ライフサイエンスコーパス: bacteriophage T7

1 perimentally tractable system, lysis time in bacteriophage T7.

2 polymerase (pol), the replicative enzyme for bacteriophage T7.

3 process that is similar to one proposed for bacteriophage T7.

4 also been found for Escherichia coli but not bacteriophage T7.

5 olymorphism data over time for four genes in bacteriophage T7.

6 mputer model for the intracellular growth of bacteriophage T7.

7 cturally simple RNA polymerase is encoded by bacteriophage T7.

8 DNA junction-selective resolving enzyme from bacteriophage T7.

9 tions among the proteins of Escherichia coli bacteriophage T7.

10 olecular bases of the packaging mechanism of bacteriophage T7.

11 the only known nucleotide kinase encoded by bacteriophage T7.

12 mple is the infection of Escherichia coli by bacteriophage T7.

13 date (VV) catalyzed by the DNA polymerase of bacteriophage T7.

14 d DNA synthesis mediated by the replisome of bacteriophage T7.

15 in a single polypeptide encoded by gene 4 of bacteriophage T7.

16 rpreting experimental evolution studies with bacteriophage T7.

17 ining the type I restriction enzyme EcoKI by bacteriophage T7 0.3 mutants leads to restriction during

18 On infection with bacteriophage T7, 20% of the minicells produced progeny

19 Bacteriophage T7 4A' protein is a DNA helicase that unwi

20 The primase fragment of the bacteriophage T7 63-kDa gene 4 helicase/primase protein

21 The gene 4 protein of bacteriophage T7, a functional hexamer, comprises DNA he

22 in Ocr (overcome classical restriction) from bacteriophage T7 acts as a mimic of DNA and inhibits all

23 n addition, the gene 10 leader sequence from bacteriophage T7 and a minicistron localized upstream of

24 is has been observed in two proteins, gp4 of bacteriophage T7 and rho of Escherichia coli.

25 resembles the single polypeptide RNAPs from bacteriophage T7 and T3, requires a separate specificity

26 rized here include family A polymerases from bacteriophage T7 and Thermus aquaticus, family B polymer

27 s of a multiprotein replication complex from bacteriophage T7 and to characterize the effect of prima

28 lar crowding using the replication system of bacteriophage T7 and we show that it affects several asp

29 Upon infection of Escherichia coli, bacteriophage T7 annexes a host protein, thioredoxin, to

30 Primase and helicase activities of bacteriophage T7 are present in a single polypeptide cod

31 Using bacteriophage T7 as a model system, we determined cryo-e

32 pproximately 650-kDa functional replisome of bacteriophage T7 assembled on DNA resembling a replicati

33 The DNA helicase encoded by gene 4 of bacteriophage T7 assembles on single-stranded DNA as a h

34 The traE gene product has been cloned into a bacteriophage T7-based transient expression system, and

35 Bacteriophage T7 belongs to the Podoviridae family and h

36 The gene 2.5 protein (gp2.5) encoded by bacteriophage T7 binds preferentially to single-stranded

37 In the replication system of bacteriophage T7 both DNA primase and DNA helicase activ

38 coli RNA polymerase and the A1 promoter from bacteriophage T7 by monitoring alterations in the intrin

39 that the gene 4 primase/helicase encoded by bacteriophage T7 can form both hexamers and heptamers.

40 nit DNA-dependent RNA polymerase (RNAP) from bacteriophage T7 catalyzes both promoter-dependent trans

41 cture of the replicative DNA polymerase from bacteriophage T7 complexed with a primer-template and a

42 Gene 1.7 of bacteriophage T7 confers sensitivity of both phage T7 an

43 The DNA helicase encoded by bacteriophage T7 consists of six identical subunits that

44 Gene 4 protein (gp4) encoded by bacteriophage T7 contains a C-terminal helicase and an N

45 The replisome of bacteriophage T7 contains a minimum of proteins, thus fa

46 ase domain of the gene 4 helicase-primase of bacteriophage T7 contains a zinc motif and a catalytic c

47 The DNA helicase encoded by gene 4 of bacteriophage T7 couples DNA unwinding to the hydrolysis

48 he replicative helicase-primase protein from bacteriophage T7 crystallized as a helical filament that

49 ent studies in the model RNA polymerase from bacteriophage T7 demonstrate that upstream duplex contac

50 ent dTTP hydrolysis by the gene 4 protein of bacteriophage T7 differ in the pathways by which these r

51 e characterize the kinetics and structure of bacteriophage T7 DNA delivery process.

