• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Lipopolysaccharide O-antigens-bacterial glycans made to measure.脂多糖 O-抗原——细菌糖的量身定制。
J Biol Chem. 2020 Jul 31;295(31):10593-10609. doi: 10.1074/jbc.REV120.009402. Epub 2020 May 18.
2
Diversity of endotoxin and its impact on pathogenesis.内毒素的多样性及其对发病机制的影响。
J Endotoxin Res. 2006;12(4):205-23. doi: 10.1179/096805106X118825.
3
The biosynthesis and biological role of lipopolysaccharide O-antigens of pathogenic Yersiniae.致病性耶尔森菌脂多糖O抗原的生物合成及生物学作用
Carbohydr Res. 2003 Nov 14;338(23):2521-9. doi: 10.1016/s0008-6215(03)00305-7.
4
Analysis of the Topology and Active-Site Residues of WbbF, a Putative O-Polysaccharide Synthase from Salmonella enterica Serovar Borreze.分析来自沙门氏菌血清型博雷泽的假定 O-多糖合成酶 WbbF 的拓扑结构和活性位点残基。
J Bacteriol. 2020 Feb 11;202(5). doi: 10.1128/JB.00625-19.
5
Lipopolysaccharide as a target for the development of novel therapeutics in gram-negative bacteria.脂多糖作为革兰氏阴性菌新型治疗药物开发的靶点。
Curr Drug Targets Infect Disord. 2001 Aug;1(2):91-106. doi: 10.2174/1568005014606143.
6
Biosynthesis and export of bacterial lipopolysaccharides.细菌脂多糖的生物合成与外排。
Annu Rev Biochem. 2014;83:99-128. doi: 10.1146/annurev-biochem-060713-035600. Epub 2014 Feb 21.
7
O-antigen structural variation: mechanisms and possible roles in animal/plant-microbe interactions.O抗原结构变异:动物/植物 - 微生物相互作用中的机制及可能作用
FEMS Microbiol Rev. 2002 Mar;26(1):17-47. doi: 10.1111/j.1574-6976.2002.tb00597.x.
8
Synthesis of lipopolysaccharide O-antigens by ABC transporter-dependent pathways.通过 ABC 转运蛋白依赖途径合成脂多糖 O-抗原。
Carbohydr Res. 2012 Jul 15;356:12-24. doi: 10.1016/j.carres.2012.02.027. Epub 2012 Mar 6.
9
Unique Regions of the Polysaccharide Copolymerase Wzz from Pseudomonas aeruginosa Are Essential for O-Specific Antigen Chain Length Control.铜绿假单胞菌多糖聚合酶 Wzz 的独特区域对于 O-特异性抗原链长控制是必需的。
J Bacteriol. 2019 Jul 10;201(15). doi: 10.1128/JB.00165-19. Print 2019 Aug 1.
10
Pseudomonas aeruginosa O-antigen chain length is determined before ligation to lipid A core.铜绿假单胞菌O抗原链的长度在与脂质A核心连接之前就已确定。
Environ Microbiol. 2002 Dec;4(12):883-97. doi: 10.1046/j.1462-2920.2002.00288.x.

引用本文的文献

1
Anti-restriction functions of injected phage proteins revealed by peeling back layers of bacterial immunity.通过逐层剖析细菌免疫揭示注入噬菌体蛋白的抗限制功能。
Nat Commun. 2025 Aug 22;16(1):7828. doi: 10.1038/s41467-025-63056-3.
2
LPS O-antigen polysaccharide length impacts outer membrane permeability of enteric gram-negative bacteria.脂多糖O抗原多糖的长度影响肠道革兰氏阴性菌的外膜通透性。
bioRxiv. 2025 Aug 15:2025.08.14.670410. doi: 10.1101/2025.08.14.670410.
3
Microbiome Shifts in Peri-Implantitis: Longitudinal Characterization of Dysbiosis and Resolution.种植体周围炎中的微生物群落变化:生态失调及其恢复的纵向特征
Int Dent J. 2025 Aug 13;75(5):100951. doi: 10.1016/j.identj.2025.100951.
4
Pseudomonas syringae Lipopolysaccharide Synthesis Gene wbpL Displays Heterogeneous Expression Within In Vitro and In Planta Populations.丁香假单胞菌脂多糖合成基因wbpL在体外和植物体内群体中表现出异质表达。
Microbiologyopen. 2025 Aug;14(4):e70031. doi: 10.1002/mbo3.70031.
5
Chain-length regulation by WzzE is necessary for, but genetically separable from, cyclic enterobacterial common antigen synthesis.WzzE对链长的调控是环状肠道细菌共同抗原合成所必需的,但在基因上可与之分离。
bioRxiv. 2025 Jun 25:2025.06.25.661564. doi: 10.1101/2025.06.25.661564.
6
MALDI O-antigen glycotyping of using DAN/DHB/K matrix.使用DAN/DHB/K基质对进行基质辅助激光解吸电离O抗原糖基分型。 (你提供的原文似乎不完整,“of”后面缺少具体所指内容)
BBA Adv. 2024 Dec 17;7:100131. doi: 10.1016/j.bbadva.2024.100131. eCollection 2025.
7
Synthesis and Evaluation of 3‑Deoxy‑d--oct-2-ulosonic Acid Derivatives to Perturb Escherichia coli Lipopolysaccharide Biosynthesis.用于干扰大肠杆菌脂多糖生物合成的3-脱氧-D-甘露糖辛酮酸衍生物的合成与评价
JACS Au. 2025 May 22;5(6):2749-2761. doi: 10.1021/jacsau.5c00338. eCollection 2025 Jun 23.
8
Fast and accurate antigen typing with Kaptive 3.使用Kaptive 3进行快速准确的抗原分型。
Microb Genom. 2025 Jun;11(6). doi: 10.1099/mgen.0.001428.
9
Genetic engineering of E. coli K-12 for heterologous carbohydrate antigen production.用于异源碳水化合物抗原生产的大肠杆菌K-12基因工程。
Microb Cell Fact. 2025 May 28;24(1):126. doi: 10.1186/s12934-025-02749-2.
10
New insights in amino sugar metabolism by the gut microbiome.肠道微生物群对氨基糖代谢的新见解。
Gut Microbes. 2025 Dec;17(1):2510462. doi: 10.1080/19490976.2025.2510462. Epub 2025 May 25.

