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Asymmetric sulfoxidation and amine binding by H64D/V68A and H64D/V68S Mb: mechanistic insight into the chiral
Shigeru Kato1, Hui-Jun Yang, Takafumi Ueno
1Department of Structural Molecular Science, The Graduate University for Advanced Studies, Okazaki 444-8585, Japan.
Journal of the American Chemical Society
|July 18, 2002
Abstract:
The H64D/V68A and H64D/V68S mutants of Myoglobin are found to oxidize thioanisole with high enantioselectivity and reactivity. These mutants are also capable of enantioselective binding of alpha-methylbenzylamine, which mimics an expected sulfoxidation intermediate. The kinetic study of the amine binding shows that the Fe-O bond cleavage in the intermediate may be the chiral discrimination step of the sulfoxidation.

