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1 n is central to the propagation of temperate phage Mu.
2 or an unusual but analogous -2 frameshift in phage Mu.
3 experimentally demonstrated in transposable phage Mu.
4 ed phage baseplate, that of Escherichia coli phage Mu.
5 tide CA found at the termini of transposable phage Mu also occurs at the termini of a large class of
6 teraction between the infecting transposable phage Mu and the host Escherichia coli replication machi
10 y the Tn3 and gamma delta resolvases and the phage Mu Gin invertase, we used substrates that provided
13 anscription from the middle promoter, Pm, of phage Mu is initiated by Escherichia coli RNA polymerase
16 ential interaction of the alpha CTD with the phage Mu middle promoter P(m) and its activator protein
17 te in its growth cycle, transcription of the phage Mu mom Promoter (Pmom) is activated by the phage g
19 fferent recombination reactions performed by phage Mu: non-replicative transposition, the pathway use
20 e CA/TG found at the termini of transposable phage Mu occurs also at the termini of a large class of
21 d-type enzyme in assays of filamentation and phage-Mu plating but resulted in reduced growth phenotyp
28 l for assembly of the functional tetramer of phage Mu transposase (MuA) on supercoiled DNA substrates
29 Tn3 resolvase and the LER synapse formed by phage Mu transposase in the case of Flp and Cre, respect
32 Here, we show that a new method based on phage Mu transposition in vitro allows convenient and co
33 mplex that carries out the chemical steps of phage Mu transposition is organized by bridging interact
35 ing about the molecular mechanism of IS1 and phage Mu transposition unexpectedly clarified how transp
39 similarities in the biochemical behavior of phage Mu wedge components and the TssF and TssG proteins