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本文引用的文献

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The use of 1H-31P GHMBC and covariance NMR to unambiguously determine phosphate ester linkages in complex polysaccharide mixtures.使用 1H-31P GHMBC 和协方差 NMR 可明确确定复杂多糖混合物中的磷酸酯键。
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Elucidation of structural and antigenic properties of pneumococcal serotype 11A, 11B, 11C, and 11F polysaccharide capsules.阐明肺炎链球菌 11A、11B、11C 和 11F 多糖荚膜的结构和抗原特性。
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A new pneumococcal serotype, 11E, has a variably inactivated wcjE gene.一种新型肺炎球菌血清型 11E,其 wcjE 基因失活情况不一。
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Amino acid 310 determines the donor substrate specificity of serogroup W-135 and Y capsule polymerases of Neisseria meningitidis.氨基酸310决定了脑膜炎奈瑟菌W-135和Y血清群荚膜聚合酶的供体底物特异性。
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Structure of the capsular polysaccharide of pneumococcal serotype 11A reveals a novel acetylglycerol that is the structural basis for 11A subtypes.肺炎球菌11A血清型荚膜多糖的结构揭示了一种新型乙酰甘油,它是11A亚型的结构基础。
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肺炎链球菌 11D 血清型具有双特异性糖基转移酶,并表达两种不同的荚膜多糖重复单元。

Streptococcus pneumoniae serotype 11D has a bispecific glycosyltransferase and expresses two different capsular polysaccharide repeating units.

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294-2170, USA.

出版信息

J Biol Chem. 2013 Jul 26;288(30):21945-54. doi: 10.1074/jbc.M113.488528. Epub 2013 Jun 4.

DOI:10.1074/jbc.M113.488528
PMID:23737526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3724649/
Abstract

Streptococcus pneumoniae (pneumococcus) expresses a capsular polysaccharide (CPS) that protects against host immunity and is synthesized by enzymes in the capsular polysaccharide synthesis (cps) locus. Serogroup 11 has six members (11A to -E) and the CPS structure of all members has been solved, except for serotype 11D. The cps loci of 11A and 11D differ by one codon (N112S) in wcrL, which putatively encodes a glycosyltransferase that adds the fourth sugar of the CPS repeating unit (RU). Gas chromatography and nuclear magnetic resonance analysis revealed that 11A and 11D PSs contain identical CPS RUs that contain αGlc as the fourth sugar. However, ∼25% of 11D CPS RUs contain instead αGlcNAc as the fourth sugar, suggesting that 11D wcrL encodes a bispecific glycosyltransferase. To test the hypothesis that codon 112 of WcrL determines enzyme specificity, and therefore the fourth sugar in the RU, we generated three isogenic pneumococcal strains with 11A cps loci containing wcrL encoding Ser-112 (MBO128) or Ala-112 (MBO130). MBO128 was serologically and biochemically identical to serotype 11D. MBO130 has a unique serologic profile; has as much αGlcNAc as 11F, 11B, and 11C CPS do; and may represent a new serotype. These findings demonstrate how pneumococci alter their CPS structure and their immunologic properties with a minimal genetic change.

摘要

肺炎链球菌(肺炎球菌)表达一种荚膜多糖(CPS),可抵抗宿主免疫,由荚膜多糖合成(cps)基因座中的酶合成。血清群 11 有六个成员(11A 至 -E),除了 11D 型外,所有成员的 CPS 结构都已解决。11A 和 11D 的 cps 基因座在 wcrL 中相差一个密码子(N112S),推测该基因编码一种糖基转移酶,可在 CPS 重复单元(RU)的第四个糖上加糖。气相色谱和核磁共振分析表明,11A 和 11D PS 含有相同的 CPS RUs,其中包含αGlc 作为第四个糖。然而,11D CPS RUs 的约 25% 含有αGlcNAc 作为第四个糖,这表明 11D wcrL 编码一种双特异性糖基转移酶。为了验证 wcrL 第 112 位密码子决定酶特异性,从而决定 RU 中的第四个糖的假说,我们生成了三个具有 11A cps 基因座的同源肺炎球菌菌株,其中 wcrL 编码丝氨酸-112(MBO128)或丙氨酸-112(MBO130)。MBO128 在血清学和生化上与 11D 型相同。MBO130 具有独特的血清学特征;与 11F、11B 和 11C CPS 一样多的αGlcNAc;并且可能代表一个新的血清型。这些发现表明肺炎球菌如何通过最小的遗传变化改变其 CPS 结构和免疫特性。