Dialysis cultures

被引:36
作者
Pörtner, R [1 ]
Märkl, H [1 ]
机构
[1] Tech Univ Hamburg, D-21071 Hamburg, Germany
关键词
D O I
10.1007/s002530051312
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
Dialysis techniques are discussed as a means for effective removal of low-molecular-mass components from fermentation broth to reach high cell density. Reactor systems and process strategies, the relevant properties of membranes and examples for high-density fermentation with dialysis, and problems related to scale-up are addressed. The dialysis technique has turned out to be very efficient and reliable for obtaining high cell densities. As in dialysis processes the membranes are not perfused, membrane clogging is not a problem as it is for micro- and ultrafiltration. By applying a "nutrient-split" feeding strategy, the loss of nutrients can be avoided and the medium is used very efficiently. The potential of dialysis cultures is demonstrated on the laboratory scale in a membrane dialysis reactor with an integrated membrane and in reactor systems with an external dialysis loop. In dialysis cultures with different microorganisms (Staphylococci, Escherichia coli, extremophilic microorganisms, Lactobacilli) the cell densities achieved were up to 30 times higher than those of other fermentation methods. The technique enables high cell densities to be attained without time-consuming medium optimization. For animal cell cultures the concept of a fixed bed coupled with dialysis proved to be very effective.
引用
收藏
页码:403 / 414
页数:12
相关论文
共 73 条
[11]  
GATJE G, 1991, APPL MICROBIOL BIOT, V34, P446, DOI 10.1007/BF00180568
[12]   INFLUENCE OF PH AND INITIAL LACTATE CONCENTRATION ON THE GROWTH OF LACTOBACILLUS-PLANTARUM [J].
GIRAUD, E ;
LELONG, B ;
RAIMBAULT, M .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1991, 36 (01) :96-99
[13]   REDUCTION OF WASTE PRODUCT EXCRETION VIA NUTRIENT CONTROL - POSSIBLE STRATEGIES FOR MAXIMIZING PRODUCT AND CELL YIELDS ON SERUM IN CULTURES OF MAMMALIAN-CELLS [J].
GLACKEN, MW ;
FLEISCHAKER, RJ ;
SINSKEY, AJ .
BIOTECHNOLOGY AND BIOENGINEERING, 1986, 28 (09) :1376-1389
[14]   HIGH-DENSITY CULTURE OF LACTOBACILLUS-CASEI BY A CROSS-FLOW CULTURE METHOD BASED ON KINETIC-PROPERTIES OF THE MICROORGANISM [J].
HAYAKAWA, K ;
SANSAWA, H ;
NAGAMUNE, T ;
ENDO, I .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1990, 70 (06) :404-408
[15]   EFFECTIVE LACTIC-ACID PRODUCTION BY 2-STAGE EXTRACTIVE FERMENTATION [J].
HONDA, H ;
TOYAMA, Y ;
TAKAHASHI, H ;
NAKAZEKO, T ;
KOBAYASHI, T .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1995, 79 (06) :589-593
[16]  
ISHII N, 1995, BIOPROCESS ENG, V13, P119, DOI 10.1007/BF00369694
[17]   INSITU PRODUCT SEPARATION IN BUTANOL FERMENTATION BY MEMBRANE-ASSISTED EXTRACTION [J].
JEON, YJ ;
LEE, YY .
ENZYME AND MICROBIAL TECHNOLOGY, 1989, 11 (09) :575-582
[18]   GROWTH AND ENERGY-CONSERVATION IN BATCH CULTURES OF PYROCOCCUS-FURIOSUS [J].
KENGEN, SWM ;
STAMS, AJM .
FEMS MICROBIOLOGY LETTERS, 1994, 117 (03) :305-309
[19]   SIMPLE FED-BATCH TECHNIQUE FOR HIGH CELL-DENSITY CULTIVATION OF ESCHERICHIA-COLI [J].
KORZ, DJ ;
RINAS, U ;
HELLMUTH, K ;
SANDERS, EA ;
DECKWER, WD .
JOURNAL OF BIOTECHNOLOGY, 1995, 39 (01) :59-65
[20]   Fermentation of extremophilic microorganisms [J].
Krahe, M ;
Antranikian, G ;
Markl, H .
FEMS MICROBIOLOGY REVIEWS, 1996, 18 (2-3) :271-285