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在粗糙脂多糖纯化过程中获得的肠杆菌共同抗原形式的新观察。

A New Look at the Enterobacterial Common Antigen Forms Obtained during Rough Lipopolysaccharides Purification.

机构信息

Laboratory of Microbial Immunochemistry and Vaccines, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla 12, 53-114 Wroclaw, Poland.

出版信息

Int J Mol Sci. 2021 Jan 12;22(2):701. doi: 10.3390/ijms22020701.

Abstract

Enterobacterial common antigen (ECA) is a conserved antigen expressed by enterobacteria. It is built by trisaccharide repeating units: →3)-α-D-Fuc4NAc-(1→4)-β-D-ManNAcA-(1→4)-α-D-GlcNAc-(1→ and occurs in three forms: as surface-bound linear polysaccharides linked to a phosphoglyceride (ECA) or lipopolysaccharide - endotoxin (ECA), and cyclic form (ECA). ECA maintains, outer membrane integrity, immunogenicity, and viability of enterobacteria. A supernatant obtained after LPS ultracentrifugation was reported as a source for ECA isolation, but it has never been assessed for detailed composition besides ECA. We used mild acid hydrolysis and gel filtration, or zwitterionic-hydrophilic interaction liquid (ZICHILIC) chromatography combined with mass spectrometry for purification, fractionation, and structural analysis of rough and R1 and K12 crude LPS preparations. Presented work is the first report concerning complex characteristic of all ECA forms present in LPS-derived supernatants. We demonstrated high heterogeneity of the supernatant-derived ECA that contaminate LPS purified by ultracentrifugation. Not only previously reported -acetylated tetrameric, pentameric, and hexameric ECA have been identified, but also devoid of lipid moiety linear ECA built from 7 to 11 repeating units. Described results were common for all selected strains. The origin of linear ECA is discussed against the current knowledge about ECA and ECA.

摘要

肠细菌共同抗原(ECA)是一种由肠细菌表达的保守抗原。它由三糖重复单位组成:→3)-α-D-Fuc4NAc-(1→4)-β-D-ManNAcA-(1→4)-α-D-GlcNAc-(1→和以三种形式存在:与磷酸甘油酯(ECA)或脂多糖-内毒素(ECA)连接的表面结合线性多糖,以及环状形式(ECA)。ECA 维持肠细菌的外膜完整性、免疫原性和活力。据报道,LPS 超速离心后的上清液是 ECA 分离的来源,但除了 ECA 之外,它的详细成分从未被评估过。我们使用弱酸水解和凝胶过滤,或两性离子-亲水相互作用液相(ZICHILIC)色谱结合质谱,对粗 LPS 制剂的 R1 和 K12 粗糙和 LPS 进行纯化、分级和结构分析。目前的工作是首次报道 LPS 衍生上清液中存在的所有 ECA 形式的复杂特征。我们证明了超速离心纯化 LPS 中污染的上清液衍生 ECA 具有高度异质性。不仅鉴定了以前报道的-乙酰化的四聚体、五聚体和六聚体 ECA,还鉴定了缺少脂质部分的由 7 到 11 个重复单位组成的线性 ECA。描述的结果在所有选定的菌株中都是常见的。针对当前关于 ECA 和 ECA 的知识,讨论了线性 ECA 的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d54/7828235/287c85093cd1/ijms-22-00701-g001.jpg

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