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1  of Escherichia coli to a virulent mutant of phage P1.
2 oter, thereby supporting the lytic growth of phage P1.
3 ective in mitigating the long-tailed somatic phage P1.
4 plementary in supporting the lytic growth of phage P1 and acid resistance of an E. coli sspA mutant.
5 her recombinases in the Int family (Cre from phage P1 and Int from Haemophilus influenzae phage HP1)
6 ional activator for the lytic development of phage P1 and is essential for stationary phase-induced a
7 E. coli MLK217 into S. typhimurium MGS-7 via phage P1 and subsequently via phage P22 into the virulen
8  of untagged mutations in the genome using a phage-P1-based gene-replacement strategy.
9 east-artificial-chromosome fragmentation and phage P1 cloning.
10                                    Using the phage P1-derived Cre/loxP recombination system, we have
11 ld-type sites if Cre protein is expressed by phage P1 during an infection.
12                               Enterobacteria phage P1 expresses two types of tail fibre, S and S'.
13                    Despite the wide usage of phage P1 for transduction, the host range and the recept
14 . coli, whereas only Y. pestis SspA supports phage P1 growth.
15                  Transduction frequency with phage P1 had been observed to be very low in Escherichia
16 t for both transcriptional activation of the phage P1 late promoter and acid resistance of E. coli.
17 E. coli and to activate transcription from a phage P1 late promoter, thereby supporting the lytic gro
18 L4 and L22 mutations into wild-type cells by phage P1-mediated transduction demonstrated that each al
19                                The temperate phage P1 packages several proteins into the virion that
20 anipulated using the generalized transducing phage P1, presumably because its extensive O antigen obs
21  are lysogenic for P1 and when infected with phage P1 produce only approximately 1% the number of inf
22           Upon induction of Cre recombinase (phage P1 recombinase), the VH and VL genes were efficien
23 sts of a promoterless derivative of cre, the phage P1 recombinase, carried on a plasmid, and two chro
24 nto the same plasmid via the two loxP sites (phage P1 recombination sites), one located downstream fr
25    Two additional peptides, derived from the phage P1 RepA protein and the E. coli HemA protein, whic
26 ily of recombinases, Flp of yeast and Cre of phage P1, show the same intrinsic chirality as lambda In
27 roteins, human mitochondrial SSB (Hsmt SSB), phage P1 SSB, and F episome-encoded SSB, as well as a Hs
28 otein was analyzed in vivo using a sensitive phage P1 transduction assay.