Wang_2014_Chem.Biol_21_257

Reference

Title : Aryl-aldehyde formation in fungal polyketides: discovery and characterization of a distinct biosynthetic mechanism - Wang_2014_Chem.Biol_21_257
Author(s) : Wang M , Beissner M , Zhao H
Ref : Chemical Biology , 21 :257 , 2014
Abstract :

Aryl-aldehydes are a common feature in fungal polyketides, which are considered to be exclusively generated by the R domain of nonreducing polyketide synthases (NR-PKSs). However, by cloning and heterologous expression of both cryptic NR-PKS and nonribosomal peptide synthase (NRPS)-like genes from Aspergillus terreus in Saccharomyces cerevisiae, we identified a distinct mechanism for aryl-aldehyde formation in which a NRPS-like protein activates and reduces an aryl-acid produced by the accompanying NR-PKS to an aryl-aldehyde. Bioinformatics study indicates that such a mechanism may be widely used throughout the fungi kingdom.

PubMedSearch : Wang_2014_Chem.Biol_21_257
PubMedID: 24412543
Gene_locus related to this paper: asptn-5moas , asptn-azpb5

Related information

Gene_locus asptn-5moas    asptn-azpb5

Citations formats

Wang M, Beissner M, Zhao H (2014)
Aryl-aldehyde formation in fungal polyketides: discovery and characterization of a distinct biosynthetic mechanism
Chemical Biology 21 :257

Wang M, Beissner M, Zhao H (2014)
Chemical Biology 21 :257