Article ID Journal Published Year Pages File Type
1391961 Chemistry & Biology 2010 14 Pages PDF
Abstract

SummaryThe 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.

► Discovery of 23 new tubulysins, showing biosynthesis is diversity oriented ► Comparative analysis of tubulysin biosynthesis in two myxobacteria ► Confirmation of the structure of pretubulysin, the first enzyme-free intermediate ► Determination of the stereochemistry of the pipecolic acid starter unit

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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