Benzodiazepine biosynthesis in Streptomyces refuineus

被引:84
作者
Hu, Yunfeng
Phelan, Vanessa
Ntai, Ioanna
Farnet, Chris M.
Zazopoulos, Emmanuel
Bachmann, Brian O. [1 ]
机构
[1] Vanderbilt Univ, Dept Chem, Nashville, TN 37204 USA
[2] Ecopia Biosci Inc, Montreal, PQ, Canada
来源
CHEMISTRY & BIOLOGY | 2007年 / 14卷 / 06期
关键词
NONRIBOSOMAL PEPTIDE SYNTHETASES; MOLECULAR CHARACTERIZATION; ADENYLATION DOMAINS; ANTHRAMYCIN; LINCOMYCIN; ANTITUMOR; GENES; SPECIFICITY; PATHWAYS;
D O I
10.1016/j.chembiol.2007.05.009
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
Anthramycin is a benzodiazepine alkaloid with potent antitumor and antibiotic activity produced by the thermophilic actinomycete Streptomyces refuineus sbsp. thermotolerans. In this study, the complete 32.5 kb gene cluster for the biosynthesis of anthramycin was identified by using a genome-scanning approach, and cluster boundaries were estimated via comparative genomics. A X-RED-mediated gene-replacement system was developed to provide supporting evidence for critical biosynthetic genes and to validate the boundaries of the proposed anthramycin gene cluster. Sequence analysis reveals that the 25 open reading frame anthramycin cluster contains genes consistent with the biosynthesis of the two halves of anthramycin: 4 methyl-3-hydroxyanthranilic acid and a "dehydroprolineacrylamide" moiety. These nonproteinogenic amino acid precursors are condensed by a two-module nonribosomal peptide synthetase (NRPS) terminated by a reductase domain, consistent with the final hemiaminal oxidation state of anthramycin.
引用
收藏
页码:691 / 701
页数:11
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