Glucose-controlled L-isoleucine fed-batch production with recombinant strains of Corynebacterium glutamicum

被引:27
作者
Kelle, R
Hermann, T
WeusterBotz, D
Eggeling, L
Kramer, R
Wandrey, C
机构
[1] Institute of Biotechnology, Research Center Jülich
[2] Institut für Biotechnologie, Forschungszentrum Jülich GmbH
关键词
Corynebacterium glutamicum; isoleucine; control; transport; fed-batch; production;
D O I
10.1016/0168-1656(96)01554-4
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
L-Isoleucine was produced in a fed-batch bioprocess with L-leucine auxotrophic Corynebacterium glutamicum strains developed by genetic engineering. An efficient supply with nutrients was achieved by applying closed-loop control of glucose as the main carbon source, with a model-based, parameter-adaptive control strategy. This control strategy is based on an extended, semi-continuous Kalman filter for process identification and a minimum variance controller. The lab scale fed-batch process with C. glutamicum SM1 and C. glutamicum DR17 pECM3::ilvA38 was characterized with respect to biomass, product and by-product accumulation. A differential analysis of growth, specific productivities, and selectivities was performed to characterize the carbon flow over process time. Characterization of L-isoleucine transport steps across the cell membrane resulted in a balance of L-isoleucine transport over process time. Up to an extracellular L-isoleucine concentration of 140 mM the cytosolic L-isoleucine, provided by the biosynthesis, was quantitatively excreted into the medium via the export carrier system. Optimized feeding profiles for L-leucine and phosphate in correlation with the on-line estimated glucose consumption were achieved up to the pilot scale (300-1 stirred tank reactor). The maximum L-isoleucine concentration was 150 mM (21 gl(-1)) with a space-time yield of 4.3 mmol l(-1) h(-1). With a 98% closed carbon balance the selectivity for isoleucine was 14%, for biomass 13%,and for CO2 68%.
引用
收藏
页码:123 / 136
页数:14
相关论文
共 26 条
[1]  
COLON GE, 1995, APPL MICROBIOL BIOT, V43, P482, DOI 10.1007/s002530050438
[2]  
COLON GE, 1995, APPL ENVIRON MICROB, V61, P74
[3]   TRANSPORT OF BRANCHED-CHAIN AMINO-ACIDS IN CORYNEBACTERIUM-GLUTAMICUM [J].
EBBIGHAUSEN, H ;
WEIL, B ;
KRAMER, R .
ARCHIVES OF MICROBIOLOGY, 1989, 151 (03) :238-244
[4]   BULK AMINO-ACID FERMENTATION - TECHNOLOGY AND COMMODITY TRADING [J].
HODGSON, J .
BIO-TECHNOLOGY, 1994, 12 (02) :152-155
[5]  
HOPPE B, 1983, CHEM UNSERER Z, V18, P73
[6]  
ISERMANN R, 1987, DIGITAL CONTROL SYST, V2
[7]   FACTORS IMPROVING L-THREONINE PRODUCTION BY A 3 L-THREONINE BIOSYNTHETIC GENES AMPLIFIED RECOMBINANT STRAIN OF BREVIBACTERIUM-LACTOFERMENTUM [J].
ISHIDA, M ;
KAWASHIMA, H ;
SATO, K ;
HASHIGUCHI, K ;
ITO, H ;
ENEI, H ;
NAKAMORI, S .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1994, 58 (04) :768-770
[8]   L-ISOLEUCINE PRODUCTION BY ANALOG-RESISTANT MUTANTS DERIVED FROM THREONINE-PRODUCING STRAIN OF CORYNEBACTERIUM-GLUTAMICUM [J].
KASE, H ;
NAKAYAMA, K .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1977, 41 (01) :109-116
[9]  
Katsumata R MT, 1986, GENET IND MICROORGAN, P217
[10]  
KELLE R, 1996, IN PRESS BIOTECHNOL