ライフサイエンスコーパス: coli

1 n aerobically respiring Escherichia coli (E. coli).

2 increases the colistin MIC of laboratory E. coli.

3 sis factor and adherent-invasive Escherichia coli.

4 as a function of growth phase in Escherichia coli.

5 otic produced by some strains of Escherichia coli.

6 east by their 1:1 orthologs from Escherichia coli.

7 or GreA inhibits break repair in Escherichia coli.

8 ysine precursor is genetically encoded in E. coli.

9 rane and periplasmic proteins of Escherichia coli.

10 a, characterized by expansion of Escherichia coli.

11 n derived from enterohemorrhagic Escherichia coli.

12 of the AcrAB-TolC efflux pump in Escherichia coli.

13 ctase activity when expressed in Escherichia coli.

14 ture, and we implemented them in Escherichia coli.

15 d in the cross-linked motifs found within E. coli.

16 rebs cycle metabolite citrate in Escherichia coli.

17 ded DNA interference activity in Escherichia coli.

18 he O-antigenic polysaccharide of Escherichia coli 120, as its p-methoxyphenyl glycoside, have been ac

19 c features of bla KPC emergence in global E. coli, 2008-2013, using both long- and short-read whole-g

20 In contrast to Escherichia coli, a model organism for chemotaxis that has 5 chemore

21 In Escherichia coli, a proteolytic system comprising the periplasmic PD

22 In Escherichia coli, about half of the transcription events are termina

23 In E. coli, activity of AasC was sensitive to triacsin C and r

24 S. aureus and B. anthracis compared with E. coli Alveolar macrophages and CD14(+) cells were overall

25 ng fast-growing bacteria such as Escherichia coli and Bacillus subtilis.

26 Escherichia coli and Enterococcus species, both indicators of fecal

27 al amino acid 5-hydroxytryptophan in both E. coli and eukaryotes, enabling efficient site-specific in

28 , which leads to overgrowth of indigenous E. coli and facilitates colonization by opportunistic patho

29 ted proteome-wide protein interactions in E. coli and HeLa cell lysates, respectively, identifying 1,

30 mechanisms of excision repair in Escherichia coli and humans and the recent genome-wide mapping of DN

31 beta-lactamase (ESBL)-producing Escherichia coli and K. pneumoniae isolates using MinION allowed suc

32 Laboratory strains of Escherichia coli and P. aeruginosa were killed by a process of conde

33 TCPs induce permeabilization of Escherichia coli and phagocytic uptake.

34 d a minimum of 5.9 and 3.1 log removal in E. coli and Phi6, respectively.

35 c coculture pairing fermentative Escherichia coli and phototrophic Rhodopseudomonas palustris.

36 e phosphoprotein cofactor (P) in Escherichia coli and purified the resulting proteins by affinity and

37 ng elongation complexes (ECs) in Escherichia coli and Saccharomyces cerevisiae and found that 1-3% of

38 ncentrations in P. ruminicola 23, whereas E. coli and Salmonella spp. responses to excess nitrogen in

39 s of larvae after challenge with Escherichia coli and Staphylococcus aureus, but had no significant e

40 and mismatches occurs bi-directionally in E. coli and that, while all MutS-recognized mismatches had

41 The test organisms were Escherichia coli and the Ebola surrogate Phi6.

42 stems support conjugative DNA transfer in E. coli and trigger P. aeruginosa T6SS killing, but not pil

43 onstituted robust blocks to both Escherichia coli and wheat germ extract translation systems, whereas

44 ndicator bacteria (FIB) Escherichia coli (E. coli) and Enterococcus spp. were enumerated using cultur

45 inhibited growth of model Gram-negative (E. coli) and Gram-positive (S. aureus) bacteria to a great

46 the abundance of FIB (Total coliforms and E. coli) and the Bacteroidales (HF183 marker) with bacteria

47 locase, EscV in enteropathogenic Escherichia coli, and cross it in strict hierarchical manner, for ex

