| Literature DB >> 27739177 |
Huihua Sun1, Wan Lin Yeo1, Yee Hwee Lim2, Xinying Chew2, Derek John Smith3,4, Bo Xue5, Kok Ping Chan2, Robert C Robinson5,6,7,8,9, Edward G Robins10, Huimin Zhao11,12, Ee Lui Ang13.
Abstract
Fluorinases offer an environmentally friendly alternative for selective fluorination under mild conditions. However, their diversity is limited in nature and they have yet to be engineered through directed evolution. Herein, we report the directed evolution of the fluorinase FlA1 for improved conversion of the non-native substrate 5'-chloro-5'-deoxyadenosine (5'-ClDA) into 5'-fluoro-5'-deoxyadenosine (5'-FDA). The evolved variants, fah2081 (A279Y) and fah2114 (F213Y, A279L), were successfully applied in the radiosynthesis of 5'-[18 F]FDA, with overall radiochemical conversion (RCC) more than 3-fold higher than wild-type FlA1. Kinetic studies of the two-step reaction revealed that the variants show a significantly improved kcat value in the conversion of 5'-ClDA into S-adenosyl-l-methionine (SAM) but a reduced kcat value in the conversion of SAM into 5'-FDA.Entities:
Keywords: biocatalysis; directed evolution; fluorinases; halogenation; radiosynthesis
Year: 2016 PMID: 27739177 DOI: 10.1002/anie.201606722
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336