Skjeldal L, Andersson K K, Grace D, Ljones T
Department of Chemistry, University of Trondheim, Dragvoll, Norway.
Biol Met. 1989;2(3):135-41. doi: 10.1007/BF01142551.
Ferredoxin from Clostridium pasteurianum substituted with two Co atoms did not give any cobalt EPR signal at 8 K as isolated, but upon reduction with sodium dithionite, a broad signal appeared with g values that indicate highspin (S = 3/2) Co(II). These signals were distinct from Co(II)-dithiothreitol signals, and disappeared upon reoxidation with air. Under anaerobic incubation of apoferredoxin with Co(II), a green derivative showed a visible spectrum typical of tetrahedral Co(II)-thiolate coordination, which shifted dramatically upon exposure to air. The 1H-NMR spectrum of the aerobically isolated protein is reported at 300 MHz; magnetic susceptibility measurements were indicative of a diamagnetic species. These spectroscopic studies indicate that Co(II)-substituted ferredoxin is oxidized to low-spin Co(III)-ferredoxin in the presence of sulfide and oxygen. The diamagnetic Co(III) state could reversibly be reduced to highspin Co(II) by sodium dithionite.
来自巴斯德梭菌的铁氧化还原蛋白用两个钴原子取代后,分离时在8K下未给出任何钴的电子顺磁共振信号,但用连二亚硫酸钠还原后,出现了一个宽信号,其g值表明为高自旋(S = 3/2)的Co(II)。这些信号与Co(II)-二硫苏糖醇信号不同,在空气中再氧化时消失。在无氧条件下,脱辅基铁氧化还原蛋白与Co(II)一起孵育,一种绿色衍生物显示出典型的四面体Co(II)-硫醇盐配位的可见光谱,暴露于空气中时该光谱会发生显著变化。有氧分离得到的蛋白质的1H-NMR光谱在300 MHz下进行了报道;磁化率测量表明是抗磁性物质。这些光谱研究表明,在存在硫化物和氧气的情况下,Co(II)取代的铁氧化还原蛋白被氧化为低自旋的Co(III)-铁氧化还原蛋白。抗磁性的Co(III)状态可以通过连二亚硫酸钠可逆地还原为高自旋的Co(II)。