Engineered reversal of the β-oxidation cycle for the synthesis of fuels and chemicals

被引:468
作者
Dellomonaco, Clementina [1 ]
Clomburg, James M. [1 ]
Miller, Elliot N. [1 ]
Gonzalez, Ramon [1 ,2 ]
机构
[1] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77005 USA
[2] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
关键词
ESCHERICHIA-COLI; FATTY-ACIDS; CLOSTRIDIUM-ACETOBUTYLICUM; MOLECULAR CHARACTERIZATION; GLYCOLYTIC FLUX; METABOLISM; ENZYME; GENES; THIOLASE; GROWTH;
D O I
10.1038/nature10333
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
Advanced (long-chain) fuels and chemicals are generated from short-chain metabolic intermediates through pathways that require carbon-chain elongation. The condensation reactions mediating this carbon-carbon bond formation can be catalysed by enzymes from the thiolase superfamily, including beta-ketoacyl-acyl-carrier protein (ACP) synthases, polyketide synthases, 3-hydroxy-3-methylglutaryl-CoA synthases, and biosynthetic thiolases(1). Pathways involving these enzymes have been exploited for fuel and chemical production, with fatty-acid biosynthesis (beta-ketoacyl-ACP synthases) attracting the most attention in recent years(2-4). Degradative thiolases, which are part of the thiolase superfamily and naturally function in the beta-oxidation of fatty acids(5,6), can also operate in the synthetic direction and thus enable carbon-chain elongation. Here we demonstrate that a functional reversal of the beta-oxidation cycle can be used as a metabolic platform for the synthesis of alcohols and carboxylic acids with various chain lengths and functionalities. This pathway operates with coenzyme A (CoA) thioester intermediates and directly uses acetylCoA for acyl-chain elongation (rather than first requiring ATP-dependent activation to malonyl-CoA), characteristics that enable product synthesis at maximum carbon and energy efficiency. The reversal of the beta-oxidation cycle was engineered in Escherichia coli and used in combination with endogenous dehydrogenases and thioesterases to synthesize n-alcohols, fatty acids and 3-hydroxy-, 3-keto- and trans-Delta(2)-carboxylic acids. The superior nature of the engineered pathway was demonstrated by producing higher-chain linear n-alcohols (C >= 4) and extracellular long-chain fatty acids (C > 10) at higher efficiency than previously reported(2,4,7-9). The ubiquitous nature of beta-oxidation, aldehyde/alcohol dehydrogenase and thioesterase enzymes has the potential to enable the efficient synthesis of these products in other industrial organisms.
引用
收藏
页码:355 / U131
页数:7
相关论文
共 40 条
[21]   Application and engineering of fatty acid biosynthesis in Escherichia coli for advanced fuels and chemicals [J].
Handke, Paul ;
Lynch, Sean A. ;
Gill, Ryan T. .
METABOLIC ENGINEERING, 2011, 13 (01) :28-37
[22]   INTERMEDIARY METABOLISM IN CLOSTRIDIUM-ACETOBUTYLICUM - LEVELS OF ENZYMES INVOLVED IN THE FORMATION OF ACETATE AND BUTYRATE [J].
HARTMANIS, MGN ;
GATENBECK, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1984, 47 (06) :1277-1283
[23]   YqhD: a broad-substrate range aldehyde reductase with various applications in production of biorenewable fuels and chemicals [J].
Jarboe, Laura R. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2011, 89 (02) :249-257
[24]   GENETIC AND MOLECULAR CHARACTERIZATION OF THE GENES INVOLVED IN SHORT-CHAIN FATTY-ACID DEGRADATION IN ESCHERICHIA-COLI - THE ATO SYSTEM [J].
JENKINS, LS ;
NUNN, WD .
JOURNAL OF BACTERIOLOGY, 1987, 169 (01) :42-52
[25]   Extracting long-chain fatty acids from a fermentation medium [J].
Lalman, JA ;
Bagley, DM .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 2004, 81 (02) :105-110
[26]   Fermentative butanol production by clostridia [J].
Lee, Sang Yup ;
Park, Jin Hwan ;
Jang, Seh Hee ;
Nielsen, Lars K. ;
Kim, Jaehyun ;
Jung, Kwang S. .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 101 (02) :209-228
[27]   A Process for Microbial Hydrocarbon Synthesis: Overproduction of Fatty Acids in Escherichia coli and Catalytic Conversion to Alkanes [J].
Lennen, Rebecca M. ;
Braden, Drew J. ;
West, Ryan M. ;
Dumesic, James A. ;
Pfleger, Brian F. .
BIOTECHNOLOGY AND BIOENGINEERING, 2010, 106 (02) :193-202
[28]   CULTURE MEDIUM FOR ENTEROBACTERIA [J].
NEIDHARDT, FC ;
BLOCH, PL ;
SMITH, DF .
JOURNAL OF BACTERIOLOGY, 1974, 119 (03) :736-747
[29]   A novel paradigm of fatty acid β-oxidation exemplified by the thioesterase-dependent partial degradation of conjugated linoleic acid that fully supports growth of Escherichia coli [J].
Nie, Lina ;
Ren, Ying ;
Janakiraman, Anuradha ;
Smith, Stuart ;
Schulz, Horst .
BIOCHEMISTRY, 2008, 47 (36) :9618-9626
[30]   GLYCOLYTIC FLUX IN ZYMOMONAS-MOBILIS - ENZYME AND METABOLITE LEVELS DURING BATCH FERMENTATION [J].
OSMAN, YA ;
CONWAY, T ;
BONETTI, SJ ;
INGRAM, LO .
JOURNAL OF BACTERIOLOGY, 1987, 169 (08) :3726-3736