Xylose utilisation by recombinant strains of Saccharomyces cerevisiae on different carbon sources
dc.contributor.author | Van Zyl W.H. | |
dc.contributor.author | Eliasson A. | |
dc.contributor.author | Hobley T. | |
dc.contributor.author | Hahn-Hagerdal B. | |
dc.date.accessioned | 2011-05-15T15:56:37Z | |
dc.date.available | 2011-05-15T15:56:37Z | |
dc.date.issued | 1999 | |
dc.description.abstract | Autoselective xylose-utilising strains of Saccharomyces cerevisiae expressing the xylose reductase (XYL1) and xylitol dehydrogenase (XYL2) genes of Pichia stipitis were constructed by replacing the chromosomal FUR1 gene with a disrupted fur1::LEU2 allele. Anaerobic fermentations with 80 g l-1 D-xylose as substrate showed a twofold higher consumption of xylose in complex medium compared to defined medium. The xylose consumption rate increased a further threefold when 20 g l-1 D-glucose or raffinose was used as co-substrate together with 50 g l-1 D-xylose. Xylose consumption was higher with raffinose as co-substrate than with glucose (85% versus 71%, respectively) after 82 h fermentations. A high initial ethanol concentration and moderate levels of glycerol and acetic acid accompanied glucose as co- substrate, whereas the ethanol concentration gradually increased with raffinose as co-substrate with no glycerol and much less acetic acid formation. | |
dc.description.version | Article | |
dc.identifier.citation | Applied Microbiology and Biotechnology | |
dc.identifier.citation | 52 | |
dc.identifier.citation | 6 | |
dc.identifier.issn | 1757598 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/9952 | |
dc.subject | acetic acid | |
dc.subject | alcohol | |
dc.subject | carbon | |
dc.subject | glucose | |
dc.subject | glycerol | |
dc.subject | oxidoreductase | |
dc.subject | raffinose | |
dc.subject | xylose | |
dc.subject | anaerobic metabolism | |
dc.subject | article | |
dc.subject | gene disruption | |
dc.subject | gene expression | |
dc.subject | nonhuman | |
dc.subject | pichia stipitis | |
dc.subject | saccharomyces cerevisiae | |
dc.subject | Acetic acid | |
dc.subject | Anaerobiosis | |
dc.subject | Chromatography, High Pressure Liquid | |
dc.subject | D-Xylulose Reductase | |
dc.subject | Endo-1,4-beta Xylanases | |
dc.subject | Ethanol | |
dc.subject | Fungal proteins | |
dc.subject | Glucose | |
dc.subject | Glycerol | |
dc.subject | Plasmids | |
dc.subject | Raffinose | |
dc.subject | Recombination, Genetic | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | Sugar alcohol dehydrogenases | |
dc.subject | Time factors | |
dc.subject | Xylose | |
dc.subject | Xylosidases | |
dc.subject | Pichia stipitis | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | Trixis | |
dc.title | Xylose utilisation by recombinant strains of Saccharomyces cerevisiae on different carbon sources | |
dc.type | Article |