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Updated: Apr 9, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Oxidative Decarboxylation of Short-Chain Fatty Acids to 1-Alkenes
Alexander Dennig1, Miriam Kuhn1, Sebastian Tassoti1
1Department of Chemistry, University of Graz, Heinrichstrasse 28, 8010 Graz (Austria).
Abstract:
The enzymatic oxidative decarboxylation of linear short-chain fatty acids (C4:0-C9:0) employing the P450 monooxygenase OleT, O2 as the oxidant, and NAD(P)H as the electron donor gave the corresponding terminal C3 to C8 alkenes with product titers of up to 0.93 g L(-1) and TTNs of >2000. Key to this process was the construction of an efficient electron-transfer chain employing putidaredoxin CamAB in combination with NAD(P)H recycling at the expense of glucose, formate, or phosphite. This system allows for the biocatalytic production of industrially important 1-alkenes, such as propene and 1-octene, from renewable resources for the first time.
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