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囊性纤维化病原体洋葱伯克霍尔德菌产生的两种不同脂多糖O抗原的结构研究和构象行为

Structural study and conformational behavior of the two different lipopolysaccharide O-antigens produced by the cystic fibrosis pathogen Burkholderia multivorans.

作者信息

Ieranò Teresa, Silipo Alba, Cescutti Paola, Leone Maria Rosaria, Rizzo Roberto, Lanzetta Rosa, Parrilli Michelangelo, Molinaro Antonio

机构信息

Dipartimento di Chimica Organica e Biochimica, Università di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia 4, 80126 Napoli, Italy.

出版信息

Chemistry. 2009 Jul 20;15(29):7156-66. doi: 10.1002/chem.200900647.

DOI:10.1002/chem.200900647
PMID:19533713
Abstract

Lipopolysaccharides (LPSs) are virulence factors expressed by gram-negative bacteria; they are among those mainly responsible for bacterial virulence. In this work we define the primary structure and the conformational features of the O-chain from the LPS produced by the highly virulent clinical isolate Burkholderia multivorans strain C1576, an opportunistic human pathogen isolated in a cystic fibrosis center and causative of an outbreak with lethal outcome. We demonstrate that the LPS from this clinical isolate consists of two O-polysaccharide chains present in different amounts and made up of repeating units, both containing deoxy sugar. Additionally, conformational studies have been performed to establish and compare the spatial arrangements of the two polysaccharides and differences in their shape have been highlighted. The comprehension of the structural and conformational features of the two repeating units may help to explain their biological significance, the molecular shape of the bacterial external surface, and the comprehension at the molecular level of the recognition mechanisms of the antibodies.

摘要

脂多糖(LPSs)是革兰氏阴性菌表达的毒力因子;它们是细菌毒力的主要成因之一。在这项工作中,我们确定了高毒力临床分离株多食伯克霍尔德菌C1576(一种在囊性纤维化中心分离出的机会性人类病原体,曾引发一次导致致命后果的疫情)产生的LPS中O链的一级结构和构象特征。我们证明,这种临床分离株的LPS由两条含量不同的O-多糖链组成,这两条链均由重复单元构成,且都含有脱氧糖。此外,还进行了构象研究,以确定并比较这两种多糖的空间排列,并突出它们形状上的差异。对这两个重复单元的结构和构象特征的理解,可能有助于解释它们的生物学意义、细菌外表面的分子形状,以及在分子水平上对抗体识别机制的理解。

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