Show simple item record

dc.contributor.authorMurphy, Kenan C.
dc.contributor.authorLewis, Laura J.
dc.date2022-08-11T08:10:03.000
dc.date.accessioned2022-08-23T16:53:34Z
dc.date.available2022-08-23T16:53:34Z
dc.date.issued1993-03-01
dc.date.submitted2008-08-04
dc.identifier.citationJ Bacteriol. 1993 Mar;175(6):1756-66.
dc.identifier.issn0021-9193 (Print)
dc.identifier.pmid8383665
dc.identifier.urihttp://hdl.handle.net/20.500.14038/42304
dc.description.abstractEscherichia coli strains bearing plasmids expressing phage P22 anti-RecBCD functions abc1 and abc2 were tested for the presence of recBC-like phenotypes. Abc2 induces moderate sensitivity to UV light in wild-type and recD mutant strains but severely sensitizes both recF and recJ mutants. Abc1 has little effect on UV sensitivity in wild-type or recF or recJ mutant hosts but increases the sensitivity of recD mutants to a UV dose of 20 J/m2 about 10-fold. Abc2 induces E. coli to segregate inviable cells during growth, interferes with the growth of lambda red gam chi+ and chi 0 phage (the effect is greater with chi+ phage), inhibits Chi and Chi-like activity as measured by lambda red gam crosses, and prevents SOS induction in response to nalidixic acid; Abc1 has no effect in these tests. Abc2, alone or with Abc1, does not allow the growth of lambda red gam in the presence of a P2 prophage but does not kill the P2 lysogenic host (as lambda Gam does). Finally, Abc2 inhibits conjugational recombination in wild-type cells to the level seen in recBC mutants. These data suggest that Abc2 inhibits the recombination-promoting ability of RecBCD but leaves the exonuclease functions intact.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=8383665&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC203970/?tool=pubmed
dc.subjectBacteriophage P22
dc.subjectBase Sequence
dc.subjectBinding Sites
dc.subjectConjugation, Genetic
dc.subjectDNA Helicases
dc.subjectDNA, Bacterial
dc.subjectEscherichia coli
dc.subjecteffects
dc.subject*Escherichia coli Proteins
dc.subjectExodeoxyribonuclease V
dc.subjectExodeoxyribonucleases
dc.subjectMolecular Sequence Data
dc.subjectNalidixic Acid
dc.subjectPlasmids
dc.subjectRecombination, Genetic
dc.subjectSOS Response (Genetics)
dc.subjectUltraviolet Rays
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleProperties of Escherichia coli expressing bacteriophage P22 Abc (anti-RecBCD) proteins, including inhibition of Chi activity
dc.typeJournal Article
dc.source.journaltitleJournal of bacteriology
dc.source.volume175
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/666
dc.identifier.contextkey564475
html.description.abstract<p>Escherichia coli strains bearing plasmids expressing phage P22 anti-RecBCD functions abc1 and abc2 were tested for the presence of recBC-like phenotypes. Abc2 induces moderate sensitivity to UV light in wild-type and recD mutant strains but severely sensitizes both recF and recJ mutants. Abc1 has little effect on UV sensitivity in wild-type or recF or recJ mutant hosts but increases the sensitivity of recD mutants to a UV dose of 20 J/m2 about 10-fold. Abc2 induces E. coli to segregate inviable cells during growth, interferes with the growth of lambda red gam chi+ and chi 0 phage (the effect is greater with chi+ phage), inhibits Chi and Chi-like activity as measured by lambda red gam crosses, and prevents SOS induction in response to nalidixic acid; Abc1 has no effect in these tests. Abc2, alone or with Abc1, does not allow the growth of lambda red gam in the presence of a P2 prophage but does not kill the P2 lysogenic host (as lambda Gam does). Finally, Abc2 inhibits conjugational recombination in wild-type cells to the level seen in recBC mutants. These data suggest that Abc2 inhibits the recombination-promoting ability of RecBCD but leaves the exonuclease functions intact.</p>
dc.identifier.submissionpathoapubs/666
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.source.pages1756-66


This item appears in the following Collection(s)

Show simple item record