Microbial 1-butanol production: Identification of non-native production routes and in silico engineering interventions

被引:36
作者
Ranganathan, Sridhar [2 ]
Maranas, Costas D. [1 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USA
基金
美国能源部;
关键词
Biofuels; Butanol; Metabolic engineering; Metabolic pathways; Strain optimization; CLOSTRIDIUM-ACETOBUTYLICUM M5; BUTANOL PRODUCTION; INFORMATION-SYSTEM; METABOLIC PATHWAYS; ESCHERICHIA-COLI; HIGHER ALCOHOLS; EXPRESSION; RECONSTRUCTION; CLONING; DEHYDROGENASE;
D O I
10.1002/biot.201000171
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The potential of engineering microorganisms with non-native pathways for the synthesis of long-chain alcohols has been identified as a promising route to biofuels. We describe computationally derived predictions for assembling pathways for the production of biofuel candidate molecules and subsequent metabolic engineering modifications that optimize product yield. A graph-based algorithm illustrates that, by culling information from BRENDA and KEGG databases, all possible pathways that link the target product with metabolites present in the production host are identified. Subsequently, we apply our recent OptForce procedure to pinpoint reaction modifications that force the imposed product yield in Escherichia coli. We demonstrate this procedure by suggesting new pathways and genetic interventions for the overproduction of 1-butanol using the metabolic model for Escherichia coli. The graph-based search method recapitulates all recent discoveries based on the 2-ketovaline intermediate and hydroxybutyryl-CoA but also pinpointes one novel pathway through thiobutanoate intermediate that to the best of our knowledge has not been explored before.
引用
收藏
页码:716 / 725
页数:10
相关论文
共 50 条
[1]   Metabolic engineering for advanced biofuels production from Escherichia coli [J].
Atsumi, Shota ;
Liao, James C. .
CURRENT OPINION IN BIOTECHNOLOGY, 2008, 19 (05) :414-419
[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]   Pathguide: a Pathway Resource List [J].
Bader, Gary D. ;
Cary, Michael P. ;
Sander, Chris .
NUCLEIC ACIDS RESEARCH, 2006, 34 :D504-D506
[5]   CHARACTERIZATION OF WILD-TYPE AND AN ACTIVE-SITE MUTANT IN ESCHERICHIA-COLI OF SHORT-CHAIN ACYL-COA DEHYDROGENASE FROM MEGASPHAERA-ELSDENII [J].
BECKER, DF ;
FUCHS, JA ;
BANFIELD, DK ;
FUNK, WD ;
MACGILLIVRAY, RTA ;
STANKOVICH, MT .
BIOCHEMISTRY, 1993, 32 (40) :10736-10742
[6]   MetaRoute: fast search for relevant metabolic routes for interactive network navigation and visualization [J].
Blum, Torsten ;
Kohlbacher, Oliver .
BIOINFORMATICS, 2008, 24 (18) :2108-2109
[7]   The impact of bacterial genomics on natural product research [J].
Bode, HB ;
Müller, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (42) :6828-6846
[8]   Cloning, sequencing, and expression of genes encoding phosphotransacetylase and acetate kinase from Clostridium acetobutylicum ATCC 824 [J].
Boynton, ZL ;
Bennett, GN ;
Rudolph, FB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (08) :2758-2766
[9]   BRENDA, AMENDA and FRENDA the enzyme information system: new content and tools in 2009 [J].
Chang, Antje ;
Scheer, Maurice ;
Grote, Andreas ;
Schomburg, Ida ;
Schomburg, Dietmar .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D588-D592
[10]   Prediction of novel synthetic pathways for the production of desired chemicals [J].
Cho, Ayoun ;
Yun, Hongseok ;
Park, Jin Hwan ;
Lee, Sang Yup ;
Park, Sunwon .
BMC SYSTEMS BIOLOGY, 2010, 4