A chemo-enzymatic oxidation cascade to activate C-H bonds with in situ generated H 2 O 2

Continuous low-level supply or in situ generation of hydrogen peroxide (H O ) is essential for the stability of unspecific peroxygenases, which are deemed ideal biocatalysts for the selective activation of C-H bonds. To envisage potential large scale applications of combined catalytic systems the re...

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Veröffentlicht in:Nature communications 2019-09, Vol.10 (1), p.4178
Hauptverfasser: Freakley, Simon J, Kochius, Svenja, van Marwijk, Jacqueline, Fenner, Caryn, Lewis, Richard J, Baldenius, Kai, Marais, Sarel S, Opperman, Diederik J, Harrison, Susan T L, Alcalde, Miguel, Smit, Martha S, Hutchings, Graham J
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Sprache:eng
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Zusammenfassung:Continuous low-level supply or in situ generation of hydrogen peroxide (H O ) is essential for the stability of unspecific peroxygenases, which are deemed ideal biocatalysts for the selective activation of C-H bonds. To envisage potential large scale applications of combined catalytic systems the reactions need to be simple, efficient and produce minimal by-products. We show that gold-palladium nanoparticles supported on TiO or carbon have sufficient activity at ambient temperature and pressure to generate H O from H and O and supply the oxidant to the engineered unspecific heme-thiolate peroxygenase PaDa-I. This tandem catalyst combination facilitates efficient oxidation of a range of C-H bonds to hydroxylated products in one reaction vessel with only water as a by-product under conditions that could be easily scaled.
ISSN:2041-1723
DOI:10.1038/s41467-019-12120-w