Format

Send to

Choose Destination
FEBS Lett. 2017 Jan;591(1):39-46. doi: 10.1002/1873-3468.12519. Epub 2016 Dec 24.

Investigating the roles of T224 and T232 in the oxidation of cinnamaldehyde catalyzed by myxobacterial CYP260B1.

Author information

1
Institut für Biochemie, Universität des Saarlandes, Saarbruecken, Germany.

Abstract

Although the oxidation of aldehydes to carboxylic acids is mainly catalyzed by aldehyde dehydrogenases in nature, cytochromes P450 are also able to perform such reactions. In this study, we demonstrate the oxidation of cinnamaldehyde to cinnamic acid by the myxobacterial CYP260B1. Following our docking studies of the aldehyde, we generated T224A and T234A mutants of CYP260B1 by site-directed mutagenesis to disrupt the substrate positioning and proton delivery, respectively. Furthermore, we used the kinetic solvent isotope effect on the steady-state turnover of the substrate to investigate the reactive intermediate capable of performing the catalysis. Our results suggest that the aldehyde oxidation occurs via a nucleophilic attack of the ferric peroxoanion.

KEYWORDS:

CYP260B1; Sorangium cellulosum So ce56; aldehyde oxidation; kinetic solvent isotope effect

PMID:
27926983
DOI:
10.1002/1873-3468.12519
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center