In the fast lane: Large-scale bacterial genome engineering

被引:18
|
作者
Feher, Tamas [1 ]
Burland, Valerie [2 ,3 ]
Posfai, Gyoergy [1 ]
机构
[1] Hungarian Acad Sci, Biol Res Ctr, Inst Biochem, H-6726 Szeged, Hungary
[2] Scarab Genom LLC, Madison, WI 53713 USA
[3] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
关键词
Genome engineering; High throughput; Bacteria; Synthetic biology; OLIGONUCLEOTIDE-DIRECTED MUTAGENESIS; MYCOPLASMA-GENITALIUM GENOME; ESCHERICHIA-COLI GENOME; READING-FRAME SELECTION; DNA MISMATCH REPAIR; GENE SYNTHESIS; CHEMICAL-SYNTHESIS; HOMOLOGOUS RECOMBINATION; MEDIATED RECOMBINATION; BACTERIOPHAGE-LAMBDA;
D O I
10.1016/j.jbiotec.2012.02.012
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
The last few years have witnessed rapid progress in bacterial genome engineering. The long-established, standard ways of DNA synthesis, modification, transfer into living cells, and incorporation into genomes have given way to more effective, large-scale, robust genome modification protocols. Expansion of these engineering capabilities is due to several factors. Key advances include: (i) progress in oligonucleotide synthesis and in vitro and in vivo assembly methods, (ii) optimization of recombineering techniques, (iii) introduction of parallel, large-scale, combinatorial, and automated genome modification procedures, and (iv) rapid identification of the modifications by barcode-based analysis and sequencing. Combination of the brute force of these techniques with sophisticated bioinformatic design and modeling opens up new avenues for the analysis of gene functions and cellular network interactions, but also in engineering more effective producer strains. This review presents a summary of recent technological advances in bacterial genome engineering. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 79
页数:8
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