48 s were successfully expressed in Escherichia coli, and eight of the nine candidates exhibited high-af

49 tin was efficiently expressed in Escherichia coli, and inhibitory assays demonstrated that it was a p

50 S. aureus and E. coli antigens were detected in immune-blotted HDM extrac

51 ating mutations of the adenomatous polyposis coli (APC) gene, whose product is an important component

52 ant for cell migration.Adenomatous polyposis coli (APC) regulates the localization of some mRNAs at c

53 unexpectedly, cyanobacteria and Escherichia coli appear to share an invariance principle to coordina

54 nnected network motifs, Escherichia coli (E. coli) appears to favor crosstalk wherein at least one of

55 Gram-negative bacteria such as Escherichia coli are protected by a complex cell envelope.

56 n 73% against B. subtilis and 67% against E. coli as compared with that of control PVDF, while aged T

57 KalbTG was produced in Escherichia coli as soluble and active enzyme in the presence of its

58 ent results in cell death, using Escherichia coli as the model organism.

59 line on sensitive and resistant strains of E.coli, as well as effects of amphotericin-B and miconazol

60 systematic 11-yr hospital-based survey of E. coli associated with bacteremia using isolates collected

61 ndogenous chromosomal DNA within Escherichia coli at 37 degrees C.

62 Using this method, we were able to detect E. coli at the concentration of approximately 10(5) CFU/mL

63 eptibility of metabolically active cells (E. coli, B. subtilis, Enterococcus, P. aeruginosa and Salmo

64 Importantly, it is also demonstrated that E. coli bacteremia initiated from translocation across the

65 aluminum foil on the UVC inactivation of E. coli bacteria and demonstrate a new radiation protection

66 tion, removal and destruction of Escherichia coli bacteria was developed onto the surface of Ag-ZnO b

67 al perturbation in a dense bath of motile E. coli bacteria.

68 n with a commensal, potentially probiotic E. coli bacteriuria strain.

69 Here, we used an Escherichia coli-based cell-free system to express a MOMP protein fr

70 ginosa BioH is more highly expressed than E. coli BioH.

71 lectin domains, was expressed in Escherichia coli BL21(lambdaDE3)pLysS cells.

72 We show that cell size in Escherichia coli can be predicted for any steady-state condition by

73 te that ribocomputing devices in Escherichia coli can evaluate two-input logic with a dynamic range u

74 recombinant CrACX2 expressed in Escherichia coli catalyzed the oxidation of fatty acyl-CoAs into tra

75 /phagocytose Candida albicans or Escherichia coli cells both ex vivo and in vivo During systemic cand

76 y in a population of independent Escherichia coli cells growing in a defined medium.

77 SIM and STORM reconstructions of Escherichia coli cells harbouring CpcA-labelled cytochrome bd 1 ubiq

78 trates at the poles and septa of Escherichia coli cells in a cardiolipin (CL)-dependent manner.

79 on of the polycation was observed to make E. coli cells more susceptible to other quaternary ammonium

80 ther, in a mixture of live and autoclaved E. coli cells our assay could detect only live cells.

81 ility and growth; and (6) ethanol-adapted E. coli cells restore the majority of these reduced activit

82 engineering, we study in living Escherichia coli cells the tripartite efflux complex CusCBA of the r

83 visiae and greater than 99.9% of Escherichia coli cells with 30 s of noncontact treatment.

84 lecules in aggregated and single Escherichia coli cells, with approximately 300 nm spatial resolution

85 macrocyclic peptide libraries produced in E. coli cells.

86 replication in primate (COS7) or Escherichia coli cells.

87 at two different temperatures in Escherichia coli cells.

88 This E. coli CEP 'interactome' provides insights into the functi

89 5 treatment reduced plasma LPS content in E. coli-challenged baboons, implying reduced complement-med

90 metalloenzymes revealed that it inhibits E. coli class II fructose bisphosphate aldolase, but not RN

91 was performed on 649 multidrug-resistant E. coli clinical isolates collected between 2011 and 2015.

