A comparative density-functional study of the reaction mechanism of the O-2-dependent coproporphyrinogen III oxidase

• Type: Article in International Scientific Journal
• Date: 2008

Authors

Pedro J Silva (Author) Other; Maria Joao Ramos (Author) FCUP

Journal

Title: Bioorganic and Medicinal Chemistry

Vol. 16

Pages: 2726-2733

ISSN: 0968-0896

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 12 Citations

Scopus - 13 Citations

Scientific classification

FOS: Natural sciences > Chemical sciences

Other information

Authenticus ID: P-004-0W0

DOI: 10.1016/j.bmc.2008.01.008

Abstract (EN): During heme biosynthesis, coproporphyrinogen III oxidase catalyzes the conversion of two propionate substituents from the highly reactive substrate coproporphyrinogen III into vinyl substituents, yielding protoporphyrinogen IX Although the crystal structure of this important enzyme has recently been reported, the reaction mechanism of this intriguing enzyme remains the subject of intense speculation, as impairment of this enzyme has been shown to be the molecular cause behind hereditary coproporphyria. We have performed DFT calculations on model systems in order to analyze several reaction mechanisms proposed for this enzyme. The results afford a full description of the different proposals and allow the rejection of a direct electron abstraction from the protonated substrate by dioxygen. We found that O-2 addition to the (preferentially deprotonated) pyrrole substrate (yielding a hydroperoxide, which then abstracts a proton from the reactive propionate substituent) is compatible with the observed experimental reaction rate, and that the reaction may then proceed through HO2- elimination, followed by decarboxylation.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 8