dinadayala, Premkumar
Sambou, Tounkang
Daffe, Mamadou
Lemassu, Anne
机构
[1] Univ Toulouse 3, Dept Mecan Mol Infect Mycobacteriennes, Inst Pharmacol & Biol Struct, UMR 5089, F-31077 Toulouse, France
[2] CNRS, F-31077 Toulouse, France
关键词
capsule; DLS; Mycobacterium tuberculosis; polysaccharide; pullulanase;
D O I
10.1093/glycob/cwn031
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
Pathogenic mycobacteria such as Mycobacterium tuberculosis, the causative agent of tuberculosis, are surrounded by a noncovalently bound capsule, whose major carbohydrate constituent is a glycogen-like alpha-glucan. In the present study we compared the structures of the extracellular polysaccharide to that of the ubiquitous intracellular glycogen. The alpha-glucan was isolated from the culture medium of Mycobacterium bovis Bacille Calmette Guerin, the vaccine strain, in which it is released whereas the intracellular glycogen was obtained after the disruption of cells. The two purified polysaccharides were eluted from permeation gel at a similar position but glycogen was less soluble and gave a more opalescent solution in water than alpha-glucan. Combination of gas chromatography-mass spectrometry analysis of partially O-methylated, partially O-acetylated alditols and NMR analysis confirmed that both polysaccharides were composed of -> 4-alpha-d-Glcp-1 -> core, substituted at some six positions with short chains. Degradation of polysaccharides with pullulanase, followed by mass spectrometry analysis of the resulting products, also showed that the two polysaccharides do not differ in terms of lengths of branching. Interestingly, application of analytical ultracentrifugation and dynamic light scattering to the mycobacterial alpha-glucan and glycogen and their enzymatic degradative products indicated that the alpha-glucan possessed a higher molecular mass and was more compact than the glycogen from the same species, allowing the formulation of working structural models for the two polysaccharides. Consistent with the models, the alpha-glucan was found to be less accessible to pullulanase, a debranching enzyme, than glycogen.
引用
收藏
页码:502 / 508
页数:7
相关论文
共 26 条
[1]   ENVIRONMENTAL CONTROL OF GLYCOGEN AND LIPID CONTENT OF MYCOBACTERIUM TUBERCULOSIS [J].
ANTOINE, AD ;
TEPPER, BS .
JOURNAL OF BACTERIOLOGY, 1969, 100 (01) :538-&
[2]   CHARACTERIZATION OF GLYCOGENS FROM MYCOBACTERIA [J].
ANTOINE, AD ;
TEPPER, BS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1969, 134 (01) :207-&
[3]   An α-glucan of Pseudallescheria boydii is involved in fungal phagocytosis and toll-like receptor activation [J].
Bittencourt, Vera Carolina B. ;
Figueiredo, Rodrigo T. ;
da Silva, Rosana B. ;
Mourao-Sa, Diego S. ;
Fernandez, Patricia L. ;
Sassaki, Guilherme L. ;
Mulloy, Barbara ;
Bozza, Marcelo T. ;
Barreto-Bergter, Eliana .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (32) :22614-22623
[4]  
BLAKENEY AB, 1985, CARBOHYD RES, V140, P319, DOI 10.1016/0008-6215(85)85132-6
[5]   DISTRIBUTION OF ALPHA-AMYLASE-RESISTANT REGIONS IN GLYCOGEN MOLECULE [J].
BRAMMER, GL ;
ROUGVIE, MA ;
FRENCH, D .
CARBOHYDRATE RESEARCH, 1972, 24 (02) :343-354
[6]  
BUEDING E, 1964, J BIOL CHEM, V239, P4018
[7]   Structural analysis of water-soluble glucans from the root of Angelica sinensis (Oliv.) Diels [J].
Cao, Wei ;
Li, Xiao-Qiang ;
Liu, Li ;
Wang, Minchang ;
Fan, Hui-Ting ;
Li, Chen ;
Lv, Zhengguang ;
Wang, Xiaojing ;
Mei, Qibing .
CARBOHYDRATE RESEARCH, 2006, 341 (11) :1870-1877
[8]   Nonopsonic binding of Mycobacterium tuberculosis to complement receptor type 3 is mediated by capsular polysaccharides and is strain dependent [J].
Cywes, C ;
Hoppe, HC ;
Daffe, M ;
Ehlers, MRW .
INFECTION AND IMMUNITY, 1997, 65 (10) :4258-4266
[9]  
Daffe M, 1998, ADV MICROB PHYSIOL, V39, P131
[10]   Revisiting the structure of the anti-neoplastic Glucans of Mycobacterium bovis Bacille Calmette-Guerin -: Structural analysis of the extracellular and boiling water extract-derived glucans of the vaccine substrains [J].
Dinadayala, P ;
Lemassu, A ;
Granovski, P ;
Cérantola, S ;
Winter, N ;
Daffé, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (13) :12369-12378