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A New Model of Pneumococcal Lipoteichoic Acid Structure Resolves Biochemical Biosynthetic and Serologic Inconsistencies of the Current Model

机译:肺炎球菌脂蛋白酸结构的新模型解决了当前模型的生化生物合成和血清学上的矛盾

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摘要

Lipoteichoic acid (LTA) is an essential bacterial membrane polysaccharide (cell wall component) that is attached to the membrane via a lipid anchor. According to the currently accepted structure of pneumococcal LTA, the polysaccharide is comprised of several repeating units, each of which starts with glucose and ends with ribitol, with the lipid anchor predicted to be Glc(β1→3)AATGal(β1→3)Glc(α1→3)-acyl2Gro, where AATGal is 2-acetamido-4-amino-2,4,6-trideoxy-d-galactose. However, this lipid anchor has not been detected in pneumococcal membranes. Furthermore, the currently accepted structure does not explain the Forssman antigen properties of LTA and predicts a molecular weight for LTA that is larger than its actual observed molecular weight. To resolve these problems, we used mass spectrometry to analyze the structure of LTA isolated from several pneumococcal strains. Our study found that the R36A pneumococcal strain produces LTA that is more representative of pneumococci than that previously characterized from the R6 strain. Analysis of LTA fragments obtained after hydrofluoric acid and nitrous treatments showed that the fragments were consistent with an LTA nonreducing terminus consisting of GalNAc(α1→3)GalNAc(β1→, which is the minimal structure for the Forssman antigen. Based on these data, we propose a revised model of LTA structure: its polysaccharide repeating unit begins with GalNAc and ends with AATGal, and its lipid anchor is Glc(α1→3)-acyl2Gro, a common lipid anchor found in pneumococcal membranes. This new model accurately predicts the observed molecular weights. The revised model should facilitate investigation of the relationship between LTA's structure and its function.
机译:脂磷壁酸(LTA)是一种必需的细菌膜多糖(细胞壁成分),它通过脂质锚定物附着在膜上。根据目前公认的肺炎球菌LTA的结构,多糖由几个重复单元组成,每个重复单元以葡萄糖开始,以核糖醇结束,脂质锚定为Glc(β1→3)AATGal(β1→3)Glc (α1→3)-酰基2Gro,其中AATGal是2-乙酰氨基-4-氨基-2,4,6-三苯氧基-d-半乳糖。然而,尚未在肺炎球菌膜中检测到该脂质锚。此外,当前接受的结构不能解释LTA的Forssman抗原特性,并且预测LTA的分子量大于其实际观察到的分子量。为了解决这些问题,我们使用质谱分析了从数种肺炎球菌菌株中分离的LTA的结构。我们的研究发现,R36A肺炎球菌菌株产生的LTA比以前从R6菌株表征的更能代表肺炎球菌。对氢氟酸和亚硝酸处理后得到的LTA片段进行分析,结果表明该片段与Forssman抗原的最小结构GalNAc(α1→3)GalNAc(β1→)组成的LTA非还原末端一致。我们提出了一个修正的LTA结构模型:它的多糖重复单元以GalNAc开始,以AATGal结尾,其脂质锚定物是Glc(α1→3)-acyl2Gro,这是在肺炎球菌膜中发现的常见脂质锚定物。观察到的分子量:修改后的模型应有助于研究LTA的结构与其功能之间的关系。

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