52 er formation, and DNA binding was studied in bacteriophage T7 DNA helicase (4A' protein).

53 Bacteriophage T7 DNA helicase is a ring-shaped hexamer t

54 Bacteriophage T7 DNA helicase requires two noncomplement

55 We present the first structural model of a bacteriophage T7 DNA helicase-DNA polymerase complex usi

56 The bacteriophage T7 DNA helicase/primase (gene 4 protein) i

57 and protease-sensitivity to the full-length bacteriophage T7 DNA ligase.

58 Bacteriophage T7 DNA polymerase (gene 5 protein, gp5) in

59 system for replicative DNA polymerases, the bacteriophage T7 DNA polymerase (gp5), encoded by gene 5

60 A modified bacteriophage T7 DNA polymerase (Sequenase) can replace

61 ctionally important conformational change in bacteriophage T7 DNA polymerase (T7 pol) that use the en

62 plicative polymerases, exonuclease-deficient bacteriophage T7 DNA polymerase (T7(-)) and HIV reverse

63 rol, to observe DNA replication catalysed by bacteriophage T7 DNA polymerase (T7DNAP) and by the Klen

64 A single copy of bacteriophage T7 DNA polymerase and DNA helicase advance

65 Bacteriophage T7 DNA polymerase efficiently incorporates

66 opposite A following all three base pairs by bacteriophage T7 DNA polymerase exo- showed burst kineti

67 We present three crystal structures of bacteriophage T7 DNA polymerase replication complexes, o

68 The three-dimensional structure of bacteriophage T7 DNA polymerase reveals the presence of

69 Bacteriophage T7 DNA polymerase shares extensive sequenc

70 ructures of the pol gamma-beta dimer and the bacteriophage T7 DNA polymerase ternary complex, which s

71 te the (+)-trans-anti-[BP]-N(2)-dG adduct by bacteriophage T7 DNA polymerase with the order of prefer

72 High fidelity DNA polymerases, such as bacteriophage T7 DNA polymerase, are predominantly block

73 The replisome consisting of bacteriophage T7 DNA polymerase, helicase, primase, and

74 s with Escherichia coli DNA polymerase I and bacteriophage T7 DNA polymerase.

75 accessory subunit and processivity factor in bacteriophage T7 DNA polymerase.

76 DNA-duplex stability affects replication by bacteriophage T7 DNA polymerase.

77 The replicative bacteriophage T7 DNA polymerase/exonuclease and the tran

78 tion kinetics of the human mitochondrial and bacteriophage T7 DNA polymerases on free-ssDNA, in compa

79 is study, we visualize fluorescently labeled bacteriophage T7 DNA polymerases within the replisome wh

80 Bacteriophage T7 DNA primase recognizes 5'-GTC-3' in sin

81 The proteins of bacteriophage T7 DNA replication mediate coordinated lea

82 than model replicative polymerases, such as bacteriophage T7(-) DNA polymerase and human immunodefic

83 aging, and molecular dynamics simulations on bacteriophage T7 DNAp and SSB, we investigated molecular

