Albracht S P, Hedderich R
Swammerdam Institute for Life Sciences, Biochemistry, University of Amsterdam, The Netherlands.
FEBS Lett. 2000 Nov 17;485(1):1-6. doi: 10.1016/s0014-5793(00)02172-4.
Hydrogenases have clear evolutionary links to the much more complex NADH-ubiquinone oxidoreductases (Complex I). Certain membrane-bound [NiFe]-hydrogenases presumably pump protons. From a detailed comparison of hydrogenases and Complex I, it is concluded here that the TYKY subunit in these enzymes is a special 2[4Fe-4S] ferredoxin, which functions as the electrical driving unit for a proton pump. The comparison further revealed that the flavodoxin fold from [NiFe]-hydrogenases is presumably conserved in the PSST subunit of Complex I. It is proposed that bovine Complex I and the soluble NAD(+)-reducing hydrogenase from Ralstonia eutropha each contain a second FMN group.
氢化酶与复杂得多的NADH-泛醌氧化还原酶(复合体I)有着明确的进化联系。某些膜结合的[NiFe] -氢化酶可能会泵送质子。通过对氢化酶和复合体I的详细比较,得出结论:这些酶中的TYKY亚基是一种特殊的2[4Fe-4S]铁氧化还原蛋白,它作为质子泵的电驱动单元发挥作用。进一步比较发现,[NiFe] -氢化酶的黄素氧还蛋白折叠结构可能在复合体I的PSST亚基中保守存在。有人提出,牛复合体I和来自嗜糖假单胞菌的可溶性NAD(+)还原氢化酶各自含有第二个FMN基团。