Effects of the changes in enzyme activities on metabolic flux redistribution around the 2-oxoglutarate branch in glutamate production by Corynebacterium glutamicum

被引:59
作者
Shimizu, H
Tanaka, H
Nakato, A
Nagahisa, K
Kimura, E
Shioya, S
机构
[1] Osaka Univ, Grad Sch Engn, Dept Biotechnol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Informat Sci & Technol, Dept Bioinformat Engn, Suita, Osaka 5650871, Japan
[3] Ajinomoto Co Inc, Fermentat & Biotechnol Lab, Kawasaki Ku, Kawasaki, Kanagawa 2108681, Japan
关键词
metabolic control analysis; flux control of glutamate over production; metabolic engineering;
D O I
10.1007/s00449-002-0307-8
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 experimental method for metabolic control analysis (MCA) was applied to the investigation of a metabolic network of glutamate production by Corynebacterium glutamicum. A metabolic reaction (MR) model was constructed and used for flux distribution analysis (MFA). The flux distribution at a key branch point, 2-oxoglutarate, was investigated in detail. Activities of isocitrate dehydrogenase (ICDH), glutamate dehydrogenase (GDH), and 2-oxoglutarate dehydrogenase complex (ODHC) around this the branch point were changed, using two genetically engineered strains (one with enhanced ICDH activity and the other with enhanced GDH activity) and by controlling environmental conditions (i.e. biotin-deficient conditions). The mole flux distribution was determined by an MR model, and the effects of the changes in the enzyme activities on the mole flux distribution were compared. Even though both GDH and ICDH activities were enhanced, the mole flux distribution was not significantly changed. When the ODHC activity was attenuated, the flux through ODHC decreased, and glutamate production was markedly increased. The flux control coefficients of the above three enzymes for glutamate production were determined based on changes in enzyme activities and the mole flux distributions. It was found that the factor with greatest impact on glutamate production in the metabolic network was obtained by attenuation of ODHC activity.
引用
收藏
页码:291 / 298
页数:8
相关论文
共 32 条
[21]   RESPONSES OF METABOLIC SYSTEMS TO LARGE CHANGES IN ENZYME-ACTIVITIES AND EFFECTORS .2. THE LINEAR TREATMENT OF BRANCHED PATHWAYS AND METABOLITE CONCENTRATIONS - ASSESSMENT OF THE GENERAL NONLINEAR CASE [J].
SMALL, JR ;
KACSER, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 213 (01) :625-640
[22]   RESPONSES OF METABOLIC SYSTEMS TO LARGE CHANGES IN ENZYME-ACTIVITIES AND EFFECTORS .1. THE LINEAR TREATMENT OF UNBRANCHED CHAINS [J].
SMALL, JR ;
KACSER, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 213 (01) :613-624
[23]   Flux amplification in complex metabolic networks [J].
Stephanopoulos, G ;
Simpson, TW .
CHEMICAL ENGINEERING SCIENCE, 1997, 52 (15) :2607-2627
[24]   NETWORK RIGIDITY AND METABOLIC ENGINEERING IN METABOLITE OVERPRODUCTION [J].
STEPHANOPOULOS, G ;
VALLINO, JJ .
SCIENCE, 1991, 252 (5013) :1675-1681
[25]  
Stephanopoulos G, 1998, METABOLIC ENG
[26]  
Takiguchi N, 1997, BIOTECHNOL BIOENG, V55, P170, DOI 10.1002/(SICI)1097-0290(19970705)55:1<170::AID-BIT18>3.0.CO
[27]  
2-Q
[28]  
Tesch M, 1999, APPL ENVIRON MICROB, V65, P1099
[29]   METABOLIC FLUX DISTRIBUTIONS IN CORYNEBACTERIUM-GLUTAMICUM DURING GROWTH AND LYSINE OVERPRODUCTION [J].
VALLINO, JJ ;
STEPHANOPOULOS, G .
BIOTECHNOLOGY AND BIOENGINEERING, 1993, 41 (06) :633-646
[30]   LINEAR CONSTRAINT RELATIONS IN BIOCHEMICAL REACTION SYSTEMS .2. DIAGNOSIS AND ESTIMATION OF GROSS ERRORS [J].
VANDERHEIJDEN, RTJM ;
ROMEIN, B ;
HEIJNEN, JJ ;
HELLINGA, C ;
LUYBEN, KCAM .
BIOTECHNOLOGY AND BIOENGINEERING, 1994, 43 (01) :11-20