Discovery of 23 Natural Tubulysins from Angiococcus disciformis An d48 and Cystobacter SBCb004

被引:55
作者
Chai, Yi [1 ]
Pistorius, Dominik [1 ]
Ullrich, Angelika [2 ]
Weissman, Kira J. [1 ]
Kazmaier, Uli [2 ]
Mueller, Rolf [1 ,3 ]
机构
[1] Univ Saarland, Dept Pharmaceut Biotechnol, D-66041 Saarbrucken, Germany
[2] Univ Saarland, Inst Organ Chem, D-66123 Saarbrucken, Germany
[3] Univ Saarland, Helmholtz Ctr Infect Res HZI, Helmholtz Inst Pharmaceut Res Saarland HIPS, D-66123 Saarbrucken, Germany
来源
CHEMISTRY & BIOLOGY | 2010年 / 17卷 / 03期
关键词
BIOSYNTHETIC GENE-CLUSTER; CATALYZED N-ALLYLATION; BIOLOGICAL EVALUATION; POTENTIAL ANTICANCER; SORANGIUM-CELLULOSUM; EPIMERIZATION DOMAIN; CLOSING METATHESIS; LIPOLYTIC ENZYMES; ASSEMBLY LINES; AMINO-ACIDS;
D O I
10.1016/j.chembiol.2010.01.016
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
The tubulysins are a family of complex peptides with promising cytotoxic activity against multi-drug-resistant tumors. To date, ten tubulysins have been described from the myxobacterial strains Angiococcus disciformis An d48 and Archangium gephyra Ar 315. We report here a third producing strain, Cystobacter sp. SBCb004. Comparison of the tubulysin biosynthetic gene clusters in SBCb004 and An d48 reveals a conserved architecture, allowing the assignment of cluster boundaries. A SBCb004 strain containing a mutant in the putative cyclodeaminase gene tubZ accumulates pretubulysin A, the proposed first enzyme-free intermediate in the pathway, whose structure we confirm by NMR. We further show, using a combination of feeding studies and structure elucidation by NMR and high-resolution tandem mass spectrometry, that SBCb004 and An d48 together biosynthesize 22 additional tubulysin derivatives. These data reveal the inherently diversity-oriented nature of the tubulysin biosynthetic pathway.
引用
收藏
页码:296 / 309
页数:14
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