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抗黑素瘤药物桦木酸的微生物转化

Microbial transformations of the antimelanoma agent betulinic acid.

作者信息

Kouzi S A, Chatterjee P, Pezzuto J M, Hamann M T

机构信息

Department of Pharmaceutics and Medicinal Chemistry, School of Pharmacy and Health Sciences, University of the Pacific, Stockton, California 95211, USA.

出版信息

J Nat Prod. 2000 Dec;63(12):1653-7. doi: 10.1021/np000343a.

Abstract

Microbial transformation studies of the antimelanoma agent betulinic acid (1) were conducted. Screening experiments showed a number of microorganisms capable of biotransforming 1. Three of these cultures, Bacillus megaterium ATCC 14581, Cunninghamella elegans ATCC 9244, and Mucor mucedo UI-4605, were selected for preparative scale transformation. Bioconversion of 1 with resting-cell suspensions of phenobarbital-induced B. megaterium ATCC 14581 resulted in the production of the known betulonic acid (2) and two new metabolites: 3beta,7beta-dihydroxy-lup-20(29)-en-28-oic acid (3) and 3beta,6alpha, 7beta-trihydroxy-lup-20(29)-en-28-oic acid (4). Biotransformation of 1 with growing cultures of C. elegans ATCC 9244 produced one new metabolite characterized as 1beta,3beta, 7beta-trihydroxy-lup-20(29)-en-28-oic acid (5). Incubation of 1 with growing cultures of M. mucedo UI-4605 afforded metabolite 3. Structure elucidation of all metabolites was based on NMR and HRMS analyses. In addition, the antimelanoma activity of metabolites 2-5 was evaluated against two human melanoma cell lines, Mel-1 (lymph node) and Mel-2 (pleural fluid).

摘要

开展了抗黑色素瘤药物桦木酸(1)的微生物转化研究。筛选实验表明有多种微生物能够对1进行生物转化。从这些微生物中挑选了三株,巨大芽孢杆菌ATCC 14581、雅致小克银汉霉ATCC 9244和匐枝根霉UI - 4605,用于制备规模的转化。用苯巴比妥诱导的巨大芽孢杆菌ATCC 14581的静息细胞悬液对1进行生物转化,产生了已知的桦木酸(2)和两种新的代谢产物:3β,7β - 二羟基 - 羽扇 - 20(29) - 烯 - 28 - 酸(3)和3β,6α,7β - 三羟基 - 羽扇 - 20(29) - 烯 - 28 - 酸(4)。用雅致小克银汉霉ATCC 9244的生长培养物对1进行生物转化,产生了一种新的代谢产物,其结构鉴定为1β,3β,7β - 三羟基 - 羽扇 - 20(29) - 烯 - 28 - 酸(5)。用匐枝根霉UI - 4605的生长培养物对1进行培养得到了代谢产物3。所有代谢产物的结构解析均基于核磁共振(NMR)和高分辨质谱(HRMS)分析。此外,还针对两种人黑色素瘤细胞系Mel - 1(淋巴结)和Mel - 2(胸水)评估了代谢产物2 - 5的抗黑色素瘤活性。

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