Katada M, Tyagi S, Nath A, Petersen R L, Gupta R K
Biochim Biophys Acta. 1979 Apr 18;584(1):149-63. doi: 10.1016/0304-4165(79)90245-9.
A new isomeric form of cobalamins is reported. The conversion of cobalamin to cobalamin (the new form) is achieved by substituting the benzimidazole base by a less bulky group like H2O or CN- and modest thermal treatment. The back conversion of adenosylcobalamin to the corresponding regular form occurs in the "base-off" form at room temperature. It seems that the corrin ring becomes quite flexible in the "base-off" form and the freer axial movement of the cobalt atom flips the corrin ring into a different conformation. The change in conformation is borne out by subtle changes in the proton magnetic resonances on the corrin ring and the base, and very marked variation in the emission Mössbauer spectra. The latter is indicative of appreciable changes in the spatial conformation in the immediate vicinity of the central metal atom. The ultraviolet-visible and infrared spectra of cobalamin are indistinguishable from those of its corresponding regular form. The new conformational isomeric species is present as an impurity in all commercially available cobalamins (including pharmaceutical preparations). It raises the question whether the cobalamins' constitute the real biologically active anti-anemic factor in humans.
报道了一种新的钴胺素异构体形式。通过用如H₂O或CN⁻等体积较小的基团取代苯并咪唑碱基并进行适度热处理,可实现钴胺素向钴胺素(新形式)的转化。腺苷钴胺素向相应常规形式的逆转化在室温下以“碱基脱离”形式发生。似乎在“碱基脱离”形式下,卟啉环变得相当灵活,钴原子更自由的轴向移动使卟啉环翻转成不同的构象。卟啉环和碱基上质子磁共振的细微变化以及发射穆斯堡尔谱的非常显著变化证实了构象的改变。后者表明中心金属原子紧邻区域的空间构象有明显变化。钴胺素的紫外可见光谱和红外光谱与其相应常规形式的光谱无法区分。这种新的构象异构体在所有市售钴胺素(包括药物制剂)中都作为杂质存在。这就提出了一个问题,即钴胺素是否构成人类真正具有生物活性的抗贫血因子。