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1 nd norovirus GII) and infectivity assays (F+ coliphage).
2 asured by culture, somatic coliphage, and F+ coliphage.
3 li infection by the Ff family of filamentous coliphage.
4 and studied in the limited context of T-even coliphages.
5 olved during infection of six newly isolated coliphages.
6 liphages (0.25 +/- 0.02 day(-1)) and somatic coliphages (0.12 +/- 0.01 day(-1)) in winter were consid
7                   The decay rates of both F+ coliphages (0.25 +/- 0.02 day(-1)) and somatic coliphage
8 omes included a homologue of the tum gene of coliphage 186, which encodes a LexA-repressed cI antirep
9  to 5.5), norovirus GII (4.6 to 5.7), and F+ coliphage (5.4 to 7.1).
10                                      For MS2 coliphage, a virus indicator, the most efficient photose
11                  In this study, the decay of coliphages, an indicator for enteric viruses, was invest
12  In contrast, soil bacteria do not propagate coliphages and hindered T4 diffusion through the biofilm
13                           The decay rates of coliphages and their uncertainties were analyzed using a
14  demonstrated that RNA-binding proteins from coliphages and yeast can function as translational repre
15 scherichia coli measured by culture, somatic coliphage, and F+ coliphage.
16 larensis LVS, Yersiniapestis F1 antigen, MS2 coliphage, and Salmonella typhimurium.
17                The lambda-related (lambdoid) coliphages are related to one another by frequent natura
18                                    Using MS2 coliphage as an internal control, the genome-wide damage
19 ompared to fecal indicator bacteria, somatic coliphage, Bacteroidales 16S rRNA marker AllBac, four hu
20                  We targeted enterobacterial coliphages because they are better than fecal indicator
21     Male-specific single-stranded RNA (FRNA) coliphages belong to the family Leviviridae.
22 5.5 and iron dose of 20 mg/L reduced the MS2 coliphage below detection limits (LRVs 6.7) in just 11.5
23                    Here, inactivation of MS2 coliphage by Fe(VI) was examined.
24 he well-studied F pilus-specific filamentous coliphages, CTXphi integrates site-specifically into its
25 nt contributors to the seasonal variation of coliphage decay.
26 s (Escherichia coli) and viral pathogens (T4 coliphage) distributed across a large network of subpopu
27   Molecules of dissimilar lengths (T2 and T7 coliphage DNA) were inserted into this region in such a
28 cosahedral, single-stranded DNA PhiX174-like coliphages do not fall into these well-defined infection
29  function in a manner similar to that of the coliphage fd protein pIII and mediate CTXphi infection a
30 1 and the morphologically distinct (class I) coliphage fd.
31          Here, we isolated and characterized coliphages from three coastal locations in the United Ki
32                        The N gene product of coliphage gamma, with a number of host proteins (Nus fac
33   Bacteriophages infecting Escherichia coli (coliphages) have been used as a proxy for faecal matter
34                           The Nun protein of coliphage HK022 arrests RNA polymerase (RNAP) in vivo an
35                           The Nun protein of coliphage HK022 excludes superinfecting lambda phage.
36    The amino-terminal arginine-rich motif of coliphage HK022 Nun binds phage lambda nascent transcrip
37                                              Coliphage HK022 Nun blocks superinfection by coliphage l
38                                          The coliphage HK022 protein Nun transcription elongation arr
39     Head assembly in the double-stranded DNA coliphage HK97 involves initially the formation of the p
40 sid) were conserved between straight phiC31, coliphage HK97, staphylococcal phage straight phiPVL, tw
41 oocysts, Bacillus atrophaeus spores, and MS2 coliphage in a model buffered water and (2) evaluate the
42 ndogenous sunlight inactivation rates of MS2 coliphage in photosensitizer-free water were measured (k
43 ovirus, norovirus genogroup II (GII), and F+ coliphage in the influent wastewater, the solid and liqu
44                                       The Ff coliphages (including M13, fd, and f1) have been intensi
45                                        In T4 coliphage infection the two enzymes are found in dNTP sy
46 shed the genomes of three new FhuA-dependent coliphages: JLBYU37, JLBYU41, and JLBYU60.
47 ntical to the structure of the tail genes of coliphages K1E, K5, and K1-5.
48 oited the novel substrate specificity of the coliphage K5 lyase in studies of the domain organization
49           The protein phosphatase encoded by coliphage lambda (PPlambda) was found to be the equivale
50                                      Like in coliphage lambda and other siphophages, a large operon i
51 ed holins S105 (3 TMDs; N(out)-C(in)) of the coliphage lambda and S68 (2 TMDs; N(in)-C(in)) of the la
52 Coliphage HK022 Nun blocks superinfection by coliphage lambda by stalling RNA polymerase (RNAP) trans
53 s specifically to block transcription of the coliphage lambda chromosome.
54 t the role of the tsp region variants of the coliphage lambda cro gene terminator, tR1, containing in
55 ere we show that the spanins of the paradigm coliphage lambda mediate efficient membrane fusion.
56                 The in vitro function of the coliphage lambda tR1 Rho-dependent terminator is governe
57  frames encoding proteins closely related to coliphage lambda's terminase protein (the large subunit)
58 gene essentiality landscape in the canonical coliphages lambda and P1.
59 domonas aeroginosa and a distant relative to coliphages like MS2 and Qbeta.