84 The bacteriophage T7 elongation complex is an excellent mode

85 We used bacteriophage T7-encoded transcription inhibitor gene pr

86 Gene 4 of bacteriophage T7 encodes a bifunctional primase-helicase

87 Gene 5 of bacteriophage T7 encodes a DNA polymerase (gp5) responsi

88 Gene 5 of bacteriophage T7 encodes a DNA polymerase essential for

89 Gene 4 of bacteriophage T7 encodes a protein (gp4) that can transl

90 Gene 2.5 of bacteriophage T7 encodes a single-stranded DNA (ssDNA)-b

91 Gene 2.5 of bacteriophage T7 encodes a single-stranded DNA-binding p

92 Gene 2.5 of bacteriophage T7 encodes a ssDNA binding protein (gp2.5)

93 Bacteriophage T7 encodes an essential inhibitor of the E

94 Bacteriophage T7 encodes its own DNA polymerase, the pro

95 Bacteriophage T7 endonuclease I selectively binds and cl

96 n interaction between the K296P mutant and a bacteriophage T7-epitope-tagged K64E mutant of dsRNA bin

97 V-1 RT reverse transcriptase (HIV-1 RT), and bacteriophage T7 exo- (T7(-)) were examined to determine

98 rus, type 1, reverse transcriptase (RT), and bacteriophage T7 exonuclease(-) (T7(-)).

99 Bacteriophage T7 expresses two forms of gene 4 protein (

100 Extension of the vaccinia virus/bacteriophage T7 expression system to CHO cells should b

101 The vaccinia virus/bacteriophage T7 expression system was adapted to Chines

102 eptide of 36.8 kDa that was confirmed in the bacteriophage T7 expression system.

103 The DNA helicase encoded by gene 4 of bacteriophage T7 forms a hexameric ring in the presence

104 scherichia coli that survive coexpression of bacteriophage T7 gene 10 and plasmid F pifA has allowed

105 The 64 amino acid residue product of bacteriophage T7 gene 2 (gp2) binds the Escherichia coli

106 Bacteriophage T7 gene 2.5 protein (gp2.5) is a single-st

107 Bacteriophage T7 gene 2.5 single-stranded DNA-binding pr

108 um nucleotide binding and oligomerization of bacteriophage T7 gene 4 helicases have been investigated

109 The bacteriophage T7 gene 4 protein (gp4) has both primase a

110 base stack of other helicases, including the bacteriophage T7 gene 4 protein and bacterial DnaB helic

111 The primase fragment of bacteriophage T7 gene 4 protein catalyzes the synthesis

112 t exhibits strong sequence homology with the bacteriophage T7 gene 4 protein primase-helicase (T7 gp4

113 ain (TBD), located in the thumb subdomain of bacteriophage T7 gene 5 DNA polymerase.

114 A crystal structure of the bacteriophage T7 gene 5 protein/Escherichia coli thiored

115 Bacteriophage T7 gene product 4 is a model hexameric hel

116 ed mutations have altered the composition of bacteriophage T7 genome and suggest that this may be a s

117 of cellular internalization of an infecting bacteriophage T7 genome has led to surprising observatio

118 In a normal infection about 850 bp of the bacteriophage T7 genome is ejected into the cell, the re

119 ensuring a high-fidelity replication of the bacteriophage T7 genome.

120 ate residue for transglycosylase activity of bacteriophage T7 gp16 is not essential for phage growth,

121 nd suggest, by comparison with the hexameric bacteriophage T7 gp4 and SV40 large T-antigen helicases,

122 the human mitochondria with high homology to bacteriophage T7 gp4 helicase-primase.

123 ctural polarity has been established for the bacteriophage T7 gp4 replicative helicase.

124 multifunctional protein encoded by gene 4 of bacteriophage T7 (gp4) provides both helicase and primas

125 The ring-shaped helicase of bacteriophage T7 (gp4), the product of gene 4, has basic

126 Bacteriophage T7 gp4A' protein is a hexameric helicase-p

127 The DNA primase of bacteriophage T7 has a zinc-binding motif that is essent

128 hin the hexameric gene 4 helicase-primase of bacteriophage T7 has been examined by using two genetica

129 he DNA polymerase encoded by gene 5 (gp5) of bacteriophage T7 has low processivity, dissociating afte

130 The DNA polymerase encoded by bacteriophage T7 has low processivity.

131 Like other bacteriophages, T7 has a singular vertex that is the sit

132 Bacteriophage T7 helicase (T7 gene 4 helicase-primase) i

133 Bacteriophage T7 helicase functions as a hexameric ring

134 The bacteriophage T7 helicase is a ring-shaped hexameric mot

135 acterized nine helicase-deficient mutants of bacteriophage T7 helicase-primase protein (4A') prepared

136 f single-stranded DNA (ssDNA) binding to the bacteriophage T7 helicase-primase, gp4A'.

