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重新审视氧化磷酸化。

Oxidative phosphorylation revisited.

作者信息

Nath Sunil, Villadsen John

机构信息

Department of Biochemical Engineering and Biotechnology, Indian Institute of Technology, Delhi, Hauz Khas, New Delhi, 110016, India; Department of Chemical and Biochemical Engineering, Technical University of Denmark, Lyngby, DK-2800, Denmark.

出版信息

Biotechnol Bioeng. 2015 Mar;112(3):429-37. doi: 10.1002/bit.25492. Epub 2015 Jan 2.

Abstract

The fundamentals of oxidative phosphorylation and photophosphorylation are revisited. New experimental data on the involvement of succinate and malate anions respectively in oxidative phosphorylation and photophosphorylation are presented. These new data offer a novel molecular mechanistic explanation for the energy coupling and ATP synthesis carried out in mitochondria and chloroplast thylakoids. The mechanism does not suffer from the flaws in Mitchell's chemiosmotic theory that have been pointed out in many studies since its first appearance 50 years ago, when it was hailed as a ground-breaking mechanistic explanation of what is perhaps the most important process in cellular energetics. The new findings fit very well with the predictions of Nath's torsional mechanism of energy transduction and ATP synthesis. It is argued that this mechanism, based on at least 15 years of experimental and theoretical work by Sunil Nath, constitutes a fundamentally different theory of the energy conversion process that eliminates all the inconsistencies in Mitchell's chemiosmotic theory pointed out by other authors. It is concluded that the energy-transducing complexes in oxidative phosphorylation and photosynthesis are proton-dicarboxylic acid anion cotransporters and not simply electrogenic proton translocators. These results necessitate revision of previous theories of biological energy transduction, coupling, and ATP synthesis. The novel molecular mechanism is extended to cover ATP synthesis in prokaryotes, in particular to alkaliphilic and haloalkaliphilic bacteria, essentially making it a complete theory addressing mechanistic, kinetic, and thermodynamic details. Finally, based on the new interpretation of oxidative phosphorylation, quantitative values for the P/O ratio, the amount of ATP generated per redox package of the reduced substrates, are calculated and compared with experimental values for fermentation on different substrates. It is our hope that the presentation of oxidative phosphorylation and photophosphorylation from a wholly new perspective will rekindle scientific discussion of a key process in bioenergetics and catalyze new avenues of research in a truly interdisciplinary field.

摘要

本文重新审视了氧化磷酸化和光合磷酸化的基本原理。文中展示了关于琥珀酸根阴离子和苹果酸根阴离子分别参与氧化磷酸化和光合磷酸化的新实验数据。这些新数据为线粒体和叶绿体类囊体中进行的能量偶联和ATP合成提供了一种全新的分子机制解释。该机制不存在米切尔化学渗透理论中的缺陷,自50年前该理论首次出现以来,许多研究都指出了这些缺陷,当时它被誉为对细胞能量学中可能是最重要过程的开创性机制解释。新发现与纳特能量转导和ATP合成的扭转机制的预测非常吻合。有人认为,基于苏尼尔·纳特至少15年的实验和理论工作,这一机制构成了一种从根本上不同的能量转换过程理论,消除了其他作者指出的米切尔化学渗透理论中的所有矛盾之处。得出的结论是,氧化磷酸化和光合作用中的能量转导复合物是质子 - 二羧酸阴离子共转运体,而不仅仅是生电质子转运体。这些结果需要对先前的生物能量转导、偶联和ATP合成理论进行修订。这种新的分子机制被扩展到涵盖原核生物中的ATP合成,特别是嗜碱和嗜盐嗜碱细菌中的ATP合成,基本上使其成为一个涉及机制、动力学和热力学细节的完整理论。最后,基于对氧化磷酸化的新解释,计算了P/O比(即每还原底物的氧化还原包产生的ATP量)的定量值,并与不同底物发酵的实验值进行了比较。我们希望从全新的角度阐述氧化磷酸化和光合磷酸化,将重新激发对生物能量学中一个关键过程的科学讨论,并催化一个真正跨学科领域的新研究途径。

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