92 Of the 649 E. coli clinical isolates, 5 (0.8%) consistently produced n

93 Escherichia coli CNT family member NupC resembles hCNT1 in permeant

94 gous expression of AfarsM1 in an Escherichia coli conferred resistance to MAs(III) but not As(III).

95 Heterologous gene expression in E. coli confirmed its functions for hydrolysis of AHLs, and

96 Escherichia coli contains at least 36 putative toxin-antitoxin gene

97 In Escherichia coli, cueR and copA are separated by two additional gene

98 Escherichia coli CusCFBA is a complex efflux system, responsible for

99 K d 11 nM) is comparable to that of the E. coli cysteine synthase complex (K d 6 nM), and both co

100 ionary divergent proteins in the Escherichia coli cytoplasm by in-cell NMR.

101 We screened Keio collection of Escherichia coli deletion mutants and revealed that deleting genes f

102 the RarA (also MgsA) protein of Escherichia coli, demonstrating that this protein functions at DNA e

103 tructured electrode by using specific anti-E.coli DNA aptamer (Kd 14nM), screened by new in-situ dev

104 is more akin to that observed in Escherichia coli dnaK mutants, rather than those in the Gram-positiv

105 ecay and a longer half-life compared with E. coli DSM1103 (6.64 +/- 0.63 h and 2.85 +/- 0.46 min vs 1

106 Fecal indicator bacteria (FIB) Escherichia coli (E. coli) and Enterococcus spp. were enumerated usi

107 arsely connected network motifs, Escherichia coli (E. coli) appears to favor crosstalk wherein at lea

108 s developed for the detection of Escherichia coli (E. coli) using the T7 bacteriophages engineered wi

109 ination in aerobically respiring Escherichia coli (E. coli).

110 Escherichia coli (Eco) 6S RNA interacts specifically with the housek

111 Enterohemorrhagic Escherichia coli (EHEC) is a commonly occurring foodborne pathogen r

112 bacter jejuni, enterohemorrhagic Escherichia coli (EHEC), or Salmonella spp.

113 with each other and with total coliforms, E. coli, enterococci, and biochemical oxygen demand (Kendal

114 this study, we initially observed that two E.coli enzymes, EcTSR and EcGCL, failed to be targeted int

115 We applied this strategy to two essential E. coli enzymes: the branched-chain aminotransferase BCAT a

116 ildren, typical enteropathogenic Escherichia coli (EPEC) is a common cause of diarrhea and is associa

117 henotypic variability in enteropathogenic E. coli (EPEC), an important human pathogen, both in virule

118 ative bacteria Escherichia coli, Escherichia coli (ESBL) (producing extended spectrum beta-lactamases

119 ainst the Gram-negative bacteria Escherichia coli, Escherichia coli (ESBL) (producing extended spectr

120 Enterotoxigenic Escherichia coli (ETEC) cause more than 500,000 deaths each year in

121 is essential for enterotoxigenic Escherichia coli (ETEC) to cause diarrhea.

122 enterocolitica, enterotoxigenic Escherichia coli (ETEC), Vibrio, and Plesiomonas shigelloides The st

123 In experiments on nonmotile E. coli exposed to polymyxin B, cell-generated frequency no

124 orylation of WRI1 using purified Escherichia coli-expressed components.

125 The Escherichia coli F element-encoded protein TraR is a distant homolog

126 re a class of cell-surface factor used by E. coli for adherence.

127 urce for future computational modeling of E. coli gene regulation, transcription, and translation.

128 In Escherichia coli, GreB is an SC protein that promotes proofreading b

129 the antibacterial effect of gentamicin on E. coli growth.

130 The NhaA crystal structure of Escherichia coli has become the paradigm for this class of secondary

131 tion of carbapenem resistance in Escherichia coli has major implications for the management of common

132 Bacteriophage lambda of Escherichia coli has two alternative life cycles after infection-hos

133 Escherichia coli have the genetic potential to use chitin as a carbo

134 periments show that the acidic tip of the E. coli Hfq CTD transiently binds the basic Sm core residue

135 toxin-prophage varphi24B on its Escherichia coli host MC1061.

