Identification and analysis of the core biosynthetic machinery of tubulysin, a potent cytotoxin with potential anticancer activity

被引:90
作者
Sandmann, A
Sasse, F
Müller, R
机构
[1] GBF German Res Ctr Biotechnol, D-38124 Braunschweig, Germany
[2] Univ Saarland, D-66041 Saarbrucken, Germany
来源
CHEMISTRY & BIOLOGY | 2004年 / 11卷 / 08期
关键词
D O I
10.1016/j.chembiol.2004.05.014
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
Myxobacteria are well known for their biosynthetic potential, especially for the production of cytotoxic compounds with potential anticancer activities. The tubulysins are currently in preclinical development. They are produced in very low quantities, and genetic manipulation of producing strains has never been accomplished. We report the development of a mariner-based transposon mutagenesis system for Angiococcus disciformis An d48. Extracts from a library of 1200 mutants were analyzed for the presence of tubulysin by a microscopic cell nucleus fragmentation bioassay. The transposition sites of four tubulysin-negative mutants were identified by vector recovery, which led to the identification and the sequencing of the corresponding core biosynthetic gene locus. Sequence analysis of more than 80,000 bp reveals an unusual multimodular hybrid polyketide synthase/peptide synthetase assembly line with a variety of unprecedented features.
引用
收藏
页码:1071 / 1079
页数:9
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