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Article
Identification of an Active Site-bound Nitrile Hydratase Intermediate through Single Turnover Stopped-flow Spectroscopy
Journal of Biological Chemistry
  • Natalie Gumataotao, Loyola University Chicago
  • Misty L. Kuhn, Loyola University Chicago
  • Natalia Hajnas, Loyola University Chicago
  • Richard C. Holz, Marquette University
Document Type
Article
Publication Date
5-31-2013
Disciplines
Abstract
Stopped-flow kinetic data were obtained for the iron-type nitrile hydratase from Rhodococcus equi TG328-2 (ReNHase) using methacrylonitrile as the substrate. Multiple turnover experiments suggest a three-step kinetic model that allows for the reversible binding of substrate, the presence of an intermediate, and the formation of product. Microscopic rate constants determined from these data are in good agreement with steady state data confirming that the stopped-flow method used was appropriate for the reaction. Single turnover stopped-flow experiments were used to identify catalytic intermediates. These data were globally fit confirming a three-step kinetic model. Independent absorption spectra acquired between 0.005 and 0.5 s of the reaction reveal a significant increase in absorbance at 375, 460, and 550 nm along with the hypsochromic shift of an Fe3+←S ligand-to-metal charge transfer band from 700 to 650 nm. The observed UV-visible absorption bands for the Fe3+-nitrile intermediate species are similar to low spin Fe3+-enzyme and model complexes bound by NO or N3−. These data provide spectroscopic evidence for the direct coordination of the nitrile substrate to the nitrile hydratase active site low spin Fe3+ center.
Comments

Journal of Biological Chemistry. Vol. 288, No. 22 (May 31, 2013): 15532-15536. DOI.

Richard C. Holz was affiliated with Loyola University-Chicago at the time of publication.

Citation Information
Natalie Gumataotao, Misty L. Kuhn, Natalia Hajnas and Richard C. Holz. "Identification of an Active Site-bound Nitrile Hydratase Intermediate through Single Turnover Stopped-flow Spectroscopy" Journal of Biological Chemistry (2013) ISSN: 0021-9258
Available at: http://works.bepress.com/richard_holz/12/