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dc.contributor.authorPeterson, Michelle E.
dc.contributor.authorDaniel, Roy M.
dc.contributor.authorDanson, Michael J.
dc.contributor.authorEisenthal, Robert
dc.date.accessioned2010-08-26T22:05:09Z
dc.date.available2010-08-26T22:05:09Z
dc.date.issued2007
dc.identifier.citationPeterson, M.E., Daniel, R.M., Danson, M.J. & Eisenthal, R. (2007). The dependence of enzyme activity on temperature: determination and validation of parameters. Biochemical Journal, 402(2), 331-337.en_NZ
dc.identifier.urihttps://hdl.handle.net/10289/4440
dc.description.abstractTraditionally, the dependence of enzyme activity on temperature has been described by a model consisting of two processes: the catalytic reaction defined by DGDaggercat, and irreversible inactivation defined by DGDaggerinact. However, such a model does not account for the observed temperature-dependent behaviour of enzymes, and a new model has been developed and validated. This model (the Equilibrium Model) describes a new mechanism by which enzymes lose activity at high temperatures, by including an inactive form of the enzyme (Einact) that is in reversible equilibrium with the active form (Eact); it is the inactive form that undergoes irreversible thermal inactivation to the thermally denatured state. This equilibrium is described by an equilibrium constant whose temperature-dependence is characterized in terms of the enthalpy of the equilibrium, DHeq, and a new thermal parameter, Teq, which is the temperature at which the concentrations of Eact and Einact are equal; Teq may therefore be regarded as the thermal equivalent of Km. Characterization of an enzyme with respect to its temperature-dependent behaviour must therefore include a determination of these intrinsic properties. The Equilibrium Model has major implications for enzymology, biotechnology and understanding the evolution of enzymes. The present study presents a new direct data-fitting method based on fitting progress curves directly to the Equilibrium Model, and assesses the robustness of this procedure and the effect of assay data on the accurate determination of Teq and its associated parameters. It also describes simpler experimental methods for their determination than have been previously available, including those required for the application of the Equilibrium Model to non-ideal enzyme reactions.en_NZ
dc.language.isoen
dc.publisherPortland Press (Online)en_NZ
dc.relation.urihttp://www.biochemj.org/bj/402/bj4020331.htmen_NZ
dc.subjectenzyme activityen_NZ
dc.subjectEquilibrium Modelen_NZ
dc.subjectkineticsen_NZ
dc.subjectstabilityen_NZ
dc.subjectthermal-dependenceen_NZ
dc.titleThe dependence of enzyme activity on temperature: determination and validation of parametersen_NZ
dc.typeJournal Articleen_NZ
dc.identifier.doi10.1042/BJ20061143en_NZ
dc.relation.isPartOfBiochemical Journalen_NZ
pubs.begin-page331en_NZ
pubs.elements-id33135
pubs.end-page337en_NZ
pubs.volume402en_NZ


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