Driving Forces Enable High-Titer Anaerobic 1-Butanol Synthesis in Escherichia coli

被引:450
作者
Shen, Claire R. [1 ]
Lan, Ethan I. [1 ,2 ]
Dekishima, Yasumasa [1 ,4 ]
Baez, Antonino [1 ]
Cho, Kwang Myung [1 ,3 ]
Liao, James C. [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Biomed Engn Interdept Program, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Genom & Prote, Los Angeles, CA 90095 USA
[4] Mitsubishi Chem Grp Sci & Technol Res Ctr Inc, Yokohama, Kanagawa, Japan
关键词
CLOSTRIDIUM-BEIJERINCKII BA101; MINERAL SALTS MEDIUM; BUTANOL PRODUCTION; TRANS-2-ENOYL-COA REDUCTASE; ACETOBUTYLICUM ATCC-824; FORMATE DEHYDROGENASE; ETHANOL-PRODUCTION; NADH AVAILABILITY; FERMENTATION; COENZYME;
D O I
10.1128/AEM.03034-10
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
1-Butanol, an important chemical feedstock and advanced biofuel, is produced by Clostridium species. Various efforts have been made to transfer the clostridial 1-butanol pathway into other microorganisms. However, in contrast to similar compounds, only limited titers of 1-butanol were attained. In this work, we constructed a modified clostridial 1-butanol pathway in Escherichia coli to provide an irreversible reaction catalyzed by trans-enoyl-coenzyme A (CoA) reductase (Ter) and created NADH and acetyl-CoA driving forces to direct the flux. We achieved high-titer (30 g/liter) and high-yield (70 to 88% of the theoretical) production of 1-butanol anaerobically, comparable to or exceeding the levels demonstrated by native producers. Without the NADH and acetyl-CoA driving forces, the Ter reaction alone only achieved about 1/10 the level of production. The engineered host platform also enables the selection of essential enzymes with better catalytic efficiency or expression by anaerobic growth rescue. These results demonstrate the importance of driving forces in the efficient production of nonnative products.
引用
收藏
页码:2905 / 2915
页数:11
相关论文
共 48 条
[1]   Structure-guided alteration of coenzyme specificity of formate dehydrogenase by saturation mutagenesis to enable efficient utilization of NADP+ [J].
Andreadeli, Aggeliki ;
Platis, Dimitris ;
Tishkov, Vladimir ;
Popov, Vladimir ;
Labrou, Nikolaos E. .
FEBS JOURNAL, 2008, 275 (15) :3859-3869
[2]   Metabolic engineering of Escherichia coli for 1-butanol production [J].
Atsumi, Shota ;
Cann, Anthony F. ;
Connor, Michael R. ;
Shen, Claire R. ;
Smith, Kevin M. ;
Brynildsen, Mark P. ;
Chou, Katherine J. Y. ;
Hanai, Taizo ;
Liao, James C. .
METABOLIC ENGINEERING, 2008, 10 (06) :305-311
[3]   Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels [J].
Atsumi, Shota ;
Hanai, Taizo ;
Liao, James C. .
NATURE, 2008, 451 (7174) :86-U13
[4]   Evolution, genomic analysis, and reconstruction of isobutanol tolerance in Escherichia coli [J].
Atsumi, Shota ;
Wu, Tung-Yun ;
Machado, Iara M. P. ;
Huang, Wei-Chih ;
Chen, Pao-Yang ;
Pellegrini, Matteo ;
Liao, James C. .
MOLECULAR SYSTEMS BIOLOGY, 2010, 6
[5]   High-flux isobutanol production using engineered Escherichia coli: a bioreactor study with in situ product removal [J].
Baez, Antonino ;
Cho, Kwang-Myung ;
Liao, James C. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2011, 90 (05) :1681-1690
[6]   Reconstructing the clostridial n-butanol metabolic pathway in Lactobacillus brevis [J].
Berezina, Oksana V. ;
Zakharova, Natalia V. ;
Brandt, Agnieszka ;
Yarotsky, Sergey V. ;
Schwarz, Wolfgang H. ;
Zverlov, Vladimir V. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2010, 87 (02) :635-646
[7]   Effect of different levels of NADH availability on metabolite distribution in Escherichia coli fermentation in minimal and complex media [J].
Berríos-Rivera, SJ ;
Sánchez, AM ;
Bennett, GN ;
San, KY .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 65 (04) :426-432
[8]   Metabolic engineering of Escherichia coli:: Increase of NADH availability by overexpressing an NAD+-dependent formate dehydrogenase [J].
Berríos-Rivera, SJ ;
Bennett, GN ;
San, KY .
METABOLIC ENGINEERING, 2002, 4 (03) :217-229
[9]   Cloning, sequencing, and expression of clustered genes encoding beta-hydroxybutyryl-coenzyme A (CoA) dehydrogenase, crotonase, and butyryl-CoA dehydrogenase from Clostridium acetobutylicum ATCC 824 [J].
Boynton, ZL ;
Bennett, GN ;
Rudolph, FB .
JOURNAL OF BACTERIOLOGY, 1996, 178 (11) :3015-3024
[10]  
BUELTER T, 2009, Patent No. 20090155869