| Literature DB >> 33169911 |
Geng Li1,2,3, Yue-Wei Guo2,3, Jeroen S Dickschat1.
Abstract
A new diterpene synthase from the actinomycete Catenulispora acidiphila was identified and the structures of its products were elucidated, including the absolute configurations by an enantioselective deuteration approach. The mechanism of the cationic terpene cyclisation cascade was deeply studied through the use of isotopically labelled substrates and of substrate analogues with partially blocked reactivity, resulting in derailment products that gave further insights into the intermediates along the cascade. Their chemistry was studied, leading to the biomimetic synthesis of a diterpenoid analogue of a brominated sesquiterpene known from the red seaweed Laurencia microcladia.Entities:
Keywords: biosynthesis; enzyme mechanisms; isotopes; substrate analogues; terpenoids
Mesh:
Substances:
Year: 2020 PMID: 33169911 PMCID: PMC7839432 DOI: 10.1002/anie.202014180
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336