Zhou_2019_Chem.Sci_10_6341

Reference

Title : Molecular mechanism of polyketide shortening inanthraquinone biosynthesis of Photorhabdus luminescens - Zhou_2019_Chem.Sci_10_6341
Author(s) : Zhou, QQ , Brauer A , Adihou H , Schmalhofer M , Saura P , Grammbitter GLC , Kaila VRI , Groll M , Bode HB
Ref : Chem Sci , 10 :6341 , 2019
Abstract :

Anthraquinones, a widely distributed class of aromatic natural products, are produced by a type II polyketidesynthase system in the Gram-negative bacterium Photorhabdus luminescens. Heterologous expression oftheantABCDEFGHI anthraquinone biosynthetic gene cluster in Escherichia coli identified AntI as an unusual lyase, catalysing terminal polyketide shortening prior to formation of the third aromatic ring. Functional in vitro and in vivo analysis of AntI using X-ray crystallography, structure-based mutagenesis, and molecular simulations revealed that AntI converts a defined octaketide to the tricyclic anthraquinone ring via retro-Claisen and Dieckmann reactions. Thus, AntI catalyses a so far unobserved multistep reaction in this PKS system.

PubMedSearch : Zhou_2019_Chem.Sci_10_6341
PubMedID:
Gene_locus related to this paper: pholl-AntI

Related information

Gene_locus pholl-AntI
Structure 6HXA

Citations formats

Zhou, QQ, Brauer A, Adihou H, Schmalhofer M, Saura P, Grammbitter GLC, Kaila VRI, Groll M, Bode HB (2019)
Molecular mechanism of polyketide shortening inanthraquinone biosynthesis of Photorhabdus luminescens
Chem Sci 10 :6341

Zhou, QQ, Brauer A, Adihou H, Schmalhofer M, Saura P, Grammbitter GLC, Kaila VRI, Groll M, Bode HB (2019)
Chem Sci 10 :6341