Closed and Open Metabolic Cycles: Transition Time
- 1 Departamento de Bioquímica, Facultad de Medicina, Instituto de Investigaciones Biomédicas Alberto Sols, UAM/CSIC, Madrid, Spain
- 2 Departamento de Bioquímica, Facultad de Medicina, Instituto de Investigaciones Biomédicas Alberto Sols, UAM/CSIC, Madrid, Spain
Abstract
A metabolic cycle can be viewed as a central core and its branches. The central core is here firstly considered as a pre-closed metabolic cycle (CMC), with a unique first substrate, but with no input or output of other components. By contrast, the metabolic cycles in nature are open metabolic cycles (OMC) with output and input of external substrates (through “metabolic branches”), modulating continuously the enzyme activities and the total concentration of their substrates thorough complex regulatory phenomena. In this work, the transition from a Closed to an Open metabolic cycle has been simulated by a consecutive entry and exit of two components through the catalytic action of two enzymes. It is known that after any alteration of the initial conditions, the cycles need a time to reach new equilibrium. We have measured the changes of transition time (T.T.) values in 81 models of CMC differing in Km or V max values. In general, the T.T. tends to be shorter in cycles with preponderant lower Km and higher V max values. Further, Mathematica refinement for the estimation of transition time from the data previously calculated can be obtained with the use of the command Interpolating Function .
- Alberty, R.A. (2011) Enzyme Kinetics, Rapid-Equilibrium Applications of Mathematica. Hoboken. http://dx.doi.org/10.1002/9780470940020
- Morris Jr., S.M. (2002) Regulation of Enzymes of the Urea Cycle and Arginine Metabolism. Annual Review of Nutrition, 22, 87-105. http://dx.doi.org/10.1146/annurev.nutr.22.110801.140547
- Albe, K.R. and Wright, B.E. (1992) Systems Analysis of the Tricarboxylic Acid Cycle in Dictyostelium discoideum. II. Control Analysis. The Journal of Biological Chemistry, 267, 3106-3114.
- Korla, K. and Mitra, C.K. (2014) Modelling the Krebs Cycle and Oxidative Phosphorylation. Journal of Biomolecular Structure and Dynamics, 32, 242-246. http://dx.doi.org/10.1080/07391102.2012.762723
- Chalhoub, E., Hanson, R.W. and Belovich, J.M. (2007) A Computer Model of Gluconeogenesis and Lipid Metabolism in the Perfused Liver. American Journal of Physiology: Endocrinology and Metabolism, 293, 1676-1686.
- Maher, A.D., Kuchel, P.W., Ortega, F., de Atauri, P., Centelles, J. and Cascante, M. (2003) Mathematical Modelling of the Urea Cycle. A Numerical Investigation into Substrate Channelling. European Journal of Biochemistry/FEBS, 270, 3953-3961.
- Bachmann, C. and Colombo, J.P. (1981) Computer Simulation of the Urea Cycle: Trials for an Appropriate Model. Enzyme, 26, 259-264.
- Günther Sillero, M.A., de Diego, A., Perez-Zuniga, F.J. and Sillero, A. (2008) Synthesis of Bisphosphonate Derivatives of ATP by T4 DNA Ligase, Ubiquitin Activating Enzyme (E1) and Other Ligases. Biochemical Pharmacology, 75, 1959-1965.
- López-Cánovas, F.J., Cánovas, F., Günther Sillero, M.A. and Sillero, A. (2010) Mathematical Model for the Ubiquitin Activating Enzyme E1. Journal of Biomedical Science and Engineering, 3, 274-286.
- López-Cánovas, F.J., Gomes, P.J. and Sillero, A. (2013) Mathematica Program: Its Use to Simulate Metabolic Irreversible Pathways and Inhibition of the First Enzyme of a Metabolic Pathway as Visuaized with the Reservoir Model. Computers in Biology and Medicine, 42, 853-864.
- García-Herrero, V., López-Cánovas, F.J. and Sillero, A. (2014) A Model Metabolic Cycle Simulated with the Mathematica Program. Journal of Biomedical Science and Engineering, 7, 286-295. http://dx.doi.org/10.4236/jbise.2014.75031
- García-Herrero, V. and Sillero, A. (2015) Pedagogical View of Model Metabolic Cycles. Biochemistry and Molecular Biology Education, 43, 468-475. http://dx.doi.org/10.1002/bmb.20920