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

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

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

34 Bacteriophage T7 belongs to the Podoviridae family and h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

53 Bacteriophage T7 DNA helicase requires two noncomplement

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

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

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

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

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

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

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

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

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

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

64 Bacteriophage T7 DNA polymerase efficiently incorporates

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

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

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

68 Bacteriophage T7 DNA polymerase shares extensive sequenc

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

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

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

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

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

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 The replicative bacteriophage T7 DNA polymerase/exonuclease and the tran

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

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

79 The proteins of bacteriophage T7 DNA replication mediate coordinated lea

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

81 The bacteriophage T7 elongation complex is an excellent mode

82 We used bacteriophage T7-encoded transcription inhibitor gene pr

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

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

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

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

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

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

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

90 Bacteriophage T7 encodes an essential inhibitor of the E

91 Bacteriophage T7 endonuclease I selectively binds and cl

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

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

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

95 Bacteriophage T7 expresses two forms of gene 4 protein (

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Bacteriophage T7 gene product 4 is a model hexameric hel

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 Bacteriophage T7 helicase functions as a hexameric ring

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

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

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

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

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

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

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

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

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

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

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

140 During bacteriophage T7 infection, the Escherichia coli RNA pol

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

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

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

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

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

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

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

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

149 Bacteriophage T7 is a well characterized member of the P

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

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

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

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

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

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

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

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

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

159 Bacteriophage T7 lysozyme binds to T7 RNA polymerase (RN

160 Bacteriophage T7 lysozyme binds to T7 RNA polymerase and

161 Bacteriophage T7 lysozyme is known to inhibit transcript

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

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

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

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

166 Bacteriophage T7 packages its double-stranded DNA genome

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

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

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

170 Bacteriophage T7 primase catalyzes the synthesis of the

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

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

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

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

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

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

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

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

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

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

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

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

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

184 Bacteriophage T7 promoters contain a consensus sequence

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 The bacteriophage T7 replisome is an economical machine that

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 The bacteriophage T7 RNA polymerase and its promoters were u

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

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

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

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

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

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

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

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

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

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

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

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

229 Bacteriophage T7 RNA polymerase is a single-subunit enzy

230 Bacteriophage T7 RNA polymerase is the best-characterize

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

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

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

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

235 Bacteriophage T7 RNA polymerase undergoes major conforma

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

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

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

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

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

241 For bacteriophage T7 RNA polymerase, transcription begins wi

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

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

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

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

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

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

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

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

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

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

252 A system of bacteriophage T7 spreading on a spatially heterogeneous

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

277 Bacteriophage T7 was challenged with either of two toxic

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

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

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

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

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

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

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

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

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