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1 ggests that they are relatively common among mycobacteriophages.
2 eric hosts and the phage L5-related group of mycobacteriophages.
3                                              Mycobacteriophages accomplish this by producing two lysi
4 ation of PA6 resembled that of the temperate mycobacteriophages, although the genome was much smaller
5 cribe what we have learned from the study of mycobacteriophages and how a holistic approach-integrati
6 luster M further expand the diversity of the mycobacteriophages and introduce novel features.
7                    Synthetic construction of mycobacteriophages and their derivatives expands the pha
8 isters can be visualized using dual-reporter mycobacteriophages and their formation prevented using r
9 ntifiable recombination proteins are rare in mycobacteriophages, and only 1 of 30 genomically charact
10                                              Mycobacteriophage are viruses that infect mycobacteria.
11                                              Mycobacteriophages are a diverse group of viruses infect
12 hat have plagued their genetic manipulation, mycobacteriophages are especially appealing subjects for
13                                              Mycobacteriophages are viruses that infect mycobacterial
14                                              Mycobacteriophages are viruses that infect mycobacterial
15 e have developed a luciferase-based reporter mycobacteriophage assay that can determine drug resistan
16 on vector can be easily adapted to different mycobacteriophage attachment sites (attB) due to its mod
17                                              Mycobacteriophage-based approaches to tuberculosis diagn
18        This study analyzes one of these, the mycobacteriophage Bethlehem DnaB intein, which we descri
19 ill facilitate postgenomic explorations into mycobacteriophage biology.
20               Three newly isolated temperate mycobacteriophages, Bongo, PegLeg, and Rey, constitute a
21 nstrates a high degree of similarity to many mycobacteriophages both morphologically and genetically.
22                           The PR promoter of mycobacteriophage BPs directs early lytic gene expressio
23                                              Mycobacteriophage Brujita is an unusual temperate phage
24 ore than 60% of the genes unrelated to other mycobacteriophages, but offers novel insights into how m
25                           Integration of the mycobacteriophage Bxb1 genome into its host chromosome i
26                          Here we report that mycobacteriophage Bxb1 integrase also mediates targeted
27                          This is mediated by mycobacteriophage Bxb1 integrase, which catalyzes recomb
28 ite-specific integration was mediated by the mycobacteriophage Bxb1 integrase-catalyzed recombination
29                                              Mycobacteriophage Bxb1 is a temperate phage of Mycobacte
30                                              Mycobacteriophage Bxb1 is a temperate phage of Mycobacte
31                                              Mycobacteriophage Bxb1 is a well-characterized virus of
32 cribe a pair of serine integrases encoded by mycobacteriophages Bxz2 and Peaches with unusual and unp
33 and Cjw1, which are distinguished from other mycobacteriophages by their possession of a Pnkp enzyme,
34        This study determined which class the mycobacteriophage Catera Gp206 and Nocardioides sp. JS61
35                                          The mycobacteriophage Catera Gp206 intein (starting with Ser
36                                          The mycobacteriophage Catera Gp206, Nocardioides sp. strain
37 , and only 1 of 30 genomically characterized mycobacteriophages (Che9c) encodes homologs of both RecE
38                             A large group of mycobacteriophages code for repressors that are unusual
39                                         Many mycobacteriophages code for their own Lsr2-related prote
40 cobacteria illustrate this model and a large mycobacteriophage collection reveals the enormous divers
41                  Genomic comparison of these mycobacteriophages contributes to our understanding of t
42 ese challenges by utilizing real-time PCR of mycobacteriophage D29 DNA to evaluate the drug resistanc
43 struction of luciferase reporter phages from mycobacteriophage D29 DNA.
44                                              Mycobacteriophage D29 is a lytic phage that infects both
45                                              Mycobacteriophage D29 is a lytic phage that infects both
46 dissection of the function and regulation of mycobacteriophage D29 Lysin A.
47 ction of Mycobacterium tuberculosis by using mycobacteriophage D29.
