Heterocomplex structure of a polyketide synthase component involved in modular backbone halogenation

Amy E. Fraley, Maria Dell, Maximilian Schmalhofer, Roy A. Meoded, Cedric Bergande, Michael Groll, Jörn Piel

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Bacterial modular polyketide synthases (PKSs) generate diverse, complex and bioactive natural products that are constructed mainly based on principles of fatty acid biosynthesis. The cytotoxic oocydin-type polyketides contain a vinyl chloride moiety introduced during polyketide chain elongation. Required for modular polyketide backbone halogenation are a non-heme iron and ɑ-ketoglutarate-dependent halogenase OocP and OocQ lacking characterized homologs. This work provides structural insights into these unusual PKS components and their interactions via a high-resolution X-ray crystallography structure of the heterocomplex. By mapping the protein-protein interactions and comparison with structures of similar halogenases, we illustrate the potential of this heterodimer complex as a replacement for the conserved homodimeric structure of homologous enzymes. The OocPQ protein pair has thus evolved as a means of stabilizing the halogenase and facilitating chemical transformations with great synthetic utility.

Original languageEnglish
Pages (from-to)565-572.e4
JournalStructure
Volume31
Issue number5
DOIs
StatePublished - 4 May 2023

Keywords

  • Halogenase
  • alpha-ketoglutarate
  • crystallography
  • heterocomplex
  • non-heme iron
  • polyketides
  • trans-AT

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