Literature DB >> 2955078

Altered phage P1 attachment to strains of Escherichia coli carrying the plasmid ColV,I-K94.

M Goodson, R J Rowbury.   

Abstract

Phages P1vir and P1cmclrf100 failed to form plaques on or multiply in Escherichia coli strains carrying the ColV,I-K94 plasmid; with P1cmclr100, the effect occurred both with phage from the lytic cycle and with that induced from a lysogen. The effect was on attachment, these P1 phages attaching poorly to ColV,I-K94+ strains. This receptor defect appeared to result mainly from the presence of ColV-encoded transfer and colicin components in the cells carrying ColV,I-K94 and it was specific to this plasmid. Phage Mu (which uses an attachment mechanism similar to that of phage P1) in the G(+) form attached to both Col- and ColV,I-K94+ strains but the G(-) form attached to neither type.

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Year:  1987        PMID: 2955078     DOI: 10.1099/0022-1317-68-7-1785

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  1 in total

1.  Strain engineering by genome mass transfer: efficient chromosomal trait transfer method utilizing donor genomic DNA and recipient recombineering hosts.

Authors:  James A Williams; Jeremy Luke; Clague Hodgson
Journal:  Mol Biotechnol       Date:  2009-05-20       Impact factor: 2.695

  1 in total

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