4.8 Article

Natural combinatorial peptide libraries in cyanobacterial symbionts of marine ascidians

Journal

NATURE CHEMICAL BIOLOGY
Volume 2, Issue 12, Pages 729-735

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nchembio829

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Funding

  1. NIGMS NIH HHS [R01 GM 071425-01A1] Funding Source: Medline

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A large family of cytotoxic cyclic peptides exemplified by the patellamides has been isolated from ascidians harboring the obligate cyanobacterial symbionts Prochloron spp.(1-5). Genome sequence analysis of these symbionts has revealed that Prochloron spp. synthesize patellamides by a ribosomal pathway(6). To understand how this pathway evolved to produce a suite of related metabolites, we analyzed 46 prochloron-containing ascidians from the tropical Pacific Ocean for the presence of patellamide biosynthetic genes and taxonomic markers. Here, we show that Prochloron spp. generate a diverse library of patellamides using small, hypervariable cassettes within a conserved genetic background. Each symbiont strain contains a single pathway, and mixtures of symbionts within ascidians lead to the accumulation of chemical libraries. We used this information to engineer the production of a new cyclic peptide in Escherichia coli, thereby demonstrating the power of comparative analysis of closely related symbiotic pathways to direct the genetic synthesis of new molecules.

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