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从一名播散性感染患者分离出的淋病奈瑟菌15253菌株产生的脂寡糖结构。淋病奈瑟菌脂寡糖新糖基化途径的证据。

The structure of lipooligosaccharide produced by Neisseria gonorrhoeae, strain 15253, isolated from a patient with disseminated infection. Evidence for a new glycosylation pathway of the gonococcal lipooligosaccharide.

作者信息

Yamasaki R, Kerwood D E, Schneider H, Quinn K P, Griffiss J M, Mandrell R E

机构信息

Department of Laboratory Medicine, University of California, San Francisco 94121.

出版信息

J Biol Chem. 1994 Dec 2;269(48):30345-51.

PMID:7982947
Abstract

We studied the structure of the lipooligosaccharide (LOS) that is produced by Neisseria gonorrhoeae, strain 15253. This strain, recovered from a patient with disseminated infection, produces predominantly a single LOS component, and its oligosaccharide (OS) structure is different from those of previously studied LOSs. Definition of this OS structure provides additional information on the LOS biosynthesis. We determined that the 15253 OS has an unusual structure: 2 lactosyl residues at its nonreducing ends shown below, [formula: see text] where KDO is 2-keto-3-deoxy-mannooctulosonic acid and Hep is heptose. Comparison of this OS structure with those determined previously indicates the presence of a new glycosylation pathway for gonococcal OS biosynthesis: elongation of a GlcNAc-linked heptose, in contrast to elongation of the other heptose by sequential addition of glycoses which results in the antigenic similarity with human glycolipids. The current study provides not only additional structural information on LOS expressed during different clinical states of infection but also evidence for the diversity of gonococcal LOS biosynthesis. This evidence may be helpful in understanding the pathogenesis involving gonococcal LOS.

摘要

我们研究了淋病奈瑟菌15253菌株产生的脂寡糖(LOS)的结构。该菌株从一名播散性感染患者中分离得到,主要产生单一的LOS成分,其寡糖(OS)结构与先前研究的LOS不同。这种OS结构的确定为LOS生物合成提供了更多信息。我们确定15253 OS具有不寻常的结构:其非还原端有2个乳糖基残基,如下所示,[化学式:见正文],其中KDO是2-酮-3-脱氧甘露辛酮酸,Hep是庚糖。将这种OS结构与先前确定的结构进行比较表明,淋球菌OS生物合成存在一种新的糖基化途径:GlcNAc连接的庚糖的延伸,这与通过依次添加糖基来延伸其他庚糖从而导致与人类糖脂具有抗原相似性的情况不同。当前的研究不仅提供了关于感染不同临床状态下表达的LOS的更多结构信息,还为淋球菌LOS生物合成的多样性提供了证据。这一证据可能有助于理解涉及淋球菌LOS的发病机制。

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