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Microb Cell Fact. 2005 Nov;4:30. Characterization of the metabolic shift between oxidative and fermentative growth in Saccharomyces cerevisiae by comparative 13C flux analysis. Frick O, Wittmann C.



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ATP production rate Maximum N/A -R01786-R04779+2.5*R01061+R01512+R00200+2.5*R00209
+2.5*R00267+2.5*R08549-R00405+1.5*R00402+2.5*R00342
+2.5*R00214
ATP production rate Minium N/A -R01786-R04779+2.5*R01061+R01512+R00200+2.5*R00209
+2.5*R08549-R00405+1.5*R00402+2.5*R00342
NADPH production rate Maximum N/A R02736+R01528+R00267+R00214
NADPH production rate Minium N/A R02736+R01528
ATP production rate Maximum N/A -R01786-R04779+2.5*R01061+R01512+R00200+2.5*R00209
+2.5*R00267+2.5*R08549-R00405+1.5*R00402+2.5*R00342
+2.5*R00214
ATP production rate Minium N/A -R01786-R04779+2.5*R01061+R01512+R00200+2.5*R00209
+2.5*R08549-R00405+1.5*R00402+2.5*R00342
NADPH production rate Maximum N/A R02736+R01528+R00267+R00214
NADPH production rate Minium N/A R02736+R01528
ATP production rate Maximum N/A -R01786-R04779+2.5*R01061+R01512+R00200+2.5*R00209
+2.5*R00267+2.5*R08549-R00405+1.5*R00402+2.5*R00342
+2.5*R00214
ATP production rate Minium N/A -R01786-R04779+2.5*R01061+R01512+R00200+2.5*R00209
+2.5*R08549-R00405+1.5*R00402+2.5*R00342
NADPH production rate Maximum N/A R02736+R01528+R00267+R00214
NADPH production rate Minium N/A R02736+R01528
Growth Condition
Strains Saccharomyces cerevisiae ATCC 32167
Genotype
Culture medium The mineral medium used for cultivation contained 2 g/L glucose, 0.5 g/L (NH4)2HPO4, 1.0 g/L (NH4)2SO4, 0.05 g/L MgSO4-7 H2O, 0.025 g/L citric acid, 0.5 g/L KCl, 0.03,g/L CaCl2-2H2O, 3 mg/L FeCl3-6 H2O, 2.1 mg/L MnSO4-H2O, 1.8 mg/L ZnSO4-7H2O, 0.5 mg/L CuSO4-5H2O, 60.3 mg/L myo-inositol, 30 mg/L Ca-pan thotenate, 6 mg/L thiamin-HCl, 1.5 mg/L pyridoxine-HCl, 0.03 mg/L biotin, and 50 mmol/L phosphate buffer (pH 6.2).
Carbon source Glucose
Growth rate 0.15/h
Case-specific description Intracellular carbon flux distribution of S.cerevisiae cultivated in chemostat on [1-13C] glucose under aerobic glucose-limited condition,corresponding to purely oxidative growth(u=0.15/h, qglc = 1.56mmol/g/h).
Growth Condition
Strains Saccharomyces cerevisiae ATCC 32167
Genotype
Culture medium The mineral medium used for cultivation contained 2 g/L glucose, 0.5 g/L (NH4)2HPO4, 1.0 g/L (NH4)2SO4, 0.05 g/L MgSO4-7 H2O, 0.025 g/L citric acid, 0.5 g/L KCl, 0.03,g/L CaCl2-2H2O, 3 mg/L FeCl3-6 H2O, 2.1 mg/L MnSO4-H2O, 1.8 mg/L ZnSO4-7H2O, 0.5 mg/L CuSO4-5H2O, 60.3 mg/L myo-inositol, 30 mg/L Ca-pan thotenate, 6 mg/L thiamin-HCl, 1.5 mg/L pyridoxine-HCl, 0.03 mg/L biotin, and 50 mmol/L phosphate buffer (pH 6.2).
Carbon source Glucose
Growth rate 0.30/h
Case-specific description Intracellular carbon flux distribution of S.cerevisiae cultivated in chemostat on [1-13C] glucose under aerobic glucose-limited condition,corresponding to respiro-fermentative growth(u=0.30/h, qglc = 4.90mmol/g/h).
Growth Condition
Strains Saccharomyces cerevisiae ATCC 32167
Genotype
Culture medium The mineral medium used for cultivation contained 2 g/L glucose, 0.5 g/L (NH4)2HPO4, 1.0 g/L (NH4)2SO4, 0.05 g/L MgSO4-7 H2O, 0.025 g/L citric acid, 0.5 g/L KCl, 0.03,g/L CaCl2-2H2O, 3 mg/L FeCl3-6 H2O, 2.1 mg/L MnSO4-H2O, 1.8 mg/L ZnSO4-7H2O, 0.5 mg/L CuSO4-5H2O, 60.3 mg/L myo-inositol, 30 mg/L Ca-pan thotenate, 6 mg/L thiamin-HCl, 1.5 mg/L pyridoxine-HCl, 0.03 mg/L biotin, and 50 mmol/L phosphate buffer (pH 6.2).
Carbon source Glucose
Growth rate 0.4/h
Case-specific description Intracellular carbon flux distribution of S.cerevisiae cultivated in chemostat on [1-13C] glucose under aerobic glucose-limited condition,corresponding to mainly fermentative growth(u=0.40/h, qglc = 8.23mmol/g/h).
Specific Rate (mmol g-1 h-1)
Glucose 1.56
Specific Rate (mmol g-1 h-1)
Glucose 4.9
Specific Rate (mmol g-1 h-1)
Glucose 8.23
Source