ライフサイエンスコーパス: Escherichia coli

1 tumor necrosis factor and adherent-invasive Escherichia coli.

2 tion levels as a function of growth phase in Escherichia coli.

3 ylate antibiotic produced by some strains of Escherichia coli.

4 l genes in yeast by their 1:1 orthologs from Escherichia coli.

5 ription factor GreA inhibits break repair in Escherichia coli.

6 d outer-membrane and periplasmic proteins of Escherichia coli.

7 to investigate the thermotactic response of Escherichia coli.

8 naerobic to aerobic growth for the bacterium Escherichia coli.

9 a Proteus mirabilis and Antibiotic resistant Escherichia coli.

10 al species outside Actinobacteria, including Escherichia coli.

11 ngle compact RNA mechanism that functions in Escherichia coli.

12 tivity against an export-deficient mutant of Escherichia coli.

13 at McC is a strong inducer of persistence in Escherichia coli.

14 he microbiota, characterized by expansion of Escherichia coli.

15 f the longest sequestration-based cascade in Escherichia coli.

16 l component of the AcrAB-TolC efflux pump in Escherichia coli.

17 s As(V) reductase activity when expressed in Escherichia coli.

18 ear architecture, and we implemented them in Escherichia coli.

19 ted by the Krebs cycle metabolite citrate in Escherichia coli.

20 to an intimin derived from enterohemorrhagic Escherichia coli.

21 vivo RNA-guided DNA interference activity in Escherichia coli.

22 related to the O-antigenic polysaccharide of Escherichia coli 120, as its p-methoxyphenyl glycoside,

23 genes (2 [8.7%] vs 19 [61.3%]; P < .001) and Escherichia coli (4 [17.4%] vs 5 [16.2%]; P = .90) were

24 The CdiA-CT toxin from uropathogenic Escherichia coli 536 is a latent tRNase that is only act

25 n a population relative to those observed in Escherichia coli (6-9) .

26 In contrast to Escherichia coli, a model organism for chemotaxis that h

27 In Escherichia coli, a proteolytic system comprising the pe

28 In Escherichia coli, a single pair of replisomes is respons

29 In Escherichia coli, about half of the transcription events

30 nst multidrug-resistant clinical isolates of Escherichia coli, Acinetobacter baumannii, Klebsiella pn

31 ith fever, urinary tract infection caused by Escherichia coli, anal lymphogranuloma venereum infectio

32 , occurs among fast-growing bacteria such as Escherichia coli and Bacillus subtilis.

33 former phylum includes pathogenic strains of Escherichia coli and Campylobacter spp. that declined in

34 e, we found that MAIT cell responses against Escherichia coli and Candida albicans displayed microbe-

35 They can be produced at large scale in Escherichia coli and could thus make secondary antibody

36 s when urinary fractions were tested against Escherichia coli and Enterococcus faecalis urinary tract

37 Escherichia coli and Enterococcus species, both indicato

38 the canonical DEDD exonucleases found in the Escherichia coli and eukaryotic replisomes.

39 t a genome-scale protein-folding network for Escherichia coli and formulate a computational model, Fo

40 w the basic mechanisms of excision repair in Escherichia coli and humans and the recent genome-wide m

41 s, human monocyte-derived macrophages killed Escherichia coli and ingested E. coli BioParticles bette

42 The system of the bacterium Escherichia coli and its virus, bacteriophage lambda, is

43 ded-spectrum beta-lactamase (ESBL)-producing Escherichia coli and K. pneumoniae isolates using MinION

44 apparent in cysteine-containing proteins in Escherichia coli and mammalian cells and is believed to

45 into proteins via amber codon suppression in Escherichia coli and mammalian cells.

46 e, we determined the population structure of Escherichia coli and of mobile genetic elements (MGEs) c

47 Escherichia coli and other Enterobacteriaceae are among

48 During biofilm formation, Escherichia coli and other Enterobacteriaceae produce an

49 Laboratory strains of Escherichia coli and P. aeruginosa were killed by a proc

50 tly produced TCPs induce permeabilization of Escherichia coli and phagocytic uptake.

