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菊欧文氏菌的渗透调节周质葡聚糖。

Osmoregulated periplasmic glucans of Erwinia chrysanthemi.

作者信息

Cogez V, Talaga P, Lemoine J, Bohin J P

机构信息

Unité de Glycobiologie Structurale et Fonctionnelle, UMR USTL-CNRS 8576, Université des Sciences et Technologies de Lille, 59655 Villeneuve d'Ascq Cedex, France.

出版信息

J Bacteriol. 2001 May;183(10):3127-33. doi: 10.1128/JB.183.10.3127-3133.2001.

Abstract

We report the initial characterization of the osmoregulated periplasmic glucans (OPGs) of Erwinia chrysanthemi. OPGs are intrinsic components of the bacterial envelope necessary to the pathogenicity of this phytopathogenic enterobacterium (F. Page, S. Altabe, N. Hugouvieux-Cotte-Pattat, J.-M. Lacroix, J. Robert-Baudouy and J.-P. Bohin, J. Bacteriol. 183:0000-0000, 2001 [companion in this issue]). OPGs were isolated by trichloracetic acid treatment and gel permeation chromatography. The synthesis of these compounds appeared to be osmoregulated, since lower amounts of OPGs were produced when bacteria were grown in media of higher osmolarities. However, a large fraction of these OPGs were recovered in the culture medium. Then, these compounds were characterized by compositional analysis, high-performance anion-exchange chromatography, matrix-assisted laser desorption mass spectrometry, and (1)H and (13)C nuclear magnetic resonance analyses. OPGs produced by E. chrysanthemi are very heterogeneous at the level of both backbone structure and substitution of these structures. The degree of polymerization of the glucose units ranges from 5 to 12. The structures are branched, with a linear backbone consisting of beta-1,2-linked glucose units to which a variable number of branches, composed of one glucose residue, are attached by beta-1,6 linkages in a random way. This glucan backbone may be substituted by O-acetyl and O-succinyl ester-linked residues.

摘要

我们报道了菊欧文氏菌渗透调节周质葡聚糖(OPGs)的初步特征。OPGs是这种植物致病肠道细菌致病性所必需的细菌包膜固有成分(F.佩奇、S.阿尔塔贝、N.于古维厄-科特-帕塔、J.-M.拉克鲁瓦、J.罗伯特-博杜伊和J.-P.博欣,《细菌学杂志》183:0000 - 0000,2001年[本期的配套文章])。通过三氯乙酸处理和凝胶渗透色谱法分离出OPGs。这些化合物的合成似乎受到渗透调节,因为当细菌在较高渗透压的培养基中生长时,产生的OPGs量较少。然而,这些OPGs的很大一部分在培养基中被回收。然后,通过成分分析、高效阴离子交换色谱法、基质辅助激光解吸质谱法以及(1)H和(13)C核磁共振分析对这些化合物进行了表征。菊欧文氏菌产生的OPGs在主链结构及其取代水平上都非常不均一。葡萄糖单元的聚合度范围为5至12。这些结构是分支的,线性主链由β - 1,2 - 连接的葡萄糖单元组成,其上连接有数量可变的由一个葡萄糖残基组成的分支,这些分支通过β - 1,6连接以随机方式连接。这种葡聚糖主链可能被O - 乙酰基和O - 琥珀酰酯连接的残基取代。

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