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...
Gespeichert in:
Veröffentlicht in: | Nature communications 2019-09, Vol.10 (1), p.4178 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |