• 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

细菌硫醇氧化还原酶——从基础研究到新的抗菌策略

Bacterial thiol oxidoreductases - from basic research to new antibacterial strategies.

作者信息

Bocian-Ostrzycka Katarzyna M, Grzeszczuk Magdalena J, Banaś Anna M, Jagusztyn-Krynicka Elżbieta Katarzyna

机构信息

Department of Bacterial Genetics, Institute of Microbiology, Faculty of Biology, University of Warsaw, Miecznikowa 1, 02-096, Warsaw, Poland.

出版信息

Appl Microbiol Biotechnol. 2017 May;101(10):3977-3989. doi: 10.1007/s00253-017-8291-8. Epub 2017 Apr 13.

DOI:10.1007/s00253-017-8291-8
PMID:28409380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5403849/
Abstract

The recent, rapid increase in bacterial antimicrobial resistance has become a major public health concern. One approach to generate new classes of antibacterials is targeting virulence rather than the viability of bacteria. Proteins of the Dsb system, which play a key role in the virulence of many pathogenic microorganisms, represent potential new drug targets. The first part of the article presents current knowledge of how the Dsb system impacts function of various protein secretion systems that influence the virulence of many pathogenic bacteria. Next, the review describes methods used to study the structure, biochemistry, and microbiology of the Dsb proteins and shows how these experiments broaden our knowledge about their function. The lessons gained from basic research have led to a specific search for inhibitors blocking the Dsb networks.

摘要

近期,细菌对抗菌药物的耐药性迅速增加,已成为一个主要的公共卫生问题。开发新型抗菌药物的一种方法是针对细菌的毒力而非其生存能力。Dsb系统的蛋白质在许多致病微生物的毒力中起关键作用,是潜在的新药物靶点。本文第一部分介绍了目前关于Dsb系统如何影响各种蛋白质分泌系统功能的知识,这些蛋白质分泌系统会影响许多致病细菌的毒力。接下来,该综述描述了用于研究Dsb蛋白质结构、生物化学和微生物学的方法,并展示了这些实验如何拓宽我们对其功能的认识。基础研究中获得的经验促使人们专门寻找阻断Dsb网络的抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbad/5403849/484d4d4fdd99/253_2017_8291_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbad/5403849/2398dafb2437/253_2017_8291_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbad/5403849/484d4d4fdd99/253_2017_8291_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbad/5403849/2398dafb2437/253_2017_8291_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbad/5403849/484d4d4fdd99/253_2017_8291_Fig2_HTML.jpg

相似文献

1
Bacterial thiol oxidoreductases - from basic research to new antibacterial strategies.细菌硫醇氧化还原酶——从基础研究到新的抗菌策略
Appl Microbiol Biotechnol. 2017 May;101(10):3977-3989. doi: 10.1007/s00253-017-8291-8. Epub 2017 Apr 13.
2
Targeting Bacterial Dsb Proteins for the Development of Anti-Virulence Agents.靶向细菌二硫键形成蛋白以开发抗毒力剂
Molecules. 2016 Jul 16;21(7):811. doi: 10.3390/molecules21070811.
3
[Type III bacterial secretion system, a promising target for the development of a new generation of antibiotic drugs].[III型细菌分泌系统,新一代抗生素药物开发的一个有前景的靶点]
Vestn Ross Akad Med Nauk. 2008(10):34-9.
4
Bacterial tyrosine kinases: novel targets for antibacterial therapy?细菌酪氨酸激酶:抗菌治疗的新靶点?
Trends Microbiol. 2009 Dec;17(12):536-43. doi: 10.1016/j.tim.2009.09.005. Epub 2009 Oct 21.
5
Protein disulfides and protein disulfide oxidoreductases in hyperthermophiles.嗜热菌中的蛋白质二硫键和蛋白质二硫键氧化还原酶。
FEBS J. 2006 Sep;273(18):4170-85. doi: 10.1111/j.1742-4658.2006.05421.x. Epub 2006 Aug 23.
6
Two-component signal transduction as potential drug targets in pathogenic bacteria.双组分信号转导系统作为病原菌药物靶点的研究进展
Curr Opin Microbiol. 2010 Apr;13(2):232-9. doi: 10.1016/j.mib.2010.01.008. Epub 2010 Feb 4.
7
Virulence as a target for antimicrobial chemotherapy.作为抗微生物化疗靶点的毒力
Expert Opin Investig Drugs. 2002 Aug;11(8):1149-59. doi: 10.1517/13543784.11.8.1149.
8
Disulfide-Bond-Forming Pathways in Gram-Positive Bacteria.革兰氏阳性菌中的二硫键形成途径
J Bacteriol. 2015 Dec 7;198(5):746-54. doi: 10.1128/JB.00769-15.
9
[Target-directed search of anti-virulence drugs].[抗毒力药物的靶向搜索]
Zh Mikrobiol Epidemiol Immunobiol. 2009 Jul-Aug(4):71-7.
10
The Extracellular Bacterial HtrA Proteins as Potential Therapeutic Targets and Vaccine Candidates.细胞外细菌HtrA蛋白作为潜在的治疗靶点和疫苗候选物。
Curr Med Chem. 2017;24(20):2174-2204. doi: 10.2174/0929867323666161223145825.

