EXTRACTIVE ACETONOBUTYLIC FERMENTATION BY COUPLING ULTRAFILTRATION AND DISTILLATION

被引:8
作者
MINIER, M
GRATELOUP, R
BLANCFERRAS, E
GOMA, G
机构
[1] Département de Génie Biochimique Et Alimentaire, Ua-Cnrs-No. 544, Institut National Des Sciences Appliquées, C.T.B.M., Toulouse, F-31077, Avenue de Rangueil
关键词
D O I
10.1002/bit.260350903
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
An extractive acetonobutylic fermentation process is developed by integrating bioproduction, Ultrafiltration, and distillation, providing simultaneous retention of biomass, selective removal of inhibitors from the permeate, as well as separation and purification of acetone–butanol–ethanol solvents. Successive batch fermentations were performed with normal pressure distillation (98°C), which permitted prolonging and enhancing (by a factor of 3) solvent production, with very few volume exchanges of medium (average dilution rate ws 0.002 h−1), and recovering on‐line concentrated solvents. Different operating conditions were also tested in order to study the presence of extracellular autolytic enzymes as inhibition factors: It was shown that, (1) extracellular autolytic activity remains low during the larger part of fermentations, even without enzyme‐inactivating thermotreatment in the distillation boiler, and (2) high‐temperature distillation causes deleterious effects to the culture medium for long duration treatments. Progressive improvements of the process were achieved, first, by managing continuous runs, providing a minimum renewal of the culture medium and, mainly, by decreasing temperature and pressure of distilation. Solvent productivity then reached 2.6 g/L h for a 0.036 h−1 average dilution rate, corresponding to a feed concentration of 156 g/L glucose actually consumed. Copyright © 1990 John Wiley & Sons, Inc.
引用
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页码:861 / 869
页数:9
相关论文
共 34 条
[1]  
AFSCHAR AS, 1985, APPL MICROBIOL BIOT, V22, P394
[2]   EFFECT OF PH AND BUTYRATE CONCENTRATION ON THE PRODUCTION OF ACETONE AND BUTANOL BY CLOSTRIDIUM-ACETOBUTYLICUM GROWN IN CONTINUOUS CULTURE [J].
BAHL, H ;
ANDERSCH, W ;
BRAUN, K ;
GOTTSCHALK, G .
EUROPEAN JOURNAL OF APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1982, 14 (01) :17-20
[3]   BACTERIOCIN PRODUCTION BY CLOSTRIDIUM-ACETOBUTYLICUM IN AN INDUSTRIAL FERMENTATION PROCESS [J].
BARBER, JM ;
ROBB, FT ;
WEBSTER, JR ;
WOODS, DR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1979, 37 (03) :433-437
[4]  
CHRISTEN P, IN PRESS BIOTECHNOL
[5]   RAPID ETHANOL FERMENTATIONS USING VACUUM AND CELL RECYCLE [J].
CYSEWSKI, GR ;
WILKE, CR .
BIOTECHNOLOGY AND BIOENGINEERING, 1977, 19 (08) :1125-1143
[6]   ACETONOBUTYLIC FERMENTATION - IMPROVEMENT OF PERFORMANCES BY COUPLING CONTINUOUS FERMENTATION AND ULTRAFILTRATION [J].
FERRAS, E ;
MINIER, M ;
GOMA, G .
BIOTECHNOLOGY AND BIOENGINEERING, 1986, 28 (04) :523-533
[7]  
Frank G.T., 1985, BIOTECHNOLOGY BIOENG, V15, P621
[8]  
GRIFFITH WL, 1983, DEV IND MICROBIOL, V24, P347
[9]   INCREASE OF SUBSTRATE CONVERSION BY PERVAPORATION IN THE CONTINUOUS BUTANOL FERMENTATION [J].
GROOT, WJ ;
SCHOUTENS, GH ;
VANBEELEN, PN ;
VANDENOEVER, CE ;
KOSSEN, NWF .
BIOTECHNOLOGY LETTERS, 1984, 6 (12) :789-792
[10]   PRODUCTION OF BUTANOL BY CLOSTRIDIUM-ACETOBUTYLICUM IN EXTRACTIVE FERMENTATION SYSTEM [J].
ISHII, S ;
TAYA, M ;
KOBAYASHI, T .
JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1985, 18 (02) :125-130