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Appl Environ Microbiol. 2004 Apr;70(4):2307-17. Molecular basis for anaerobic growth of Saccharomyces cerevisiae on xylose, investigated by global gene expression and metabolic flux analysis. Sonderegger M, Jeppsson M, Hahn-Hagerdal B, et al.



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Font-size: Color: Global color
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 6.96 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 33.5 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 30.18 R02736+R01528
Growth Condition
Strains Saccharomyces cerevisiae TMB3001
Genotype (CEN.PK 113-7A [MATa his3-Delta1 MAL2-8c SUC2] his3::YIpXR/XDH/XK)
Culture medium Cultures were stored in aliquots supplemented with 15% glycerol at -80 Celsius and were revived by growth in YPD medium (10 g of yeast extract per liter, 20 g of peptone per liter, 20 g of glucose per liter). All cultures used for physiological and DNA microarray experiments were grown in minimal medium. For anaerobic cultivation,the medium was supplemented with ethanol-dissolved ergosterol (Fluka) and Tween 80 (Sigma) at final concentrations of 0.01 and 0.42 g/liter, respectively.
Carbon source Glucose
Growth rate 0.05/h
Case-specific description Molar carbon fluxes during anaerobic exponential batch growth of TMB3001 on 10 g of glucose per liter.
Growth Condition
Strains Saccharomyces cerevisiae C1
Genotype (CEN.PK 113-7A [MATa his3-Delta1 MAL2-8c SUC2] his3::YIpXR/XDH/XK)
Culture medium Cultures were stored in aliquots supplemented with 15% glycerol at -80 Celsius and were revived by growth in YPD medium (10 g of yeast extract per liter, 20 g of peptone per liter, 20 g of glucose per liter). All cultures used for physiological and DNA microarray experiments were grown in minimal medium. For anaerobic cultivation,the medium was supplemented with ethanol-dissolved ergosterol (Fluka) and Tween 80 (Sigma) at final concentrations of 0.01 and 0.42 g/liter, respectively.
Carbon source Xylose
Growth rate 0.05/h
Case-specific description Molar carbon fluxes during anaerobic exponential batch growth of C1 on 10 g of xylose per liter.
Growth Condition
Strains Saccharomyces cerevisiae C1
Genotype (CEN.PK 113-7A [MATa his3-Delta1 MAL2-8c SUC2] his3::YIpXR/XDH/XK)
Culture medium Cultures were stored in aliquots supplemented with 15% glycerol at -80 Celsius and were revived by growth in YPD medium (10 g of yeast extract per liter, 20 g of peptone per liter, 20 g of glucose per liter). All cultures used for physiological and DNA microarray experiments were grown in minimal medium. For anaerobic cultivation,the medium was supplemented with ethanol-dissolved ergosterol (Fluka) and Tween 80 (Sigma) at final concentrations of 0.01 and 0.42 g/liter, respectively.
Carbon source Xylose
Growth rate 0.05/h
Case-specific description Molar carbon fluxes during 10 g of xylose per liter plus 0.5 g of acetoin per liter.
Specific Rate (mmol g-1 h-1)
glucose 0.41
xylose 0.497
Specific Rate (mmol g-1 h-1)
glucose 0.267
xylose 0.323
Specific Rate (mmol g-1 h-1)
glucose 3.47
xylose 4.246
Source