137 a single-subunit RNA polymerase (RNAP) from bacteriophage T7, implementing all-atom molecular dynami

138 genome reveals that it is closely related to bacteriophage T7 in both genome organization and sequenc

139 rapid size and titre analysis of unlabelled bacteriophage T7 in both salt solution and mouse blood p

140 e of the DNA polymerase encoded by gene 5 of bacteriophage T7, in a complex with its processivity fac

141 In bacteriophage T7-infected cells, the product of viral ge

142 ysiological metabolism in a crude extract of bacteriophage T7-infected cells.

143 rary was prepared from RNA synthesized after bacteriophage T7 infection and the sequence of bacteriop

144 o plays a role in protecting E. coli against bacteriophage T7 infection by limiting the dGTP required

145 talytic activity is known to increase during bacteriophage T7 infection, reflecting the expression of

146 During bacteriophage T7 infection, the Escherichia coli RNA pol

147 Bacteriophage T7 infects Escherichia coli, and despite e

148 Ocr, the first protein expressed by bacteriophage T7, inhibits type Iota DNA restriction enz

149 Gene 6 protein of bacteriophage T7 is a 5'-3'-exonuclease specific for dsD

150 Endonuclease I of bacteriophage T7 is a DNA junction-resolving enzyme.

151 (overcome classical restriction) protein of bacteriophage T7 is a molecular mimic of double-stranded

152 Gene 5 protein (gp5) of bacteriophage T7 is a non-processive DNA polymerase, whi

153 Gene 5 protein (gp5) of bacteriophage T7 is a non-processive DNA polymerase.

154 The RNA polymerase (RNAP) of bacteriophage T7 is a single subunit enzyme that can tra

155 The gene 2.5 protein (gp2.5) of bacteriophage T7 is a single-stranded DNA (ssDNA) bindin

156 Bacteriophage T7 is a well characterized member of the P

157 The single-subunit RNA polymerase (RNAP) of bacteriophage T7 is able to perform all steps of transcr

158 n extracts of Escherichia coli infected with bacteriophage T7 is able to repair double-strand breaks

159 Gene 2.5 of bacteriophage T7 is an essential gene that encodes a sin

160 Gene 2.5 of bacteriophage T7 is an essential gene that encodes a sin

161 A synthesis in the DNA replication system of bacteriophage T7 is catalyzed by the primase domain of t

162 ngle-stranded DNA (ssDNA) binding protein of bacteriophage T7 is essential for T7 DNA replication and

163 The replicative polymerase of bacteriophage T7 is structurally and mechanistically wel

164 The Ocr protein of bacteriophage T7 is the most studied DNA mimic and funct

165 The ocr protein, the product of gene 0.3 of bacteriophage T7, is a structural mimic of the phosphate

166 Bacteriophage T7 lysozyme binds to T7 RNA polymerase (RN

167 Bacteriophage T7 lysozyme binds to T7 RNA polymerase and

168 Bacteriophage T7 lysozyme is known to inhibit transcript

169 In bacteriophage T7, movement of either the DNA helicase or

170 kin to those identified in the processing of bacteriophage T7 mRNAs.

171 The product of gene 0.3 of bacteriophage T7, ocr, is a potent inhibitor of type I D

172 other in vitro display technologies such as bacteriophage T7 or mRNA display.

