• 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

厌氧培养的大肠杆菌细胞中NADH脱氢酶I和二甲基亚砜还原酶的H⁺/e⁻化学计量学

H+/e- stoichiometry for NADH dehydrogenase I and dimethyl sulfoxide reductase in anaerobically grown Escherichia coli cells.

作者信息

Bogachev A V, Murtazina R A, Skulachev V P

机构信息

Department of Bioenergetics, A.N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Russia.

出版信息

J Bacteriol. 1996 Nov;178(21):6233-7. doi: 10.1128/jb.178.21.6233-6237.1996.

DOI:10.1128/jb.178.21.6233-6237.1996
PMID:8892824
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178495/
Abstract

Anaerobically grown Escherichia coli cells were shown to acidify the reaction medium in response to oxygen or dimethyl sulfoxide (DMSO) pulses, with the H+/e- stoichiometry being close to 2.5 and 1.5, respectively. In the presence of the NADH dehydrogenase I (NDH-I) inhibitor 8-methyl-N-vanillyl-6-nonenamide (capsaicin) or in mutants lacking NDH-I, this ratio decreased to 1 for O2 and to 0 for DMSO. These data suggest that (i) the H+/e- stoichiometry for E. coli NDH-I is at least 1.5 and (ii) the DMSO reductase does not generate a proton motive force.

摘要

厌氧培养的大肠杆菌细胞在氧气或二甲基亚砜(DMSO)脉冲刺激下会使反应培养基酸化,H⁺/e⁻化学计量比分别接近2.5和1.5。在存在NADH脱氢酶I(NDH-I)抑制剂8-甲基-N-香草基-6-壬酰胺(辣椒素)时,或在缺乏NDH-I的突变体中,该比例对于氧气降至1,对于DMSO降至0。这些数据表明:(i)大肠杆菌NDH-I的H⁺/e⁻化学计量比至少为1.5;(ii)DMSO还原酶不会产生质子动力。

相似文献

1
H+/e- stoichiometry for NADH dehydrogenase I and dimethyl sulfoxide reductase in anaerobically grown Escherichia coli cells.厌氧培养的大肠杆菌细胞中NADH脱氢酶I和二甲基亚砜还原酶的H⁺/e⁻化学计量学
J Bacteriol. 1996 Nov;178(21):6233-7. doi: 10.1128/jb.178.21.6233-6237.1996.
2
Dimethyl sulfoxide reductase activity by anaerobically grown Escherichia coli HB101.厌氧培养的大肠杆菌HB101的二甲基亚砜还原酶活性。
J Bacteriol. 1985 Jun;162(3):1151-5. doi: 10.1128/jb.162.3.1151-1155.1985.
3
Molecular cloning and expression of the Escherichia coli dimethyl sulfoxide reductase operon.大肠杆菌二甲基亚砜还原酶操纵子的分子克隆与表达
J Bacteriol. 1988 Apr;170(4):1511-8. doi: 10.1128/jb.170.4.1511-1518.1988.
4
Requirement for the proton-pumping NADH dehydrogenase I of Escherichia coli in respiration of NADH to fumarate and its bioenergetic implications.大肠杆菌质子泵NADH脱氢酶I在NADH呼吸生成延胡索酸过程中的需求及其生物能量学意义。
Eur J Biochem. 1997 Feb 15;244(1):155-60. doi: 10.1111/j.1432-1033.1997.00155.x.
5
Dimethyl sulfoxide reductase is not required for trimethylamine N-oxide reduction in Escherichia coli.
FEMS Microbiol Lett. 1991 Oct 15;67(3):255-9. doi: 10.1016/0378-1097(91)90485-s.
6
Proton translocation coupled to dimethyl sulfoxide reduction in anaerobically grown Escherichia coli HB101.在厌氧培养的大肠杆菌HB101中,质子转运与二甲基亚砜还原相偶联。
J Bacteriol. 1985 Jul;163(1):369-75. doi: 10.1128/jb.163.1.369-375.1985.
7
Purification and properties of Escherichia coli dimethyl sulfoxide reductase, an iron-sulfur molybdoenzyme with broad substrate specificity.大肠杆菌二甲基亚砜还原酶的纯化及性质,一种具有广泛底物特异性的铁硫钼酶。
J Bacteriol. 1988 Apr;170(4):1505-10. doi: 10.1128/jb.170.4.1505-1510.1988.
8
Studies on the proton-translocating NADH:ubiquinone oxidoreductases of mitochondria and Escherichia coli using the inhibitor 1,10-phenanthroline.
FEBS Lett. 1994 Feb 14;339(1-2):142-6. doi: 10.1016/0014-5793(94)80402-8.
9
Characterization of an NADH-linked cupric reductase activity from the Escherichia coli respiratory chain.大肠杆菌呼吸链中一种与NADH相关的铜还原酶活性的表征。
Arch Biochem Biophys. 1999 Oct 15;370(2):143-50. doi: 10.1006/abbi.1999.1398.
10
Effect of microaerophilic cell growth conditions on expression of the aerobic (cyoABCDE and cydAB) and anaerobic (narGHJI, frdABCD, and dmsABC) respiratory pathway genes in Escherichia coli.微需氧细胞生长条件对大肠杆菌中需氧呼吸途径基因(cyoABCDE和cydAB)及厌氧呼吸途径基因(narGHJI、frdABCD和dmsABC)表达的影响。
J Bacteriol. 1996 Feb;178(4):1094-8. doi: 10.1128/jb.178.4.1094-1098.1996.

