ライフサイエンスコーパス: coliphage

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 liphages (0.25 +/- 0.02 day(-1)) and somatic coliphages (0.12 +/- 0.01 day(-1)) in winter were consid

5 The decay rates of both F+ coliphages (0.25 +/- 0.02 day(-1)) and somatic coliphage

6 omes included a homologue of the tum gene of coliphage 186, which encodes a LexA-repressed cI antirep

7 to 5.5), norovirus GII (4.6 to 5.7), and F+ coliphage (5.4 to 7.1).

8 In this study, the decay of coliphages, an indicator for enteric viruses, was invest

9 In contrast, soil bacteria do not propagate coliphages and hindered T4 diffusion through the biofilm

10 The decay rates of coliphages and their uncertainties were analyzed using a

11 demonstrated that RNA-binding proteins from coliphages and yeast can function as translational repre

12 scherichia coli measured by culture, somatic coliphage, and F+ coliphage.

13 larensis LVS, Yersiniapestis F1 antigen, MS2 coliphage, and Salmonella typhimurium.

14 The lambda-related (lambdoid) coliphages are related to one another by frequent natura

15 ompared to fecal indicator bacteria, somatic coliphage, Bacteroidales 16S rRNA marker AllBac, four hu

16 Male-specific single-stranded RNA (FRNA) coliphages belong to the family Leviviridae.

17 Here, inactivation of MS2 coliphage by Fe(VI) was examined.

18 he well-studied F pilus-specific filamentous coliphages, CTXphi integrates site-specifically into its

19 nt contributors to the seasonal variation of coliphage decay.

20 s (Escherichia coli) and viral pathogens (T4 coliphage) distributed across a large network of subpopu

21 Molecules of dissimilar lengths (T2 and T7 coliphage DNA) were inserted into this region in such a

22 cosahedral, single-stranded DNA PhiX174-like coliphages do not fall into these well-defined infection

23 function in a manner similar to that of the coliphage fd protein pIII and mediate CTXphi infection a

24 1 and the morphologically distinct (class I) coliphage fd.

25 The N gene product of coliphage gamma, with a number of host proteins (Nus fac

26 The Nun protein of coliphage HK022 arrests RNA polymerase (RNAP) in vivo an

27 The Nun protein of coliphage HK022 excludes superinfecting lambda phage.

28 The amino-terminal arginine-rich motif of coliphage HK022 Nun binds phage lambda nascent transcrip

29 Coliphage HK022 Nun blocks superinfection by coliphage l

30 The coliphage HK022 protein Nun transcription elongation arr

31 Head assembly in the double-stranded DNA coliphage HK97 involves initially the formation of the p

32 sid) were conserved between straight phiC31, coliphage HK97, staphylococcal phage straight phiPVL, tw

33 ndogenous sunlight inactivation rates of MS2 coliphage in photosensitizer-free water were measured (k

34 ovirus, norovirus genogroup II (GII), and F+ coliphage in the influent wastewater, the solid and liqu

35 In T4 coliphage infection the two enzymes are found in dNTP sy

36 ntical to the structure of the tail genes of coliphages K1E, K5, and K1-5.

37 oited the novel substrate specificity of the coliphage K5 lyase in studies of the domain organization

38 The protein phosphatase encoded by coliphage lambda (PPlambda) was found to be the equivale

39 Like in coliphage lambda and other siphophages, a large operon i

40 ed holins S105 (3 TMDs; N(out)-C(in)) of the coliphage lambda and S68 (2 TMDs; N(in)-C(in)) of the la

41 Coliphage HK022 Nun blocks superinfection by coliphage lambda by stalling RNA polymerase (RNAP) trans

42 s specifically to block transcription of the coliphage lambda chromosome.

43 t the role of the tsp region variants of the coliphage lambda cro gene terminator, tR1, containing in

44 ere we show that the spanins of the paradigm coliphage lambda mediate efficient membrane fusion.

45 The in vitro function of the coliphage lambda tR1 Rho-dependent terminator is governe

46 frames encoding proteins closely related to coliphage lambda's terminase protein (the large subunit)

47 domonas aeroginosa and a distant relative to coliphages like MS2 and Qbeta.