136 -bound state, exemplified by the Escherichia coli Hsp70 DnaK, the interdomain linker is flexible.

137 o control their activity against Escherichia coli in both directions with light in the visible region

138 ned the prevalence of pathogenic Escherichia coli in poultry and poultry products; however, limited d

139 We detected E. coli in source water (25%), stored water (77%), child ha

140 ght to be a major source of nutrients for E. coli in the gut.

141 almost completely retained the pathogenic E. coli in the subsurface, suggesting that utilizing sand m

142 nhibit macrophage activation by nonviable E. coli In total, this study shows that cathelicidins do no

143 RA101295 reduced the E. coli-induced "oxidative burst," as well as leukocyte act

144 romal cells reduce the severity of rodent E. coli-induced acute respiratory distress syndrome.

145 RA101295 strongly inhibited E. coli-induced complement activation both in vitro and in

146 -mesenchymal stem/stromal cells to reduce E. coli-induced oxidant injury.

147 Mechanisms that allow for a persistent E. coli infection are not fully understood.

148 E. coli infection stimulated proliferation of granulopoieti

149 t with different timing, both FXa/PCPS and E coli infusion led to robust thrombin and plasmin generat

150 cholate siderophore expressed by Escherichia coli, inhibited PMA-induced generation of reactive oxyge

151 r of hydrogen peroxide in anoxic Escherichia coli Intriguingly, ccp transcription requires both the p

152 Escherichia coli is a leading cause of bacterial mastitis in dairy c

153 on in Pseudomonas sp. compared to that in E. coli is due to the dilution effect of different pathways

154 The Tat system of Escherichia coli is made up of TatA, TatB, and TatC components.

155 Cell division in Escherichia coli is mediated by a large protein complex called the d

156 Ammonium assimilation in Escherichia coli is regulated by two paralogous proteins (GlnB and G

157 d optimisation of HBc particle yield from E. coli is required to improve laboratory-scale productivit

158 The NhaA antiporter of Escherichia coli is the best studied member of the Na(+)/H(+) exchan

159 isolates, we sequenced 600 C. jejuni and C. coli isolates from various stages of poultry processing

160 Human C. coli isolates were likely to originate from chickens (56

161 network of 122 sequence type 131 (ST131) E. coli isolates.

162 tures of Bacillus licheniformis, Escherichia coli JM109, and Lactobacillus reuteri ATCC PTA 4659.

163 was more effective than PEf1 in infecting E. coli K-12 in pure cultures, PEf1 was 20-fold more effect

164 in suppressing a model enteric bacterium (E. coli K-12) in mixtures with soil bacteria (Pseudomonas p

165 ent DNA damage (SOS) response in Escherichia coli K-12, despite the fact that pressure cannot comprom

166 summarizes experimental data for Escherichia coli K-12, the best-studied bacterial model organism.

167 in animals colonized at P2 but not at P9, E. coli K1 bacteria gain access to the enterocyte surface i

168 O157:H7 was 3.3 fold higher than that of E. coli K12 in all biochar-amended sand columns.

169 ed lysis protein, Lys(M), of the Escherichia coli levivirus M (5) .

170 (+)-dependent DNA ligase family (Escherichia coli LigA), captured as their respective Michaelis compl

171 inflammatory response induced by Escherichia coli lipopolysaccharide (LPS), a Toll-like receptor (TLR

172 ainst the spoilage food bacteria Escherichia coli, Listeria monocytogenes, Staphylococcus aureus and

173 t the 2.6-A crystal structure of Escherichia coli Lnt.

174 erved in an NMR structure of the Escherichia coli LpoA N domain.

175 enome encodes two orthologues of Escherichia coli LpxL.

