Cyclic peptide production using a macrocyclase with enhanced substrate promiscuity and relaxed recognition determinants.

Chem Commun (Camb)

Marine Biodiscovery Centre, Department of Chemistry, University of Aberdeen, Meston Walk, Aberdeen AB24 3UE, UK. and Institute of Medical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK and Pharmacognosy Department, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt.

Published: September 2017

Macrocyclic peptides have promising therapeutic potential but the scaling up of their chemical synthesis is challenging. The cyanobactin macrocyclase PatG is an efficient tool for production but is limited to substrates containing 6-11 amino acids and at least one thiazoline or proline. Here we report a new cyanobactin macrocyclase that can cyclize longer peptide substrates and those not containing proline/thiazoline and thus allows exploring a wider chemical diversity.

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Source
http://dx.doi.org/10.1039/c7cc05913bDOI Listing

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