Physiologic mechanisms of sequential products synthesis in 1,3-propanediol fed-batch fermentation by Klebsiella pneumoniae

被引:50
作者
Zheng, Zong-Ming [1 ]
Xu, Yun-Zhen [1 ]
Liu, Hong-Juan [2 ]
Guo, Ni-Ni [1 ]
Cai, Zhong-Zhen [3 ]
Liu, De-Hua [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing, Peoples R China
[3] Xinjiang Univ, Coll Life Sci & Technol, Urumqi, Peoples R China
关键词
metabolic flux; enzymatic activity; 1,3-propanediol; internal redox state; fed-batch;
D O I
10.1002/bit.21830
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
The glycerol fed-batch fermentation by Klebsiella pneumoniae CGMCC 1.6366 exhibited the sequential synthesis of products, including acetate, 1,3-propanediol (1,3-PD), 2,3-butanediol, ethanol, succinate, and lactate. The dominant flux distribution was shifted from acetate formation to 1,3-PD formation in early-exponential growth phase and then to lactate synthesis in late-exponential growth phase. The underlying physiological mechanism of the above observations has been investigated via the related enzymes, nucleotide, and intermediary metabolites analysis. The carbon flow shift is dictated by the intrinsic physiological state and enzymatic activity regulation. Especially, the internal redox state could serve as a rate-controlling factor for 1,3-PD production. The q(1,3-PD) formation was the combined outcomes of regulations of glycerol dehydratase activity and internal redox balancing. The q(ethanol)/q(acetate) ratios demonstrated the flexible adaptation mechanism of K. pneumoniae preferring ATP generation in early-exponential growth phase. A low PEP to pyruvate ratio corresponded LDH activity increase, leading to lactate accumulation in stationary phase.
引用
收藏
页码:923 / 932
页数:10
相关论文
共 49 条
[1]  
Ahrens K, 1998, BIOTECHNOL BIOENG, V59, P544, DOI 10.1002/(SICI)1097-0290(19980905)59:5<544::AID-BIT3>3.0.CO
[2]  
2-A
[3]   Physiologic mechanisms involved in accumulation of 3-hydroxypropionaldehyde during fermentation of glycerol by Enterobacter agglomerans [J].
Barbirato, F ;
Soucaille, P ;
Bories, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (12) :4405-4409
[4]   Anaerobic pathways of glycerol dissimilation by Enterobacter agglomerans CNCM 1210: Limitations and regulations [J].
Barbirato, F ;
Astruc, S ;
Soucaille, P ;
Camarasa, C ;
Salmon, JM ;
Bories, A .
MICROBIOLOGY-UK, 1997, 143 :2423-2432
[5]   IMPROVED CYCLING ASSAY FOR NICOTINAMIDE ADENINE-DINUCLEOTIDE [J].
BERNOFSKY, C ;
SWAN, M .
ANALYTICAL BIOCHEMISTRY, 1973, 53 (02) :452-458
[6]   Correlation between growth rates, EIIACrr phosphorylation, and intracellular cyclic AMP levels in Escherichia coli K-12 [J].
Bettenbrock, Katja ;
Sauter, Thomas ;
Jahreis, Knut ;
Kremling, Andreas ;
Lengeler, Joseph W. ;
Gilles, Ernst-Dieter .
JOURNAL OF BACTERIOLOGY, 2007, 189 (19) :6891-6900
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]   Changes in size of intracellular pools of coenzyme A and its thioesters in Escherichia coli K-12 cells to various carbon sources and stresses [J].
Chohnan, S ;
Izawa, H ;
Nishihara, H ;
Takamura, Y .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1998, 62 (06) :1122-1128
[9]   ESCHERICHIA-COLI MUTANTS WITH ALTERED CONTROL OF ALCOHOL-DEHYDROGENASE AND NITRATE REDUCTASE [J].
CLARK, D ;
CRONAN, JE .
JOURNAL OF BACTERIOLOGY, 1980, 141 (01) :177-183
[10]   Metabolic control analysis of glycerol synthesis in Saccharomyces cerevisiae [J].
Cronwright, GR ;
Rohwer, JM ;
Prior, BA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (09) :4448-4456