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1 eric hosts and the phage L5-related group of mycobacteriophages.
3 ation of PA6 resembled that of the temperate mycobacteriophages, although the genome was much smaller
5 ntifiable recombination proteins are rare in mycobacteriophages, and only 1 of 30 genomically charact
7 hat have plagued their genetic manipulation, mycobacteriophages are especially appealing subjects for
10 on vector can be easily adapted to different mycobacteriophage attachment sites (attB) due to its mod
15 nstrates a high degree of similarity to many mycobacteriophages both morphologically and genetically.
18 ore than 60% of the genes unrelated to other mycobacteriophages, but offers novel insights into how m
22 ite-specific integration was mediated by the mycobacteriophage Bxb1 integrase-catalyzed recombination
25 cribe a pair of serine integrases encoded by mycobacteriophages Bxz2 and Peaches with unusual and unp
26 and Cjw1, which are distinguished from other mycobacteriophages by their possession of a Pnkp enzyme,
30 , and only 1 of 30 genomically characterized mycobacteriophages (Che9c) encodes homologs of both RecE
32 ese challenges by utilizing real-time PCR of mycobacteriophage D29 DNA to evaluate the drug resistanc
38 onally replicating shuttle phasmids from the mycobacteriophages D29 and TM4 that enable efficient del
39 of the phams have sequence similarity to non-mycobacteriophage database entries, and fewer than 10% o
41 e system by identification and expression of mycobacteriophage-encoded recombination proteins, adapti
45 hermosensitive mutations were created in the mycobacteriophage genome that allow replication at 30 de
48 eplete with novel genes not present in other mycobacteriophage genomes, and although most are of unkn
49 literature estimates, extrapolating from 14 mycobacteriophage genomes, suggesting that two billion p
51 describe a functional genomic dissection of mycobacteriophage Giles, in which the virion proteins ar
53 tic determination of the genome sequences of mycobacteriophages has revealed the presence of several
54 70 complete genome sequences available, the mycobacteriophages have provided a wealth of information
57 of a Pnkp enzyme, are also unique among the mycobacteriophages in their specification of putative RN
58 f features not previously described in other mycobacteriophages, including noncanonical genome archit
61 ycobacterial lysis, a Giles DeltalysB mutant mycobacteriophage is viable, but defective in the normal
64 ning the phage attachment site attP from the mycobacteriophage L5 genome and additionally containing
73 that shares a similar genome organization to mycobacteriophage L5, although the two phages are hetero
74 that it is a close relative of the temperate mycobacteriophage L5, and is presumably a non-temperate
75 that it is a close relative of the temperate mycobacteriophage L5, whose sequence has been described
78 logy of Bxb1 particles is similar to that of mycobacteriophages L5 and D29, although Bxb1 differs fro
81 e previously described a luciferase reporter mycobacteriophage (LRP) assay that can detect Mycobacter
86 P protocol is the ability of the recombinant mycobacteriophage phAE40 to infect a variety of Mycobact
88 hermore, rarefaction analysis shows that the mycobacteriophage population is not closed, and there is
89 cobacteriophages, which-together with the 83 mycobacteriophages previously reported-represent the lar
92 , and new methods for simple construction of mycobacteriophage recombinants will facilitate postgenom
94 Characterization of ten Cluster N temperate mycobacteriophages revealed at least five distinct proph
95 The genomic sequences of ten newly isolated mycobacteriophages suggest that the bacteriophage popula
103 ere the complete genome sequences of 138 new mycobacteriophages, which-together with the 83 mycobacte
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