A Unique Tryptophan C‐Prenyltransferase from the Kawaguchipeptin Biosynthetic Pathway. Issue 11 (5th February 2016)

• Record Type: Journal Article
• Authors: Parajuli, Anirudra; Kwak, Daniel H.; Dalponte, Luca; Leikoski, Niina; Galica, Tomas; Umeobika, Ugochukwu; Trembleau, Laurent; Bent, Andrew; Sivonen, Kaarina; Wahlsten, Matti; Wang, Hao; Rizzi, Ermanno; De Bellis, Gianluca; Naismith, James; Jaspars, Marcel; Liu, Xinyu; Houssen, Wael; Fewer, David Peter
• Is Part Of: Angewandte Chemie international edition. Volume 55:Issue 11(2016)
• Page Start: 3596
• Page End: 3599
• Publication Date: 2016-02-05
• Subjects: biosynthesis -- cyanobactins -- peptides -- prenylation -- prenyltransferases; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201509920
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Cyanobactins are a rapidly growing family of linear and cyclic peptides produced by cyanobacteria. Kawaguchipeptins A and B, two macrocyclic undecapeptides reported earlier from Microcystis aeruginosa NIES‐88, are shown to be products of the cyanobactin biosynthetic pathway. The 9 kb kawaguchipeptin ( kgp ) gene cluster was identified in a 5.26 Mb draft genome of Microcystis aeruginosa NIES‐88. We verified that this gene cluster is responsible for the production of the kawaguchipeptins through heterologous expression of the kgp gene cluster in Escherichia coli . The KgpF prenyltransferase was overexpressed and was shown to prenylate C‐3 of Trp residues in both linear and cyclic peptides in vitro. Our findings serve to further enhance the structural diversity of cyanobactins to include tryptophan‐prenylated cyclic peptides. Abstract : The macrocyclic undecapeptides Kawaguchipeptin A and B from Microcystis aeruginosa NIES‐88 were shown to be products of the cyanobactin biosynthetic pathway. The 9 kb kawaguchipeptin (kgp) gene cluster was identified as being responsible for their production through heterologous expression in Escherichia coli, and the KgpF prenyltransferase was shown to prenylate C‐3 of Trp residues in both linear and cyclic peptides in vitro.