Literature DB >> 6743248

The kinetics of consecutive enzyme reactions. The design of coupled assays and the temporal response of pathways.

J S Easterby.   

Abstract

A regime is proposed for the design of coupled enzyme assays in which auxiliary enzymes are added at concentrations proportional to their Km values. Under these conditions it is possible to calculate the complete time course of the assay including the time required for the system to approach its steady state. The consequence of increasing the number of coupling enzymes is shown to be a considerable decrease in time required to reach the steady state provided that the overall transient time remains the same. The method is extended to the general consideration of pathways and shows that pathways of the same length exhibit identical temporal responses provided that the units of concentration and time used are based on the steady-state concentration of intermediates and the transient time respectively. An unexpected finding is that increasing the number of intermediates in a pathway can decrease the time required to enter a steady state.

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Year:  1984        PMID: 6743248      PMCID: PMC1153552          DOI: 10.1042/bj2190843

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  5 in total

1.  Transient time of the pyruvate kinase-lactate dehydrogenase system of rabbit muscle in vitro.

Authors:  B Hess; B Wurster
Journal:  FEBS Lett       Date:  1970-07-29       Impact factor: 4.124

2.  The kinetics of coupled enzyme reactions. Applications to the assay of glucokinase, with glucose 6-phosphate dehydrogenase as coupling enzyme.

Authors:  A C Storer; A Cornish-Bowden
Journal:  Biochem J       Date:  1974-07       Impact factor: 3.857

3.  A kinetic analysis of coupled enzyme assays.

Authors:  W R McClure
Journal:  Biochemistry       Date:  1969-07       Impact factor: 3.162

4.  Coupled enzyme assays: a general expression for the transient.

Authors:  J S Easterby
Journal:  Biochim Biophys Acta       Date:  1973-02-15

5.  A generalized theory of the transition time for sequential enzyme reactions.

Authors:  J S Easterby
Journal:  Biochem J       Date:  1981-10-01       Impact factor: 3.857

  5 in total
  10 in total

1.  Transition time control analysis of a glycolytic system under different glucose concentrations. Control of transition time versus control of flux.

Authors:  N V Torres; E Meléndez-Hevia
Journal:  Mol Cell Biochem       Date:  1992-06-26       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

3.  Control analysis of transition times in metabolic systems.

Authors:  E Meléndez-Hevia; N V Torres; J Sicilia; H Kacser
Journal:  Biochem J       Date:  1990-01-01       Impact factor: 3.857

4.  Transient times in linear metabolic pathways under constant affinity constraints.

Authors:  M Lloréns; J C Nuño; F Montero
Journal:  Biochem J       Date:  1997-10-15       Impact factor: 3.857

5.  Study of the flux and transition time control coefficient profiles in a metabolic system in vitro and the effect of an external stimulator.

Authors:  N V Torres; R Souto; E Meléndez-Hevia
Journal:  Biochem J       Date:  1989-06-15       Impact factor: 3.857

6.  Transient-time analysis of substrate-channelling in interacting enzyme systems.

Authors:  J Ovádi; P Tompa; B Vértessy; F Orosz; T Keleti; G R Welch
Journal:  Biochem J       Date:  1989-01-01       Impact factor: 3.857

7.  The effect of feedback on pathway transient response.

Authors:  J S Easterby
Journal:  Biochem J       Date:  1986-02-01       Impact factor: 3.857

8.  Excess-substrate inhibition in enzymology and high-dose inhibition in pharmacology: a reinterpretation [corrected].

Authors:  P W Kühl
Journal:  Biochem J       Date:  1994-02-15       Impact factor: 3.857

9.  Kinetic study of an enzymic cycling system coupled to an enzymic step: determination of alkaline phosphatase activity.

Authors:  E Valero; R Varón; F García-Carmona
Journal:  Biochem J       Date:  1995-07-01       Impact factor: 3.857

10.  Kinetic studies of Escherichia coli AlkB using a new fluorescence-based assay for DNA demethylation.

Authors:  Todd W Roy; A S Bhagwat
Journal:  Nucleic Acids Res       Date:  2007-11-14       Impact factor: 16.971

  10 in total

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