A rapid and reliable strategy for chromosomal integration of gene(s) with multiple copies
出版年份 2015 全文链接
标题
A rapid and reliable strategy for chromosomal integration of gene(s) with multiple copies
作者
关键词
-
出版物
Scientific Reports
Volume 5, Issue 1, Pages -
出版商
Springer Nature
发表日期
2015-04-08
DOI
10.1038/srep09684
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- High-Efficiency Scarless Genetic Modification in Escherichia coli by Using Lambda Red Recombination and I-SceI Cleavage
- (2014) Junjie Yang et al. APPLIED AND ENVIRONMENTAL MICROBIOLOGY
- Construction of an l-serine producing Escherichia coli via metabolic engineering
- (2014) Pengfei Gu et al. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY
- Rapid one-step inactivation of single or multiple genes inEscherichia coli
- (2013) Chan Woo Song et al. Biotechnology Journal
- A new simple method for introducing an unmarked mutation into a large gene of non-competent Gram-negative bacteria by FLP/FRT recombination
- (2013) Masahito Ishikawa et al. BMC MICROBIOLOGY
- Tools for advanced and targeted genetic manipulation of the β-lactam antibiotic producer Acremonium chrysogenum
- (2013) S. Bloemendal et al. JOURNAL OF BIOTECHNOLOGY
- Metabolic and pathway engineering to influence native and altered erythromycin production through E. coli
- (2013) Ming Jiang et al. METABOLIC ENGINEERING
- Construction of Escherichia coli strains with chromosomally integrated expression cassettes for the synthesis of 2′-fucosyllactose
- (2013) Florian Baumgärtner et al. Microbial Cell Factories
- Knock-in/Knock-out (KIKO) vectors for rapid integration of large DNA sequences, including whole metabolic pathways, onto the Escherichia coli chromosome at well-characterised loci
- (2013) Suriana Sabri et al. Microbial Cell Factories
- Characterization of 582 natural and synthetic terminators and quantification of their design constraints
- (2013) Ying-Ja Chen et al. NATURE METHODS
- Quantifying Translational Coupling in E. coli Synthetic Operons Using RBS Modulation and Fluorescent Reporters
- (2013) Ayelet Levin-Karp et al. ACS Synthetic Biology
- One-Step Cloning and Chromosomal Integration of DNA
- (2013) François St-Pierre et al. ACS Synthetic Biology
- One-Step Sequence- and Ligation-Independent Cloning as a Rapid and Versatile Cloning Method for Functional Genomics Studies
- (2012) Jae-Yeon Jeong et al. APPLIED AND ENVIRONMENTAL MICROBIOLOGY
- Adjusting the attB Site in Donor Plasmid Improves the Efficiency of ΦC31 Integrase System
- (2012) Fei Xie et al. DNA AND CELL BIOLOGY
- A PCR-free cloning method for the targeted φ80 Int-mediated integration of any long DNA fragment, bracketed with meganuclease recognition sites, into the Escherichia coli chromosome
- (2012) Anna A. Ublinskaya et al. JOURNAL OF MICROBIOLOGICAL METHODS
- A strategy of gene overexpression based on tandem repetitive promoters in Escherichia coli
- (2012) Mingji Li et al. Microbial Cell Factories
- One-step of tryptophan attenuator inactivation and promoter swapping to improve the production of L-tryptophan in Escherichia coli
- (2012) Pengfei Gu et al. Microbial Cell Factories
- Genome-scale promoter engineering by coselection MAGE
- (2012) Harris H Wang et al. NATURE METHODS
- Automated Design of Genetic Toggle Switches with Predetermined Bistability
- (2012) Shuobing Chen et al. ACS Synthetic Biology
- Modular Engineering of l-Tyrosine Production in Escherichia coli
- (2011) Darmawi Juminaga et al. APPLIED AND ENVIRONMENTAL MICROBIOLOGY
- A mini-Mu transposon-based method for multiple DNA fragment integration into bacterial genomes
- (2010) Xiao-Xing Wei et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- Site-specific chromosomal integration of large synthetic constructs
- (2010) Thomas E. Kuhlman et al. NUCLEIC ACIDS RESEARCH
- Programming cells by multiplex genome engineering and accelerated evolution
- (2009) Harris H. Wang et al. NATURE
- Stabilized gene duplication enables long-term selection-free heterologous pathway expression
- (2009) Keith E J Tyo et al. NATURE BIOTECHNOLOGY
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