引用本文的文献

1
Advancements of paper-based sensors for antibiotic-resistant bacterial species identification.用于鉴定耐抗生素细菌种类的纸质传感器的进展
NPJ Biosens. 2024;1(1):17. doi: 10.1038/s44328-024-00016-9. Epub 2024 Dec 13.
2
Exploring the inhibitory potential of -designed small peptides on Hp0231 (DsbK), a periplasmic oxidoreductase involved in disulfide bond formation.探索设计的小肽对Hp0231(DsbK)的抑制潜力,Hp0231是一种参与二硫键形成的周质氧化还原酶。
Front Mol Biosci. 2024 Jan 11;10:1335704. doi: 10.3389/fmolb.2023.1335704. eCollection 2023.
3
Space and time on the membrane: modelling Type VI secretion system dynamics as a state-dependent random walk.

本文引用的文献

1
Engineering of Helicobacter pylori Dimeric Oxidoreductase DsbK (HP0231).幽门螺杆菌二聚体氧化还原酶DsbK(HP0231)的工程改造
Front Microbiol. 2016 Jul 26;7:1158. doi: 10.3389/fmicb.2016.01158. eCollection 2016.
2
Human commensals producing a novel antibiotic impair pathogen colonization.人类共生菌产生新型抗生素可破坏病原体定植。
Nature. 2016 Jul 28;535(7613):511-6. doi: 10.1038/nature18634.
3
Helicobacter pylori HP0231 Influences Bacterial Virulence and Is Essential for Gastric Colonization.幽门螺杆菌HP0231影响细菌毒力且对胃部定植至关重要。
膜上的空间与时间:将VI型分泌系统动力学建模为状态依赖的随机游走
R Soc Open Sci. 2023 Nov 1;10(11):230284. doi: 10.1098/rsos.230284. eCollection 2023 Nov.
4
Quantitative Proteomic Analysis of Cyanide and Mercury Detoxification by Pseudomonas pseudoalcaligenes CECT 5344.假单胞菌属 Pseudomonas pseudoalcaligenes CECT 5344 对氰化物和汞解毒的定量蛋白质组学分析。
Microbiol Spectr. 2023 Aug 17;11(4):e0055323. doi: 10.1128/spectrum.00553-23. Epub 2023 Jul 11.
5
Functional Analysis of Hypothetical Proteins of Reveals the Presence of Virulence Factors and Growth-Related Enzymes With Therapeutic Potential.[某种生物]假定蛋白质的功能分析揭示了具有治疗潜力的毒力因子和生长相关酶的存在。 (这里原文中“of”后面缺少具体所指生物,翻译时补充了“某种生物”,以使译文更完整)
Bioinform Biol Insights. 2022 Nov 9;16:11779322221136002. doi: 10.1177/11779322221136002. eCollection 2022.
6
The suppressor of copper sensitivity protein C from Caulobacter crescentus is a trimeric disulfide isomerase that binds copper(I) with subpicomolar affinity.铜敏感蛋白 C 的抑制剂来自新月柄杆菌,是一种三聚体二硫键异构酶,能以皮摩尔级亲和力结合铜(I)。
Acta Crystallogr D Struct Biol. 2022 Mar 1;78(Pt 3):337-352. doi: 10.1107/S2059798322000729. Epub 2022 Feb 21.
7
NapB Restores cytochrome c biosynthesis in bacterial dsbD-deficient mutants.NapB 恢复细菌 dsbD 缺陷型突变体中的细胞色素 c 生物合成。
Commun Biol. 2022 Jan 21;5(1):87. doi: 10.1038/s42003-022-03034-3.
