Literature DB >> 17928131

Three mechanisms and rapid-equilibrium rate equations for a type of reductase reaction.

Robert A Alberty1.   

Abstract

Rapid-equilibrium rate equations for enzyme-catalyzed reactions are especially useful when the mechanism involves a number of pKs, but they are also useful when some reactants have stoichiometric numbers greater than one or hydrogen ions are produced or consumed in the rate-determining step. The pH dependencies of limiting velocities, Michaelis constants, and reaction velocities for the forward reaction are discussed for two examples of reductase reactions of the type mR + O -> products, where R is the reductant and O is the oxidant. For the nitrate reductase reaction (EC 1.9.6.1), m = 2 and two hydrogen ions are consumed. For the nitrite-ferredoxin reductase reaction (EC 1.7.7.1), m = 6 and eight hydrogen ions are consumed. The expressions for the limiting velocities, Michaelis constants, and rate equations for the forward reaction are derived for two ordered mechanisms and the random mechanism. Three Mathematica programs are used to make plots of kinetic parameters as functions of pH and three-dimensional plots of rapid-equilibrium velocities as functions of [O] and [R] for arbitrary sets of input parameters.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17928131     DOI: 10.1016/j.bpc.2007.09.005

Source DB:  PubMed          Journal:  Biophys Chem        ISSN: 0301-4622            Impact factor:   2.352


  2 in total

1.  Rapid-equilibrium rate equations for the enzymatic catalysis of A+B=P+Q over a range of pH.

Authors:  Robert A Alberty
Journal:  Biophys Chem       Date:  2007-11-12       Impact factor: 2.352

2.  Determination of kinetic parameters of enzyme-catalyzed reaction a + B + C --> products with the minimum number of velocity measurements.

Authors:  Robert A Alberty
Journal:  J Phys Chem B       Date:  2009-01-29       Impact factor: 2.991

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.