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大环内酯苷元的生物糖基化。I. 5-O-麦卡糖基纳波内酯和9-二氢-5-O-麦卡糖基纳波内酯的分离与表征。

Biological glycosidation of macrolide aglycones. I. Isolation and characterization of 5-O-mycaminosyl narbonolide and 9-dihydro-5-O-mycaminosyl narbonolide.

作者信息

Maezawa I, Kinumaki A, Suzuki M

出版信息

J Antibiot (Tokyo). 1976 Nov;29(11):1203-8. doi: 10.7164/antibiotics.29.1203.

Abstract

Glycosidation of narbonolide with mycaminose was attempted by feeding narbonolide during the fermentation of a parent or a mutant strain of Streptomyces platensis, a producer of 16-membered macrolide antibiotics, platenomycins. As a result, two new compounds I and II were isolated from the fermentation broth and identified as 5-O-mycaminosyl narbonolide (I) and 9-dihydro-5-O-mycaminosyl narbonolide (II), respectively. Physicochemical and antimicrobial properties of I and II are also referred to.

摘要

通过在16元大环内酯类抗生素普拉特链霉菌素(platenomycins)的亲本或突变菌株发酵过程中加入纳波内酯(narbonolide),尝试将纳波内酯与枝链霉糖(mycaminose)进行糖基化反应。结果,从发酵液中分离出两种新化合物I和II,分别鉴定为5-O-枝链霉糖基纳波内酯(I)和9-二氢-5-O-枝链霉糖基纳波内酯(II)。文中还提到了I和II的物理化学性质和抗菌特性。

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