CONTINUOUS ETHANOL-PRODUCTION FROM RAW STARCH USING A REVERSIBLY SOLUBLE AUTOPRECIPITATING AMYLASE AND FLOCCULATING YEAST-CELLS

被引:22
作者
HOSHINO, K
TANIGUCHI, M
MARUMOTO, H
FUJII, M
机构
[1] NIIGATA UNIV,FAC ENGN,DEPT CHEM ENGN,NIIGATA 95021,JAPAN
[2] NIIGATA UNIV,GRAD SCH NAT SCI & TECHNOL,NIIGATA 95021,JAPAN
来源
JOURNAL OF FERMENTATION AND BIOENGINEERING | 1990年 / 69卷 / 04期
关键词
D O I
10.1016/0922-338X(90)90218-L
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Direct ethanol production from raw starch was performed continuously using a combination of a reversibly soluble-autoprecipitating amylase (D-AS) in which Dabiase K-27 was immobilized covalently on an enteric coating polymer (hydroxypropyl methylcellulose acetate succinate, AS) as a carrier, and a flocculating yeast. Continuous production was carried out using a reactor equipped with a mixing vessel and a separation vessel. D-AS and the yeast were separated continuously from the product solution by self-sedimentation in the separation vessel and they were utilized repeatedly. In the continuous saccharification of raw starch by D-AS alone, the glucose productivity was about 3.6 g/l/h at a dilution rate (D) of 0.1 h-1. In the continuous ethanol production from raw starch by a combination of D-AS and flocculating yeast cells, high ethanol productivity up to 2.0 g/l/h was achieved at D=0.1 h-1. Although the enzymatic activity of D-AS is inactivated due to insolubilization of the enzyme by the accumulation of NaCl produced in controlling the pH in the reactor, it is possible to recover the D-AS enzymatic activity by removing the NaCl. This continuous fermentation system suggests a potential for effective ethanol production from raw starch, and it may be widely applicable in heterogeneous culture systems using solid substrates other than raw starch. © 1990.
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页码:228 / 233
页数:6
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