Publication | Open Access
Merging Whole‐cell Biosynthesis of Styrene and Transition‐metal Catalyzed Derivatization Reactions
23
Citations
47
References
2021
Year
EngineeringChemistryWhole‐cell BiocatalysisBiosynthesisNatural Product BiosynthesisIsolated EnzymesHomogeneous CatalysisChemical BiotechnologyTransition‐metal CatalysisBiochemistryBiocatalysisDiversity-oriented SynthesisCatalysisWhole‐cell BiosynthesisCatalytic SynthesisBiomolecular EngineeringAlkene MetathesisNatural SciencesWhole Cell Biocatalysis
Abstract The approach of combining enzymatic and transition‐metal catalysis has been focused almost exclusively on using purified, isolated enzymes. The use of whole‐cell biocatalysis, instead of isolated enzymes, with transition‐metal catalysis, however, has been investigated only sparsely to date. Herein we present the development of two transition‐metal catalyzed reactions used to derivatize styrene obtained from whole‐cell biosynthesis. Using a biocompatible ruthenium cross‐metathesis catalyst up to 1.5 mM stilbene could be obtained in the presence of E. coli , which simultaneously produced styrene. Using palladium catalysts and arylboronic acids, titers of up to 1 mM of several stilbene derivatives were obtained. These two transition‐metal catalyzed reactions are valuable additions to the toolbox of combined whole‐cell biocatalysis and transition‐metal catalysis, offering the possibility to supplement biosynthetic pathways with the chemical versatility of abiological transition‐metal catalysis.
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