首页> 美国卫生研究院文献>ChemistryOpen >Structural Elucidation of the O-Antigen Polysaccharide from Escherichia coli O181
【2h】

Structural Elucidation of the O-Antigen Polysaccharide from Escherichia coli O181

机译:大肠杆菌O181中O抗原多糖的结构解析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Shiga-toxin-producing Escherichia coli (STEC) is an important pathogen associated to food-borne infection in humans; strains of E. coli O181, isolated from human cases of diarrhea, have been classified as belonging to this pathotype. Herein, the structure of the O-antigen polysaccharide (PS) from E. coli O181 has been investigated. The sugar analysis showed quinovosamine (QuiN), glucosamine (GlcN), galactosamine (GalN), and glucose (Glc) as major components. Analysis of the high-resolution mass spectrum of the oligosaccharide (OS), obtained by dephosphorylation of the O-deacetylated PS with aqueous 48 % hydrofluoric acid, revealed a pentasaccharide composed of two QuiNAc, one GlcNAc, one GalNAc, and one Glc residue. The 1H and 13C NMR chemical shift assignments of the OS were carried out using 1 D and 2 D NMR experiments, and the OS was sequenced using a combination of tandem mass spectrometry (MS/MS) data and NMR 13C NMR glycosylation shifts. The structure of the native PS was determined using NMR spectroscopy, and it consists of branched pentasaccharide repeating units joined by phosphodiester linkages: →4)[α-l-QuipNAc-(1→3)]-α-d-GalpNAc6Ac-(1→6)-α-d-Glcp-(1→P-4)-α-l-QuipNAc-(1→3)-β-d-GlcpNAc-(1→; the O-acetyl groups represent 0.4 equivalents per repeating unit. Both the OS and PSs exhibit rare conformational behavior since two of the five anomeric proton resonances could only be observed at an elevated temperature.
机译:产生志贺毒素的大肠杆菌(STEC)是与人类食源性感染相关的重要病原体。从人类腹泻病例中分离出的大肠杆菌O181菌株已被归类为该病型。在此,已经研究了来自大肠杆菌O181的O-抗原多糖(PS)的结构。糖分分析显示喹诺酮胺(QuiN),葡糖胺(GlcN),半乳糖胺(GalN)和葡萄糖(Glc)是主要成分。通过用48%的氢氟酸水溶液对O-脱乙酰化的PS进行磷酸化而获得的寡糖(OS)的高分辨率质谱分析表明,五糖由两个QuiNAc,一个GlcNAc,一个GalNAc和一个Glc残基组成。使用1 D和2 D NMR实验进行OS的 1 H和 13 C NMR化学位移分配,并结合串联质谱对OS进行测序光谱(MS / MS)数据和NMR 13 C NMR糖基化位移。天然PS的结构是使用NMR光谱确定的,它由通过磷酸二酯键连接的分支的五糖重复单元组成:→4)[α-l-QuipNAc-((1→3)]-α-d-GalpNAc6Ac-(1 →6)-α-d-GlcpNA-(1→P-4)-α-l-QuipNAc-(1→3)-β-d-GlcpNAc-(1→; O-乙酰基每次重复表示0.4当量OS和PS均表现出罕见的构象行为,因为只有在升高的温度下才能观察到五个异头质子共振中的两个。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号