Literature DB >> 2998050

In vitro packaging of plasmid DNA oligomers by Salmonella phage P22: independence of the pac site, and evidence for the termination cut in vitro.

W Behnisch, H Schmieger.   

Abstract

In vitro packaging experiments with phage P22 using artificially ligated plasmid concatemers have shown that the pac site is not necessary for DNA packaging although in vivo this initiation signal is indispensable. This indicates that the phage-coded protein gp3 also executes other important functions during phage maturation in addition to the recognition of pac, or that its site specificity is lost in vitro. It has been shown previously that gp3 is necessary for in vitro packaging. Further, it was demonstrated that DNA which is only 74% of headful size cannot be packaged. Oversized DNA, however, is cut in vitro to unit length.

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Year:  1985        PMID: 2998050     DOI: 10.1016/0042-6822(85)90273-9

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  3 in total

1.  Molecular analysis of the packaging signal in bacteriophage CP-T1 of Vibrio cholerae.

Authors:  A Guidolin; P A Manning
Journal:  Mol Gen Genet       Date:  1988-06

2.  Selection of bacterial pac sites recognized by Salmonella phage P22.

Authors:  W Vogel; H Schmieger
Journal:  Mol Gen Genet       Date:  1986-12

3.  Subunit conformations and assembly states of a DNA-translocating motor: the terminase of bacteriophage P22.

Authors:  Daniel Nemecek; Eddie B Gilcrease; Sebyung Kang; Peter E Prevelige; Sherwood Casjens; George J Thomas
Journal:  J Mol Biol       Date:  2007-09-20       Impact factor: 5.469

  3 in total

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