The Use of Affinity Chromatography to Study Proteins Involved in Bacteriophage T4 Genetic Recombination
Tim Formosa, Bruce Alberts
Abstract
Tim Formosa, Bruce Alberts
Abstract
Bacteriophage T4 is a large virus that has been val-uable for studies of molecular genetic mechanisms. For the past 10 years, this laboratory has been making a focussed effort to study all of its DNA replication pro-teins (Alberts et al. 1983). However, an extremely high level of genetic recombination also occurs during T4 infections, estimated to result from an average of about 25 crossovers per genome quivalent of DNA (Stahl et al. 1964). This recombination appears to be largely in-dependent of the Escherichia coli host cell's genetic re-combination system: Few differences in recombination frequency have been observed when comparing infec-tions in wild-type strains of E. coli with infections in strains deficient in various recombination functions, including cells with lesions at the recA locus (Mortel-
OpenAlex reports 49 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Bacteriophage T4 is a large virus that has been val-uable for studies of molecular genetic mechanisms. For the past 10 years, this laboratory has been making a focussed effort to study all of its DNA replication pro-teins (Alberts et al. 1983). However, an extremely high level of genetic recombination also occurs during T4 infections, estimated to result from an average of about 25 crossovers per genome quivalent of DNA (Stahl et al. 1964). This recombination appears to be largely in-dependent of the Escherichia coli host cell's genetic re-combination system: Few differences in recombination frequency have been observed when comparing infec-tions in wild-type strains of E. coli with infections in strains deficient in various recombination functions, including cells with lesions at the recA locus (Mortel-
Key concepts: RecBCD, Recombination, FLP-FRT recombination, Escherichia coli, Genetic recombination, Genetics, Bacteriophage, Biology