African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12487

Full Length Research Paper

Modeling metabolic response to changes of enzyme amount in yeast glycolysis

Xuelian Yang1,2, Lin Xu1 and Ming Yan1*
1College of Biotechnology and Pharmaceutical Engineering,Nanjing University of Technology, XinMoFan Road,Nanjing,Jiangs,210009,China. 2Beijing Higher Institution Engineering Research Center of Food Additives and Ingredients,Beijing Technology & Business University,Beijing 100048,China.
Email: [email protected], [email protected]

  •  Accepted: 17 August 2010
  •  Published: 11 October 2010

Abstract

Based on the work of Hynne et al. (2001), in an in silico model of glycolysis,Saccharomyces cerevisiae is established by introducing an enzyme amount multiple factor (É‘) into the kinetic equations. The model is aimed to predict the metabolic response to the change of enzyme amount. With the help of É‘, the amounts of twelve enzymes were altered by different multiples from their initial values. Then twenty metabolite concentrations were monitored and analyzed. The prediction of metabolite levels accord with the experimental result and understanding of bioprocess. It also suggested that the metabolic response to dropping enzyme amounts was stronger than the increasing concentrations. Besides, two different trends of change in the metabolite levels appeared apparently, which are correspond with the network structure. Therefore, for regulating the metabolite levels through changing enzyme amount, not only biochemical characteristic but also location of enzymes in the network should be considered.

 

Key words: Glycolysis, yeast, metabolites level, enzyme perturbation, kinetic model.

Abbreviation

EtOH, Ethanol; HK, hexokinase; GAPDH, glyceraldehyde-3- phosphate dehydrogenase; ADH, alcohol dehydrogenase; TIM, triose phosphate isomerase; lpGlyc, lumped glycerol formation reaction; PDC, pyruvate decarboxylase; ALD, aldolase; PFK, phosphofructokinase; PK, pyruvate kinase;PGI, phosphoglucose isomerase; lpPEP, phosphoenol pyruvate formation reaction.