Flux prediction using artificial neural network (ANN) for the upper part of glycolysis.

Journal: PloS one
PMID:

Abstract

The selection of optimal enzyme concentration in multienzyme cascade reactions for the highest product yield in practice is very expensive and time-consuming process. The modelling of biological pathways is a difficult process because of the complexity of the system. The mathematical modelling of the system using an analytical approach depends on the many parameters of enzymes which rely on tedious and expensive experiments. The artificial neural network (ANN) method has been successively applied in different fields of science to perform complex functions. In this study, ANN models were trained to predict the flux for the upper part of glycolysis as inferred by NADH consumption, using four enzyme concentrations i.e., phosphoglucoisomerase, phosphofructokinase, fructose-bisphosphate-aldolase, triose-phosphate-isomerase. Out of three ANN algorithms, the neuralnet package with two activation functions, "logistic" and "tanh" were implemented. The prediction of the flux was very efficient: RMSE and R2 were 0.847, 0.93 and 0.804, 0.94 respectively for logistic and tanh functions using a cross validation procedure. This study showed that a systemic approach such as ANN could be used for accurate prediction of the flux through the metabolic pathway. This could help to save a lot of time and costs, particularly from an industrial perspective. The R-code is available at: https://github.com/DSIMB/ANN-Glycolysis-Flux-Prediction.

Authors

  • Anamya Ajjolli Nagaraja
    LE2P, Laboratory of Energy, Electronics and Processes EA 4079, Faculty of Sciences and Technology, University of La Reunion, France.
  • Nicolas Fontaine
    PEACCEL, Protein Engineering Accelerator, Paris, France.
  • Mathieu Delsaut
    LE2P, Laboratory of Energy, Electronics and Processes EA 4079, Faculty of Sciences and Technology, University of La Reunion, France.
  • Philippe Charton
    DSIMB, INSERM, UMR S-1134, Laboratory of ExcellenceLABEX GR, Faculty of Sciences and Technology, University of La Reunion & University Paris Diderot, Paris, France.
  • Cedric Damour
    LE2P, Laboratory of Energy, Electronics and Processes EA 4079, Faculty of Sciences and Technology, University of La Reunion, France.
  • Bernard Offmann
    UFIP, UMR 6286 CNRS, UFR Sciences et Techniques, Université de Nantes, Nantes, France.
  • Brigitte Grondin-Perez
    LE2P, Laboratory of Energy, Electronics and Processes EA 4079, Faculty of Sciences and Technology, University of La Reunion, France.
  • Frédéric Cadet
    PEACCEL, Protein Engineering Accelerator, Paris, France. frederic.cadet@peaccel.com.