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作 者:范铭琦[1] 沈依群[1] 胡小玲[1] 范瑾[1]
机构地区:[1]江苏省微生物研究所
出 处:《中国抗生素杂志》1998年第3期178-185,共8页Chinese Journal of Antibiotics
摘 要:用大孔吸附型树脂对西索米星原料药进行分离,极性小组分首先被洗脱。用高效液相色谱法测定了分离前后的西索米星纯度,发现可从84%提高到92%。此外还建立了用硅胶薄层层析检测小组分的方法,并用阳离子交换树脂对小组分进行了分离。采用上述方法可分离得6种小组分。再用Am-berliteCG-50、CM-SephadexC-25等精制,得各小组分的精制品,经冷冻干燥后进行结构测定。其中含量最多的NAT-1、UK-1与庆大霉素A和加洛糖胺同质,NAT-4与庆大霉素A1的文献报道相符;而NAT-2、UK-2经MS、1H-NMR、13C-NMR测定。The complex of minor components was isolated from sisomicin bulk material by macroporous adsorption resin. Then, the polar minor components were eluated first. They were separated into six components by ion exchange resin; and the purity of sisomicin increased from 84% to 92%. We performed an experimental study of the method for the identification of minor compo nents by the use of thin layer chromatography. Each minor component was purified by repeated ionexchange chromatographic processes. Finally, NAT 1 and UK 1 were identified as gentamicin A and garamine and NAT 4 was identified as gentamicin A 1by comparing with reported MS, 1H NMR and 13 C NMR data. NAT 2 and UK 1 were inferred as new pseudodisuccharides by 1H NMR, 13 C NMR and mass spectroscopic studies.
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