Li_2016_Chembiochem_17_904

Reference

Title : Biosynthesis of LL-Z1272beta: Discovery of a New Member of NRPS-like Enzymes for Aryl-Aldehyde Formation - Li_2016_Chembiochem_17_904
Author(s) : Li C , Matsuda Y , Gao H , Hu D , Yao XS , Abe I
Ref : Chembiochem , 17 :904 , 2016
Abstract :

LL-Z1272beta (1) is a prenylated aryl-aldehyde produced by several fungi; it also serves as a key pathway intermediate for many fungal meroterpenoids. Despite its importance in the biosynthesis of natural products, the molecular basis for the biosynthesis of 1 has yet to be elucidated. Here we identified the biosynthetic gene cluster for 1 from Stachybotrys bisbyi PYH05-7, and elucidated the biosynthetic route to 1. The biosynthesis involves a polyketide synthase, a prenyltransferase, and a nonribosomal peptide synthetase (NRPS)-like enzyme, which is responsible for the generation of the aldehyde functionality. Interestingly, the NRPS-like enzyme only accepts the farnesylated substrate to catalyze the carboxylate reduction; this represents a new example of a substrate for adenylation domains.

PubMedSearch : Li_2016_Chembiochem_17_904
PubMedID: 26972702
Gene_locus related to this paper: stabi-stba

Related information

Gene_locus stabi-stba

Citations formats

Li C, Matsuda Y, Gao H, Hu D, Yao XS, Abe I (2016)
Biosynthesis of LL-Z1272beta: Discovery of a New Member of NRPS-like Enzymes for Aryl-Aldehyde Formation
Chembiochem 17 :904

Li C, Matsuda Y, Gao H, Hu D, Yao XS, Abe I (2016)
Chembiochem 17 :904