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大肠杆菌菌株2513(R4核心型)和F653(R3核心型)去酰化脂多糖的结构分析

Structural analysis of deacylated lipopolysaccharide of Escherichia coli strains 2513 (R4 core-type) and F653 (R3 core-type).

作者信息

Müller-Loennies Sven, Lindner Buko, Brade Helmut

机构信息

Borstel Research Center, Center for Medicine and Biosciences, Borstel, Germany.

出版信息

Eur J Biochem. 2002 Dec;269(23):5982-91. doi: 10.1046/j.1432-1033.2002.03322.x.

Abstract

Lipopolysaccharide (LPS) of Escherichia coli strain 2513 (R4 core-type) yielded after alkaline deacylation one major oligosaccharide by high-performance anion-exchange chromatography (HPAEC) which had a molecular mass of 2486.59 Da as determined by electrospray ionization mass spectrometry. This was in accordance with the calculated molecular mass of a tetraphosphorylated dodecasaccharide of the composition shown below. NMR-analyses identified the chemical structure as where l-alpha-d-Hep is l-glycero-alpha-d-manno-heptopyranose and Kdo is 3-deoxy-alpha-d-manno-oct-2-ulopyranosylonic acid and all hexoses are present as d-pyranoses. We have also isolated the complete core-oligosaccharides of E. coli F653 LPS for which only preliminary data were available and investigated the deacylated LPS by NMR and MS. The proposed structure determined previously by methylation analysis was confirmed and is shown below. In addition we have quantified the side-chain heptose substitution of the inner core with GlcpN ( approximately 30%) and confirmed that this sugar is only present when the phosphate at the second l,d-Hepp residue is absent.

摘要

大肠杆菌2513株(R4核心型)的脂多糖(LPS)经碱性脱酰基处理后,通过高效阴离子交换色谱(HPAEC)得到一种主要的寡糖,经电喷雾电离质谱测定其分子量为2486.59 Da。这与如下所示组成的四磷酸化十二糖的计算分子量相符。核磁共振分析确定其化学结构为,其中l-α-d-Hep为l-甘油-α-d-甘露庚吡喃糖,Kdo为3-脱氧-α-d-甘露-2-辛酮糖醛酸,所有己糖均以d-吡喃糖形式存在。我们还分离出了大肠杆菌F653 LPS的完整核心寡糖,之前仅有其初步数据,并用核磁共振和质谱对脱酰基LPS进行了研究。先前通过甲基化分析确定的结构得到了证实,如下所示。此外,我们还对内核心中GlcpN(约30%)的侧链庚糖取代进行了定量,并证实只有当第二个l,d-Hepp残基处的磷酸不存在时,这种糖才会出现。

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