Exploring modular reengineering strategies to redesign the teicoplanin non-ribosomal peptide synthetase

Milda Kaniusaite, Robert J. A. Goode, Julien Tailhades, Ralf B. Schittenhelm, Max J. Cryle

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Non-ribosomal peptide synthesis is an important biosynthesis pathway in secondary metabolism. In this study we have investigated modularisation and redesign strategies for the glycopeptide antibiotic teicoplanin. Using the relocation or exchange of domains within the NRPS modules, we have identified how to initiate peptide biosynthesis and explored the requirements for the functional reengineering of both the condensation/adenylation domain and epimerisation/condensation domain interfaces. We have also demonstrated strategies that ensure communication between isolated NRPS modules, leading to new peptide assembly pathways. This provides important insights into NRPS reengineering of glycopeptide antibiotic biosynthesis and has broad implications for the redesign of other NRPS systems.

Original languageEnglish
Pages (from-to)9443-9458
Number of pages16
JournalChemical Science
Volume11
Issue number35
DOIs
Publication statusPublished - 21 Sep 2020

Cite this