173 Bacteriophage T7 packages its double-stranded DNA genome

174 The gene 4 protein of bacteriophage T7 plays a central role in DNA replication

175 ding protein (gp2.5), encoded by gene 2.5 of bacteriophage T7, plays an essential role in DNA replica

176 In contrast, bacteriophage T7 Pol generates NTS mutations predominant

177 expression levels in 6,348 experiments using bacteriophage T7 polymerase to synthesize messenger RNA

178 Bacteriophage T7 primase catalyzes the synthesis of the

179 We report a crystal structure of bacteriophage T7 primase that reveals its two domains an

180 ment that the mitochondrial DNA helicase and bacteriophage T7 primase-helicase share physical feature

181 equence and functional similarities with the bacteriophage T7 primase-helicase.

182 Limited proteolysis of bacteriophage T7 primase/helicase with endoproteinase Gl

183 ilayer structure of the portal vertex of the bacteriophage T7 procapsid, the recipient of T7 DNA in p

184 ces for COR15am and COR6.6 were fused to the bacteriophage T7 promoter and expressed in Escherichia c

185 nd highly unstable when transcribed from the bacteriophage T7 promoter at 37 degrees C.

186 FLP recombinase gene under the control of a bacteriophage T7 promoter, (ii) it confers kanamycin res

187 ne) of Escherichia coli deformylase behind a bacteriophage T7 promoter, we have, however, been able t

188 cloned under control of the strong inducible bacteriophage T7 promoter, yet induction did not yield d

189 d in a single plasmid under the control of a bacteriophage T7 promoter.

190 0) or p55gag (pTMIgag) gene regulated by the bacteriophage T7 promoter.

191 ia coli and expressed under the control of a bacteriophage T7 promoter.

192 Bacteriophage T7 promoters contain a consensus sequence

193 rcular and linear M13 double-stranded DNA by bacteriophage T7 proteins have been examined by electron

194 The gene 4 proteins of bacteriophage T7 provide both primase and helicase activ

195 The gene 4 protein of bacteriophage T7 provides both helicase and primase acti

196 The 63 kDa gene 4 protein of bacteriophage T7 provides both helicase and primase acti

197 Gene 4 protein (gp4) of bacteriophage T7 provides two essential functions at the

198 The two substrates examined are based on the bacteriophage T7 R1.1 RNase III processing signal.

199 The 63-kDa gene 4 primase of bacteriophage T7 recognizes a core trinucleotide sequenc

200 ligate three-component system comprising the bacteriophage T7-related mitochondrial RNA polymerase, t

201 Bacteriophage T7 relies on its own RNA polymerase (RNAp)

202 we have demonstrated that the passage of the bacteriophage T7 replication complex is blocked in vitro

203 In the bacteriophage T7 replication system, DNA primase is enco

204 olling Okazaki fragment initiation using the bacteriophage T7 replication system.

205 proach to visualize this coordination in the bacteriophage T7 replisome by simultaneously monitoring

206 nd ensemble methods, we demonstrate that the bacteriophage T7 replisome is able to directly replicate

207 The bacteriophage T7 replisome is an economical machine that

208 nation-dependent replication promoted by the bacteriophage T7 replisome was disrupted by substitution

209 tructure of an ATP-dependent DNA ligase from bacteriophage T7 revealed that the protein comprised two

210 on-denaturing agarose gel electrophoresis of bacteriophage T7 reveals two states of the mature T7 cap

211 on-deficient vaccinia virus MVA encoding the bacteriophage T7 RNA polymerase (MVA/T7).

212 common reaction conditions and components on bacteriophage T7 RNA polymerase (RNAP) activity using a

213 To form a functional open complex, bacteriophage T7 RNA polymerase (RNAP) binds to its prom

214 The region in bacteriophage T7 RNA polymerase (RNAP) comprising residu

215 We have identified mutants of bacteriophage T7 RNA polymerase (RNAP) that are altered

216 elongation complex (EC), the single-subunit bacteriophage T7 RNA polymerase (RNAP) undergoes dramati

217 (2)-epsilon G acts as a partial block to the bacteriophage T7 RNA polymerase (RNAP), which allows nuc

218 known to cause pausing and/or termination by bacteriophage T7 RNA polymerase (RNAP).