176 olution, we obtained a mutant of Escherichia coli LS5218 with functional deletions of fadE and atoC t

177 h for de novo sequencing using whole cell E. coli lysate.

178 J cm(-2) ) toward Gram-negative bacteria E. coli, making it a remarkably efficient optically mediate

179 metabolic engineering system in Escherichia coli Members of the TPS-c subfamily were characterized a

180 Predictive cysteine cross-linking in E. coli membranes and PELDOR measurements along the transpo

181 EcoCyc now supports running and modifying E. coli metabolic models directly on the EcoCyc website.

182 we show here for representative Escherichia coli mRNAs that 35%-50% of each transcript is diphospho

183 es tend to target modified DNA sites, and E. coli Mrr activity was previously shown to be elicited by

184 on of the large conductance MS channel of E. coli, (MscL), in DHBs.

185 f omega and its role in assembly of RNAP, E. coli mutants lacking rpoZ (codes for omega) are viable d

186 ebsiella pneumoniae (n = 1,127), Escherichia coli (n = 149), and Enterobacter cloacae (n = 110).

187 ansporter CopA has been known in Escherichia coli, no gene for its chaperone had been identified.

188 chanistic and systemic levels in Escherichia coli Numerous important insights on DNA repair were obta

189 The E coli O-antigen is a promising vaccine target.

190 In 2011 Escherichia coli O104:H4 caused an outbreak with >800 cases of hemol

191 etection of the food contaminant Escherichia coli O157:H7 (E. coli O157:H7) in complex food products

192 E. coli O157:H7 is an enterohemorrhagic bacteria responsibl

193 Shiga toxin-producing Escherichia coli O157:H7 primarily resides in cattle asymptomaticall

194 (2) The retention of E. coli O157:H7 was 3.3 fold higher than that of E. coli K1

195 ood contaminant Escherichia coli O157:H7 (E. coli O157:H7) in complex food products due to the recent

196 of integral membrane proteins in Escherichia coli often yields insufficient quantities of purifiable

197 ng the transmembrane beta-barrel Escherichia coli OmpLA as a scaffold protein.

198 middle of the beta barrel of the Escherichia coli OMPs OmpLA and EspP creates an energy barrier that

199 on of CsrA to gene expression in Escherichia coli on a global scale.

200 s decreased disinfection efficacy against E. coli on heavy-duty tarp but does prevent splashing, whic

201 we performed a genetic screen in Escherichia coli on the LCFA, oleate, and compared our results with

202 somerase and RNase H activity in Escherichia coli or Saccharomyces cerevisiae caused R-loop accumulat

203 n inactivated along with ExoI in Escherichia coli, or Sae2 in eukaryotes, palindromic amplifications

204 functional traits in N. meningitidis and E. coli Our study indicates that the expression of NMB0419

205 eria (Pseudomonas aeruginosa and Escherichia coli) over time through lag and log growth phases and fo

206 acids using the transmembrane beta-barrel E. coli PagP as a scaffold protein.

207 phagocytic uptake of bacterial (Escherichia coli) particles by (i) capturing along the filopodial sh

208 tudy quantifies the transport of Escherichia coli pathogenic O157:H7 and nonpathogenic K12 strains in

209 fects of membrane thickness, the Escherichia coli periplasmic chaperones Skp and SurA, and BamA, the

210 In a buffer solution, E. coli PI-7 displayed a longer lag phase prior to decay an

211 the C-terminal D4 domain of the Escherichia coli polysaccharide transporter Wza.

212 To contextualize ST131 within the broader E. coli population associated with disease, we used genomic

213 We modelled this scenario using Escherichia coli populations producing colicins, an antibiotic that

214 Using available data for Escherichia coli protein solubility in a cell-free expression system

215 eveloped methodology was then applied for E. coli quantification in water samples using nanomaterial

216 OMCCs from the A. tumefaciens VirB/VirD4, E. coli R388 Trw, and Bordetella pertussis Ptl systems supp

217 n, without affecting host phagocytosis of E. coli RA101295 treatment reduced plasma LPS content in E.