引用本文的文献

1
Respiratory complex I with charge symmetry in the membrane arm pumps protons.具有膜臂电荷对称性的呼吸复合物 I 泵质子。
Proc Natl Acad Sci U S A. 2022 Jul 5;119(27):e2123090119. doi: 10.1073/pnas.2123090119. Epub 2022 Jun 27.
2
Paracoccus denitrificans: a genetically tractable model system for studying respiratory complex I.脱氮副球菌:研究呼吸复合物 I 的遗传上可操作的模型系统。
Sci Rep. 2021 May 12;11(1):10143. doi: 10.1038/s41598-021-89575-9.
3
Metabolic energy conservation for fermentative product formation.代谢能量守恒与发酵产物形成。
Microb Biotechnol. 2021 May;14(3):829-858. doi: 10.1111/1751-7915.13746. Epub 2021 Jan 13.
4
Spotlight on the Energy Harvest of Electroactive Microorganisms: The Impact of the Applied Anode Potential.电活性微生物能量获取聚焦:外加阳极电位的影响
Front Microbiol. 2019 Jun 26;10:1352. doi: 10.3389/fmicb.2019.01352. eCollection 2019.
5
Respiratory Complex I in and Pumps Four Protons across the Membrane for Every NADH Oxidized.呼吸链复合体I每氧化一分子NADH可将四个质子泵过膜。
J Biol Chem. 2017 Mar 24;292(12):4987-4995. doi: 10.1074/jbc.M116.771899. Epub 2017 Feb 7.
6
Roles of subunit NuoL in the proton pumping coupling mechanism of NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli.亚基NuoL在大肠杆菌NADH:泛醌氧化还原酶(复合体I)质子泵浦偶联机制中的作用
J Biochem. 2016 Oct;160(4):205-215. doi: 10.1093/jb/mvw027. Epub 2016 Apr 26.
7
Roles of semiquinone species in proton pumping mechanism by complex I.半醌类物质在复合体I质子泵浦机制中的作用。
J Bioenerg Biomembr. 2014 Aug;46(4):269-77. doi: 10.1007/s10863-014-9557-9. Epub 2014 Jul 31.
8
On the mechanism of respiratory complex I.关于呼吸复合体I的机制。
J Bioenerg Biomembr. 2014 Aug;46(4):255-68. doi: 10.1007/s10863-014-9566-8. Epub 2014 Jul 15.
9
Analysis of Escherichia coli mutants with a linear respiratory chain.具有线性呼吸链的大肠杆菌突变体分析。
PLoS One. 2014 Jan 27;9(1):e87307. doi: 10.1371/journal.pone.0087307. eCollection 2014.
10
Evidence for a key role of cytochrome bo3 oxidase in respiratory energy metabolism of Gluconobacter oxydans.证明细胞色素 bo3 氧化酶在氧化葡萄糖杆菌呼吸能量代谢中的关键作用。
J Bacteriol. 2013 Sep;195(18):4210-20. doi: 10.1128/JB.00470-13. Epub 2013 Jul 12.

