The biosynthetic gene cluster for the antitumor rebeccamycin:: Characterization and generation of indolocarbazole derivatives

被引:185
作者
Sánchez, C
Butovich, IA
Braña, AF
Rohr, J
Méndez, C
Salas, JA
机构
[1] Med Univ S Carolina, Coll Pharm, Dept Pharmaceut Sci, Charleston, SC 29425 USA
[2] Univ Oviedo, Dept Biol Func, Oviedo 33006, Spain
[3] Univ Oviedo, Inst Univ Oncol Principado Asturias, Oviedo 33006, Spain
来源
CHEMISTRY & BIOLOGY | 2002年 / 9卷 / 04期
关键词
D O I
10.1016/S1074-5521(02)00126-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rebeccamycin, a halogenated natural product of the indolocarbazole family, is produced by Saccharothrix aerocolonigenes ATCC39243. Several rebeccamycin analogues, which target DNA topoisomerase I or II, have already entered clinical trials as anticancer drugs. Using as a probe an internal fragment of ngt, a Saccharothrix aerocolonigenes gene encoding an indolocarbazole N-glycosyltransferase, we isolated a DNA region that directed the biosynthesis of rebeccamycin when introduced into Streptomyces albus. Sequence analysis of 25.6 kb revealed genes for indolocarbazole core formation, halogenation, glycosylation, and sugar methylation, as well as a regulatory gene and two resistance/secretion genes. Heterologous expression of subsets of these genes resulted in production of deschloro-rebeccamycin, 4'-demethyl-deschloro-rebeccamycin, and deschloro-rebeccamycin aglycone. The cloned genes should help to elucidate the molecular basis for indolocarbazole biosynthesis and set the stage for the generation of novel indolocarbazole analogues by genetic engineering.
引用
收藏
页码:519 / 531
页数:13
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