51 tic anaerobic coculture pairing fermentative Escherichia coli and phototrophic Rhodopseudomonas palus

52 on with oral beta-glucuronidase derived from Escherichia coli and pretreatment with vancomycin and im

53 e bactericidal, killing approximately 90% of Escherichia coli and Pseudomonas aeruginosa cells within

54 hlorobaculum limnaeum strain DSMZ 1677(T) in Escherichia coli and purified the enzyme under anoxic co

55 ector and the phosphoprotein cofactor (P) in Escherichia coli and purified the resulting proteins by

56 y transcribing elongation complexes (ECs) in Escherichia coli and Saccharomyces cerevisiae and found

57 activity in vitro and rescued the growth of Escherichia coli and Saccharomyces cerevisiae strains wi

58 -resolution crystal structures of GusRs from Escherichia coli and Salmonella enterica in complexes wi

59 Of the 1,982 Escherichia coli and Shigella sp. isolates analyzed in t

60 urvival rates of larvae after challenge with Escherichia coli and Staphylococcus aureus, but had no s

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

62 We show that the mesophile Escherichia coli and the extremophile Shewanella piezoto

63 e, we used both the export chaperone SecB of Escherichia coli and the tripartite TAC system of Mycoba

64 A) and m1G constituted robust blocks to both Escherichia coli and wheat germ extract translation syst

65 to the translocase, EscV in enteropathogenic Escherichia coli, and cross it in strict hierarchical ma

66 ive sequences were successfully expressed in Escherichia coli, and eight of the nine candidates exhib

67 ny proteins associated with the cell wall of Escherichia coli, and for some of these proteins the dis

68 This cystatin was efficiently expressed in Escherichia coli, and inhibitory assays demonstrated tha

69 tro in live bacteria (Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa) relative t

70 Urinary Escherichia coli antibiograms were compared between inst

71 Quite unexpectedly, cyanobacteria and Escherichia coli appear to share an invariance principle

72 The FRET changes observed in Escherichia coli are more complicated, where FRET-increa

73 Gram-negative bacteria such as Escherichia coli are protected by a complex cell envelop

74 KalbTG was produced in Escherichia coli as soluble and active enzyme in the pre

75 oprim treatment results in cell death, using Escherichia coli as the model organism.

76 tested for bacteria-killing capacity against Escherichia coli, as a functional assay of immune functi

77 Escherichia coli associated with urinary tract infection

78 id DNA and endogenous chromosomal DNA within Escherichia coli at 37 degrees C.

79 biosensors for electrochemical detection of Escherichia coli B.

80 of binary fission in model bacteria such as Escherichia coli, Bacillus subtilis, and Caulobacter cre

81 rgeted detection, removal and destruction of Escherichia coli bacteria was developed onto the surface

82 Here, we used an Escherichia coli-based cell-free system to express a MOM

83 dified NTF was combined with codon-optimized Escherichia coli BirA in a single T-DNA construct.

84 ic neck and lectin domains, was expressed in Escherichia coli BL21(lambdaDE3)pLysS cells.

85 Infection of Escherichia coli by the T7 phage leads to rapid and sele

86 w that the evolution of multi-drug-resistant Escherichia coli can be manipulated in vitro by administ

87 We show that cell size in Escherichia coli can be predicted for any steady-state c

88 We demonstrate that ribocomputing devices in Escherichia coli can evaluate two-input logic with a dyn

89 The purified recombinant CrACX2 expressed in Escherichia coli catalyzed the oxidation of fatty acyl-C

90 ells to kill/phagocytose Candida albicans or Escherichia coli cells both ex vivo and in vivo During s

91 heterogeneity in a population of independent Escherichia coli cells growing in a defined medium.

92 SIM and STORM reconstructions of Escherichia coli cells harbouring CpcA-labelled cytochro

93 ProP concentrates at the poles and septa of Escherichia coli cells in a cardiolipin (CL)-dependent m

94 and genetic engineering, we study in living Escherichia coli cells the tripartite efflux complex Cus

95 romyces cerevisiae and greater than 99.9% of Escherichia coli cells with 30 s of noncontact treatment

96 map small molecules in aggregated and single Escherichia coli cells, with approximately 300 nm spatia

97 vectors for replication in primate (COS7) or Escherichia coli cells.

98 usion with the potential for imaging in live Escherichia coli cells.

99 le spectrum at two different temperatures in Escherichia coli cells.

100 Escherichia coli CNT family member NupC resembles hCNT1

101 lls were more frequent upon stimulation with Escherichia coli compared with healthy controls.

102 lymeric adhesive organelles of uropathogenic Escherichia coli composed of DraE subunits, responsible

103 The cytokinetic division ring of Escherichia coli comprises filaments of FtsZ tethered to

104 Heterologous expression of AfarsM1 in an Escherichia coli conferred resistance to MAs(III) but no

105 Escherichia coli contains at least 36 putative toxin-ant

106 In Escherichia coli, CpxRA senses and responds to envelope

107 The Escherichia coli CSP genes CspA and CspB were modified t

108 In Escherichia coli, cueR and copA are separated by two add

109 icial samples (including synthetic miRNA and Escherichia coli cultures) and biological samples (human

110 Escherichia coli CusCFBA is a complex efflux system, res

111 three evolutionary divergent proteins in the Escherichia coli cytoplasm by in-cell NMR.