218 rystal structures of full length Escherichia coli RapZ at 3.40 A and 3.25 A, and its isolated C-termi

219 differences in clustering between native E. coli receptors, with the TM sequence of better-clusterin

220 th) efficacy for particulate and Escherichia coli removal under simulated real-world usage.

221 py (CoSMoS) to follow the exchange of the E. coli replicative DNA polymerase Pol IIIcore with the tra

222 providing the molecular basis for how the E. coli replisome can maintain high processivity and yet po

223 In vitro studies of reconstituted E. coli replisomes have attributed this remarkable processi

224 in the bacterial cytoplasm of an Escherichia coli reporter strain.

225 2.80; 95% CI, 1.65-4.74) and in Escherichia coli-resistant infections (OR, 2.28; 95% CI, 1.32-3.96).

226 ne (oxyBAC) present in this gene array in E. coli resulted in formation of BDMA from BACs at a rate o

227 Arg-213 as a crucial residue on Escherichia coli RF2 for discriminating guanine in the third positio

228 S531 of Escherichia coli RNA polymerase (RNAP) beta subunit is a part of RNA

229 The Escherichia coli RNA polymerase (RNAP) is a multisubunit protein com

230 ere, we present the structure of Escherichia coli RNA polymerase complexed with NusG.

231 er or proofreading hydrolysis by Escherichia coli RNAP.

232 targets, including latex beads, Escherichia coli, Salmonella typhimurium, and Mycobacterium tubercul

233 1 K pneumoniae samples and 77 (19%) of 402 E coli samples were carbapenemase (KPC, NDM, OXA-48-like,

234 s and an in vivo baboon model of Escherichia coli sepsis.

235 The Escherichia coli sequence type 648 complex (STc648) is an emerging l

236 itive and 99.3% specific for detection of E. coli serotype O:157.

237 E. coli single strand (ss) DNA binding protein (SSB) is an

238 mary biosynthetic determinant of Escherichia coli size and present evidence supporting a similar role

239 in the in vivo environment of an Escherichia coli SSO, their development was based on structure-activ

240 lera toxin, or heat-stable enterotoxin of E. coli (STa toxin), with IC50 down to approximately 5 nM.

241 tize high-density populations of Escherichia coli, Staphylococcus aureus, and Mycobacterium smegmatis

242 ed a suitable bacterial selection system (E. coli strain BW5Delta).

243 wca operon caused a persistent-infection E. coli strain to become sensitive to complement-mediated k

244 the antibiotic cefotaxime in an Escherichia coli strain with a high mistranslation rate.

245 Using a novobiocin-sensitive Escherichia coli strain with a leaky outer membrane, we identified a

246 Using a DeltasdhE E. coli strain, we show that the requirement for the assemb

247 c DNA from lambda bacteriophage, Escherichia coli (strain K12, MG1655) and Mus musculus (female BALB/

248 We sequenced the genomes of the E. coli strains and report genes unique to the two phenotyp

249 Although industrial Escherichia coli strains efficiently use glucose, their ability to u

250 Among them, nine E. coli strains possess an epidemic pCSZ4-like IncX4 plasmi

251 01] times more likely to harbor resistant E. coli strains than layer farms.

252 nterococci, fewer environmentally adapted E. coli strains were isolated on selective media containing

253 measured fitness of approximately 14,000 E. coli strains, each expressing a reporter gene with a uni

254 ition and statistical tools, to determine E. coli susceptibility within a few minutes to different an

255 has the potential to allow the versatile E. coli system to be employed as an exciting new carbon cap

256 es discrete intramolecular cross-links of E. coli TatC involving both its N- and C-tails.

257 te residue in the transmembrane region of E. coli TatC, which when modified by DCCD interferes with t

258 times more of soluble protein in Escherichia coli than fusions with several conventional tags.

