CRISPR/Cas9 advances engineering of microbial cell factories

被引:149
作者
Jakociunas, Tadas [1 ]
Jensen, Michael K. [1 ]
Keasling, Jay D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Tech Univ Denmark, Novo Nordisk Fdn Ctr Biosustainabil, Lyngby, Denmark
[2] Joint BioEnergy Inst, Emeryville, CA USA
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Biol Syst & Engn Div, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
关键词
Genome editing; Metabolic engineering; CRISPR/Cas9; Recombineering; Yeast; Bacteria; DOUBLE-STRAND BREAKS; HETEROLOGOUS GENE-EXPRESSION; ESCHERICHIA-COLI GENOME; SPENT SULFITE LIQUOR; SACCHAROMYCES-CEREVISIAE; HOMOLOGOUS RECOMBINATION; HIGH-THROUGHPUT; IN-VIVO; CHROMOSOMAL INTEGRATION; PLASMID CONSTRUCTION;
D O I
10.1016/j.ymben.2015.12.003
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
One of the key drivers for successful metabolic engineering in microbes is the efficacy by which genomes can be edited. As such there are many methods to choose from when aiming to modify genomes, especially those of model organisms like yeast and bacteria. In recent years, clustered regularly interspaced palindromic repeats (CRISPR) and its associated proteins (Cas) have become the method of choice for precision genome engineering in many organisms due to their orthogonality, versatility and efficacy. Here we review the strategies adopted for implementation of RNA-guided CRISPR/Cas9 genome editing with special emphasis on their application for metabolic engineering of yeast and bacteria. Also, examples of how nuclease-deficient Cas9 has been applied for RNA-guided transcriptional regulation of target genes will be reviewed, as well as tools available for computer-aided design of guide-RNAs will be highlighted. Finally, this review will provide a perspective on the immediate challenges and opportunities foreseen by the use of CRISPR/Cas9 genome engineering and regulation in the context of metabolic engineering. (C) 2015 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:44 / 59
页数:16
相关论文
共 196 条
  • [1] Isoprenoid Pathway Optimization for Taxol Precursor Overproduction in Escherichia coli
    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
    [J]. SCIENCE, 2010, 330 (6000) : 70 - 74
  • [2] Virus population dynamics and acquired virus resistance in natural microbial communities
    Andersson, Anders F.
    Banfield, Jillian F.
    [J]. SCIENCE, 2008, 320 (5879) : 1047 - 1050
  • [3] Optimization of the mevalonate-based isoprenoid biosynthetic pathway in Escherichia coli for production of the anti-malarial drug precursor amorpha-4,11-diene
    Anthony, Jennifer R.
    Anthony, Larry C.
    Nowroozi, Farnaz
    Kwon, Gina
    Newman, Jack D.
    Keasling, Jay D.
    [J]. METABOLIC ENGINEERING, 2009, 11 (01) : 13 - 19
  • [4] Enhancement of Farnesyl Diphosphate Pool as Direct Precursor of Sesquiterpenes Through Metabolic Engineering of the Mevalonate Pathway in Saccharomyces cerevisiae
    Asadollahi, Mohammad A.
    Maury, Jerome
    Schalk, Michel
    Clark, Anthony
    Nielsen, Jens
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2010, 106 (01) : 86 - 96
  • [5] Homology-Integrated CRISPR-Cas (HI-CRISPR) System for One-Step Multigene Disruption in Saccharomyces cerevisiae
    Bao, Zehua
    Xiao, Han
    Lang, Jing
    Zhang, Lu
    Xiong, Xiong
    Sun, Ning
    Si, Tong
    Zhao, Huimin
    [J]. ACS SYNTHETIC BIOLOGY, 2015, 4 (05): : 585 - 594
  • [6] CRISPR provides acquired resistance against viruses in prokaryotes
    Barrangou, Rodolphe
    Fremaux, Christophe
    Deveau, Helene
    Richards, Melissa
    Boyaval, Patrick
    Moineau, Sylvain
    Romero, Dennis A.
    Horvath, Philippe
    [J]. SCIENCE, 2007, 315 (5819) : 1709 - 1712
  • [7] PLASMID-ENCODED PROTEIN - THE PRINCIPAL FACTOR IN THE METABOLIC BURDEN ASSOCIATED WITH RECOMBINANT BACTERIA
    BENTLEY, WE
    MIRJALILI, N
    ANDERSEN, DC
    DAVIS, RH
    KOMPALA, DS
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 1990, 35 (07) : 668 - 681
  • [8] Efficient gene targeting in Drosophila with zinc-finger nucleases
    Beumer, K
    Bhattacharyya, G
    Bibikova, M
    Trautman, JK
    Carroll, D
    [J]. GENETICS, 2006, 172 (04) : 2391 - 2403
  • [9] Bibikova M, 2002, GENETICS, V161, P1169
  • [10] Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system
    Bikard, David
    Jiang, Wenyan
    Samai, Poulami
    Hochschild, Ann
    Zhang, Feng
    Marraffini, Luciano A.
    [J]. NUCLEIC ACIDS RESEARCH, 2013, 41 (15) : 7429 - 7437