112 We screened Keio collection of Escherichia coli deletion mutants and revealed that dele

113 Analysis of activity in Escherichia coli DeltacobB revealed that the probe can r

114 activity of the RarA (also MgsA) protein of Escherichia coli, demonstrating that this protein functi

115 y question concerning the catalytic cycle of Escherichia coli dihydrofolate reductase (ecDHFR) is whe

116 nzimidazoles have been synthesized and their Escherichia coli DNA topoisomerase I inhibition, binding

117 disruption is more akin to that observed in Escherichia coli dnaK mutants, rather than those in the

118 3C2Tx modified membranes were tested against Escherichia coli (E. coli) and Bacillus subtilis (B. sub

119 Fecal indicator bacteria (FIB) Escherichia coli (E. coli) and Enterococcus spp. were en

120 y between sparsely connected network motifs, Escherichia coli (E. coli) appears to favor crosstalk wh

121 n that Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) species are abundant bacteria

122 al method was developed for the detection of Escherichia coli (E. coli) using the T7 bacteriophages e

123 Hg(II) coordination in aerobically respiring Escherichia coli (E. coli).

124 enum-containing formate dehydrogenase H from Escherichia coli (EcFDH-H) is a powerful model system fo

125 Escherichia coli (Eco) 6S RNA interacts specifically wit

126 odborne pathogens, such as enterohemorrhagic Escherichia coli (EHEC) and Salmonella enterica serovar

127 Enterohemorrhagic Escherichia coli (EHEC) is a commonly occurring foodborn

128 Enterohemorrhagic Escherichia coli (EHEC) is a diarrheagenic pathogen that

129 ning Campylobacter jejuni, enterohemorrhagic Escherichia coli (EHEC), or Salmonella spp.

130 d urinary tract infections (CAUTI) caused by Escherichia coli, Enterococcus, and Staphylococcus aureu

131 on (Clostridium difficile, enteroaggregative Escherichia coli, enteropathogenic E. coli, and enteroto

132 effacing pathogens such as enteropathogenic Escherichia coli (EPEC) and Citrobacter rodentium during

133 In children, typical enteropathogenic Escherichia coli (EPEC) is a common cause of diarrhea an

134 tected by the GI panel were enteropathogenic Escherichia coli (EPEC, n = 21), norovirus (n = 21), rot

135 the Gram-negative bacteria Escherichia coli, Escherichia coli (ESBL) (producing extended spectrum bet

136 alis, and against the Gram-negative bacteria Escherichia coli, Escherichia coli (ESBL) (producing ext

137 Enterotoxigenic Escherichia coli (ETEC) cause more than 500,000 deaths e

138 l intestine is essential for enterotoxigenic Escherichia coli (ETEC) to cause diarrhea.

139 of Yersinia enterocolitica, enterotoxigenic Escherichia coli (ETEC), Vibrio, and Plesiomonas shigell

140 Extraintestinal pathogenic Escherichia coli (ExPEC), so named because this pathotyp

141 ndent phosphorylation of WRI1 using purified Escherichia coli-expressed components.

142 The Escherichia coli F element-encoded protein TraR is a dis

143 Here we present genetic evidence that in Escherichia coli, FtsA antagonizes FtsZ protofilament bu

144 nd a H(+) across the cytoplasmic membrane of Escherichia coli (galactoside/H(+) symport).

145 When contacted with the model bacterium Escherichia coli, GO nanosheets with vertical orientatio

146 In Escherichia coli, GreB is an SC protein that promotes pr

147 el was the re-engineering of the 23S rRNA of Escherichia coli, guided by the use of a phosphorylated

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

149 he dissemination of carbapenem resistance in Escherichia coli has major implications for the manageme

150 Bacteriophage lambda of Escherichia coli has two alternative life cycles after i

151 Escherichia coli have the genetic potential to use chiti

152 Using an Escherichia coli heterologous sterol expression system,

153 erised Shiga toxin-prophage varphi24B on its Escherichia coli host MC1061.

