A R Poteete

Summary

Affiliation: University of Massachusetts Medical Center
Country: USA

Publications

  1. pmc Alteration of T4 lysozyme structure by second-site reversion of deleterious mutations
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical Center, Worcester 01655, USA
    Protein Sci 6:2418-25. 1997
  2. pmc Roles of RuvC and RecG in phage lambda red-mediated recombination
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
    J Bacteriol 181:5402-8. 1999
  3. pmc Genetic requirements of phage lambda red-mediated gene replacement in Escherichia coli K-12
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
    J Bacteriol 182:2336-40. 2000
  4. ncbi request reprint PCR-mediated gene replacement in Escherichia coli
    K C Murphy
    Department of Molecular Genetics and Microbiology University of Massachusetts Medical School, Worcester, MA 01655, USA
    Gene 246:321-30. 2000
  5. ncbi request reprint What makes the bacteriophage lambda Red system useful for genetic engineering: molecular mechanism and biological function
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA
    FEMS Microbiol Lett 201:9-14. 2001
  6. pmc Superinfection exclusion (sieB) genes of bacteriophages P22 and lambda
    K Ranade
    Department of Molecular Genetics and Microbiology, University of Massachusetts, Worcester 01655
    J Bacteriol 175:4712-8. 1993

Collaborators

Detail Information

Publications6

  1. pmc Alteration of T4 lysozyme structure by second-site reversion of deleterious mutations
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical Center, Worcester 01655, USA
    Protein Sci 6:2418-25. 1997
    ..Some variants of proteins bearing primary substitutions at the positions of Asp 20 and Ala 98 are inferred to have significantly altered structures...
  2. pmc Roles of RuvC and RecG in phage lambda red-mediated recombination
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
    J Bacteriol 181:5402-8. 1999
    ..However, in all cases, the frequency of Red-mediated recombination was higher in recG than in recG+. These observations favor models in which RecG tends to push invading 3'-ended strands back out of recombination intermediates...
  3. pmc Genetic requirements of phage lambda red-mediated gene replacement in Escherichia coli K-12
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
    J Bacteriol 182:2336-40. 2000
    ..Expression of a gene(s) from the nin region of phage lambda partially complemented both the viability and recombination defects of the recF, recO, and recR mutants and the recombination defect of ruvC but not of ruvAB or recQ mutants...
  4. ncbi request reprint PCR-mediated gene replacement in Escherichia coli
    K C Murphy
    Department of Molecular Genetics and Microbiology University of Massachusetts Medical School, Worcester, MA 01655, USA
    Gene 246:321-30. 2000
    ..coli. Three of these replacements were performed without prior cloning of the genes...
  5. ncbi request reprint What makes the bacteriophage lambda Red system useful for genetic engineering: molecular mechanism and biological function
    A R Poteete
    Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA
    FEMS Microbiol Lett 201:9-14. 2001
    ..The role of high-frequency double-strand break repair/recombination in the life cycle of the lambdoid phages is discussed...
  6. pmc Superinfection exclusion (sieB) genes of bacteriophages P22 and lambda
    K Ranade
    Department of Molecular Genetics and Microbiology, University of Massachusetts, Worcester 01655
    J Bacteriol 175:4712-8. 1993
    ..The sieB promoter thus identified was inactivated by a 2-base substitution in its -10 hexamer. The sieB gene of coliphage lambda was also identified. The promoter for lambda sieB was identified by homology to that of P22 sieB...