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λ Recombineering Used to Engineer the Genome of Phage T7
by
Court, Donald L.
, Adhya, Sankar
, Rattray, Alison J.
, Jensen, Jordan D.
, Parks, Adam R.
in
Antibiotics
/ Artificial chromosomes
/ bacteriophage engineering
/ bacteriophage genetics
/ Cloning
/ Deoxyribonucleic acid
/ DNA
/ E coli
/ Gene expression
/ Genetic engineering
/ Genomes
/ In vivo methods and tests
/ Infections
/ Mutation
/ phage therapy
/ Phages
/ Recombination
/ recombineering
/ RNA polymerase
/ Transfection
/ Virulence
2020
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λ Recombineering Used to Engineer the Genome of Phage T7
by
Court, Donald L.
, Adhya, Sankar
, Rattray, Alison J.
, Jensen, Jordan D.
, Parks, Adam R.
in
Antibiotics
/ Artificial chromosomes
/ bacteriophage engineering
/ bacteriophage genetics
/ Cloning
/ Deoxyribonucleic acid
/ DNA
/ E coli
/ Gene expression
/ Genetic engineering
/ Genomes
/ In vivo methods and tests
/ Infections
/ Mutation
/ phage therapy
/ Phages
/ Recombination
/ recombineering
/ RNA polymerase
/ Transfection
/ Virulence
2020
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Do you wish to request the book?
λ Recombineering Used to Engineer the Genome of Phage T7
by
Court, Donald L.
, Adhya, Sankar
, Rattray, Alison J.
, Jensen, Jordan D.
, Parks, Adam R.
in
Antibiotics
/ Artificial chromosomes
/ bacteriophage engineering
/ bacteriophage genetics
/ Cloning
/ Deoxyribonucleic acid
/ DNA
/ E coli
/ Gene expression
/ Genetic engineering
/ Genomes
/ In vivo methods and tests
/ Infections
/ Mutation
/ phage therapy
/ Phages
/ Recombination
/ recombineering
/ RNA polymerase
/ Transfection
/ Virulence
2020
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Journal Article
λ Recombineering Used to Engineer the Genome of Phage T7
2020
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Overview
Bacteriophage T7 and T7-like bacteriophages are valuable genetic models for lytic phage biology that have heretofore been intractable with in vivo genetic engineering methods. This manuscript describes that the presence of λ Red recombination proteins makes in vivo recombineering of T7 possible, so that single base changes and whole gene replacements on the T7 genome can be made. Red recombination functions also increase the efficiency of T7 genome DNA transfection of cells by ~100-fold. Likewise, Red function enables two other T7-like bacteriophages that do not normally propagate in E. coli to be recovered following genome transfection. These results constitute major technical advances in the speed and efficiency of bacteriophage T7 engineering and will aid in the rapid development of new phage variants for a variety of applications.
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