Metabolic Flux Analysis Elucidates the Importance of the Acid-Formation Pathways in Regulating Solvent Production by Clostridium acetobutylicum

被引:78
作者
Desai, Ruchir P. [1 ]
Harris, Latonia M. [1 ]
Welker, Neil E. [2 ]
Papoutsakis, Eleftherios T. [1 ]
机构
[1] Northwestern Univ, Dept Chem Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Biochem Cell Biol & Mol Biol, Evanston, IL USA
关键词
D O I
10.1006/mben.1999.0118
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
Metabolic flux analysis was used to investigate the roles of the acid formation pathways in Clostridium acetobutylicum. The acid formation pathways were revealed to serve different roles in wildtype fermentations than previously expected. Specifically, enzymes known to catalyze butyrate formation were found to uptake butyrate without concomitant production of acetone. This role was further corroborated by flux analysis of a recombinant strain overexpressing the butyrate formation enzymes. Analysis of wildtype fermentation data also revealed an important role for the acetate formation enzymes, namely the cycling of carbon between acetate and acetylCoA during the stationary phase. Next, metabolic flux analysis was used to compare the patterns of activity in two butyrate kinase deficient strains of C. acetobutylicum. The strain developed by gene inactivation, PJC4BK, exhibited a shift in acid formation fluxes toward acetate while the strain developed by antisense RNA strategies, 824(pRD4), did not exhibit such a shift. However, both strains exhibited altered solvent formation patterns. PJC4BK exhibited a strong transient enhancement of solvent formation fluxes. In contrast, 824(pRD4) exhibited relatively lower levels of solvent formation fluxes, although fluxes were sustained over a longer period of time. (C) 1999 Academic Press
引用
收藏
页码:206 / 213
页数:8
相关论文
共 15 条
[1]  
Chen CK, 1999, APPL ENVIRON MICROB, V65, P499
[2]  
Desai RP, 1999, APPL ENVIRON MICROB, V65, P936
[3]   Stoichiometric modeling of Clostridium acetobutylicum fermentations with non-linear constraints [J].
Desai, RP ;
Nielsen, LK ;
Papoutsakis, ET .
JOURNAL OF BIOTECHNOLOGY, 1999, 71 (1-3) :191-205
[4]   Genetic manipulation of acid formation pathways by gene inactivation in Clostridium acetobutylicum ATCC 824 [J].
Green, EM ;
Boynton, ZL ;
Harris, LM ;
Rudolph, FB ;
Papoutsakis, ET ;
Bennett, GN .
MICROBIOLOGY-SGM, 1996, 142 :2079-2086
[5]  
HARTMANIS MGN, 1984, APPL MICROBIOL BIOT, V20, P66
[6]   SOLVENTOGENESIS IN CLOSTRIDIUM-ACETOBUTYLICUM FERMENTATIONS RELATED TO CARBOXYLIC-ACID AND PROTON CONCENTRATIONS [J].
HUSEMANN, MHW ;
PAPOUTSAKIS, ET .
BIOTECHNOLOGY AND BIOENGINEERING, 1988, 32 (07) :843-852
[7]   ACETONE-BUTANOL FERMENTATION REVISITED [J].
JONES, DT ;
WOODS, DR .
MICROBIOLOGICAL REVIEWS, 1986, 50 (04) :484-524
[8]   EQUATIONS AND CALCULATIONS FOR FERMENTATIONS OF BUTYRIC-ACID BACTERIA [J].
PAPOUTSAKIS, ET .
BIOTECHNOLOGY AND BIOENGINEERING, 1984, 26 (02) :174-187
[9]   THE EFFECT OF PH ON NITROGEN SUPPLY, CELL-LYSIS, AND SOLVENT PRODUCTION IN FERMENTATIONS OF CLOSTRIDIUM-ACETOBUTYLICUM [J].
ROOS, JW ;
MCLAUGHLIN, JK ;
PAPOUTSAKIS, ET .
BIOTECHNOLOGY AND BIOENGINEERING, 1985, 27 (05) :681-694
[10]   NETWORK RIGIDITY AND METABOLIC ENGINEERING IN METABOLITE OVERPRODUCTION [J].
STEPHANOPOULOS, G ;
VALLINO, JJ .
SCIENCE, 1991, 252 (5013) :1675-1681