Enzyme kinetics has undergone very rapid growth and development during the past fifteen years and has been well received by the biochemical community. A cursory glance at the current biochem ical literature reveals the increasing popularity of enzyme ki netics1 yet, there are very few books available to guide the enzymologist who wishes to conduct kinetic experiments. This monograph was undertaken to provide the fledgling kineticist with an outline of contemporary initial rate enzyme kinetics. A large portion of the material contained in this book is presented in a second-year, graduate-level…mehr
Enzyme kinetics has undergone very rapid growth and development during the past fifteen years and has been well received by the biochemical community. A cursory glance at the current biochem ical literature reveals the increasing popularity of enzyme ki netics1 yet, there are very few books available to guide the enzymologist who wishes to conduct kinetic experiments. This monograph was undertaken to provide the fledgling kineticist with an outline of contemporary initial rate enzyme kinetics. A large portion of the material contained in this book is presented in a second-year, graduate-level course in biochemistry at Iowa State University. I have found that the presentation in this course has enabled students without a strong background in math ematics to undertake initial rate studies at the research bench. The monograph obviously is more comprehensive than any course could be, and should permit similar accomplishment. As the title implies, the major emphasis of this monograph is on initial rate enzyme kinetics. I considered at length the advis ability of including chapters on integrated rate equations and on the theory and application of rapid reaction kinetics, such as rapid-mixing stopped-flow, and temperature-jump kinetics. These, however, are topics that would require a good deal of space to develop if they were to be helpful to the beginner.Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Produktdetails
Produktdetails
Molecular Biology, Biochemistry and Biophysics Molekularbiologie, Biochemie und Biophysik 22
I Nomenclature, Definitions, and Evolution of the Kinetic Mechanism.- A. Nomenclature.- B. Evolution of Initial Rate Kinetics.- References.- II Derivation of Initial Velocity Rate Equations.- A. Definitions and Derivations.- B. The Equilibrium Assumption.- C. Derivation of Complex Steady-State Rate Equations.- D. Derivation of the Rate Equation Using the Rapid Equilibrium Assumption.- E. Derivation of Initial Rate Equations Using a Combination of Equilibrium and Steady-State Assumptions.- F. Derivation of Steady-State Rate Equations by Using the Digital Computer.- References.- III Experimental Protocol and Plotting of Kinetic Data.- A. General Considerations.- B. Analysis of Radioactive Substrates and Determination of Radiopurity.- C. pH Effects.- D. Substrate Concentration.- E. Studies of Forward and Reverse Reactions.- F. Studies of Nucleotide Dependent Enzymic Reactions.- G. The Kinetic Assay.- H. Plotting Methods.- I. Graphical Procedures.- J. The Point of Convergence of Sequential Double Reciprocal Plots as a Criterion of Kinetic Mechanism.- K. Protocol and Data Plotting for Three Substrate Systems.- L. Graphical Methods for Differentiating between Steady-State and Equilibrium Ordered Bi Bi Mechanisms.- References.- IV Use of Competitive Substrate Analogs and Alternative Substrates for Studying Kinetic Mechanisms.- A. Competitive Inhibition.- B. Partial Competitive Inhibition.- C. Noncompetitive Inhibition.- D. Ucompetitive Inhibition.- E. Nonlinear Enzyme Inhibition.- F. The Use of Substrate Analogs for Studying Kinetic Mechanisms.- G. Cleland's Rules for Dead End Inhibition.- H. The Stereochemical Nature of Enzyme and Substrate Interaction.- I. Kinetics of Enzyme Specificity.- J. The Kinetics of Transition State Analogs.- References.- V Product, Substrate, andAlternative Substrate Inhibition.- A. Product Inhibition Experiments.- B. Substrate Inhibition.- C. Alternative Substrate Inhibition.- D. Alternative Product Inhibition.- E. Multisite Ping Pong Mechanisms.- F. Enzymes with Identical Substrate-Product Pairs.- References.- VI Isotope Exchange.- A. Abortive Complex Formation.- B. Derivation of Rate Equations.- C. Substrate Synergism.- D. Calculation of Kinetic Parameters.- E. Experimental Protocol.- F. Isotope-Trapping.- References.- VII Isomerization Mechanisms and the ? and Haldane Relationships.- A. The ? Relationships.- B. The Haldane Relationships.- C. Isomerization Mechanisms.- References.- VIII The Effect of Temperature and pH on Enzyme Activity.- A. Effect of pH on Enzyme Kinetics.- B. The Effect of Temperature on Enzyme Catalyzed Reactions.- References.- IX Cooperativity and Allostery.- A. Cooperativity.- B. Molecular Models.- C. Kinetic Models.- D. Allostery.- E. Product Effects.- References.- Appendix I Rate Equations, Determinants, and Haldane Expressions for Some Common Kinetic Mechanisms.- Appendix II A Computer Program for Deriving Enzyme Rate Equations.- Appendix III Plotting and Statistical Analysis of Kinetic Data Using the OMNITAB Program.
