The mechanism of oxygen sensing by the global transcriptional regulator FNR
全局转录调节因子 FNR 的氧传感机制
基本信息
- 批准号:BB/G018960/1
- 负责人:
- 金额:$ 35.19万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2010
- 资助国家:英国
- 起止时间:2010 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Bacteria inhabit almost every environmental niche on Earth, including some that are so harsh that many other forms of life cannot survive. This success is at least in part due to the ability of bacteria to adapt to changes in environment, and this adaptation is rooted in their capacity to alter patterns of gene expression in response to external and internal cues. A key environmental parameter that is monitored by many bacteria is oxygen concentration. We are particularly interested in the bacterium Escherichia coli (E. coli). One of its remarkable properties is that it is able to thrive both in the presence and absence of oxygen. To do this it has to dramatically alter its metabolism, but this has consequences because without oxygen the potential for energy conservation and growth are limited compared to when oxygen is present. To test whether oxygen is present E. coli uses a protein called FNR, which acts as an oxygen sensor. It has a special co-factor called an iron-sulfur cluster that reacts with oxygen in a way that switches FNR off. In the 'off-state' (no iron-sulfur cluster) FNR cannot bind to DNA to activate expression of genes that are used during growth in the absence of oxygen. When there is no oxygen the iron-sulfur remains associated with FNR and so the protein can bind to DNA and activate expression of genes that are needed for growth in the absence of oxygen. For the last few years we have studied the reaction of oxygen with the FNR iron-sulfur cluster. These studies have revealed the complex biochemistry of the reaction and how this makes the FNR protein an exquisitely sensitive oxygen sensor. However, our studies have raised even more questions. We now propose to address some of these by determining the molecular choreography of the reaction of oxygen with the FNR iron-sulfur cluster and how this leads to altered DNA-binding properties. We will also investigate how the potentially toxic reaction products are managed by the cell, and why some bacteria have more than one FNR protein; could it be that different FNR proteins have evolved to operate in different ranges of oxygen concentration? The work is important at several levels. It will allow us to understand more about a basic biological process that is fundamental for the virulent properties of many bacterial pathogens, such as Salmonella and E. coli. It will provide new insight and a deeper understanding of an ancient class of proteins that evolved in an anaerobic world. It has wider significance for how signal perception and signal transduction are linked in a ubiquitous family of bacterial gene regulators. And finally, it offers possibilities of designing molecular switches that will respond to changes in oxygen levels for use in biotechnology.
细菌几乎栖息在地球上的每一个生态位,包括一些恶劣到许多其他形式的生命无法生存的环境。这种成功至少部分是由于细菌适应环境变化的能力,这种适应植根于它们根据外部和内部线索改变基因表达模式的能力。许多细菌监测的一个关键环境参数是氧浓度。我们对大肠杆菌(E. coli)特别感兴趣。它的一个显著特性是它能够在有氧和没有氧的情况下茁壮成长。要做到这一点,它必须极大地改变它的新陈代谢,但这有后果,因为没有氧气,与有氧气时相比,能量节约和生长的潜力是有限的。为了测试是否有氧气存在,大肠杆菌使用一种叫做FNR的蛋白质,它起到氧气传感器的作用。它有一种特殊的辅助因子,叫做铁硫簇,它与氧反应,以一种关闭FNR的方式。在“关闭状态”(没有铁硫簇)下,FNR不能与DNA结合以激活在缺氧条件下生长过程中使用的基因表达。当没有氧气时,铁硫仍然与FNR相关,因此蛋白质可以与DNA结合,并激活在缺乏氧气的情况下生长所需的基因表达。在过去的几年里,我们研究了氧与FNR铁硫团簇的反应。这些研究揭示了该反应的复杂生物化学原理,以及FNR蛋白是如何成为极其敏感的氧传感器的。然而,我们的研究提出了更多的问题。我们现在建议通过确定氧与FNR铁硫簇反应的分子编排以及这如何导致dna结合特性的改变来解决其中的一些问题。我们还将研究细胞如何管理潜在毒性反应产物,以及为什么一些细菌具有多个FNR蛋白;是不是不同的FNR蛋白已经进化到在不同的氧浓度范围内工作?这项工作在几个层面上都很重要。它将使我们更多地了解一个基本的生物过程,这是许多细菌病原体(如沙门氏菌和大肠杆菌)毒性特性的基础。它将为在厌氧环境中进化的一类古老蛋白质提供新的见解和更深入的理解。这对于信号感知和信号转导如何在一个无处不在的细菌基因调控家族中联系起来具有更广泛的意义。最后,它提供了设计分子开关的可能性,这种开关将对用于生物技术的氧气水平的变化作出反应。
项目成果
期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Systems analysis of transcription factor activities in environments with stable and dynamic oxygen concentrations.
