Literature DB >> 9089640

A simple mechanism decreasing free metabolite pool size in static spatial channelling.

B Korzeniewski1, P A Quant.   

Abstract

We propose a simple mechanism which enables decrease of the free pool of channelled metabolite in static spatial channelling, when the concentration of the enzyme consuming the channelled metabolite is greater than the concentration of the enzyme producing this metabolite. Spatial channelling occurs between two enzymes when the common metabolite is released to a small space between these enzymes and does not from a ternary covalent complex with them, as is the case in covalent (dynamic or static) channelling. The mechanism proposed is qualitatively independent of rate constants, metabolite concentrations as well as other kinetic properties and is quantitatively significant for all physiologically relevant conditions. Calculations show that the free metabolite pool must decrease, when the concentration of the enzyme consuming the channelled metabolite is greater than the enzyme producing it. This mechanism is much more effective than increase in the concentration (or rate constant) of the enzyme consuming the metabolite in the absence of spatial channelling.

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Year:  1997        PMID: 9089640     DOI: 10.1023/a:1006882029611

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  14 in total

Review 1.  Enzyme-enzyme interactions and their metabolic role.

Authors:  P A Srere; J Ovadi
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Review 2.  Physiological significance of metabolic channelling.

Authors:  J Ovádi
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3.  Channelling can decrease pool size.

Authors:  P Mendes; D B Kell; H V Westerhoff
Journal:  Eur J Biochem       Date:  1992-02-15

4.  Failure of channelling to maintain low concentrations of metabolic intermediates.

Authors:  A Cornish-Bowden
Journal:  Eur J Biochem       Date:  1991-01-01

Review 5.  Complexes of sequential metabolic enzymes.

Authors:  P A Srere
Journal:  Annu Rev Biochem       Date:  1987       Impact factor: 23.643

Review 6.  Kinetic and physico-chemical analysis of enzyme complexes and their possible role in the control of metabolism.

Authors:  T Keleti; J Ovádi; J Batke
Journal:  Prog Biophys Mol Biol       Date:  1989       Impact factor: 3.667

7.  Intermediates of peroxisomal beta-oxidation. A study of the fatty acyl-CoA esters which accumulate during peroxisomal beta-oxidation of [U-14C]hexadecanoate.

Authors:  K Bartlett; R Hovik; S Eaton; N J Watmough; H Osmundsen
Journal:  Biochem J       Date:  1990-08-15       Impact factor: 3.857

8.  Channelling can affect concentrations of metabolic intermediates at constant net flux: artefact or reality?

Authors:  A Cornish-Bowden; M L Cárdenas
Journal:  Eur J Biochem       Date:  1993-04-01

Review 9.  A minimal hypothesis for membrane-linked free-energy transduction. The role of independent, small coupling units.

Authors:  H V Westerhoff; B A Melandri; G Venturoli; G F Azzone; D B Kell
Journal:  Biochim Biophys Acta       Date:  1984-12-17

10.  Intramitochondrial control of the oxidation of hexadecanoate in skeletal muscle. A study of the acyl-CoA esters which accumulate during rat skeletal-muscle mitochondrial beta-oxidation of [U-14C]hexadecanoate and [U-14C]hexadecanoyl-carnitine.

Authors:  S Eaton; A K Bhuiyan; R S Kler; D M Turnbull; K Bartlett
Journal:  Biochem J       Date:  1993-01-01       Impact factor: 3.857

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  1 in total

1.  Does metabolite channeling accelerate enzyme-catalyzed cascade reactions?

Authors:  Liubov Poshyvailo; Eric von Lieres; Svyatoslav Kondrat
Journal:  PLoS One       Date:  2017-02-24       Impact factor: 3.240

  1 in total

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