219 Bacteriophage T7 RNA polymerase (T7 RNAP) is commonly us

220 Bacteriophage T7 RNA polymerase (T7 RNAP) is widely used

221 ns, IVT of mRNA is typically performed using bacteriophage T7 RNA polymerase (T7 RNAP) owing to its a

222 To address this, we modified bacteriophage T7 RNA polymerase (T7 RNAP) to create a li

223 To make messenger RNA transcripts, bacteriophage T7 RNA polymerase (T7 RNAP) undergoes a tr

224 We have used bacteriophage T7 RNA polymerase (T7RNAP) to study the tr

225 scription by Gal4, (ii) transcription by the bacteriophage T7 RNA polymerase (T7RNAP), and (iii) FLP-

226 binding kinetics between single molecules of bacteriophage T7 RNA polymerase and DNA, as a function o

227 ecifically modified O(6)-meG DNA template by bacteriophage T7 RNA polymerase and human RNA polymerase

228 The bacteriophage T7 RNA polymerase and its promoters were u

229 developed to control the expression of both bacteriophage T7 RNA polymerase and recombinant gene(s)

230 d a copy of the ORF under the control of the bacteriophage T7 RNA polymerase and the Escherichia coli

231 T7) which constitutively express cytoplasmic bacteriophage T7 RNA polymerase and which are derived fr

232 dvantage of an experimental system that uses bacteriophage T7 RNA polymerase as a probe for aspects o

233 The mechanism of bacteriophage T7 RNA polymerase binding to its promoter

234 ven membrane proteins in an Escherichia coli-bacteriophage T7 RNA polymerase expression system.

235 and 'non-replicating' vectors, encoding the bacteriophage T7 RNA polymerase for transcription of rec

236 uced nucleosome sliding and transcription by bacteriophage T7 RNA polymerase from the nucleosomal tem

237 ed, which carries a chromosomally integrated bacteriophage T7 RNA polymerase gene expressed from a la

238 a recombinant vaccinia virus expressing the bacteriophage T7 RNA polymerase in the presence of the D

239 HSP82 gene to be exclusively transcribed by bacteriophage T7 RNA polymerase in vivo.

240 We show here that transcription by the bacteriophage T7 RNA polymerase increases the deaminatio

241 Bacteriophage T7 RNA polymerase is a single-subunit enzy

242 Bacteriophage T7 RNA polymerase is the best-characterize

243 Transcription by bacteriophage T7 RNA polymerase occurs in three stages c

244 uctures of transcription complexes formed by bacteriophage T7 RNA polymerase reveal a nucleotide-addi

245 the initiation of transcription in the model bacteriophage T7 RNA polymerase system, the simplest pos

246 Using bacteriophage T7 RNA polymerase to install poly(G) tails

247 Bacteriophage T7 RNA polymerase undergoes major conforma

248 omoter binding and open complex formation in bacteriophage T7 RNA polymerase was investigated using 2

249 tic mechanism of transcription initiation by bacteriophage T7 RNA polymerase was investigated using t

250 yeast transcriptional activator GAL4 and for bacteriophage T7 RNA polymerase were inserted into the b

251 In the present study the gene for bacteriophage T7 RNA polymerase, implanted with a eukary

252 Unlike the salt-sensitive bacteriophage T7 RNA polymerase, this marine RNA polymer

253 For bacteriophage T7 RNA polymerase, transcription begins wi

254 sion of cell death by the combination of the bacteriophage T7 RNA polymerase-lysozyme system and an i

255 ly synthesized siRNAs are siRNAs produced by bacteriophage T7 RNA polymerase.

256 y used for in vitro run-off RNA synthesis is bacteriophage T7 RNA polymerase.

257 rly steps during transcription initiation by bacteriophage T7 RNA polymerase.

258 es of transcription past these lesions using bacteriophage T7 RNA polymerase.

