Improvement in the bioreactor specific productivity by coupling continuous reactor with repeated fed-batch reactor for acetone-butanol-ethanol production

被引:13
作者
Setlhaku, Mpho [1 ]
Brunberg, Sina [1 ]
Villa, Eva del Amor [1 ]
Wichmann, Rolf [1 ]
机构
[1] TU Dortmund, Dept Biochem & Chem Engn, Biochem Engn Lab, D-44227 Dortmund, Germany
关键词
ABE; Clostridium acetobutylicum; Two-stage continuous fermentation; Repeated fed-batch; Specific product rate; Volumetric productivity; 2-STAGE CONTINUOUS FERMENTATION; IMMOBILIZED CLOSTRIDIUM-ACETOBUTYLICUM; SOLVENT PRODUCTION; CHEMOSTAT CULTURE; ABE-FERMENTATION; 1ST STAGE; BEIJERINCKII; GROWTH; INHIBITION; SUBSTRATE;
D O I
10.1016/j.jbiotec.2012.04.004
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
In comparison to the different fermentation modes for the production of acetone, butanol and ethanol (ABE) researched to date, the continuous fermentation is the most economically favored. Continuous fermentation with two or more reactor cascade is reported to be the most efficient as it results in a more stable solvent production process. In this work, it is shown that a continuous (first-stage) reactor coupled to a repeated fed-batch (second stage) is superior to batch and fed-batch fermentations, including two-stage continuous fermentation. This is due to the efficient catalyst use, reported through the specific product rate and rapid glucose consumption rate. High solvents are produced at 19.4 g(ABE) l(-1), with volumetric productivities of 0.92 g(butanol) l(-1) h(-1) and 1.47 g(ABE) l(-1) h(-1). The bioreactor specific productivities of 0.62 and 0.39 g g(-1) (cdw) h(-1) obtained show a high catalyst activity. This new process mode has not been reported before in the development of ABE fermentation and it shows great potential and superiority to the existing fermentation methods. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:147 / 152
页数:6
相关论文
共 45 条
[1]  
AFSCHAR AS, 1985, APPL MICROBIOL BIOT, V22, P394
[2]   LEVEL OF ENZYMES INVOLVED IN ACETATE, BUTYRATE, ACETONE AND BUTANOL FORMATION BY CLOSTRIDIUM-ACETOBUTYLICUM [J].
ANDERSCH, W ;
BAHL, H ;
GOTTSCHALK, G .
EUROPEAN JOURNAL OF APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1983, 18 (06) :327-332
[3]  
[Anonymous], [No title captured]
[4]   CONTINUOUS PRODUCTION OF ACETONE AND BUTANOL BY CLOSTRIDIUM-ACETOBUTYLICUM IN A 2-STAGE PHOSPHATE LIMITED CHEMOSTAT [J].
BAHL, H ;
ANDERSCH, W ;
GOTTSCHALK, G .
EUROPEAN JOURNAL OF APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1982, 15 (04) :201-205
[5]   INHIBITOR EFFECT OF PRODUCTS OF METABOLISM ON GROWTH OF CLOSTRIDIUM-ACETOBUTYLICUM [J].
BALLONGUE, J ;
MASION, E ;
AMINE, J ;
PETITDEMANGE, H ;
GAY, R .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1987, 26 (06) :568-573
[6]  
Braun K., 1982, APPL MICROBIOL BIOT, V14, P17
[7]  
Clarke K.G., 1987, BIOTECHNOL BIOENG, V32, P538
[8]   The genes for butanol and acetone formation in Clostridium acetobutylicum ATCC 824 reside on a large plasmid whose loss leads to degeneration of the strain [J].
Cornillot, E ;
Nair, RV ;
Papoutsakis, ET ;
Soucaille, P .
JOURNAL OF BACTERIOLOGY, 1997, 179 (17) :5442-5447
[9]   New insights and novel developments in clostridial acetone/butanol/isopropanol fermentation [J].
Dürre, P .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1998, 49 (06) :639-648
[10]   CONTINUOUS PRODUCT RECOVERY BY INSITU GAS STRIPPING CONDENSATION DURING SOLVENT PRODUCTION FROM WHEY PERMEATE USING CLOSTRIDIUM-ACETOBUTYLICUM [J].
ENNIS, BM ;
MARSHALL, CT ;
MADDOX, IS ;
PATERSON, AHJ .
BIOTECHNOLOGY LETTERS, 1986, 8 (10) :725-730