60                              The majority of coliphages lost at least 10-60% of the capsid protein mi
61 viously shown to be the target of the Sgl of coliphage M.
62 age (designated CTXphi), which is related to coliphage M13.
63 ce for translational activation of the Qbeta coliphage maturation cistron, mediated by the presence o
64 bited similar mass recovery as commonly used coliphage MS2 and were 7-fold better transported than kn
65                          Detailed studies on coliphage MS2 coat protein-mediated translational repres
66 eviously characterized relatives such as the coliphages MS2 and Qbeta.
67 face properties of six marine phages and two coliphages (MS2, T4) on transport in sand-filled percola
68 ncytial virus (RSV), rhinovirus (RV), and F+ coliphage/MS2.
69 nome shares synteny and gene similarity with coliphage N15 and vibriophages VP882 and VHML, suggestin
70                               Similar to the coliphage N4 gp2 protein, Drc likely binds locally unwou
71                                              Coliphage N4 infection leads to shut-off of host DNA rep
72 Unlike other characterized phages, the lytic coliphage N4 must inject the 360-kDa virion RNA polymera
73                                              Coliphage N4 virion RNA polymerase (vRNAP), the most dis
74                                              Coliphage N4 virion RNA polymerase (vRNAP), which is inj
75                                              Coliphage N4 virion-encapsidated RNA polymerase (vRNAP)
76                                              Coliphage N4-coded, virion-encapsidated RNA polymerase (
77 y phages, one of which became the classic T3 coliphage of Demerec and Fano.
78 trastrain transduction experiments with both coliphage P1 and Salmonella phage P22.
79 rm, the prototype SAR endolysin, Lyz(P1), of coliphage P1, has an active-site Cys covalently blocked
80 Y is the putative holin gene of the paradigm coliphage P2 and encodes a 93-amino-acid protein.
81 ke phage family, with strong similarities to coliphages P2 and 186 and some similarity to the retronp
82 SaPI1 and 80alpha is similar to that between coliphages P4 and P2.
83                                              Coliphage phi X174 encodes a single lysis protein, E, a
84 out with endospores of Bacillus subtilis and coliphage phiX174 over a distance of 25 m in an alluvial
85 III-N1 and V. cholerae TolA-C are similar to coliphage pIII-N1 and E. coli TolA-C, respectively, yet
86     Classification of purified large (60 nm) coliphage PR772 particles leads to broad peaks, due to b
87 7 diverged from its common ancestor with the coliphage prior to the ancient split between these gener
88 through domain, a 850 nucleotide hairpin, in coliphage Q beta genomic RNA.
89 quenced and annotated the T4-like genomes of coliphage RB16 (a close relative of RB43), A. salmonicid
90 ves of the bacteriophage T4, including three coliphages (RB43, RB49 and RB69), three Aeromonas salmon
91                         HK022 is a temperate coliphage related to phage lambda.
92                                        HK022 coliphage site-specific recombinase Integrase (Int) can
93                                          RNA coliphage SP was propagated for several generations on a
94                 Our analyses reveal that the coliphage species are a monophyletic group consisting of
95 ns, is significantly more closely related to coliphage T3 than to T7.
96 the efficacy of polyvalent phage PEf1 versus coliphage T4 in suppressing a model enteric bacterium (E
97                                              Coliphage T4 Pnkp is a bifunctional polynucleotide 5'-ki
98 il metagenomic DNA library(3) with the lytic coliphage T4 to isolate clones carrying protective genes
99                      t is the holin gene for coliphage T4, encoding a 218-amino-acid (aa) protein ess
100 MDa baseplate, dramatically smaller than the coliphage T4.
101 equences of the packaging/terminase genes of coliphages T4 and RB49 and vibriophages KVP40 and KVP20
102 y characterized in model systems provided by coliphages T4 and T7.
103                 The 90-nm-diameter capsid of coliphage T5 is organized with T=13 icosahedral geometry
104 le expression vector utilizing a promoter of coliphage T5, P(N25) and a derivative of the IncW broad-
105 nt and organization clearly place SP6 in the coliphage T7 group of phages, but there is approximately
106          phiA1122 is very closely related to coliphage T7; the two genomes are colinear, and the geno
107 haring of conserved structural modules among coliphage tail-fiber genes to which gp37 was previously
108    Here, we build on the recent discovery of coliphages that have the outer membrane (OM) lipopolysac
109                    However, the diversity of coliphages that is present in seawater remains largely u
110  E. coli, intestinal enterococci and somatic coliphages through cultivation and for human (BacH) and
111  Here, we investigated the resistance of MS2 coliphage to inactivation by chlorine dioxide (ClO2).
112           Bacillus atrophaeus spores and MS2 coliphage treated with bromine and chlorine were reduced
113 am-positive and Gram-negative bacteria, MS-2 coliphage virus, and ovalbumin protein species.
114                         The test for somatic coliphage was a relatively strong predictor of the prese
115  reduction of both male specific and somatic coliphages was seen at specific ozone doses as low as 0.
116 g a suite of thirty environmentally-isolated coliphages, we demonstrate multi-layered and robust phag
117 ), but the decay rates of male-specific (F+) coliphages were not significantly different between sunl
118 nts revealed that the decay rates of somatic coliphages were significantly higher in sunlight (1.29 +
119 remely facile reduction of P1 suggested that coliphages with myovirus morphology may not be conservat

 
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