Benson N, Farrar J A, McEwan A G, Thomson A J
Centre for Metalloprotein Spectroscopy and Biology, School of Chemical Sciences, University of East Anglia, Norwich, UK.
FEBS Lett. 1992 Jul 28;307(2):169-72. doi: 10.1016/0014-5793(92)80760-e.
Dimethylsulphoxide (DMSO) reductase from R. capsulatus contains a molybdenum-pterin cofactor at its active site. As prepared the molybdenum is in the 6+ oxidation state, devoid of EPR signals. Stepwise reduction generates an EPR signal characteristic of Mo(V) having hyperfine coupling to a single proton and integrating to less than 25% of the total molybdenum. The low temperature MCD spectrum shows oppositely signed bands between approximately 550-700 nm. These bands are assigned as dithiolene-to-Mo(V) charge transitions. A simple theoretical model can satisfactorily account for the bands in the MCD spectrum. No evidence is found for cysteine coordination to Mo(V).
来自荚膜红细菌的二甲基亚砜(DMSO)还原酶在其活性位点含有一个钼蝶呤辅因子。制备好的钼处于6 +氧化态,没有电子顺磁共振(EPR)信号。逐步还原会产生具有与单个质子超精细偶合且积分小于总钼量25%的Mo(V)特征的EPR信号。低温磁圆二色性(MCD)光谱在大约550 - 700纳米之间显示出符号相反的谱带。这些谱带被指定为二硫烯到Mo(V)的电荷跃迁。一个简单的理论模型可以令人满意地解释MCD光谱中的谱带。未发现半胱氨酸与Mo(V)配位的证据。