• 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

大肠杆菌Δfur突变体在稳定期显示出低HPII过氧化氢酶活性。

Escherichia coli deltafur mutant displays low HPII catalase activity in stationary phase.

作者信息

Benov Ludmil, Sequeira Fatima

机构信息

Department of Biochemistry, Faculty of Medicine, Kuwait University, Kuwait.

出版信息

Redox Rep. 2003;8(6):379-83. doi: 10.1179/135100003225003357.

DOI:10.1179/135100003225003357
PMID:14980071
Abstract

Iron is among the most important micronutrients used by bacteria. As a partner of the Fenton reaction, however, iron potentiates oxygen toxicity. Strict regulation of iron metabolism, and its coupling with regulation of defenses against oxidative stress, is an essential factor for life in the presence of oxygen. In Escherichia coli, iron metabolism is regulated by the Fur protein. A Fur-deficient mutant, in stationary phase, displayed about 30y-fold lower HPII activity than the respective, Fur-proficient parental strain. Deletion of fur seems to affect HPII catalase specifically, since the mutant was capable of inducing HPI catalase when challenged with H(2)O(2). Low HPII catalase activity appears to be among the reasons for hydrogen peroxide hypersensitivity of the deltafur mutant.

摘要

铁是细菌所使用的最重要的微量营养素之一。然而,作为芬顿反应的参与者,铁会增强氧毒性。严格调控铁代谢,并将其与抗氧化应激防御的调控相结合,是在有氧环境中生存的关键因素。在大肠杆菌中,铁代谢由Fur蛋白调控。处于稳定期的Fur缺陷型突变体的HPII活性比相应的Fur功能正常的亲本菌株低约30倍。fur基因的缺失似乎特异性地影响HPII过氧化氢酶,因为该突变体在用H₂O₂刺激时能够诱导HPI过氧化氢酶。低HPII过氧化氢酶活性似乎是Δfur突变体对过氧化氢超敏的原因之一。

相似文献

1
Escherichia coli deltafur mutant displays low HPII catalase activity in stationary phase.大肠杆菌Δfur突变体在稳定期显示出低HPII过氧化氢酶活性。
Redox Rep. 2003;8(6):379-83. doi: 10.1179/135100003225003357.
2
Reduced hydroperoxidase (HPI and HPII) activity in the Deltafur mutant contributes to increased sensitivity to UVA radiation in Escherichia coli.Deltafur突变体中氢过氧化物酶(HPI和HPII)活性降低导致大肠杆菌对紫外线辐射的敏感性增加。
J Photochem Photobiol B. 2005 May 13;79(2):151-7. doi: 10.1016/j.jphotobiol.2005.01.003.
3
Growth of Escherichia coli in iron-enriched medium increases HPI catalase activity.大肠杆菌在富含铁的培养基中生长会增加HPI过氧化氢酶活性。
J Biochem Mol Biol. 2003 Nov 30;36(6):608-10. doi: 10.5483/bmbrep.2003.36.6.608.
4
Contributions of ferric uptake regulator Fur to the sensitivity and oxidative response of Acinetobacter baumannii to antibiotics.铁摄取调节因子 Fur 对鲍曼不动杆菌对抗生素敏感性和氧化应激反应的贡献。
Microb Pathog. 2018 Jun;119:35-41. doi: 10.1016/j.micpath.2018.03.060. Epub 2018 Mar 31.
5
Regulation of hydroperoxidase (catalase) expression in Escherichia coli.大肠杆菌中氢过氧化物酶(过氧化氢酶)表达的调控
FEMS Microbiol Lett. 1995 Sep 1;131(2):113-9. doi: 10.1111/j.1574-6968.1995.tb07764.x.
6
Submicromolar hydrogen peroxide disrupts the ability of Fur protein to control free-iron levels in Escherichia coli.亚微摩尔浓度的过氧化氢会破坏铁摄取调节蛋白(Fur)控制大肠杆菌中游离铁水平的能力。
Mol Microbiol. 2007 May;64(3):822-30. doi: 10.1111/j.1365-2958.2007.05701.x.
7
Hypochlorous acid stress in Escherichia coli: resistance, DNA damage, and comparison with hydrogen peroxide stress.大肠杆菌中的次氯酸应激:抗性、DNA损伤以及与过氧化氢应激的比较。
J Bacteriol. 1996 Nov;178(21):6145-50. doi: 10.1128/jb.178.21.6145-6150.1996.
8
RpoS- and OxyR-independent induction of HPI catalase at stationary phase in Escherichia coli and identification of rpoS mutations in common laboratory strains.大肠杆菌稳定期RpoS和OxyR非依赖性诱导HPI过氧化氢酶及常见实验室菌株中rpoS突变的鉴定
J Bacteriol. 1997 Jul;179(13):4158-63. doi: 10.1128/jb.179.13.4158-4163.1997.
9
Up-expression of NapA and other oxidative stress proteins is a compensatory response to loss of major Helicobacter pylori stress resistance factors.NapA和其他氧化应激蛋白的上调表达是对幽门螺杆菌主要应激抗性因子丧失的一种补偿性反应。
Free Radic Res. 2005 Nov;39(11):1173-82. doi: 10.1080/10715760500306729.
10
Substantial DNA damage from submicromolar intracellular hydrogen peroxide detected in Hpx- mutants of Escherichia coli.在大肠杆菌的Hpx-突变体中检测到亚微摩尔浓度的细胞内过氧化氢造成的大量DNA损伤。
Proc Natl Acad Sci U S A. 2005 Jun 28;102(26):9317-22. doi: 10.1073/pnas.0502051102. Epub 2005 Jun 20.

引用本文的文献

1
Manipulating Intracellular Oxidative Conditions to Enhance Porphyrin Production in .通过调控细胞内氧化条件提高卟啉产量
Bioengineering (Basel). 2025 Jan 17;12(1):83. doi: 10.3390/bioengineering12010083.
2
Effects of the Quinone Oxidoreductase WrbA on Biofilm Formation and Oxidative Stress.醌氧化还原酶WrbA对生物膜形成和氧化应激的影响
Antioxidants (Basel). 2021 Jun 6;10(6):919. doi: 10.3390/antiox10060919.
3
Small RNA ArcZ Regulates Oxidative Stress Response Genes and Regulons in .小RNA ArcZ调节氧化应激反应基因及调控子
Front Microbiol. 2019 Nov 29;10:2775. doi: 10.3389/fmicb.2019.02775. eCollection 2019.
4
Transcriptional regulation by Ferric Uptake Regulator (Fur) in pathogenic bacteria.致病细菌中铁摄取调节因子(Fur)的转录调控。
Front Cell Infect Microbiol. 2013 Oct 2;3:59. doi: 10.3389/fcimb.2013.00059. eCollection 2013.
5
Regulation of catalase-peroxidase KatG is OxyR dependent and Fur independent in Caulobacter crescentus.新月柄杆菌中过氧化氢酶-过氧化物酶 KatG 的调控依赖于 OxyR 而不依赖于 Fur。
J Bacteriol. 2011 Apr;193(7):1734-44. doi: 10.1128/JB.01339-10. Epub 2011 Jan 21.