259 Here, we designed a genetic screen around E. coli that identified high-affinity cytochrome bd oxidase

260 al pathogens, including enterohemorrhagic E. coli The mechanisms that allow pathogens to target these

261 In some cases (e.g., Escherichia coli) the gene is not located within a biotin synthetic

262 to produce hFGF21 efficiently in Escherichia coli, the expression and solubility of hFGF21 were teste

263 When applied to Escherichia coli, the regulation network constructed by our proposed

264 lutamate is the major monovalent anion in E. coli, these results suggest that SSB likely binds to ssD

265 tance 100-fold when expressed in Escherichia coli This qualifies ClpG as a potential persistence and

266 SrtA expression was achieved in Escherichia coli through molecular engineering, including manipulati

267 t we exposed growing colonies of Escherichia coli to a virulent mutant of phage P1.

268 We subjected Escherichia coli to an antibiotic to obtain motile cells of differen

269 cycle resulted in increased resistance of E. coli to PGRP killing.

270 ructure of full-length ZntB from Escherichia coli together with the results of isothermal titration c

271 at the highly conserved Tyr-86 residue in E. coli TrmD is essential to discriminate between 3',5'-cAM

272 on of suppressor tRNA species in Escherichia coli; tRNAs with 8/4 or 9/3 structures efficiently inser

273 Here we show that the Escherichia coli UbiD enzyme, which is implicated in ubiquinone bios

274 was 20-fold more effective in suppressing E. coli under simulated multispecies biofilm conditions bec

275 s (UTIs) caused by uropathogenic Escherichia coli (UPEC) affect 150 million people annually.

276 pels intracellular uropathogenic Escherichia coli (UPEC) from their intracellular niche.

277 Uropathogenic Escherichia coli (UPEC), the predominant cause of urinary tract infe

278 We detected escherichelin during clinical E. coli urinary tract infection (UTI) and experimental huma

279 lobacter species other than C. jejuni and C. coli using a filtration method and microaerobic conditio

280 y (11.9 kb encoding 10 genes) in Escherichia coli using a highly error-prone microchip-synthesized ol

281 duction of alpha-methyl acids in Escherichia coli using these enzymes allows the construction of micr

282 e T4 infects the bacterial host (Escherichia coli) using an efficient genomic delivery machine that i

283 ed for the detection of Escherichia coli (E. coli) using the T7 bacteriophages engineered with lacZ o

284 elve experimental populations of Escherichia coli, using whole-genome metagenomic sequencing at five

285 ality, and the incidence of UTIs caused by E coli vaccine serotypes in each group.

286 rescent protein (GFP)-expressing Escherichia coli was cultured onto PAR4-AP-modified titanium with an

287 nuclear cell (PBMC) responses to Escherichia coli was employed.

288 The quantification of Escherichia coli was investigated with standard and nanomaterial amp

289 nstituting bilin biosynthesis in Escherichia coli was modified to utilize HY2 from the streptophyte a

290 deoxyoctulosonate (Kdo)-lipid A domain in E. coli was necessary to facilitate chemical structure anal

291 y-forming units per mL of vaccine-serotype E coli was noted in the vaccine compared with the placebo

292 rica, Klebsiella pneumoniae, and Escherichia coli We compare patterns of selection operating on IGRs

293 sphatidylserine [PCPS]) vs LD100 Escherichia coli We found that, albeit with different timing, both F

294 ization of the MsrQ protein from Escherichia coli We optimized conditions for the overexpression and

295 tudies using Cryptosporidium and Escherichia coli, we show that failure to consider biphasic pathogen

296 ng a chemical genomics screen in Escherichia coli, we uncover a mode of action for DTPs-the disruptio

297 mplex that can also be formed in Escherichia coli when it is co-expressed with genes encoding PEB bio

298 nidase (beta-glucur) are both produced by E. coli, while beta-glucosidase (beta-gluco) is produced by

299 By examining replisomes in live E. coli with fluorescence microscopy, we found that the Pol

300 lysis activity of an amidase expressed in E. coli with three different substrates.