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本文引用的文献

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Structure and mechanism of mitochondrial electron transport chain.线粒体电子传递链的结构与机制。
Biomed J. 2018 Feb;41(1):9-20. doi: 10.1016/j.bj.2017.12.001. Epub 2018 Mar 26.
2
On the nature of organic and inorganic centers that bifurcate electrons, coupling exergonic and endergonic oxidation-reduction reactions.关于使电子分叉、偶联放能和吸能氧化还原反应的有机和无机中心的性质。
Chem Commun (Camb). 2018 Apr 19;54(33):4091-4099. doi: 10.1039/c8cc01530a.
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Flavin-Based Electron Bifurcation, Ferredoxin, Flavodoxin, and Anaerobic Respiration With Protons (Ech) or NAD (Rnf) as Electron Acceptors: A Historical Review.以黄素为基础的电子分叉、铁氧化还原蛋白、黄素氧化还原蛋白以及以质子(Ech)或NAD(Rnf)作为电子受体的无氧呼吸:历史回顾
Front Microbiol. 2018 Mar 14;9:401. doi: 10.3389/fmicb.2018.00401. eCollection 2018.
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Flavin-Based Electron Bifurcation, A New Mechanism of Biological Energy Coupling.基于黄素的电子分支:生物能量耦合的新机制。
Chem Rev. 2018 Apr 11;118(7):3862-3886. doi: 10.1021/acs.chemrev.7b00707. Epub 2018 Mar 21.
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Molecular basis of the flavin-based electron-bifurcating caffeyl-CoA reductase reaction.基于黄素的电子分叉咖啡酰辅酶 A 还原酶反应的分子基础。
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The semiquinone swing in the bifurcating electron transferring flavoprotein/butyryl-CoA dehydrogenase complex from Clostridium difficile.双歧电子转移黄素蛋白/丁酰基辅酶 A 脱氢酶复合物中来自艰难梭菌的半醌摆动。
Nat Commun. 2017 Nov 17;8(1):1577. doi: 10.1038/s41467-017-01746-3.
7
H/D exchange mass spectrometry and statistical coupling analysis reveal a role for allostery in a ferredoxin-dependent bifurcating transhydrogenase catalytic cycle.H/D 交换质谱和统计偶联分析揭示变构作用在依赖于铁氧还蛋白的分叉氢载体酶催化循环中的作用。
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Electron Bifurcation: Thermodynamics and Kinetics of Two-Electron Brokering in Biological Redox Chemistry.电子分支:生物氧化还原化学中两电子代理的热力学和动力学。
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Methanogenic heterodisulfide reductase (HdrABC-MvhAGD) uses two noncubane [4Fe-4S] clusters for reduction.产甲烷异二硫键还原酶 (HdrABC-MvhAGD) 使用两个非立方烷 [4Fe-4S] 簇进行还原。
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Defining Electron Bifurcation in the Electron-Transferring Flavoprotein Family.确定电子传递黄素蛋白家族中的电子分叉
J Bacteriol. 2017 Oct 3;199(21). doi: 10.1128/JB.00440-17. Print 2017 Nov 1.

电子分裂的新纪元。

A new era for electron bifurcation.

机构信息

Institute of Biological Chemistry, Washington State University, Pullman WA 99163, United States; Pacific Northwest National Laboratory, Richland, WA 99352, United States.

Department of Chemistry and Department of Physics, Duke University, Durham, NC 27708, United States; Department of Biochemistry, Duke University, Durham, NC 27710, United States.

出版信息

Curr Opin Chem Biol. 2018 Dec;47:32-38. doi: 10.1016/j.cbpa.2018.07.026. Epub 2018 Aug 1.

DOI:10.1016/j.cbpa.2018.07.026
PMID:30077080
原文链接:
https://pmc.ncbi.nlm.nih.gov/articles/PMC9113080/
Abstract

Electron bifurcation, or the coupling of exergonic and endergonic oxidation-reduction reactions, was discovered by Peter Mitchell and provides an elegant mechanism to rationalize and understand the logic that underpins the Q cycle of the respiratory chain. Thought to be a unique reaction of respiratory complex III for nearly 40 years, about a decade ago Wolfgang Buckel and Rudolf Thauer discovered that flavin-based electron bifurcation is also an important component of anaerobic microbial metabolism. Their discovery spawned a surge of research activity, providing a basis to understand flavin-based bifurcation, forging fundamental parallels with Mitchell's Q cycle and leading to the proposal of metal-based bifurcating enzymes. New insights into the mechanism of electron bifurcation provide a foundation to establish the unifying principles and essential elements of this fascinating biochemical phenomenon.

摘要

电子分支,或释能和吸能氧化还原反应的偶联,由彼得·米切尔(Peter Mitchell)发现,为合理化和理解呼吸链 Q 循环的逻辑提供了一个优雅的机制。电子分支被认为是呼吸复合物 III 的独特反应近 40 年,大约十年前,沃尔夫冈·布克尔(Wolfgang Buckel)和鲁道夫·萨瑟(Rudolf Thauer)发现黄素基电子分支也是厌氧微生物代谢的重要组成部分。他们的发现引发了研究热潮,为理解黄素基分支提供了基础,与米切尔的 Q 循环建立了基本的平行关系,并导致了基于金属的分支酶的提出。对电子分支机制的新见解为建立这一迷人生化现象的统一原则和基本要素提供了基础。