Lactose/whey utilization and ethanol production by transformed Saccharomyces cerevisiae cells
β Scribed by Danilo Porro; Enzo Martegani; Bianca Maria Ranzi; Lilia Alberghina
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 629 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0006-3592
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β¦ Synopsis
Strains of Saccharornyces cerevisiae transformed with a multicopy expression vector bearing both the Escherichia coli P-galactosidase gene under the control of the upstream activating sequence of the GALI-10 genes and the GAL4 activator gene release part of P-galactosidase in the growth medium. This release is due to cell lysis of the older mother cells; the enzyme maintains its activity in buffered growth media. Fermentation studies with transformed yeast strains showed that the release of @-galactosidase allowed an ef- ficient growth on buffered media containing lactose as carbon source as well as on whey-based media. The transformed strains utilized up to 95% of the lactose and a high growth yield was obtained in rich media. High productions of ethanol were also observed in stationary phase after growth in lactose minimal media.
π SIMILAR VOLUMES
Genetically engineered Saccharomyces cerevisiae strains that express Escherichia coli p-galactosidase gene are able to bioconvert lactose or whey into fructose-1.6diphosphate (FDP). High FDP yields from whey were obtained with an appropriate ratio between cell concentration and inorganic phosphate.
Alcohol fermentation of lactose was investigated using a recombinant flocculating Saccharomyces cerevisiae, expressing the LAC4 (coding for β€-galactosidase) and LAC12 (coding for lactose permease) genes of Kluyveromyces marxianus. Data on yeast fermentation and growth on a medium containing lactose