An efficient method of selectable marker gene excision by Xer recombination for gene replacement in bacterial chromosomes.
about
Antibiotic-free selection in biotherapeutics: now and foreverA system of vectors for Bacillus subtilis spore surface displayXer recombinase and genome integrity in Helicobacter pylori, a pathogen without topoisomerase IVCurrent development in genetic engineering strategies of Bacillus species.Molecular strategy for survival at a critical high temperature in Eschierichia coli.Genome-wide analysis of phosphorylated PhoP binding to chromosomal DNA reveals several novel features of the PhoPR-mediated phosphate limitation response in Bacillus subtilis.Disruption of Escherichia coli Nissle 1917 K5 capsule biosynthesis, through loss of distinct kfi genes, modulates interaction with intestinal epithelial cells and impact on cell health.Development of an efficient autoinducible expression system by promoter engineering in Bacillus subtilisConstruction and development of an auto-regulatory gene expression system in Bacillus subtilis.OLE RNA protects extremophilic bacteria from alcohol toxicityProgress in Bacillus subtilis Spore Surface Display Technology towards Environment, Vaccine Development, and Biocatalysis.Efficient and simple generation of multiple unmarked gene deletions in Mycobacterium smegmatisMob/oriT, a mobilizable site-specific recombination system for unmarked genetic manipulation in Bacillus thuringiensis and Bacillus cereus.The dif/Xer recombination systems in proteobacteria.Gene replacement techniques for Escherichia coli genome modification.Live to cheat another day: bacterial dormancy facilitates the social exploitation of β-lactamases.Genome engineering using a synthetic gene circuit in Bacillus subtilis.Editing of the Bacillus subtilis Genome by the CRISPR-Cas9 System.Characterization of pABVA01, a plasmid encoding the OXA-24 carbapenemase from Italian isolates of Acinetobacter baumannii.Xer site-specific recombination, an efficient tool to introduce unmarked deletions into mycobacteria.Development of a repressible mycobacterial promoter system based on two transcriptional repressors.A highly unstable transcript makes CwlO D,L-endopeptidase expression responsive to growth conditions in Bacillus subtilisBiological Containment of Genetically Modified Bacillus subtilis.Proteomic analysis of Bacillus subtilis strains engineered for improved production of heterologous proteins.Metabolic Engineering of Escherichia coli K12 for Homofermentative Production of L-Lactate from Xylose.An extracellular aminopeptidase encoded by the ywaD gene plays an important role in supplying nitrogen nutrition for the growth of Bacillus subtilis 168.Evaluation of genetic manipulation strategies on D-lactate production by Escherichia coli.Genome Editing Method for the Anaerobic Magnetotactic Bacterium Desulfovibrio magneticus RS-1
P2860
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P2860
An efficient method of selectable marker gene excision by Xer recombination for gene replacement in bacterial chromosomes.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
An efficient method of selecta ...... ment in bacterial chromosomes.
@en
An efficient method of selecta ...... ment in bacterial chromosomes.
@nl
type
label
An efficient method of selecta ...... ment in bacterial chromosomes.
@en
An efficient method of selecta ...... ment in bacterial chromosomes.
@nl
prefLabel
An efficient method of selecta ...... ment in bacterial chromosomes.
@en
An efficient method of selecta ...... ment in bacterial chromosomes.
@nl
P2860
P1476
An efficient method of selecta ...... ment in bacterial chromosomes.
@en
P2093
Alexandra E Bloor
Rocky M Cranenburgh
P2860
P304
P356
10.1128/AEM.72.4.2520-2525.2006
P407
P577
2006-04-01T00:00:00Z