Literature DB >> 6548935

Theory and practical application of coupled enzyme reactions: one and two auxiliary enzymes.

S P Brooks, T Espinola, C H Suelter.   

Abstract

An extended and practical set of equations which describe coupled enzyme reactions is presented. The mathematical treatment relies on two assumptions: (a) the rate of the primary enzyme reaction is constant and (b) the reverse reactions are negligible. The treatment leads to the development of new equations which relate the time required for the concentration of a reaction intermediate to reach a defined fraction of its steady-state concentration to the kinetic parameters of the enzymes when mutarotation of one of the intermediates does not occur. The new equations reduce to those previously derived when the steady-state concentration of the intermediate is small compared with its Km value. A method for minimizing the cost of the two auxiliary enzyme system is also provided.

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Year:  1984        PMID: 6548935     DOI: 10.1139/o84-121

Source DB:  PubMed          Journal:  Can J Biochem Cell Biol        ISSN: 0714-7511


  2 in total

1.  A kinetic description of sequential, reversible, Michaelis-Menten reactions: practical application of theory to metabolic pathways.

Authors:  S P Brooks; K B Storey
Journal:  Mol Cell Biochem       Date:  1992-09-22       Impact factor: 3.396

2.  Analysis and characterization of transition states in metabolic systems. Transition times and the passivity of the output flux.

Authors:  N V Torres; J Sicilia; E Meléndez-Hevia
Journal:  Biochem J       Date:  1991-05-15       Impact factor: 3.857

  2 in total

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