4.1 Article

Genome Mining Expands the Chemical Diversity of the Cyanobactin Family to Include Highly Modified Linear Peptides

Journal

CHEMISTRY & BIOLOGY
Volume 20, Issue 8, Pages 1033-1043

Publisher

CELL PRESS
DOI: 10.1016/j.chembiol.2013.06.015

Keywords

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Funding

  1. Academy of Finland [118637, 258827, 259505]
  2. Helsinki University [788/51/2010]
  3. Office of Science of the US Department of Energy [DE-AC02-05CH11231]
  4. Academy of Finland (AKA) [258827, 259505, 259505, 258827] Funding Source: Academy of Finland (AKA)

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Ribosomal peptides are produced through the posttranslational modification of short precursor peptides. Cyanobactins are a growing family of cyclic ribosomal peptides produced by cyanobacteria. However, a broad systematic survey of the genetic capacity to produce cyanobactins is lacking. Here we report the identification of 31 cyanobactin gene clusters from 126 genomes of cyanobacteria. Genome mining suggested a complex evolutionary history defined by horizontal gene transfer and rapid diversification of precursor genes. Extensive chemical analyses demonstrated that some cyanobacteria produce short linear cyanobactins with a chain length ranging from three to five amino acids. The linear peptides were N-prenylated and O-methylated on the N and C termini, respectively, and named aeruginosamide and viridisamide. These findings broaden the structural diversity of the cyanobactin family to include highly modified linear peptides with rare posttranslational modifications.

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