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Genome Mining of Alkaloidal Terpenoids from a Hybrid Terpene and Nonribosomal Peptide Biosynthetic Pathway.
- Source :
-
Journal of the American Chemical Society [J Am Chem Soc] 2020 Jan 15; Vol. 142 (2), pp. 710-714. Date of Electronic Publication: 2020 Jan 03. - Publication Year :
- 2020
-
Abstract
- Biosynthetic pathways containing multiple core enzymes have potential to produce structurally complex natural products. Here we mined a fungal gene cluster that contains two predicted terpene cyclases (TCs) and a nonribosomal peptide synthetase (NRPS). We showed the flv pathway produces flavunoidine 1 , an alkaloidal terpenoid. The core of 1 is a tetracyclic, cage-like, and oxygenated sesquiterpene that is connected to dimethylcadaverine via a C-N bond and is acylated with 5,5-dimethyl-l-pipecolate. The roles of all flv enzymes are established on the basis of metabolite analysis from heterologous expression.
- Subjects :
- Ribosomes chemistry
Alkaloids chemistry
Genome
Peptides chemistry
Terpenes chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5126
- Volume :
- 142
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of the American Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- 31885262
- Full Text :
- https://doi.org/10.1021/jacs.9b13046