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Combinatorial Biosynthesis of (+)-Daurichromenic Acid and Its Halogenated Analogue.

Authors :
Okada M
Saito K
Wong CP
Li C
Wang D
Iijima M
Taura F
Kurosaki F
Awakawa T
Abe I
Source :
Organic letters [Org Lett] 2017 Jun 16; Vol. 19 (12), pp. 3183-3186. Date of Electronic Publication: 2017 May 25.
Publication Year :
2017

Abstract

Daurichromenic acid is a meroterpenoid with various pharmacological activities that is biosynthesized from grifolic acid in Rhododendron dauricum. Heterologous expression of grifolic acid synthases from Stachybotrys bisbyi and a daurichromenic acid synthase from R. dauricum in Aspergillus oryzae mediated three-step combinatorial biosynthesis of (+)-daurichromenic acid through enantioselective 6-endo-trig cyclization. Additional introduction of a halogenase from Fusarium sp. into the strain resulted in the biosynthesis of (+)-5-chlorodaurichromenic acid, which exceeds the antibacterial activity of the original compounds.

Details

Language :
English
ISSN :
1523-7052
Volume :
19
Issue :
12
Database :
MEDLINE
Journal :
Organic letters
Publication Type :
Academic Journal
Accession number :
28541042
Full Text :
https://doi.org/10.1021/acs.orglett.7b01288