α-Olefins are important precursors for many chemical
products
such as lubricants and detergents. The biocatalytic reaction has become
a new approach to synthesizing α-olefins from biobased feedstocks
such as fatty acids. Two enzymes, pyranose-2-oxidase (P2O) and cytochrome
P450-OleTJE (OleTJE), are coupled to form a
cascade reaction in which the first P2O-catalyzed reaction generates
H2O2, which is a cosubstrate for the second
OleTJE-catalyzed reaction to convert fatty acids into α-olefins.
In this work, we developed multienzyme immobilization protocols that
colocalize the two enzymes onto graphene oxide (GO) in close proximity,
enabling efficient diffusion of H2O2 between
the reactions. The coimmobilized enzymes on GO exhibited enhanced
productivity with a relative activity of 143% as compared to that
of the free enzymes. Also, liquid–liquid extraction (LLE) was
used to recover α-olefins and facilitate enzyme reuse. When
employing LLE with dodecane as a solvent, the overall production increased
by 2.47-fold compared to the conventional condition of using free
enzymes with ethyl acetate as a solvent.