Cape Jonathan L, Bowman Michael K, Kramer David M
Institute of Biological Chemistry, Washington State University, 289 Clark Hall, Pullman, WA 99164-6314, USA.
Trends Plant Sci. 2006 Jan;11(1):46-55. doi: 10.1016/j.tplants.2005.11.007. Epub 2005 Dec 13.
The cytochrome (cyt) bc(1), b(6)f and related complexes are central components of the respiratory and photosynthetic electron transport chains. These complexes carry out an extraordinary sequence of electron and proton transfer reactions that conserve redox energy in the form of a trans-membrane proton motive force for use in synthesizing ATP and other processes. Thirty years ago, Peter Mitchell proposed a general turnover mechanism for these complexes, which he called the Q-cycle. Since that time, many opposing schemes have challenged the Q-cycle but, with the accumulation of large amounts of biochemical, kinetic, thermodynamic and high-resolution structural data, the Q-cycle has triumphed as the accepted model, although some of the intermediate steps are poorly understood and still controversial. One of the major research questions concerning the cyt bc(1) and b(6)f complexes is how these enzymes suppress deleterious and dissipative side reactions. In particular, most Q-cycle models involve reactive semiquinone radical intermediates that can reduce O(2) to superoxide and lead to cellular oxidative stress. Current models to explain the avoidance of side reactions involve unprecedented or unusual enzyme mechanisms, the testing of which will involve new theoretical and experimental approaches.
细胞色素(cyt)bc(1)、b(6)f及相关复合物是呼吸和光合电子传递链的核心组成部分。这些复合物执行一系列非凡的电子和质子转移反应,以跨膜质子动力的形式保存氧化还原能量,用于合成ATP及其他过程。三十年前,彼得·米切尔提出了这些复合物的一种通用周转机制,他称之为Q循环。从那时起,许多相反的方案对Q循环提出了挑战,但是,随着大量生化、动力学、热力学和高分辨率结构数据的积累,Q循环已作为被接受的模型取得了胜利,尽管一些中间步骤仍了解甚少且存在争议。关于细胞色素bc(1)和b(6)f复合物的主要研究问题之一是这些酶如何抑制有害的和耗散性的副反应。特别是,大多数Q循环模型涉及反应性半醌自由基中间体,其可将O(2)还原为超氧化物并导致细胞氧化应激。目前解释避免副反应的模型涉及前所未有的或不寻常的酶机制,对其进行测试将需要新的理论和实验方法。