Divergence of multimodular polyketide synthases revealed by a didomain structure

Jianting Zheng, Darren C. Gay, Borries Demeler, Mark A. White, Adrian T. Keatinge-Clay

Research output: Contribution to journalArticle

50 Scopus citations

Abstract

The enoylreductase (ER) is the final common enzyme from modular polyketide synthases (PKSs) to be structurally characterized. The 3.0 Å-resolution structure of the didomain comprising the ketoreductase (KR) and ER from the second module of the spinosyn PKS reveals that ER shares an ∼600- Å2 interface with KR distinct from that of the related mammalian fatty acid synthase (FAS). In contrast to the ER domains of the mammalian FAS, the ER domains of the second module of the spinosyn PKS do not make contact across the two-fold axis of the synthase. This monomeric organization may have been necessary in the evolution of multimodular PKSs to enable acyl carrier proteins to access each of their cognate enzymes. The isolated ER domain showed activity toward a substrate analog, enabling us to determine the contributions of its active site residues.

Original languageEnglish (US)
Pages (from-to)615-621
Number of pages7
JournalNature Chemical Biology
Volume8
Issue number7
DOIs
StatePublished - Jul 2012

    Fingerprint

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this