1 ouble-strand DNA end-binding protein, Gam of
bacteriophage Mu.
2 e bound to a strong gyrase binding site from
bacteriophage Mu.
3 mechanism underlying target immunity by the
bacteriophage Mu.
4 ed to a maximum of 2 kb and mutagenized with
bacteriophage Mud.
5 rt the complete 36,717 bp genome sequence of
bacteriophage Mu and provide an analysis of the sequence
6 cialized activities of genetic elements like
bacteriophage Mu and the F plasmid.
7 quence specificity of the invertase Gin from
bacteriophage Mu and Tn3 resolvase from Escherichia coli
8 The
bacteriophage Mu C gene encodes a 16.5 kDa site-specific
9 Originally discovered in the
bacteriophage Mu DNA inversion system gin, Fis (Factor f
10 Initiation of
bacteriophage Mu DNA replication by transposition requir
11 richia coli plays two distinct functions for
bacteriophage Mu DNA replication by transposition.
12 at this primosome plays an essential role in
bacteriophage Mu DNA replication by transposition.
13 Bacteriophage Mu DNA synthesis is initiated during trans
14 Replication of
bacteriophage Mu DNA, a process requiring efficient syna
15 The repressor protein of
bacteriophage Mu establishes and maintains lysogeny by s
16 The immunity repressor (Rep) of
bacteriophage Mu establishes and maintains lysogeny by s
17 The repressor of
bacteriophage Mu functions in the establishment and main
18 is located midway between the termini of the
bacteriophage Mu genome and is required for efficient re
19 The
bacteriophage Mu genome contains a centrally located str
20 hia coli chromosome for the insertion of the
bacteriophage Mu genome.
21 The C-terminal domain (CTD) of
bacteriophage Mu immunity repressor (Rep) regulates DNA
22 Rapid degradation of the
bacteriophage Mu immunity repressor can be induced in tr
23 The
bacteriophage Mu immunity repressor is a conformationall
24 infected cells revealed enhanced regions of
bacteriophage Mu insertion near the ends of HIV-1 cDNA,
25 Lytic development of
bacteriophage Mu is controlled by a regulatory cascade a
26 ial for replicative DNA transposition by the
bacteriophage Mu,
is an ATPase that assembles into a pol
27 Transcription of the
bacteriophage Mu mom operon is strongly repressed by the
28 Transcription of the
bacteriophage Mu mom operon requires transactivation by
29 Gene expression during lytic development of
bacteriophage Mu occurs in three phases: early, middle,
30 Lytic development of
bacteriophage Mu proceeds through three phases of transc
31 Bacteriophage Mu replicates as a transposable element, e
32 Conversion of
bacteriophage Mu repressor to ClpXP-sensitive form corre
33 Middle transcription of
bacteriophage Mu requires Escherichia coli RNA polymeras
34 Middle transcription of
bacteriophage Mu requires Escherichia coli RNA polymeras
35 anscription from the middle promoter, Pm, of
bacteriophage Mu requires the phage-encoded activator pr
36 ons in an N-terminal 70-amino acid domain of
bacteriophage Mu'
s repressor cause temperature-sensitive
37 The transposition of
bacteriophage Mu serves as a model system for understand
38 The
bacteriophage Mu strong gyrase site (SGS) is required fo
39 The
bacteriophage Mu strong gyrase site (SGS), required for
40 Like enteric
bacteriophage Mu,
the BcepMu genomic DNA is flanked by v
41 he MuA transposase mediates transposition of
bacteriophage Mu through two distinct mechanisms.
42 amines the contribution of domain II beta of
bacteriophage Mu transposase (A protein), a subdomain of
43 During transposition
bacteriophage Mu transposase (MuA) catalyzes the transfe
44 ity to the better understood turnover of the
bacteriophage Mu transposase and functions of integrase
45 ntegrase, avian sarcoma virus integrase, and
bacteriophage Mu transposase.
46 To trigger
bacteriophage Mu transposition and replication in respon
47 helicase DnaB for replisome assembly during
bacteriophage Mu transposition and replication.
48 Studies of
bacteriophage Mu transposition paved the way for underst
49 Transposition of
bacteriophage Mu uses two DNA cleavage sites and six tra
50 Target specificity for
bacteriophage Mu was studied using a new phage derivativ