Combinatorial genetic perturbation to refine metabolic circuits for producing biofuels and biochemicals

被引:22
作者
Kim, Hyo Jin
Turner, Timothy Lee
Jin, Yong-Su [1 ]
机构
[1] Univ Illinois, Inst Genom Biol, Urbana, IL 61801 USA
关键词
Combinatorial library; Inverse metabolic engineering; Metabolic circuit; Biofuel; Biochemical; ARTIFICIAL TRANSCRIPTION FACTORS; SACCHAROMYCES-CEREVISIAE; ESCHERICHIA-COLI; CELLULOSIC ETHANOL; PROMOTER LIBRARY; MUTAGENESIS STRATEGIES; LYCOPENE BIOSYNTHESIS; PHENOTYPIC ALTERATION; SYSTEMS BIOLOGY; EXPRESSION;
D O I
10.1016/j.biotechadv.2013.03.010
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
Recent advances in metabolic engineering have enabled microbial factories to compete with conventional processes for producing fuels and chemicals. Both rational and combinatorial approaches coupled with synthetic and systematic tools play central roles in metabolic engineering to create and improve a selected microbial phenotype. Compared to knowledge-based rational approaches, combinatorial approaches exploiting biological diversity and high-throughput screening have been demonstrated as more effective tools for improving various phenotypes of interest. In particular, identification of unprecedented targets to rewire metabolic circuits for maximizing yield and productivity of a target chemical has been made possible. This review highlights general principles and the features of the combinatorial approaches using various libraries to implement desired phenotypes for strain improvement. In addition, recent applications that harnessed the combinatorial approaches to produce biofuels and biochemicals will be discussed. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:976 / 985
页数:10
相关论文
共 99 条
[1]   Isoprenoid Pathway Optimization for Taxol Precursor Overproduction in Escherichia coli [J].
Ajikumar, Parayil Kumaran ;
Xiao, Wen-Hai ;
Tyo, Keith E. J. ;
Wang, Yong ;
Simeon, Fritz ;
Leonard, Effendi ;
Mucha, Oliver ;
Phon, Too Heng ;
Pfeifer, Blaine ;
Stephanopoulos, Gregory .
SCIENCE, 2010, 330 (6000) :70-74
[2]   Tuning genetic control through promoter engineering [J].
Alper, H ;
Fischer, C ;
Nevoigt, E ;
Stephanopoulos, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12678-12683
[3]   Identifying gene targets for the metabolic engineering of lycopene biosynthesis in Escherichia coli [J].
Alper, H ;
Jin, YS ;
Moxley, JF ;
Stephanopoulos, G .
METABOLIC ENGINEERING, 2005, 7 (03) :155-164
[4]   Construction of lycopene-overproducing E-coli strains by combining systematic and combinatorial gene knockout targets [J].
Alper, H ;
Miyaoku, K ;
Stephanopoulos, G .
NATURE BIOTECHNOLOGY, 2005, 23 (05) :612-616
[5]   Uncovering the gene knockout landscape for improved lycopene production in E. coli [J].
Alper, Hal ;
Stephanopoulos, Gregory .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2008, 78 (05) :801-810
[6]   Global transcription machinery engineering: A new approach for improving cellular phenotype [J].
Alper, Hal ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (03) :258-267
[7]   Engineering yeast transcription machinery for improved ethanol tolerance and production [J].
Alper, Hal ;
Moxley, Joel ;
Nevoigt, Elke ;
Fink, Gerald R. ;
Stephanopoulos, Gregory .
SCIENCE, 2006, 314 (5805) :1565-1568
[8]   Engineering for biofuels: exploiting innate microbial capacity or importing biosynthetic potential? [J].
Alper, Hal ;
Stephanopoulos, Gregory .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (10) :715-723
[9]   Mutagenesis strategies in zebrafish for identifying genes involved in development and disease [J].
Amsterdam, Adam ;
Hopkins, Nancy .
TRENDS IN GENETICS, 2006, 22 (09) :473-478
[10]   Modular design of artificial transcription factors [J].
Ansari, AZ ;
Mapp, AK .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (06) :765-772