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首页> 外文期刊>Glycobiology >Characterization of the lipopolysaccharide from Pasteurella multocida Heddleston serovar 9: Identification of a proposed bi-functionaln dTDP-3-acetamido-3,6-dideoxy-α-d-glucose biosynthesis enzyme
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Characterization of the lipopolysaccharide from Pasteurella multocida Heddleston serovar 9: Identification of a proposed bi-functionaln dTDP-3-acetamido-3,6-dideoxy-α-d-glucose biosynthesis enzyme

机译:多杀性巴斯德氏菌Heddleston血清型9的脂多糖的表征:拟议的双功能dTDP-3-acetamido-3,6-dideoxy-α-d-葡萄糖生物合成酶的鉴定

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摘要

Pasteurella multocida strains are classified into 16 different lipopolysaccharide (LPS) serovars using the Heddleston serotyping scheme. Ongoing studies in our laboratories on the LPS aim to determine the core oligosaccharide (OS) structures expressed by each of the Heddleston type strains and identify the genes and transferases required for the biosynthesis of the serovar-specific OSs. In this study, we have determined the core OS of the LPS expressed by the Heddleston serovar 9 type strain, P2095. Structural information was established by a combination of monosaccharide and methylation analyses, nuclear magnetic resonance spectroscopy and mass spectrometry revealing the following structure: . The serovar 9 OS contains an inner core that is conserved among P. multocida strains with an elaborate outer core extension containing rhamnose (Rha), a d-glycero-d-manno isomer of heptose, and the unusual deoxyamino sugar, 3-acetamido-3,6-dideoxy-α-d-glucose (Qui3NAc). Genetic analyses of the LPS outer core biosynthesis locus revealed that in addition to the glycosyltransferases predicted to transfer the sugars to the nascent LPS molecule, the locus also contained the complete set of genes required for the biosynthesis of the nucleotide sugar donors dTDP-Rha and dTDP-Qui3NAc. One of the genes identified as part of the dTDP-Qui3NAc biosynthesis pathway, qdtD, encodes a proposed bi-functional enzyme with N-terminal amino acid identity to dTDP-4-oxo-6-deoxy-d-glucose-3,4-oxoisomerase and C-terminal amino acid identity to dTDP-3-oxo-6-deoxy-α-d-glucose transacetylase.
机译:使用Heddleston血清分型方案,将多杀巴斯德氏菌菌株分为16种不同的脂多糖(LPS)血清型。我们实验室中正在进行的有关LPS的研究旨在确定每种Heddleston型菌株表达的核心寡糖(OS)结构,并鉴定血清素特异性OS的生物合成所需的基因和转移酶。在这项研究中,我们确定了Heddleston血清型9型菌株P2095所表达的LPS的核心OS。通过单糖和甲基化分析,核磁共振波谱和质谱相结合,建立了结构信息,揭示了以下结构:血清型9 OS包含一个内核,该内核在多杀毕赤酵母菌株中具有保守性,其外核延伸复杂,含有鼠李糖(Rha),庚糖的d-甘油-d-甘露糖异构体和不常见的脱氧氨基糖3-acetamido- 3,6-二脱氧-α-d-葡萄糖(Qui3NAc)。 LPS外部核心生物合成基因座的遗传分析表明,除了预计将糖转移到新生LPS分子上的糖基转移酶外,该基因座还包含核苷酸糖供体dTDP-Rha和dTDP的生物合成所需的全套基因。 -Qui3NAc。被鉴定为dTDP-Qui3NAc生物合成途径一部分的基因之一qdtD,编码一种拟议的双功能酶,其与dTDP-4-oxo-6-deoxy-d-glucose-3,4-的N末端氨基酸相同。氧代异构酶和C端氨基酸与dTDP-3-oxo-6-脱氧-α-d-葡萄糖转乙酰基酶相同。

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  • 来源
    《Glycobiology》 |2012年第3期|p.332-344|共13页
  • 作者

    Andrew D Cox;

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    Monash University, @%@, Canada @%@To whom correspondence should be addressed: Tel: @%@;

    Fax: @%@;

    e-mail:;

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