48 age (designated CTXphi), which is related to coliphage M13.

49 ce for translational activation of the Qbeta coliphage maturation cistron, mediated by the presence o

50 bited similar mass recovery as commonly used coliphage MS2 and were 7-fold better transported than kn

51 Detailed studies on coliphage MS2 coat protein-mediated translational repres

52 eviously characterized relatives such as the coliphages MS2 and Qbeta.

53 face properties of six marine phages and two coliphages (MS2, T4) on transport in sand-filled percola

54 nome shares synteny and gene similarity with coliphage N15 and vibriophages VP882 and VHML, suggestin

55 Coliphage N4 infection leads to shut-off of host DNA rep

56 Unlike other characterized phages, the lytic coliphage N4 must inject the 360-kDa virion RNA polymera

57 Coliphage N4 virion RNA polymerase (vRNAP), the most dis

58 Coliphage N4 virion RNA polymerase (vRNAP), which is inj

59 Coliphage N4 virion-encapsidated RNA polymerase (vRNAP)

60 Coliphage N4-coded, virion-encapsidated RNA polymerase (

61 y phages, one of which became the classic T3 coliphage of Demerec and Fano.

62 trastrain transduction experiments with both coliphage P1 and Salmonella phage P22.

63 rm, the prototype SAR endolysin, Lyz(P1), of coliphage P1, has an active-site Cys covalently blocked

64 Y is the putative holin gene of the paradigm coliphage P2 and encodes a 93-amino-acid protein.

65 ke phage family, with strong similarities to coliphages P2 and 186 and some similarity to the retronp

66 SaPI1 and 80alpha is similar to that between coliphages P4 and P2.

67 Coliphage phi X174 encodes a single lysis protein, E, a

68 III-N1 and V. cholerae TolA-C are similar to coliphage pIII-N1 and E. coli TolA-C, respectively, yet

69 7 diverged from its common ancestor with the coliphage prior to the ancient split between these gener

70 through domain, a 850 nucleotide hairpin, in coliphage Q beta genomic RNA.

71 quenced and annotated the T4-like genomes of coliphage RB16 (a close relative of RB43), A. salmonicid

72 ves of the bacteriophage T4, including three coliphages (RB43, RB49 and RB69), three Aeromonas salmon

73 HK022 is a temperate coliphage related to phage lambda.

74 RNA coliphage SP was propagated for several generations on a

75 Our analyses reveal that the coliphage species are a monophyletic group consisting of

76 ns, is significantly more closely related to coliphage T3 than to T7.

77 the efficacy of polyvalent phage PEf1 versus coliphage T4 in suppressing a model enteric bacterium (E

78 Coliphage T4 Pnkp is a bifunctional polynucleotide 5'-ki

79 t is the holin gene for coliphage T4, encoding a 218-amino-acid (aa) protein ess

80 equences of the packaging/terminase genes of coliphages T4 and RB49 and vibriophages KVP40 and KVP20

81 y characterized in model systems provided by coliphages T4 and T7.

82 The 90-nm-diameter capsid of coliphage T5 is organized with T=13 icosahedral geometry

83 le expression vector utilizing a promoter of coliphage T5, P(N25) and a derivative of the IncW broad-

84 nt and organization clearly place SP6 in the coliphage T7 group of phages, but there is approximately

85 phiA1122 is very closely related to coliphage T7; the two genomes are colinear, and the geno

86 haring of conserved structural modules among coliphage tail-fiber genes to which gp37 was previously

87 E. coli, intestinal enterococci and somatic coliphages through cultivation and for human (BacH) and

88 Here, we investigated the resistance of MS2 coliphage to inactivation by chlorine dioxide (ClO2).

89 am-positive and Gram-negative bacteria, MS-2 coliphage virus, and ovalbumin protein species.

90 The test for somatic coliphage was a relatively strong predictor of the prese

91 ), but the decay rates of male-specific (F+) coliphages were not significantly different between sunl

92 nts revealed that the decay rates of somatic coliphages were significantly higher in sunlight (1.29 +