本文引用的文献

1
Assembly of Bacterial Capsular Polysaccharides and Exopolysaccharides.细菌荚膜多糖和胞外多糖的组装。
Annu Rev Microbiol. 2020 Sep 8;74:521-543. doi: 10.1146/annurev-micro-011420-075607. Epub 2020 Jul 17.
2
A bifunctional O-antigen polymerase structure reveals a new glycosyltransferase family.双功能 O-抗原聚合酶结构揭示了一个新的糖基转移酶家族。
Nat Chem Biol. 2020 Apr;16(4):450-457. doi: 10.1038/s41589-020-0494-0. Epub 2020 Mar 9.
3
Detection of Transport Intermediates in the Peptidoglycan Flippase MurJ Identifies Residues Essential for Conformational Cycling.检测肽聚糖翻转酶 MurJ 中的转运中间体可鉴定对构象循环至关重要的残基。
J Am Chem Soc. 2020 Mar 25;142(12):5482-5486. doi: 10.1021/jacs.9b12185. Epub 2020 Mar 11.
4
Structure and mechanism of the ER-based glucosyltransferase ALG6.内质网基葡萄糖基转移酶 ALG6 的结构与机制
Nature. 2020 Mar;579(7799):443-447. doi: 10.1038/s41586-020-2044-z. Epub 2020 Feb 26.
5
Outer membrane protein size and LPS O-antigen define protective antibody targeting to the Salmonella surface.外膜蛋白大小和 LPS O-抗原决定了针对沙门氏菌表面的保护性抗体的靶向性。
Nat Commun. 2020 Feb 12;11(1):851. doi: 10.1038/s41467-020-14655-9.
6
The O-Antigen Epitope Governs Susceptibility to Colistin in Salmonella enterica.O 抗原表位决定了肠道沙门氏菌对黏菌素的易感性。
mBio. 2020 Jan 28;11(1):e02831-19. doi: 10.1128/mBio.02831-19.
7
One or two membranes? Diderm Firmicutes challenge the Gram-positive/Gram-negative divide.一层还是两层膜?Firmicutes 挑战革兰氏阳性/阴性划分。
Mol Microbiol. 2020 Mar;113(3):659-671. doi: 10.1111/mmi.14469.
8
In Situ Structure of an Intact Lipopolysaccharide-Bound Bacterial Surface Layer.完整脂多糖结合细菌表面层的原位结构。
Cell. 2020 Jan 23;180(2):348-358.e15. doi: 10.1016/j.cell.2019.12.006. Epub 2019 Dec 26.
9
Structure and Ligand-Binding Properties of the O Antigen ABC Transporter Carbohydrate-Binding Domain.O 抗原 ABC 转运蛋白碳水化合物结合域的结构和配体结合特性。
Structure. 2020 Feb 4;28(2):252-258.e2. doi: 10.1016/j.str.2019.11.020. Epub 2019 Dec 23.
10
Cytosolic Gram-negative bacteria prevent apoptosis by inhibition of effector caspases through lipopolysaccharide.胞质革兰氏阴性菌通过脂多糖抑制效应半胱天冬酶来防止细胞凋亡。
Nat Microbiol. 2020 Feb;5(2):354-367. doi: 10.1038/s41564-019-0620-5. Epub 2019 Dec 23.

脂多糖 O-抗原——细菌糖的量身定制。

Lipopolysaccharide O-antigens-bacterial glycans made to measure.

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.

出版信息

J Biol Chem. 2020 Jul 31;295(31):10593-10609. doi: 10.1074/jbc.REV120.009402. Epub 2020 May 18.

DOI:10.1074/jbc.REV120.009402
PMID:32424042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7397119/
Abstract

Lipopolysaccharides are critical components of bacterial outer membranes. The more conserved lipid A part of the lipopolysaccharide molecule is a major element in the permeability barrier imposed by the outer membrane and offers a pathogen-associated molecular pattern recognized by innate immune systems. In contrast, the long-chain O-antigen polysaccharide (O-PS) shows remarkable structural diversity and fulfills a range of functions, depending on bacterial lifestyles. O-PS production is vital for the success of clinically important Gram-negative pathogens. The biological properties and functions of O-PSs are mostly independent of specific structures, but the size distribution of O-PS chains is particularly important in many contexts. Despite the vast O-PS chemical diversity, most are produced in bacterial cells by two assembly strategies, and the different mechanisms employed in these pathways to regulate chain-length distribution are emerging. Here, we review our current understanding of the mechanisms involved in regulating O-PS chain-length distribution and discuss their impact on microbial cell biology.

摘要

脂多糖是细菌外膜的重要组成部分。脂多糖分子中更保守的脂质 A 部分是外膜所施加的通透性屏障的主要组成部分,并提供了先天免疫系统识别的病原体相关分子模式。相比之下,长链 O-抗原多糖(O-PS)表现出显著的结构多样性,并根据细菌的生活方式发挥多种功能。O-PS 的产生对于临床重要的革兰氏阴性病原体的成功至关重要。O-PS 的生物学特性和功能在很大程度上与其特定结构无关,但 O-PS 链的大小分布在许多情况下尤为重要。尽管 O-PS 的化学多样性非常广泛,但大多数都是由两种组装策略在细菌细胞中产生的,而这些途径中用于调节链长分布的不同机制正在逐渐浮现。在这里,我们回顾了我们对调节 O-PS 链长分布的机制的理解,并讨论了它们对微生物细胞生物学的影响。