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Microb Cell Fact. 2012 Oct;11:138. Metabolic engineering of the purine biosynthetic pathway in Corynebacterium glutamicum results in increased intracellular pool sizes of IMP and hypoxanthine. Peifer S, Barduhn T, Zimmet S, et al.



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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 148.2 R02736+R01528+R00267+R00214
NADPH production rate Minium 89.8 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 265.1 R02736+R01528+R00267+R00214
NADPH production rate Minium 195.6 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 186.3 R02736+R01528+R00267+R00214
NADPH production rate Minium 58.6 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 305 R02736+R01528+R00267+R00214
NADPH production rate Minium 196 R02736+R01528
Growth Condition
Strains Corynebacterium glutamicum ATCC 13032
Genotype Wild type.
Culture medium The first precultures were grown on complex media (pH6.8) containing per liter: 10.0g glucose,2.5g NaCl,2.0g urea,5.0g yeast extract,5.0g beef extract,5.0g polypeptone and 20.0g casamino acids.For agar plates,the complex medium was supplemented with 20.0g/L agar. Second precultures and main cultures were grown on minimal medium (pH 7.2) containing per liter: 15.0g glucose,4.0g KH2PO4,16.0g Na2HPO4,500mg MgCl2-6H2O,300mg 3,4-dihydroxibenzoic acid,100mg CaCl2-2H2O,100ug cyanocobalamin,750ug thiamine,4ug pyridoxal phosphate,100ug biotin,400ug calcium pantothenate,2ug folic acid,400ug nicotinic acid,200ug 4-aminobenzoic acid,400ug pyridoxine-HCl,2mg inositol,10mg FeCl2-4H2O,1mg ZnCl2,100ug CuCl2,20ug NiCl2-6H2O,20ug Na2MoO4-2H2O,500ug boric acid,100ug KI, 100ug CoCl2-6H2O and 10 mg MnCl2-4H2O.
Carbon source Glucose
Growth rate 0.443/h
Case-specific description Intracellular carbon flux distributions with corresponding standard deviations of the central metabolism of the wild type C.glutamicum ATCC 13032.
Growth Condition
Strains Corynebacterium glutamicum delta pgi
Genotype deletion of the pgi gene(NCgl0817)
Culture medium The first precultures were grown on complex media (pH6.8) containing per liter: 10.0g glucose,2.5g NaCl,2.0g urea,5.0g yeast extract,5.0g beef extract,5.0g polypeptone and 20.0g casamino acids.For agar plates,the complex medium was supplemented with 20.0g/L agar. Second precultures and main cultures were grown on minimal medium (pH 7.2) containing per liter: 15.0g glucose,4.0g KH2PO4,16.0g Na2HPO4,500mg MgCl2-6H2O,300mg 3,4-dihydroxibenzoic acid,100mg CaCl2-2H2O,100ug cyanocobalamin,750ug thiamine,4ug pyridoxal phosphate,100ug biotin,400ug calcium pantothenate,2ug folic acid,400ug nicotinic acid,200ug 4-aminobenzoic acid,400ug pyridoxine-HCl,2mg inositol,10mg FeCl2-4H2O,1mg ZnCl2,100ug CuCl2,20ug NiCl2-6H2O,20ug Na2MoO4-2H2O,500ug boric acid,100ug KI, 100ug CoCl2-6H2O and 10 mg MnCl2-4H2O.
Carbon source Glucose
Growth rate 0.376/h
Case-specific description Intracellular carbon flux distributions with corresponding standard deviations of the central metabolism of mutant strains C.glutamicum delta pgi.
Growth Condition
Strains Corynebacterium glutamicum delta purA delta guaB2
Genotype double deletion of purA and guaB2 genes
Culture medium The first precultures were grown on complex media (pH6.8) containing per liter: 10.0g glucose,2.5g NaCl,2.0g urea,5.0g yeast extract,5.0g beef extract,5.0g polypeptone and 20.0g casamino acids.For agar plates,the complex medium was supplemented with 20.0g/L agar. Second precultures and main cultures were grown on minimal medium (pH 7.2) containing per liter: 15.0g glucose,4.0g KH2PO4,16.0g Na2HPO4,500mg MgCl2-6H2O,300mg 3,4-dihydroxibenzoic acid,100mg CaCl2-2H2O,100ug cyanocobalamin,750ug thiamine,4ug pyridoxal phosphate,100ug biotin,400ug calcium pantothenate,2ug folic acid,400ug nicotinic acid,200ug 4-aminobenzoic acid,400ug pyridoxine-HCl,2mg inositol,10mg FeCl2-4H2O,1mg ZnCl2,100ug CuCl2,20ug NiCl2-6H2O,20ug Na2MoO4-2H2O,500ug boric acid,100ug KI, 100ug CoCl2-6H2O and 10 mg MnCl2-4H2O.
Carbon source Glucose
Growth rate 0.317/h
Case-specific description Intracellular carbon flux distributions with corresponding standard deviations of the central metabolism of C.glutamicum delta purA delta guaB2.
Growth Condition
Strains Corynebacterium glutamicum delta purA delta guaB2 purFK348Q delta pgi
Genotype deletion of purA,guaB2 and pgi genes and allelic amino acid substitution K348Q in the purF gene
Culture medium The first precultures were grown on complex media (pH6.8) containing per liter: 10.0g glucose,2.5g NaCl,2.0g urea,5.0g yeast extract,5.0g beef extract,5.0g polypeptone and 20.0g casamino acids.For agar plates,the complex medium was supplemented with 20.0g/L agar. Second precultures and main cultures were grown on minimal medium (pH 7.2) containing per liter: 15.0g glucose,4.0g KH2PO4,16.0g Na2HPO4,500mg MgCl2-6H2O,300mg 3,4-dihydroxibenzoic acid,100mg CaCl2-2H2O,100ug cyanocobalamin,750ug thiamine,4ug pyridoxal phosphate,100ug biotin,400ug calcium pantothenate,2ug folic acid,400ug nicotinic acid,200ug 4-aminobenzoic acid,400ug pyridoxine-HCl,2mg inositol,10mg FeCl2-4H2O,1mg ZnCl2,100ug CuCl2,20ug NiCl2-6H2O,20ug Na2MoO4-2H2O,500ug boric acid,100ug KI, 100ug CoCl2-6H2O and 10 mg MnCl2-4H2O.
Carbon source Glucose
Growth rate 0.146/h
Case-specific description Intracellular carbon flux distributions with corresponding standard deviations of the central metabolism of C.glutamicum delta purA delta guaB2 purFK348Q delta pgi.
Specific Rate (mmol g-1 h-1)
glucose 4.67
Specific Rate (mmol g-1 h-1)
glucose 4.18
Specific Rate (mmol g-1 h-1)
glucose 4.24
Specific Rate (mmol g-1 h-1)
glucose 1.29
Source