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Solution and Computational Studies of Kinetic Isotope Effects in Flavoprotein and Quinoprotein Catalyzed Substrate Oxidations as Probes of Enzymic Hydrogen Tunneling and Mechanism
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Solution and Computational Studies of Kinetic Isotope Effects in Flavoprotein and Quinoprotein Catalyzed Substrate Oxidations as Probes of Enzymic Hydrogen Tunneling and Mechanism book
Solution and Computational Studies of Kinetic Isotope Effects in Flavoprotein and Quinoprotein Catalyzed Substrate Oxidations as Probes of Enzymic Hydrogen Tunneling and Mechanism
DOI link for Solution and Computational Studies of Kinetic Isotope Effects in Flavoprotein and Quinoprotein Catalyzed Substrate Oxidations as Probes of Enzymic Hydrogen Tunneling and Mechanism
Solution and Computational Studies of Kinetic Isotope Effects in Flavoprotein and Quinoprotein Catalyzed Substrate Oxidations as Probes of Enzymic Hydrogen Tunneling and Mechanism book
ABSTRACT
I. Enzymic H-Tunneling and Kinetic Isotope Effects ........................................................ 671
A. Stopped-Flow Methods to Access the Half-Reactions
of Flavoenzymes and Quinoproteins ....................................................................... 672
II. Interpreting Temperature Dependence of Isotope Effects in Terms
of H-Tunneling................................................................................................................. 673
III. H-Tunneling in Flavoenzymes PETN Reductase and MR ............................................. 675
IV. H-Tunneling in TTQ-Dependent MADH and AADH .................................................... 678
V. Computational Studies of Substrate Oxidation in TTQ-Dependent
Amine Dehydrogenases ................................................................................................... 679
VI. H-Tunneling in Flavoprotein Amine Dehydrogenases: TSOX and
Engineering Gated Motion in TMADH .......................................................................... 682
VII. Concluding Remarks........................................................................................................ 685
Acknowledgments ........................................................................................................................ 685
References..................................................................................................................................... 685
Kinetic isotope effects (KIEs) are powerful probes of H-transfer reactions and have provided
evidence for nonclassical transfer of the H nucleus in enzymes (see Chapter 28 by Kohen in this
volume for a detailed discussion of the use of KIEs to identify tunneling regimes). Early
studies of H-transfer by quantum tunneling focused on deviations from values predicted by
semi-classical models (in which zero point energies, but not tunneling, have been taken into
account): KIEs, Swain-Schaad relationships
[exp
. 3:26; where k
, k
, and k
are the
rates of transfer for protium, deuterium and tritium, respectively] or Arrhenius prefactor ratios
(q1 for a reaction proceeding purely by tunneling, ,1 for moderate tunneling). For a more
detailed discussion see, for example, Chapter 28 by Kohen in this volume. Early examples in
which H-tunneling was inferred from measurements of KIEs include yeast alcohol
dehydrogenase,
bovine serum amine oxidase,
horse liver alcohol dehydrogenase,
and
monoamine oxidase.