Catalytic Mechanism of Heme Oxygenase through EPR and ENDOR of Cryoreduced Oxy-Heme Oxygenase and Its Asp 140 Mutants

• Published in: Journal of the American Chemical Society 2002-02, Vol.124 (8), p.1798-1808
• Main Authors: Davydov, Roman, Kofman, Viktoria, Fujii, Hiroshi, Yoshida, Tadashi, Ikeda-Saito, Masao, Hoffman, Brian M
• Format: Article
• Language: English
• Subjects: Aspartic Acid - chemistry; Aspartic Acid - genetics; Biological and medical sciences; Catalysis; Electron Spin Resonance Spectroscopy; Fundamental and applied biological sciences. Psychology; Heme - chemistry; Heme - metabolism; Heme Oxygenase (Decyclizing) - chemistry; Heme Oxygenase (Decyclizing) - genetics; Heme Oxygenase (Decyclizing) - metabolism; Models, Molecular; Molecular and cellular biology; Mutation; Nuclear Magnetic Resonance, Biomolecular; Oxidation-Reduction
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja0122391

Heme oxygenase (HO) catalyzes the O2- and NADPH-cytochrome P450 reductase-dependent conversion of heme to biliverdin, Fe, and CO through a process in which the heme participates both as a prosthetic group and as a substrate. In the present study, we have generated a detailed reaction cycle for the first monooxygenation step of HO catalysis, conversion of the heme to α-meso-hydroxyheme. We employed EPR (using both 16O2 and 17O2) and 1H, 14N ENDOR spectroscopies to characterize the intermediates generated by 77 K radiolytic cryoreduction and subsequent annealing of wild-type oxy-HO and D140A, F mutants. One-electron cryoreduction of oxy-HO yields a hydroperoxoferri-HO with g-tensor, g = [2.37, 2.187, 1.924]. Annealing of this species to 200 K is accompanied by spectroscopic changes that include the appearance of a new 1H ENDOR signal, reflecting rearrangements in the active site. Kinetic measurements at 214 K reveal that the annealed hydroperoxoferri-HO species, denoted R, generates the ferri-α-meso-hydroxyheme product in a first-order reaction. Disruption of the H-bonding network within the distal pocket of HO by the alanine and phenylalanine mutations of residue D140 prevents product formation. The hydroperoxoferri-HO (D140A) instead undergoes heterolytic cleavage of the O−O bond, ultimately yielding an EPR-silent compound II-like species that does not form product. These results, which agree with earlier suggestions, establish that hydroperoxoferri-HO is indeed the reactive species, directly forming the α-meso-hydroxyheme product by attack of the distal OH of the hydroperoxo moiety at the heme α-carbon.