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Chapter

Solution and Computational Studies of Kinetic Isotope Effects in Flavoprotein and Quinoprotein Catalyzed Substrate Oxidations as Probes of Enzymic Hydrogen Tunneling and Mechanism

Chapter

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

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

Edited ByAmnon Kohen, Hans-Heinrich Limbach
BookIsotope Effects In Chemistry and Biology

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Edition 1st Edition
First Published 2005
Imprint CRC Press
Pages 20
eBook ISBN 9780429116131

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.

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