48 onally replicating shuttle phasmids from the mycobacteriophages D29 and TM4 that enable efficient del
49 of the phams have sequence similarity to non-mycobacteriophage database entries, and fewer than 10% o
50      We developed a 48 h luciferase reporter mycobacteriophage drug susceptibility testing (LRM-DST)
51 rived single-stranded DNA recombineering and mycobacteriophage-encoded proteins.
52 e system by identification and expression of mycobacteriophage-encoded recombination proteins, adapti
53                          The 1,885 sequenced mycobacteriophages encompass over 200,000 genes in 7,300
54                                              Mycobacteriophages encounter a unique problem among phag
55 aracterized the virulence of three different mycobacteriophages (Fionnbharth, Muddy, and D29), alone
56 atic investigation of the virulence of three mycobacteriophages, Fionnbharth, Muddy, and D29, and the
57 lowed by incubation with 10(3) PFU/ml of D29 mycobacteriophage for 24 h and then real-time PCR.
58  193 unrelated genes encoded by 13 different mycobacteriophages for their ability to impair the growt
59                                     Although mycobacteriophage genes exhibit a smaller average size t
60 e limitations-together with the abundance of mycobacteriophage genes of unknown function-could be add
61                       We identified 45 (23%) mycobacteriophage genes that are toxic when expressed.
62 hermosensitive mutations were created in the mycobacteriophage genome that allow replication at 30 de
63 However, the relatively high G+C% content of mycobacteriophage genomes (64.1%) can be challenging for
64 A set of 2,600 fully sequenced and annotated mycobacteriophage genomes and the development of tools f
65                              More than 1,400 mycobacteriophage genomes have been sequenced, coding fo
66                                      Ten new mycobacteriophage genomes presented by show that most ph
67 se chemistry, the reconstruction of complete mycobacteriophage genomes using High-Complexity Golden G
68 eplete with novel genes not present in other mycobacteriophage genomes, and although most are of unkn
69  literature estimates, extrapolating from 14 mycobacteriophage genomes, suggesting that two billion p
70                        Analysis of the novel mycobacteriophage Giles genome not only extends our curr
71  describe a functional genomic dissection of mycobacteriophage Giles, in which the virion proteins ar
72                          Here we investigate mycobacteriophage Giles-host protein-protein interaction
73 tic determination of the genome sequences of mycobacteriophages has revealed the presence of several
74  70 complete genome sequences available, the mycobacteriophages have provided a wealth of information
75                                              Mycobacteriophages have provided key tools for tuberculo
76                                The cluster M mycobacteriophages have siphoviral morphologies with unu
77  we provide the X-ray crystal structure of a mycobacteriophage immunity repressor bound to DNA, which
78  of a Pnkp enzyme, are also unique among the mycobacteriophages in their specification of putative RN
79 f features not previously described in other mycobacteriophages, including noncanonical genome archit
80                                              Mycobacteriophages infect and replicate in viable bacter
81  to visualize the spatiotemporal dynamics of mycobacteriophage infection in single cells and populati
82                                              Mycobacteriophage infection of M. leprae was shown using
83   These results inform us on the dynamics of mycobacteriophage infections, both alone and in cocktail
84  eight-gene cluster has strong similarity to mycobacteriophage integrase sequences.
85 ycobacterial lysis, a Giles DeltalysB mutant mycobacteriophage is viable, but defective in the normal
86                                              Mycobacteriophage L5 accomplishes this by an atypical ph
87                       The well-characterized mycobacteriophage L5 forms stable lysogens in Mycobacter
88 ning the phage attachment site attP from the mycobacteriophage L5 genome and additionally containing
89                      The genome of temperate mycobacteriophage L5 integrates into the chromosomes of
90                                              Mycobacteriophage L5 integrates into the genome of Mycob
91                                The temperate mycobacteriophage L5 integrates site specifically into t
92                            Lysogenization of mycobacteriophage L5 involves integration of the phage g
93                                              Mycobacteriophage L5 is a temperate phage that forms lys
94                                              Mycobacteriophage L5 is a well-characterized temperate p
95                               Integration of mycobacteriophage L5 is catalyzed by a phage-encoded int
96                               Integration of mycobacteriophage L5 requires the mycobacterial integrat
97 that shares a similar genome organization to mycobacteriophage L5, although the two phages are hetero
98 that it is a close relative of the temperate mycobacteriophage L5, and is presumably a non-temperate
99 that it is a close relative of the temperate mycobacteriophage L5, whose sequence has been described
100  tuberculosis that stimulates integration of mycobacteriophage L5.
