Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Intermediate in the O−O Bond Cleavage Reaction of an Extradiol Dioxygenase

Journal Article · · Biochemistry-US
DOI:https://doi.org/10.1021/bi801459q· OSTI ID:1006981

The reactive oxy intermediate of the catalytic cycle of extradiol aromatic ring-cleaving dioxygenases is formed by binding the catecholic substrate and O{sub 2} in adjacent ligand positions of the active site metal [usually Fe(II)]. This intermediate and the following Fe(II)-alkylperoxo intermediate resulting from oxygen attack on the substrate have been previously characterized in a crystal of homoprotocatechuate 2,3-dioxygenase (HPCD). Here a subsequent intermediate in which the O-O bond is broken to yield a gem diol species is structurally characterized. This new intermediate is stabilized in the crystal by using the alternative substrate, 4-sulfonylcatechol, and the Glu323Leu variant of HPCD, which alters the crystal packing.

Research Organization:
Advanced Photon Source (APS), Argonne National Laboratory (ANL), Argonne, IL (US)
Sponsoring Organization:
USDOE
OSTI ID:
1006981
Journal Information:
Biochemistry-US, Journal Name: Biochemistry-US Journal Issue: (43) ; 10, 2008 Vol. 47; ISSN 0006-2960; ISSN BICHAW
Country of Publication:
United States
Language:
ENGLISH

Similar Records

Nuclear Resonance Vibrational Spectroscopy Definition of O2 Intermediates in an Extradiol Dioxygenase: Correlation to Crystallography and Reactivity
Journal Article · Sun Nov 11 23:00:00 EST 2018 · Journal of the American Chemical Society · OSTI ID:1490963

Crystal structures of alkylperoxo and anhydride intermediates in an intradiol ring-cleaving dioxygenase
Journal Article · Sun Dec 28 23:00:00 EST 2014 · Proceedings of the National Academy of Sciences of the United States of America · OSTI ID:1170026