259 ined evidence that open complex formation in bacteriophage T7 RNA polymerase:promoter binary complexe

260 ced in vitro-transcribed mRNAs using several bacteriophage T7 RNA polymerases, including one wild-typ

261 ssay to quantify transcription elongation by bacteriophage T7 RNAP on small, circular DNA templates a

262 dent RNA polymerases, mammalian RNAP III and bacteriophage T7 RNAP.

263 The 80-kDa gene 5 protein encoded by bacteriophage T7 shares significant amino acid homology

264 ed as well as the steady-state population of bacteriophage T7-specific transcripts were examined for

265 A system of bacteriophage T7 spreading on a spatially heterogeneous

266 eplication loops by individual replisomes of bacteriophage T7 supporting coordinated DNA replication.

267 in minutes after infecting Escherichia coli, bacteriophage T7 synthesizes many copies of its genomic

268 Rpo41 is homologous to the single-subunit bacteriophage T7/T3 RNAP.

269 olymerase (RNAP) is highly homologous to the bacteriophage T7/T3 RNAP.

270 single-polypeptide-chain RNA polymerase from bacteriophage T7 (T7RNAP), like other RNA polymerases, u

271 The six bacteriophage T7 tail fibers, homo-trimers of gene produ

272 tal structure of TTPA resembles those of the bacteriophage T7 tail protein gp11 and gp4 of bacterioph

273 a simulation based on experimental data from bacteriophage T7 that computes the developmental cycle o

274 Syn5 is homologous to bacteriophage T7 that infects Escherichia coli.

275 ndonuclease I is a 149 amino acid protein of bacteriophage T7 that is a Holliday junction-resolving e

276 fficiency of a replicative DNA helicase from bacteriophage T7 that is a member of a class of helicase

277 I is a junction-resolving enzyme encoded by bacteriophage T7, that selectively binds and cleaves fou

278 In bacteriophage T7 the gene 2.5 single-stranded DNA-bindin

279 Two proteins encoded by bacteriophage T7, the gene 2.5 single-stranded DNA bindi

280 as a result of an internal protein unique to bacteriophage T7, the T7 genome may be significantly mor

281 h medium selectively inhibits the ability of bacteriophage T7 to infect Escherichia coli by inhibitin

282 A deficiency in the primase of bacteriophage T7 to synthesize primers can be overcome b

283 overexpressed in Escherichia coli by using a bacteriophage T7 transient expression system, and a prot

284 The ring-shaped helicase of bacteriophage T7 translocates along single-stranded (ss)

285 han residues are dispersed in the primase of bacteriophage T7: Trp-42 in the ZBD and Trp-69, -97, -14

286 Here, we show that bacteriophage T7 undergoes apparent stress-induced mutag

287 DNA polymerase from bacteriophage T7 undergoes large, substrate-induced conf

288 esses, the DNA helicase encoded by gene 4 of bacteriophage T7 uses dTTP most efficiently.

289 of the zinc-binding domain of DNA primase of bacteriophage T7 using a bacterial homolog from Geobacil

290 uantified such changes in growing plaques of bacteriophage T7 using a digital imaging system.

291 Bacteriophage T7 was challenged with either of two toxic

292 A large population of the DNA bacteriophage T7 was grown with a mutagen, producing a g

293 n extracts of Escherichia coli infected with bacteriophage T7 was used to monitor repair of double-st

294 n extracts of Escherichia coli infected with bacteriophage T7 was used to study the mechanism of doub

295 stem based on Escherichia coli infected with bacteriophage T7 was used to test for involvement of hos

296 es the protein of the head-tail connector of bacteriophage T7, was expressed in Escherichia coli.

297 d mutations have influenced the evolution of bacteriophage T7, we analyzed its genome for a bias in b

298 Two lines of the bacteriophage T7 were grown to fix mutations indiscrimin

299 taining the scaffolding and head proteins of bacteriophage T7 were isolated after both proteins were

300 HaeII restriction fragments of the DNA from bacteriophage T7, which range in length from 474 to 6514