(Q52643348)

5 May 2018

title

A method for generating precise gene deletions and insertions in Escherichia coli. (English)

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5 May 2018

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Qi-Ming Zhou

1

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5 May 2018

Dong-Jie Fan

2

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5 May 2018

Jiang-Bi Xie

3

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5 May 2018

Chuan-Peng Liu

4

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5 May 2018

Jun-Mei Zhou

5

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5 May 2018

publication date

8 January 2010

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5 May 2018

World Journal of Microbiology and Biotechnology

published in

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5 May 2018

volume

26

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5 May 2018

issue

7

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5 May 2018

page(s)

1323-1329

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5 May 2018

https://scigraph.springernature.com/pub.10.1007/s11274-009-0305-y

exact match

0 references

cites work

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https://api.crossref.org/works/10.1007%2FS11274-009-0305-Y

Thermal unfolding of Escherichia coli trigger factor studied by ultra-sensitive differential scanning calorimetry.

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https://api.crossref.org/works/10.1007%2FS11274-009-0305-Y

Structural rearrangements and the unfolding mechanism of a Trigger Factor mutant studied by multiple structural probes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11274-009-0305-Y

New method for generating deletions and gene replacements in Escherichia coli

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11274-009-0305-Y

Methods for generating precise deletions and insertions in the genome of wild-type Escherichia coli: application to open reading frame characterization

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https://api.crossref.org/works/10.1007%2FS11274-009-0305-Y

Trigger factor-assisted folding of bovine carbonic anhydrase II.

21 January 2018

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An 11.8 kDa proteolytic fragment of the E. coli trigger factor represents the domain carrying the peptidyl-prolyl cis/trans isomerase activity.

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A global regulatory role of gluconeogenic genes in Escherichia coli revealed by transcriptome network analysis.

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Gene replacement with linear DNA fragments in wild-type Escherichia coli: enhancement by Chi sites

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A new logic for DNA engineering using recombination in Escherichia coli

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A new method for generating point mutations in bacterial artificial chromosomes by homologous recombination in Escherichia coli

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Structure of trigger factor binding domain in biologically homologous complex with eubacterial ribosome reveals its chaperone action

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DNA cloning by homologous recombination in Escherichia coli

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Versatile suicide vectors which allow direct selection for gene replacement in gram-negative bacteria.

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An efficient recombination system for chromosome engineering in Escherichia coli

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A single-step transconjugation system for the introduction of unmarked deletions into Actinobacillus pleuropneumoniae serotype 7 using a sucrose sensitivity marker.

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Highly efficient method for introducing successive multiple scarless gene deletions and markerless gene insertions into the Yersinia pestis chromosome

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Markerless gene replacement in Escherichia coli stimulated by a double-strand break in the chromosome

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Antibiotic marker modifications of lambda Red and FLP helper plasmids, pKD46 and pCP20, for inactivation of chromosomal genes using PCR products in multidrug-resistant strains.

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Genetic engineering using homologous recombination

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Construction of targeted single copy lac fusions using lambda Red and FLP-mediated site-specific recombination in bacteria

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The amino-terminal 118 amino acids of Escherichia coli trigger factor constitute a domain that is necessary and sufficient for binding to ribosomes.

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Gene replacement with linear DNA in electroporated wild-type Escherichia coli

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The C-terminal domain of Escherichia coli trigger factor represents the central module of its chaperone activity.

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Combination of overlapping bacterial artificial chromosomes by a two-step recombinogenic engineering method

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Modular structure of the trigger factor required for high activity in protein folding.

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One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products

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Epitope tagging of chromosomal genes in Salmonella

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Modification of human beta-globin locus PAC clones by homologous recombination in Escherichia coli

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12 December 2020

10.1007/S11274-009-0305-Y

Identifiers

DOI

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5 May 2018

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5 May 2018