8
Identification and characterization of two drug-like fragments that bind to the same cryptic binding pocket of Burkholderia pseudomallei DsbA.鉴定并表征两个类似药物的片段,它们与伯克霍尔德氏菌 DsbA 的同一个隐匿结合口袋结合。
Acta Crystallogr D Struct Biol. 2022 Jan 1;78(Pt 1):75-90. doi: 10.1107/S2059798321011475.
9
Antibacterial Profile of a Microbicidal Agent Targeting Tyrosine Phosphatases and Redox Thiols, Novel Drug Targets.一种靶向酪氨酸磷酸酶和氧化还原硫醇(新型药物靶点)的杀菌剂的抗菌谱
Antibiotics (Basel). 2021 Oct 27;10(11):1310. doi: 10.3390/antibiotics10111310.
10
Antibiofilm Activity of Heather and Manuka Honeys and Antivirulence Potential of Some of Their Constituents on the DsbA1 Enzyme of .石南蜂蜜和麦卢卡蜂蜜的抗生物膜活性及其某些成分对……的DsbA1酶的抗毒力潜力
Antibiotics (Basel). 2020 Dec 15;9(12):911. doi: 10.3390/antibiotics9120911.
PLoS One. 2016 May 3;11(5):e0154643. doi: 10.1371/journal.pone.0154643. eCollection 2016.
4
Components of the type six secretion system are substrates of Francisella tularensis Schu S4 DsbA-like FipB protein.VI型分泌系统的组分是土拉弗朗西斯菌Schu S4 DsbA样FipB蛋白的底物。
Virulence. 2016 Nov 16;7(8):882-894. doi: 10.1080/21505594.2016.1168550. Epub 2016 Mar 30.
5
Bacterial Secretion Systems: An Overview.细菌分泌系统:概述。
Microbiol Spectr. 2016 Feb;4(1). doi: 10.1128/microbiolspec.VMBF-0012-2015.
6
Type VI secretion and anti-host effectors.VI 型分泌系统和抗宿主效应因子。
Curr Opin Microbiol. 2016 Feb;29:81-93. doi: 10.1016/j.mib.2015.11.006. Epub 2015 Dec 24.
7
Formation of an Intramolecular Periplasmic Disulfide Bond in TcpP Protects TcpP and TcpH from Degradation in Vibrio cholerae.TcpP中分子内周质二硫键的形成可保护霍乱弧菌中的TcpP和TcpH不被降解。
J Bacteriol. 2015 Nov 16;198(3):498-509. doi: 10.1128/JB.00338-15. Print 2016 Feb 1.
8
Soft Computing Methods for Disulfide Connectivity Prediction.用于二硫键连接预测的软计算方法
Evol Bioinform Online. 2015 Oct 20;11:223-9. doi: 10.4137/EBO.S25349. eCollection 2015.
9
Functional and evolutionary analyses of Helicobacter pylori HP0231 (DsbK) protein with strong oxidative and chaperone activity characterized by a highly diverged dimerization domain.幽门螺杆菌HP0231(DsbK)蛋白的功能与进化分析,该蛋白具有强氧化和伴侣活性,其特征为高度分化的二聚化结构域。
Front Microbiol. 2015 Oct 8;6:1065. doi: 10.3389/fmicb.2015.01065. eCollection 2015.
10
Structure and multistate function of the transmembrane electron transporter CcdA.跨膜电子转运蛋白CcdA的结构与多态功能
Nat Struct Mol Biol. 2015 Oct;22(10):809-14. doi: 10.1038/nsmb.3099. Epub 2015 Sep 21.