I Nomenclature, Definitions, and Evolution of the Kinetic Mechanism.- A. Nomenclature.- B. Evolution of Initial Rate Kinetics.- References.- II Derivation of Initial Velocity Rate Equations.- A. Definitions and Derivations.- B. The Equilibrium Assumption.- C. Derivation of Complex Steady-State Rate Equations.- D. Derivation of the Rate Equation Using the Rapid Equilibrium Assumption.- E. Derivation of Initial Rate Equations Using a Combination of Equilibrium and Steady-State Assumptions.- F. Derivation of Steady-State Rate Equations by Using the Digital Computer.- References.- III Experimental Protocol and Plotting of Kinetic Data.- A. General Considerations.- B. Analysis of Radioactive Substrates and Determination of Radiopurity.- C. pH Effects.- D. Substrate Concentration.- E. Studies of Forward and Reverse Reactions.- F. Studies of Nucleotide Dependent Enzymic Reactions.- G. The Kinetic Assay.- H. Plotting Methods.- I. Graphical Procedures.- J. The Point of Convergence of Sequential Double Reciprocal Plots as a Criterion of Kinetic Mechanism.- K. Protocol and Data Plotting for Three Substrate Systems.- L. Graphical Methods for Differentiating between Steady-State and Equilibrium Ordered Bi Bi Mechanisms.- References.- IV Use of Competitive Substrate Analogs and Alternative Substrates for Studying Kinetic Mechanisms.- A. Competitive Inhibition.- B. Partial Competitive Inhibition.- C. Noncompetitive Inhibition.- D. Ucompetitive Inhibition.- E. Nonlinear Enzyme Inhibition.- F. The Use of Substrate Analogs for Studying Kinetic Mechanisms.- G. Cleland's Rules for Dead End Inhibition.- H. The Stereochemical Nature of Enzyme and Substrate Interaction.- I. Kinetics of Enzyme Specificity.- J. The Kinetics of Transition State Analogs.- References.- V Product, Substrate, andAlternative Substrate Inhibition.- A. Product Inhibition Experiments.- B. Substrate Inhibition.- C. Alternative Substrate Inhibition.- D. Alternative Product Inhibition.- E. Multisite Ping Pong Mechanisms.- F. Enzymes with Identical Substrate-Product Pairs.- References.- VI Isotope Exchange.- A. Abortive Complex Formation.- B. Derivation of Rate Equations.- C. Substrate Synergism.- D. Calculation of Kinetic Parameters.- E. Experimental Protocol.- F. Isotope-Trapping.- References.- VII Isomerization Mechanisms and the ? and Haldane Relationships.- A. The ? Relationships.- B. The Haldane Relationships.- C. Isomerization Mechanisms.- References.- VIII The Effect of Temperature and pH on Enzyme Activity.- A. Effect of pH on Enzyme Kinetics.- B. The Effect of Temperature on Enzyme Catalyzed Reactions.- References.- IX Cooperativity and Allostery.- A. Cooperativity.- B. Molecular Models.- C. Kinetic Models.- D. Allostery.- E. Product Effects.- References.- Appendix I Rate Equations, Determinants, and Haldane Expressions for Some Common Kinetic Mechanisms.- Appendix II A Computer Program for Deriving Enzyme Rate Equations.- Appendix III Plotting and Statistical Analysis of Kinetic Data Using the OMNITAB Program.
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