Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
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Strategies used for genetically modifying bacterial genome: site-directed mutagenesis, gene inactivation, and gene over-expressionCapsular glucan and intracellular glycogen of Mycobacterium tuberculosis: biosynthesis and impact on the persistence in miceEffects of Pyrogallol on Growth and Cytotoxicity of Wild-Type and katG Mutant Strains of Vibrio vulnificusGenetic tools for allelic replacement in Burkholderia species.Novel system for efficient isolation of Clostridium double-crossover allelic exchange mutants enabling markerless chromosomal gene deletions and DNA integration.Instability of pathogenicity islands in uropathogenic Escherichia coli 536.Use of rpsL as a Counterselectable Marker in Borrelia burgdorferiA rapid and simple method for constructing stable mutants of Acinetobacter baumanniiMobilisation and remobilisation of a large archetypal pathogenicity island of uropathogenic Escherichia coli in vitro support the role of conjugation for horizontal transfer of genomic islands.Repression of aerobic leukotoxin transcription by integration host factor in Aggregatibacter actinomycetemcomitansIntroduction of the six major genomic deletions of modified vaccinia virus Ankara (MVA) into the parental vaccinia virus is not sufficient to reproduce an MVA-like phenotype in cell culture and in mice.The Actinomyces oris type 2 fimbrial shaft FimA mediates co-aggregation with oral streptococci, adherence to red blood cells and biofilm development.Markerless gene deletion system for sphingomonads.A suitable streptomycin-resistant mutant for constructing unmarked in-frame gene deletions using rpsL as a counter-selection marker.Genome-based metabolic engineering of Mannheimia succiniciproducens for succinic acid production.mazF, a novel counter-selectable marker for unmarked chromosomal manipulation in Bacillus subtilis.The synchrony phenotype persists after elimination of multiple GATC sites from the dnaA promoter of Escherichia coli.The cyclic-AMP receptor protein (CRP) regulon in Aggregatibacter actinomycetemcomitans includes leukotoxinAdvances in genetic manipulation of obligate intracellular bacterial pathogensA modified Janus cassette (Sweet Janus) to improve allelic replacement efficiency by high-stringency negative selection in Streptococcus pneumoniae.Developing Universal Genetic Tools for Rapid and Efficient Deletion Mutation in Vibrio Species Based on Suicide T-Vectors Carrying a Novel Counterselectable Marker, vmi480Targeted Curing of All Lysogenic Bacteriophage from Streptococcus pyogenes Using a Novel Counter-selection TechniqueIn-Frame Deletions Allow Functional Characterization of Complex Cellulose Degradation Phenotypes in Cellvibrio japonicus.Two systems for targeted gene deletion in Coxiella burnetiiLambda Red-mediated Recombineering in the Attaching and Effacing Pathogen Escherichia albertiipyrF as a Counterselectable Marker for Unmarked Genetic Manipulations in Treponema denticola.Investigation of the Genetics and Biochemistry of Roseobacticide Production in the Roseobacter Clade Bacterium Phaeobacter inhibens.Tools for functional postgenomic analysis of listeria monocytogenes.Construction of new cloning, lacZ reporter and scarless-markerless suicide vectors for genetic studies in Aggregatibacter actinomycetemcomitans.Mlc is a transcriptional activator with a key role in integrating cyclic AMP receptor protein and integration host factor regulation of leukotoxin RNA synthesis in Aggregatibacter actinomycetemcomitans.A new simple method for introducing an unmarked mutation into a large gene of non-competent Gram-negative bacteria by FLP/FRT recombinationHigh-Efficiency, Two-Step Scarless-Markerless Genome Genetic Modification in Salmonella enterica.Precision-engineering the Pseudomonas aeruginosa genome with two-step allelic exchange.Multigene disruption in undomesticated Bacillus subtilis ATCC 6051a using the CRISPR/Cas9 system.Stabilization of the Virulence Plasmid pSLT of Salmonella Typhimurium by Three Maintenance Systems and Its Evaluation by Using a New Stability Test.Improved antibiotic-free DNA vaccine vectors utilizing a novel RNA based plasmid selection system.Bacterial cellular engineering by genome editing and gene silencingA versatile one-step CRISPR-Cas9 based approach to plasmid-curing.Promotion and Rescue of Intracellular Brucella neotomae Replication during Coinfection with Legionella pneumophilaAn Effective Counterselection System for Listeria monocytogenes and Its Use To Characterize the Monocin Genomic Region of Strain 10403S.
P2860
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P2860
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@en
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@nl
type
label
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@en
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@nl
prefLabel
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@en
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@nl
P2093
P2860
P1476
Counterselectable markers: untapped tools for bacterial genetics and pathogenesis.
@en
P2093
P2860
P304
P407
P577
1998-09-01T00:00:00Z