This paper reports on photoenzymatic cascade reactions to transform unsaturated fatty acids into enantiomerically pure secondary fatty alcohols. The process involves a two-step approach: stereoselective hydration of the C=C double bond using oleate hydratases, followed by decarboxylation of the intermediate hydroxy acids using a photoactivated decarboxylase. A wide range of unsaturated fatty acids were successfully converted into enantiomerically pure fatty alcohols using this one-pot method.
Publisher
Nature Communications
Published On
May 07, 2020
Authors
Wuyuan Zhang, Jeong-Hoo Lee, Sabry H. H. Younes, Fabio Tonin, Peter-Leon Hagedoorn, Harald Pichler, Yoonjin Baeg, Jin-Byung Park, Robert Kourist, Frank Hollmann
Tags
photoenzymatic reactions
fatty acids
secondary fatty alcohols
stereoselective hydration
decarboxylation
biotechnology
one-pot method
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