Genetic Manipulation of Lytic Bacteriophages with BRED: Bacteriophage Recombineering of Electroporated DNA
We describe a recombineering-based method for the genetic manipulation of lytically replicating bacteriophages, focusing on mycobacteriophages. The approach utilizes recombineering-proficient strains of Mycobacterium smegmatis and employs a cotransformation strategy with purified phage genomic DNA a...
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Humana Press Inc.
2019
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| LEADER | 11500caa a22011897a 4500 | ||
|---|---|---|---|
| 001 | PAPER-25809 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518205756.0 | ||
| 008 | 190410s2019 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-85058900261 | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 100 | 1 | |a Marinelli, L.J. | |
| 245 | 1 | 0 | |a Genetic Manipulation of Lytic Bacteriophages with BRED: Bacteriophage Recombineering of Electroporated DNA |
| 260 | |b Humana Press Inc. |c 2019 | ||
| 270 | 1 | 0 | |m Marinelli, L.J.; Division of Dermatology, Department of Medicine, David Geffen School of Medicine, University of California, Los AngelesUnited States; email: laurajmarinelli@gmail.com |
| 506 | |2 openaire |e Política editorial | ||
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| 504 | |a Shin, H., Lee, J.H., Yoon, H., Kang, D.H., Ryu, S., Genomic investigation of lysogen formation and host lysis systems of the Salmonella temperate bacteriophage SPN9CC (2014) Appl Environ Microbiol, 80, p. 374 | ||
| 504 | |a Swaminathan, S., Rapid engineering of bacterial artificial chromosomes using oligonucleotides (2001) Genesis, 29, p. 14 | ||
| 520 | 3 | |a We describe a recombineering-based method for the genetic manipulation of lytically replicating bacteriophages, focusing on mycobacteriophages. The approach utilizes recombineering-proficient strains of Mycobacterium smegmatis and employs a cotransformation strategy with purified phage genomic DNA and a mutagenic substrate, which selects for only those cells that are competent to take up DNA. The cotransformation method, combined with the high rates of recombination obtained in M. smegmatis recombineering strains, allows for the efficient and rapid generation of bacteriophage mutants. © 2019, Springer Science+Business Media, LLC, part of Springer Nature. |l eng | |
| 593 | |a Division of Dermatology, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States | ||
| 593 | |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, IQUIBICEN-CONICET, Buenos Aires, Argentina | ||
| 593 | |a Laboratorio “Bacteriófagos y Aplicaciones Biotecnológicas”, Departamento de Química Biológica, FCEyN, UBA, Ciudad Universitaria, Ciudad Autónoma de Buenos Aires, Argentina | ||
| 593 | |a Department of Biological Sciences and Pittsburgh Bacteriophage Institute, University of Pittsburgh, Pittsburgh, PA, United States | ||
| 690 | 1 | 0 | |a BRED |
| 690 | 1 | 0 | |a ELECTROPORATION |
| 690 | 1 | 0 | |a MYCOBACTERIA |
| 690 | 1 | 0 | |a MYCOBACTERIOPHAGE |
| 690 | 1 | 0 | |a RECOMBINEERING |
| 690 | 1 | 0 | |a BACTERIOPHAGE DNA |
| 690 | 1 | 0 | |a GENOMIC DNA |
| 690 | 1 | 0 | |a OLIGONUCLEOTIDE |
| 690 | 1 | 0 | |a RAC PROTEIN |
| 690 | 1 | 0 | |a RECOMBINANT PROTEIN |
| 690 | 1 | 0 | |a RECT PROTEIN |
| 690 | 1 | 0 | |a BACTERIOPHAGE RECOMBINEERING OF ELECTROPORATED DNA |
| 690 | 1 | 0 | |a BACTERIUM CULTURE |
| 690 | 1 | 0 | |a ELECTROPORATION |
| 690 | 1 | 0 | |a GENETIC ENGINEERING |
| 690 | 1 | 0 | |a GENETIC MANIPULATION |
| 690 | 1 | 0 | |a GENETIC RECOMBINATION |
| 690 | 1 | 0 | |a METHODOLOGY |
| 690 | 1 | 0 | |a MUTANT |
| 690 | 1 | 0 | |a MYCOBACTERIOPHAGE |
| 690 | 1 | 0 | |a MYCOBACTERIUM SMEGMATIS |
| 690 | 1 | 0 | |a NATURAL SCIENCE |
| 690 | 1 | 0 | |a NONHUMAN |
| 690 | 1 | 0 | |a POLYMERASE CHAIN REACTION |
| 690 | 1 | 0 | |a PROPHAGE |
| 690 | 1 | 0 | |a RECOMBINEERING |
| 700 | 1 | |a Piuri, M. | |
| 700 | 1 | |a Hatfull, G.F. | |
| 773 | 0 | |d Humana Press Inc., 2019 |g v. 1898 |h pp. 69-80 |p Methods Mol. Biol. |x 10643745 |t Methods in Molecular Biology | |
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