Doherty G M, Mayhew S G, Malthouse J P
Department of Biochemistry, University College Dublin, Ireland.
Biochem J. 1993 Aug 15;294 ( Pt 1)(Pt 1):215-8. doi: 10.1042/bj2940215.
The thiol group of the flavodoxin from Clostridium pasteurianum has been cyanylated in a single step using [cyanato-13C]2-nitro-5-thiocyanatobenzoic acid. This chemical modification increases the dissociation constant of the apoflavodoxin-FMN complex 10-fold from 0.33 +/- 0.15 nM to 2.9 +/- 1.3 nM. The thiocyanate carbons of the cyanylated cysteine residue of apoflavodoxin and flavodoxin had chemical shift values of 114.7 and 112.3 p.p.m. respectively. From these chemical shifts we conclude that the binding of FMN by the cyanylated apoflavodoxin causes a decrease in the polarity and/or hydrogen bonding capacity of the environment of the thiocyanate group. We compare these results with those obtained from similar studies on the cyanylated apoflavodoxin and flavodoxin from Megasphaera elsdenii and we discuss how FMN binding and cyanylation perturb the structures of apoflavodoxins from Megasphaera elsdenii and Clostridium pasteurianum.
利用[氰基-13C]2-硝基-5-硫氰基苯甲酸,已一步法对巴氏芽孢梭菌黄素氧还蛋白的巯基进行了氰化。这种化学修饰使脱辅基黄素氧还蛋白-FMN复合物的解离常数从0.33±0.15 nM增加了10倍,达到2.9±1.3 nM。脱辅基黄素氧还蛋白和黄素氧还蛋白的氰化半胱氨酸残基的硫氰酸酯碳的化学位移值分别为114.7和112.3 ppm。根据这些化学位移,我们得出结论,氰化脱辅基黄素氧还蛋白与FMN的结合导致硫氰酸酯基团环境的极性和/或氢键结合能力降低。我们将这些结果与从对埃氏巨球型菌的氰化脱辅基黄素氧还蛋白和黄素氧还蛋白的类似研究中获得的结果进行比较,并讨论FMN结合和氰化如何扰乱埃氏巨球型菌和巴氏芽孢梭菌脱辅基黄素氧还蛋白的结构。