- DOI:10.1098/rsob.120091
- 发表时间:2012-07
- 期刊:
- 影响因子:5.8
- 作者:Rolfe MD;Ocone A;Stapleton MR;Hall S;Trotter EW;Poole RK;Sanguinetti G;Green J;SysMO-SUMO Consortium
- 通讯作者:SysMO-SUMO Consortium
Structure-function relationships of the Mycobacterium tuberculosis transcription factor WhiB1.
- DOI:10.1371/journal.pone.0040407
- 发表时间:2012
- 期刊:
- 影响因子:3.7
- 作者:Smith LJ;Stapleton MR;Buxton RS;Green J
- 通讯作者:Green J
Three Pseudomonas putida FNR Family Proteins with Different Sensitivities to O2.
- DOI:10.1074/jbc.m115.654079
- 发表时间:2015-07-03
- 期刊:
- 影响因子:0
- 作者:Ibrahim SA;Crack JC;Rolfe MD;Borrero-de Acuña JM;Thomson AJ;Le Brun NE;Schobert M;Stapleton MR;Green J
- 通讯作者:Green J
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J Green其他文献
Questioning the usefulness of 24-hour recall of exclusive breastfeeding
质疑 24 小时回忆纯母乳喂养的有用性
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
K Nanishi;J Green;A Shibanuma;H Hongo - 通讯作者:
H Hongo
Effects of magnesium supplementation on erythrocyte cation transport in diuretic-treated hypertensives
- DOI:
10.1016/s0271-5317(89)80151-4 - 发表时间:
1989-11-01 - 期刊:
- 影响因子:
- 作者:
MB Zemel;J Green;PC Zemel;F Douglas;R Geiser;JR Sowers - 通讯作者:
JR Sowers
EE735 A New Post-Diagnostic Psycho-Education and Acceptance and Commitment Therapy Program for Caregivers of Children Recently Diagnosed With Autism Spectrum Disorder (REACH-ASD): A Trial-Based Cost-Effectiveness Analysis
EE735 一项针对近期被诊断患有自闭症谱系障碍儿童的照顾者的新的诊断后心理教育与接受与承诺疗法方案(REACH-ASD):一项基于试验的成本效益分析
- DOI:
10.1016/j.jval.2024.10.1015 - 发表时间:
2024-12-01 - 期刊:
- 影响因子:6.000
- 作者:
G Shields;A Rowlandson;L Davies;K Leadbitter;J Green - 通讯作者:
J Green
Substrate specificity of soluble methane monooxygenase: Mechanistic implications
- DOI:
10.1016/s0021-9258(19)84627-6 - 发表时间:
1989-10-25 - 期刊:
- 影响因子:
- 作者:
J Green;H Dalton - 通讯作者:
H Dalton
EE232 Collecting Economic Data From Global Autism Spectrum Disorder (ASD) Research: A Comparison From the UK and India
EE232 从全球自闭症谱系障碍(ASD)研究中收集经济数据:来自英国和印度的比较
- DOI:
10.1016/j.jval.2024.10.514 - 发表时间:
2024-12-01 - 期刊:
- 影响因子:6.000
- 作者:
R Roy;G Shields;P Verma;SS Dash;D Jangra;J Green;K Leadbitter;G Divan - 通讯作者:
G Divan
J Green的其他文献
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{{ truncateString('J Green', 18)}}的其他基金
Enhanced Biofuel Production via Integrated Microbubble Technology
通过集成微泡技术提高生物燃料生产
- 批准号:
EP/N011511/1 - 财政年份:2016
- 资助金额:
$ 35.19万 - 项目类别:
Research Grant
Crossing biological membranes: Engineering the cell-environment interface to improve process efficiency
穿过生物膜:设计细胞-环境界面以提高过程效率
- 批准号:
BB/L013703/1 - 财政年份:2014
- 资助金额:
$ 35.19万 - 项目类别:
Research Grant
A new pathway for iron-sulfur cluster repair
铁硫簇修复的新途径
- 批准号:
BB/L008114/1 - 财政年份:2014
- 资助金额:
$ 35.19万 - 项目类别:
Research Grant
Integrating cAMP- and nitric oxide- signalling in Mycobacterium tuberculosis: novel regulatory networks that challenge established paradigms
在结核分枝杆菌中整合 cAMP 和一氧化氮信号传导:挑战既定范例的新型调控网络
- 批准号:
BB/K000071/1 - 财政年份:2012
- 资助金额:
$ 35.19万 - 项目类别:
Research Grant
Characterization of an anaerobic Escherichia coli K-12 cyclic-di-GMP phosphodiesterase
厌氧大肠杆菌 K-12 环二 GMP 磷酸二酯酶的表征
- 批准号:
BB/G006024/1 - 财政年份:2009
- 资助金额:
$ 35.19万 - 项目类别:
Research Grant
The Escherichia coli YfiD protein: an oxygen and acidity responsive regulator of carbon flux
大肠杆菌 YfiD 蛋白:碳通量的氧和酸度响应调节剂
- 批准号:
BB/E019943/1 - 财政年份:2007
- 资助金额:
$ 35.19万 - 项目类别:
Research Grant
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