| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10161329 | Biochemical Engineering Journal | 2005 | 29 Pages |
Abstract
For both of the systems studied the pathway utilization and relative flux distributions obtained from MFA are in good agreement with reported E. coli gene expression profiles at different stages of growth and during recombinant protein overexpression.
Keywords
OxaloacetateTCAlysCMetEgndAcCoAPEPgltAF6PADPSDHCd-Ribulose-5-phosphateMDHdGTPdCTPUTPdATPCTPrPITTPPYRaKGGTPNH3PPCNAPDHP/Oxylulose-5-phosphateFBAIPTGppGppRECPASPX5P6-phosphogluconate dehydrogenaseRecombinant DNAPEP carboxylaseFUMα-ketoglutarateAdenosine TriphosphateATPadenosine diphosphateaspartateAmmoniaAcetateAcetic acidEscherichia coliUridine triphosphateOxygenAcetohydroxy acid isomeroreductaseisopropyl-β-d-thiogalactopyranosideMetabolic flux analysisPlasmid copy numberthymidine triphosphatedeoxycytidine triphosphatedeoxyadenosine triphosphatedeoxyguanosine triphosphateMicrobial growthsuccinate dehydrogenaseCitrate synthaseCytidine triphosphateFructose 1,6-diphosphateFructose 6-phosphatePhosphatephosphoenolpyruvatephosphoenolpyruvate carboxykinaseFumarateMethionine synthasemalate dehydrogenaseNADHnicotinamide adenine dinucleotidenicotinamide adenine dinucleotide phosphateMFABatch processingRecombinant proteinPyruvateGluglutamateGlucose isomeraseGlucose kinaseGlkGuanosine triphosphate
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Pınar Ãzkan, Berna Sariyar, F. Ãzde Ãtkür, UÄur Akman, Amable Hortaçsu,