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蜡样芽孢杆菌ATCC 14579中UDP-D-奎诺糖胺的生物合成

The Biosynthesis of UDP-D-QuiNAc in Bacillus cereus ATCC 14579.

作者信息

Hwang Soyoun, Aronov Avi, Bar-Peled Maor

机构信息

Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia, United States of America.

Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia, United States of America; Departments of Plant Biology, University of Georgia, Athens, Georgia, United States of America.

出版信息

PLoS One. 2015 Jul 24;10(7):e0133790. doi: 10.1371/journal.pone.0133790. eCollection 2015.

Abstract

N-acetylquinovosamine (2-acetamido-2,6-di-deoxy-D-glucose, QuiNAc) is a relatively rare amino sugar residue found in glycans of few pathogenic gram-negative bacteria where it can play a role in infection. However, little is known about QuiNAc-related polysaccharides in gram-positive bacteria. In a routine screen for bacillus glycan grown at defined medium, it was surprising to identify a QuiNAc residue in polysaccharides isolated from this gram-positive bacterium. To gain insight into the biosynthesis of these glycans, we report the identification of an operon in Bacillus cereus ATCC 14579 that contains two genes encoding activities not previously described in gram-positive bacteria. One gene encodes a UDP-N-acetylglucosamine C4,6-dehydratase, (abbreviated Pdeg) that converts UDP-GlcNAc to UDP-4-keto-4,6-D-deoxy-GlcNAc (UDP-2-acetamido-2,6-dideoxy-α-D-xylo-4-hexulose); and the second encodes a UDP-4-reductase (abbr. Preq) that converts UDP-4-keto-4,6-D-deoxy-GlcNAc to UDP-N-acetyl-quinovosamine in the presence of NADPH. Biochemical studies established that the sequential Pdeg and Preq reaction product is UDP-D-QuiNAc as determined by mass spectrometry and one- and two-dimensional NMR experiments. Also, unambiguous evidence for the conversions of the dehydratase product, UDP-α-D-4-keto-4,6-deoxy-GlcNAc, to UDP-α-D-QuiNAc was obtained using real-time 1H-NMR spectroscopy and mass spectrometry. The two genes overlap by 4 nucleotides and similar operon organization and identical gene sequences were also identified in a few other Bacillus species suggesting they may have similar roles in the lifecycle of this class of bacteria important to human health. Our results provide new information about the ability of Bacilli to form UDP-QuiNAc and will provide insight to evaluate their role in the biology of Bacillus.

摘要

N-乙酰奎诺糖胺(2-乙酰氨基-2,6-二脱氧-D-葡萄糖,QuiNAc)是一种相对罕见的氨基糖残基,存在于少数致病性革兰氏阴性菌的聚糖中,在感染过程中发挥作用。然而,关于革兰氏阳性菌中与QuiNAc相关的多糖知之甚少。在对在特定培养基中生长的芽孢杆菌聚糖进行的常规筛选中,从这种革兰氏阳性菌分离出的多糖中鉴定出一个QuiNAc残基,这令人惊讶。为了深入了解这些聚糖的生物合成,我们报告了在蜡样芽孢杆菌ATCC 14579中鉴定出一个操纵子,该操纵子包含两个编码革兰氏阳性菌中以前未描述的活性的基因。一个基因编码UDP-N-乙酰葡糖胺C4,6-脱水酶(缩写为Pdeg),它将UDP-GlcNAc转化为UDP-4-酮-4,6-D-脱氧-GlcNAc(UDP-2-乙酰氨基-2,6-二脱氧-α-D-木酮糖-4-己酮糖);另一个基因编码UDP-4-还原酶(缩写为Preq),它在NADPH存在下将UDP-4-酮-4,6-D-脱氧-GlcNAc转化为UDP-N-乙酰奎诺糖胺。生化研究表明,通过质谱以及一维和二维核磁共振实验确定,连续的Pdeg和Preq反应产物是UDP-D-QuiNAc。此外,使用实时1H-NMR光谱和质谱获得了脱水酶产物UDP-α-D-4-酮-4,6-脱氧-GlcNAc转化为UDP-α-D-QuiNAc的确凿证据。这两个基因重叠4个核苷酸,在其他一些芽孢杆菌物种中也鉴定出了类似的操纵子组织和相同的基因序列,表明它们在这类对人类健康重要的细菌的生命周期中可能具有相似的作用。我们的结果提供了关于芽孢杆菌形成UDP-QuiNAc能力的新信息,并将有助于深入了解它们在芽孢杆菌生物学中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/968c/4514872/c3a9b7753b59/pone.0133790.g001.jpg

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