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A model of yeast glycolysis based on a consistent kinetic characterisation of all its enzymes

Authors :
Manchester Centre for Integrative Systems Biology [research center]
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group) [research center]
BBSRC / EPSRC [sponsor]
Smallbone, Kieran(*)
Messiha, Hanan L.(*)
Carroll, Kathleen M.(*)
Winder, Catherine L.(*)
Malys, Naglis(*)
Dunn, Warwick B.
Murabito, Ettore
Swainston, Neil
Dada, Joseph O.
Khan, Farid
Pir, Pinar
Simeonidis, Vangelis
Spasic, Irena
Wishart, Jill
Weichart, Dieter
Hayes, Neil W.
Jameson, Daniel
Broomhead, David S.
Oliver, Stephen G.
Gaskell, Simon J.
McCarthy, John E.G.
Paton, Norman W.
Westerhoff, Hans V.
Kell, Douglas B.
Mendes, Pedro
Manchester Centre for Integrative Systems Biology [research center]
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group) [research center]
BBSRC / EPSRC [sponsor]
Smallbone, Kieran(*)
Messiha, Hanan L.(*)
Carroll, Kathleen M.(*)
Winder, Catherine L.(*)
Malys, Naglis(*)
Dunn, Warwick B.
Murabito, Ettore
Swainston, Neil
Dada, Joseph O.
Khan, Farid
Pir, Pinar
Simeonidis, Vangelis
Spasic, Irena
Wishart, Jill
Weichart, Dieter
Hayes, Neil W.
Jameson, Daniel
Broomhead, David S.
Oliver, Stephen G.
Gaskell, Simon J.
McCarthy, John E.G.
Paton, Norman W.
Westerhoff, Hans V.
Kell, Douglas B.
Mendes, Pedro
Publication Year :
2013

Abstract

We present an experimental and computational pipeline for the generation of kinetic models of metabolism, and demonstrate its application to glycolysis in Saccharomyces cerevisiae. Starting from an approximate mathematical model, we employ a ‘‘cycle of knowledge’’ strategy, identifying the steps with most control over flux. Kinetic parameters of the individual isoenzymes within these steps are measured experimentally under a standardised set of conditions. Experimental strategies are applied to establish a set of in vivo concentrations for isoenzymes and metabolites. The data are integrated into a mathematical model that is used to predict a new set of metabolite concentrations and reevaluate the control properties of the system. This bottom-up modelling study reveals that control over the metabolic network most directly involved in yeast glycolysis is more widely distributed than previously thought.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn906075324
Document Type :
Electronic Resource