Lee Hyun Ju, Reimann Joachim, Huang Yafei, Adelroth Pia
Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
Biochim Biophys Acta. 2012 Apr;1817(4):537-44. doi: 10.1016/j.bbabio.2011.10.007. Epub 2011 Oct 26.
Heme-copper oxidases (HCuOs) terminate the respiratory chain in mitochondria and most bacteria. They are transmembrane proteins that catalyse the reduction of oxygen and use the liberated free energy to maintain a proton-motive force across the membrane. The HCuO superfamily has been divided into the oxygen-reducing A-, B- and C-type oxidases as well as the bacterial NO reductases (NOR), catalysing the reduction of NO in the denitrification process. Proton transfer to the catalytic site in the mitochondrial-like A family occurs through two well-defined pathways termed the D- and K-pathways. The B, C, and NOR families differ in the pathways as well as the mechanisms for proton transfer to the active site and across the membrane. Recent structural and functional investigations, focussing on proton transfer in the B, C and NOR families will be discussed in this review.
血红素铜氧化酶(HCuOs)在线粒体和大多数细菌中终止呼吸链。它们是跨膜蛋白,催化氧气还原,并利用释放的自由能维持跨膜质子动力势。HCuO超家族已被分为氧还原A型、B型和C型氧化酶以及细菌一氧化氮还原酶(NOR),后者在反硝化过程中催化一氧化氮的还原。质子通过两条明确的途径转移到线粒体样A家族的催化位点,这两条途径被称为D途径和K途径。B、C和NOR家族在质子转移到活性位点以及跨膜的途径和机制上有所不同。本综述将讨论最近聚焦于B、C和NOR家族质子转移的结构和功能研究。