Metabolic engineering of Escherichia coli using CRISPR-Cas9 meditated genome editing

被引:335
作者
Li, Yifan [1 ,2 ,3 ]
Lin, Zhenquan [1 ,2 ,3 ]
Huang, Can [1 ,2 ,3 ]
Zhang, Yan [1 ,2 ,3 ]
Wang, Zhiwen [1 ,2 ,3 ]
Tang, Ya-Jie [4 ]
Chen, Tao [1 ,2 ,3 ]
Zhao, Xueming [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Minist Educ, Key Lab Syst Bioengn, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn, SynBio Res Platform, Tianjin, Peoples R China
[3] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[4] Hubei Univ Technol, Key Lab Fermentat Engn, Minist Educ, Wuhan 430068, Peoples R China
基金
中国国家自然科学基金;
关键词
CRISPR/Cas9; Genome editing; Combinatorial metabolic engineering; beta-Carotene; ISOPRENOID PATHWAY; BETA-CAROTENE; OPTIMIZATION; GENE; REPLACEMENT; OVERPRODUCTION; RECOMBINATION; SYSTEMS;
D O I
10.1016/j.ymben.2015.06.006
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
Engineering cellular metabolism for improved production of valuable chemicals requires extensive modulation of bacterial genome to explore complex genetic spaces. Here, we report the development of a CRISPR-Cas9 based method for iterative genome editing and metabolic engineering of Escherichia coli This system enables us to introduce various types of genomic modifications with near 100% editing efficiency and to introduce three mutations simultaneously. We also found that cells with intact mismatch repair system had reduced chance to escape CRISPR mediated cleavage and yielded increased editing efficiency. To demonstrate its potential, we used our method to integrate the beta-carotene synthetic pathway into the genome and to optimize the methylerythritol-phosphate (MEP) pathway and central metabolic pathways for beta-carotene overproduction. We collectively tested 33 genomic modifications and constructed more than 100 genetic variants for combinatorially exploring the metabolic landscape. Our best producer contained15 targeted mutations and produced 2.0 g/L beta-carotene in fed-batch fermentation. (C) 2015 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:13 / 21
页数:9
相关论文
共 53 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]   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
[3]  
Bao Z., 2014, ACS SYNTH BIOL
[4]   Harnessing Yarrowia lipolytica lipogenesis to create a platform for lipid and biofuel production [J].
Blazeck, John ;
Hill, Andrew ;
Liu, Leqian ;
Knight, Rebecca ;
Miller, Jarrett ;
Pan, Anny ;
Otoupal, Peter ;
Alper, Hal S. .
NATURE COMMUNICATIONS, 2014, 5
[5]   Enhanced multiplex genome engineering through co-operative oligonucleotide co-selection [J].
Carr, Peter A. ;
Wang, Harris H. ;
Sterling, Bram ;
Isaacs, Farren J. ;
Lajoie, Marc J. ;
Xu, George ;
Church, George M. ;
Jacobson, Joseph M. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (17) :e132
[6]   In Silico Identification of Gene Amplification Targets for Improvement of Lycopene Production [J].
Choi, Hyung Seok ;
Lee, Sang Yup ;
Kim, Tae Yong ;
Woo, Han Min .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2010, 76 (10) :3097-3105
[7]   High-Efficiency Multiplex Genome Editing of Streptomyces Species Using an Engineered CRISPR/Cas System [J].
Cobb, Ryan E. ;
Wang, Yajie ;
Zhao, Huimin .
ACS SYNTHETIC BIOLOGY, 2015, 4 (06) :723-728
[8]   Enhanced levels of λ red-mediated recombinants in mismatch repair mutants [J].
Costantino, N ;
Court, DL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15748-15753
[9]   One step DNA assembly for combinatorial metabolic engineering [J].
Coussement, Pieter ;
Maertens, Jo ;
Beauprez, Joeri ;
Van Bellegem, Wouter ;
De Mey, Marjan .
METABOLIC ENGINEERING, 2014, 23 :70-77
[10]   One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products [J].
Datsenko, KA ;
Wanner, BL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6640-6645