101 megmatis whose product confers resistance to mycobacteriophages L5 and D29 when overproduced.
102 logy of Bxb1 particles is similar to that of mycobacteriophages L5 and D29, although Bxb1 differs fro
103 cterium smegmatis that confers resistance to mycobacteriophages L5 and D29.
104 element phiRv2, and compare them to those of mycobacteriophages L5 and D29.
105     We developed a novel luciferase reporter mycobacteriophage (LRM) based phenotypic DST method usin
106 d the application of the luciferase reporter mycobacteriophage (LRM) for drug screening.
107 e previously described a luciferase reporter mycobacteriophage (LRP) assay that can detect Mycobacter
108           The utility of luciferase reporter mycobacteriophages (LRPs) for detection, identification,
109 ains encoding up to three kill switches: two mycobacteriophage lysin operons negatively regulated by
110                                     Tmp's of mycobacteriophages may thus have acquired these motifs i
111                               We demonstrate mycobacteriophage-mediated introduction of foreign DNA u
112                                              Mycobacteriophages (MPs) have been gaining interest in r
113 u homologs in Corndog and Omega, two related mycobacteriophages of Mycobacterium smegmatis.
114                            Here we show that mycobacteriophages Omega and Cjw1 and vibriophage KVP40
115 P protocol is the ability of the recombinant mycobacteriophage phAE40 to infect a variety of Mycobact
116 and characterize the gp82 protein encoded by mycobacteriophage Phaedrus.
117                 We developed a more powerful mycobacteriophage (Phi(2)GFP10) with a fluorescent repor
118 ing potential drug targets and for exploring mycobacteriophage physiology.
119 hermore, rarefaction analysis shows that the mycobacteriophage population is not closed, and there is
120                                              Mycobacteriophages preferentially adsorb at Mycobacteriu
121 cobacteriophages, which-together with the 83 mycobacteriophages previously reported-represent the lar
122                              Upon infection, mycobacteriophages produce lysins that catalyze cell wal
123          Although the attachment site DNA of mycobacteriophage Pukovnik is likely to contain four sit
124 , and new methods for simple construction of mycobacteriophage recombinants will facilitate postgenom
125                                              Mycobacteriophages represent a genetically diverse group
126  Characterization of ten Cluster N temperate mycobacteriophages revealed at least five distinct proph
127                                              Mycobacteriophages show considerable potential as therap
128                                              Mycobacteriophages show promise as therapeutic agents fo
129  The genomic sequences of ten newly isolated mycobacteriophages suggest that the bacteriophage popula
130                                              Mycobacteriophages-the viruses of mycobacterial hosts-pr
131                                              Mycobacteriophages thus present a massive reservoir of g
132 on of foreign DNA using the broad-host range mycobacteriophage TM4 and the application of the lucifer
133 Here we focussed on the WhiB-like protein of mycobacteriophage TM4, WhiBTM4.
134                                Many of these mycobacteriophage Tmp's contain small motifs with sequen
135                     Thirdly, it is the first mycobacteriophage to be described that forms a large pro
136                        We engineered the TM4 mycobacteriophage to express green enhanced nanolucifera
137 quirements responsible for the attachment of mycobacteriophage to the host cell wall.
138                The predominant morphotype of mycobacteriophage virions has a DNA-containing capsid at
139                                              Mycobacteriophages, viruses that can infect bacteria suc
140                                          Two mycobacteriophages were administered intravenously to a
141                               TM4 is a lytic mycobacteriophage which infects mycobacteria of clinical
142 ere the complete genome sequences of 138 new mycobacteriophages, which-together with the 83 mycobacte

 
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