| Literature DB >> 28146322 |
Patrick Rabe1, Jan Rinkel1, Etilia Dolja1, Thomas Schmitz1, Britta Nubbemeyer1, T Hoang Luu1, Jeroen S Dickschat1.
Abstract
The mechanisms of two diterpene cyclases from streptomycetes-one with an unknown product that was identified as the spirocyclic hydrocarbon spiroviolene and one with the known product tsukubadiene-were investigated in detail by isotope labeling experiments. Although the structures of the products were very different, the cyclization mechanisms of both enzymes proceed through the same initial cyclization reactions, before they diverge towards the individual products, which is reflected in the close phylogenetic relationship of the enzymes.Entities:
Keywords: NMR spectroscopy; biosynthesis; isotopes; reaction mechanisms; terpenes
Mesh:
Substances:
Year: 2017 PMID: 28146322 DOI: 10.1002/anie.201612439
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336