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环境和生物膜依赖性变化对蜡样芽胞杆菌次生细胞壁多糖的影响。

Environmental and biofilm-dependent changes in a Bacillus cereus secondary cell wall polysaccharide.

机构信息

Université de Lille1, Unité de Glycobiologie Structurale et Fonctionnelle, F-59650 Villeneuve d'Ascq, France.

出版信息

J Biol Chem. 2011 Sep 9;286(36):31250-62. doi: 10.1074/jbc.M111.249821. Epub 2011 Jul 22.

Abstract

Bacterial species from the Bacillus genus, including Bacillus cereus and Bacillus anthracis, synthesize secondary cell wall polymers (SCWP) covalently associated to the peptidoglycan through a phospho-diester linkage. Although such components were observed in a wide panel of B. cereus and B. anthracis strains, the effect of culture conditions or of bacterial growth state on their synthesis has never been addressed. Herein we show that B. cereus ATCC 14579 can synthesize not only one, as previously reported, but two structurally unrelated secondary cell wall polymers (SCWP) polysaccharides. The first of these SCWP, →4)[GlcNAc(β1-3)]GlcNAc(β1-6)[Glc(β1-3)][ManNAc(α1-4)]GalNAc(α1-4)ManNAc(β1→, although presenting an original sequence, fits to the already described the canonical sequence motif of SCWP. In contrast, the second polysaccharide was made up by a totally original sequence, →6)Gal(α1-2)(2-R-hydroxyglutar-5-ylamido)Fuc2NAc4N(α1-6)GlcNAc(β1→, which no equivalent has ever been identified in the Bacillus genus. In addition, we established that the syntheses of these two polysaccharides were differently regulated. The first one is constantly expressed at the surface of the bacteria, whereas the expression of the second is tightly regulated by culture conditions and growth states, planktonic, or biofilm.

摘要

芽孢杆菌属中的细菌物种,包括蜡状芽孢杆菌和炭疽芽孢杆菌,通过磷酸二酯键将与肽聚糖共价结合的次级细胞壁聚合物(SCWP)合成。尽管在广泛的蜡状芽孢杆菌和炭疽芽孢杆菌菌株中观察到了这些成分,但培养条件或细菌生长状态对它们合成的影响从未被涉及。本文表明,蜡状芽孢杆菌 ATCC 14579 不仅可以合成一种,如先前报道的,而是两种结构上无关的次级细胞壁聚合物(SCWP)多糖。这些 SCWP 中的第一种,→4)[GlcNAc(β1-3)]GlcNAc(β1-6)[Glc(β1-3)][ManNAc(α1-4)]GalNAc(α1-4)ManNAc(β1→,尽管具有原始序列,但符合已描述的 SCWP 规范序列基序。相比之下,第二种多糖由完全原始的序列组成,→6)Gal(α1-2)(2-R-羟基戊二酸-5-酰胺基)Fuc2NAc4N(α1-6)GlcNAc(β1→,在芽孢杆菌属中从未识别出其等效物。此外,我们确定了这两种多糖的合成受到不同的调控。第一种在细菌表面不断表达,而第二种的表达则受到培养条件和生长状态(浮游或生物膜)的严格调控。

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