Andres Y, MacCordick H J, Hubert J C
Laboratoire de Microbiologie, Institut Le Bel, Université Louis Pasteur, Strasbourg, France.
Biol Met. 1991;4(4):207-10. doi: 10.1007/BF01141182.
The interaction of cations of group IIIb elements (Sc, Y, La) with mycobactin S in ethanol leads to the formation of 1:1 complexes which closely resemble the known aluminium compound with respect to ultraviolet absorption and fluorescence emission spectra. Determination of molar stoichiometry by spectrophotometry shows that this method can be conveniently applied to the estimation of purity in mycobactin samples. Hydrolytic dissociation measurements based on aqueous extraction of the labelled complexes in heterogeneous phase indicate a pronounced gradation in cation-binding stability, which increases from La (rapid and complete dissociation) to sc (approximately 24% dissociation under similar conditions). The observed properties of the complexes are rationalized by semi-empirical model calculations, which suggest that ionic radius effects resulting from interaction of the IIIb cations with mycobactin S would not favour octahedral coordination of these elements as in the stable Fe(III) complex.
IIIb族元素(钪、钇、镧)的阳离子与乙醇中的分枝杆菌素S相互作用,会形成1:1的配合物。就紫外吸收和荧光发射光谱而言,这些配合物与已知的铝化合物极为相似。通过分光光度法测定摩尔化学计量比表明,该方法可方便地用于估算分枝杆菌素样品的纯度。基于在非均相相中对标记配合物进行水相萃取的水解解离测量表明,阳离子结合稳定性存在明显的梯度变化,从镧(快速且完全解离)到钪(在类似条件下约24%解离)逐渐增加。配合物的观察性质通过半经验模型计算得到合理解释,这表明IIIb族阳离子与分枝杆菌素S相互作用产生的离子半径效应不利于这些元素像在稳定的铁(III)配合物中那样形成八面体配位。