## Abstract A mathematical model for direct alcohol fermentation from starch was proposed using an amylaseβproducing recombinant yeast, __Saccharomyces cerevisiae__ SR93. This model consisted of the reaction rate equations for glucoamylase synthesis in the recombinant yeast, starch degradation by a
Ethanol production from raw starch by a recombinant yeast having saccharification and fermentation activities
β Scribed by Yoshitoshi Nakamura; Tatsuro Sawada; Akihiro Komatsu
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2002
- Tongue
- English
- Weight
- 187 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0268-2575
- DOI
- 10.1002/jctb.681
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β¦ Synopsis
Abstract
In order to develop a method for converting raw starch into ethanol efficiently, direct fermentation of ozonized raw starch using a recombinant yeast was investigated. Ozonolysis was carried out as a pretreatment to convert raw starch into ethanol rapidly and efficiently, and then the effect of the ozone degradation conditions on the degree of polymerization and the amount of amylose in a raw starch was determined. Since the degree of polymerization was low and the amount of amylose was high, raw starch treated with an ozone concentration of 40βgm^β3^ and an ozonation time of 30βmin was the material chosen for alcohol fermentation. Though the recombinant yeast could not convert the untreated raw starch, it converted the soluble starch and the ozonized raw starch at a comparatively high yield into ethanol. About 56% of the ozonized raw starch decomposed, and the ethanol concentration obtained from the ozonized raw starch was markedly greater than that obtained from untreated raw starch. The dynamic behavior of cell growth, substrate degradation, and ethanol production was examined in a continuous culture under various dilution rates, and the optimal dilution rate, ie 0.15βh^β1^, was determined for maximizing the ethanol productivity (amount of ethanol produced per unit time).
Β© 2002 Society of Chemical Industry
π SIMILAR VOLUMES
Alcohol fermentation of starch was investigated using a direct starch fermenting yeast, Saccharomyces cerevisiae SR93, constructed by integrating a glucoamylase- producing gene (STA1) into the chromosome of Saccharomyces cerevisiae SH1089. The glucoamylase was con- stitutively produced by the recomb