Display cellulolytic enzymes on Saccharomyces cerevisiae cell surface by using Flo1p as an anchor protein for cellulosic ethanol production / 生物工程学报
Chinese Journal of Biotechnology
;
(12): 1401-1413, 2014.
Artículo
en Chino
| WPRIM
| ID: wpr-345584
ABSTRACT
In this study, we constructed a yeast consortium surface-display expression system by using Flo1 as an anchor protein. Endoglucanase II (EGII) and cellobiohydrolase II (CBHII) from Trichoderma reesei, and β3-glucosidase 1 (BGLI) from Aspergillus aculeatus were immobilized on Saccharomyces cerevisiae Y5. We constructed the cellulose-displaying expression yeast consortium (Y5/fEGIIY5/fCBHIIY5/fBGLI = 111) and investigated the enzymatic ability and ethanol fermentation. The displayed cellulolytic enzymes was stabile during the 96-h fermentation. The yeast consortium produced 0.77 g/L ethanol from 10 g/L phosphoric acid swollen cellulose (PASC) within 96 h. The yield (in grams of ethanol produced per gram of carbohydrate consumed) was 0.35 g/g, which correspond to 68.6% of the theoretical yield.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Unión Proteica
/
Aspergillus
/
Saccharomyces cerevisiae
/
Trichoderma
/
Celulasa
/
Celulosa
/
Proteínas de Saccharomyces cerevisiae
/
Lectinas de Unión a Manosa
/
Celulosa 1,4-beta-Celobiosidasa
/
Etanol
Idioma:
Chino
Revista:
Chinese Journal of Biotechnology
Año:
2014
Tipo del documento:
Artículo
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