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 |
Gene_locus | pholl-AntI |
Structure | 6HXA |
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