本文引用的文献

1
Role of uncoupled and non-coupled oxidations in maintenance of safely low levels of oxygen and its one-electron reductants.
Q Rev Biophys. 1996 May;29(2):169-202. doi: 10.1017/s0033583500005795.
2
Demonstration of separate genetic loci encoding distinct membrane-bound respiratory NADH dehydrogenases in Escherichia coli.在大肠杆菌中编码不同膜结合呼吸型NADH脱氢酶的独立基因座的证明。
J Bacteriol. 1993 May;175(10):3013-9. doi: 10.1128/jb.175.10.3013-3019.1993.
3
Escherichia coli mutants lacking NADH dehydrogenase I have a competitive disadvantage in stationary phase.缺乏NADH脱氢酶I的大肠杆菌突变体在稳定期具有竞争劣势。
J Bacteriol. 1993 Sep;175(17):5642-7. doi: 10.1128/jb.175.17.5642-5647.1993.
4
Kinetics, control, and mechanism of ubiquinone reduction by the mammalian respiratory chain-linked NADH-ubiquinone reductase.哺乳动物呼吸链相关的NADH-泛醌还原酶催化泛醌还原的动力学、调控及机制
J Bioenerg Biomembr. 1993 Aug;25(4):367-75. doi: 10.1007/BF00762462.
5
Bacterial NADH-quinone oxidoreductases: iron-sulfur clusters and related problems.细菌NADH-醌氧化还原酶:铁硫簇及相关问题。
J Bioenerg Biomembr. 1993 Aug;25(4):347-56. doi: 10.1007/BF00762460.
6
Isolation and characterization of the proton-translocating NADH: ubiquinone oxidoreductase from Escherichia coli.来自大肠杆菌的质子转运型NADH:泛醌氧化还原酶的分离与特性分析
Eur J Biochem. 1995 Jun 1;230(2):538-48. doi: 10.1111/j.1432-1033.1995.tb20594.x.
7
Transcriptional regulation of the proton translocating NADH dehydrogenase genes (nuoA-N) of Escherichia coli by electron acceptors, electron donors and gene regulators.电子受体、电子供体和基因调控因子对大肠杆菌质子转运型NADH脱氢酶基因(nuoA-N)的转录调控
Mol Microbiol. 1995 May;16(3):521-34. doi: 10.1111/j.1365-2958.1995.tb02416.x.
8
The respiratory chains of Escherichia coli.大肠杆菌的呼吸链
Microbiol Rev. 1984 Sep;48(3):222-71. doi: 10.1128/mr.48.3.222-271.1984.
9
Two protons are pumped from the mitochondrial matrix per electron transferred between NADH and ubiquinone.在NADH和泛醌之间每转移一个电子,就有两个质子从线粒体基质泵出。
FEBS Lett. 1984 Apr 24;169(2):300-4. doi: 10.1016/0014-5793(84)80338-5.
10
Thermodynamic limits to the ATP/site stoichiometries of oxidative phosphorylation by rat liver mitochondria.大鼠肝脏线粒体氧化磷酸化过程中ATP/位点化学计量的热力学极限
J Biol Chem. 1984 Mar 10;259(5):3058-63.