Brief Communication abstract


Nature Chemical Biology 4, 341 - 343 (2008)
Published online: 20 April 2008 | doi:10.1038/nchembio.84

A global assembly line for cyanobactins

Mohamed S Donia1, Jacques Ravel2 & Eric W Schmidt1

Top

More than 100 cyclic peptides harboring heterocyclized residues are known from marine ascidians, sponges and different genera of cyanobacteria. Here, we report an assembly line responsible for the biosynthesis of these diverse peptides, now called cyanobactins, both in symbiotic and free-living cyanobacteria. By comparing five new cyanobactin biosynthetic clusters, we produced the prenylated antitumor preclinical candidate trunkamide in Escherichia coli culture using genetic engineering.

Top
  1. Department of Medicinal Chemistry, University of Utah, 30 South 2000 East, Room 201, Salt Lake City, Utah 84112, USA.
  2. Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201, USA.

Correspondence to: Eric W Schmidt1 e-mail: ews1@utah.edu



MORE ARTICLES LIKE THIS

These links to content published by NPG are automatically generated.

NEWS AND VIEWS

Combinatorial biosynthesis in symbiotic bacteria

Nature Chemical Biology News and Views (01 Dec 2006)


Extra navigation

Subscribe to Nature Chemical Biology

Subscribe

Open Innovation Challenges

naturejobs