ATP drives direct photosynthetic production of 1-butanol in cyanobacteria

被引:267
作者
Lan, Ethan I. [1 ,2 ]
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
基金
美国国家科学基金会;
关键词
biofuel; malonyl-CoA; metabolic engineering; synthetic biology; ESCHERICHIA-COLI; EXPRESSION; COENZYME; BIOSYNTHESIS; BUTANOL; COA; DEHYDROGENASE; METABOLISM; ENZYME; GENES;
D O I
10.1073/pnas.1200074109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While conservation of ATP is often a desirable trait for microbial production of chemicals, we demonstrate that additional consumption of ATP may be beneficial to drive product formation in a nonnatural pathway. Although production of 1-butanol by the fermentative coenzyme A (CoA)-dependent pathway using the reversal of beta-oxidation exists in nature and has been demonstrated in various organisms, the first step of the pathway, condensation of two molecules of acetyl-CoA to acetoacetyl-CoA, is thermodynamically unfavorable. Here, we show that artificially engineered ATP consumption through a pathway modification can drive this reaction forward and enables for the first time the direct photosynthetic production of 1-butanol from cyanobacteria Synechococcus elongatus PCC 7942. We further demonstrated that substitution of bifunctional aldehyde/alcohol dehydrogenase (AdhE2) with separate butyraldehyde dehydrogenase (Bldh) and NADPH-dependent alcohol dehydrogenase (YqhD) increased 1-butanol production by 4-fold. These results demonstrated the importance of ATP and cofactor driving forces as a design principle to alter metabolic flux.
引用
收藏
页码:6018 / 6023
页数:6
相关论文
共 50 条
[1]   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
[2]   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
[3]   Direct photosynthetic recycling of carbon dioxide to isobutyraldehyde [J].
Atsumi, Shota ;
Higashide, Wendy ;
Liao, James C. .
NATURE BIOTECHNOLOGY, 2009, 27 (12) :1177-U142
[4]   Directed Evolution of Methanococcus jannaschii Citramalate Synthase for Biosynthesis of 1-Propanol and 1-Butanol by Escherichia coli [J].
Atsumi, Shota ;
Liao, James C. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (24) :7802-7808
[5]   Engineered ketol-acid reductoisomerase and alcohol dehydrogenase enable anaerobic 2-methylpropan-1-ol production at theoretical yield in Escherichia coli [J].
Bastian, Sabine ;
Liu, Xiang ;
Meyerowitz, Joseph T. ;
Snow, Christopher D. ;
Chen, Mike M. Y. ;
Arnold, Frances H. .
METABOLIC ENGINEERING, 2011, 13 (03) :345-352
[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]   Enzyme mechanism as a kinetic control element for designing synthetic biofuel pathways [J].
Bond-Watts, Brooks B. ;
Bellerose, Robert J. ;
Chang, Michelle C. Y. .
NATURE CHEMICAL BIOLOGY, 2011, 7 (04) :222-227
[8]   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
[9]   EXPRESSION OF THE PSBDII GENE IN SYNECHOCOCCUS SP STRAIN-PCC-7942 REQUIRES SEQUENCES DOWNSTREAM OF THE TRANSCRIPTION START SITE [J].
BUSTOS, SA ;
GOLDEN, SS .
JOURNAL OF BACTERIOLOGY, 1991, 173 (23) :7525-7533
[10]   Engineering the metabolism of Escherichia coli W3110 for the conversion of sugar to redox-neutral and oxidized products:: Homoacetate production [J].
Causey, TB ;
Zhou, S ;
Shanmugam, KT ;
Ingram, LO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :825-832