154 hesion molecule (MAM) from the gut commensal Escherichia coli HS (MAM(HS)), which contains an array o

155 , in the ADP-bound state, exemplified by the Escherichia coli Hsp70 DnaK, the interdomain linker is f

156 e, we show that chicken cathelicidin-2 kills Escherichia coli in an immunogenically silent fashion.

157 allowed us to control their activity against Escherichia coli in both directions with light in the vi

158 D structures of sigma1.1 are available: from Escherichia coli in complex with RNAP and from T. mariti

159 s have examined the prevalence of pathogenic Escherichia coli in poultry and poultry products; howeve

160 We engineered colony-wide DNA cycling in Escherichia coli in the form of plasmid copy number osci

161 al role in protecting flies against systemic Escherichia coli infection.

162 Ent), a catecholate siderophore expressed by Escherichia coli, inhibited PMA-induced generation of re

163 cant degrader of hydrogen peroxide in anoxic Escherichia coli Intriguingly, ccp transcription require

164 Escherichia coli is a commensal or pathogenic bacterium

165 Escherichia coli is a leading cause of bacterial mastiti

166 The Tat system of Escherichia coli is made up of TatA, TatB, and TatC comp

167 Cell division in Escherichia coli is mediated by a large protein complex

168 ZipA protein from Escherichia coli is one of the essential components of t

169 Ammonium assimilation in Escherichia coli is regulated by two paralogous proteins

170 Nucleotide excision repair in Escherichia coli is stimulated by transcription, specifi

171 The NhaA antiporter of Escherichia coli is the best studied member of the Na(+)

172 irection switching in the flagellar motor of Escherichia coli is under the control of a complex on th

173 ternary mixtures of Bacillus licheniformis, Escherichia coli JM109, and Lactobacillus reuteri ATCC P

174 The Escherichia coli K-12 nrf operon encodes a periplasmic n

175 RecA-dependent DNA damage (SOS) response in Escherichia coli K-12, despite the fact that pressure ca

176 ollects and summarizes experimental data for Escherichia coli K-12, the best-studied bacterial model

177 pendency of neonatal systemic infection with Escherichia coli K1 can be replicated in the neonatal ra

178 Gram-negative species-Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, and Pseudomonas

179 olderia pseudomallei, Chlamydia trachomatis, Escherichia coli, Klebsiella pneumoniae, Legionella pneu

180 f an unrelated lysis protein, Lys(M), of the Escherichia coli levivirus M (5) .

181 and the NAD(+)-dependent DNA ligase family (Escherichia coli LigA), captured as their respective Mic

182 tructural similarities with the bifunctional Escherichia coli lipopolysaccharide (LPS) O antigen regu

183 inhibit the inflammatory response induced by Escherichia coli lipopolysaccharide (LPS), a Toll-like r

184 ons (MBC) against the spoilage food bacteria Escherichia coli, Listeria monocytogenes, Staphylococcus

185 re, we report the 2.6-A crystal structure of Escherichia coli Lnt.

186 rom that observed in an NMR structure of the Escherichia coli LpoA N domain.

187 f various P. aeruginosa and, for comparison, Escherichia coli LPS environments on the physical proper

188 pathogen's genome encodes two orthologues of Escherichia coli LpxL.

189 adaptive evolution, we obtained a mutant of Escherichia coli LS5218 with functional deletions of fad

190 Current vaccines to Escherichia coli mastitis have shown some albeit limited

191 in a modular metabolic engineering system in Escherichia coli Members of the TPS-c subfamily were cha

192 novel assay, we show here for representative Escherichia coli mRNAs that 35%-50% of each transcript

193 We identified Escherichia coli mutants that demonstrated increased mem

194 road spectrum antibacterial activity against Escherichia coli, Mycobacterium smegmatis, Staphylococcu

195 tified in Klebsiella pneumoniae (n = 1,127), Escherichia coli (n = 149), and Enterobacter cloacae (n

196 we present structures of the CDI toxin from Escherichia coli NC101 in ternary complex with its cogna

197 opper ion transporter CopA has been known in Escherichia coli, no gene for its chaperone had been ide

198 s at both mechanistic and systemic levels in Escherichia coli Numerous important insights on DNA repa

199 In 2011 Escherichia coli O104:H4 caused an outbreak with >800 ca

200 or for the detection of the food contaminant Escherichia coli O157:H7 (E. coli O157:H7) in complex fo

201 Shiga toxin-producing Escherichia coli O157:H7 primarily resides in cattle asy

202 rexpression of integral membrane proteins in Escherichia coli often yields insufficient quantities of

203 ty scale using the transmembrane beta-barrel Escherichia coli OmpLA as a scaffold protein.

204 ue near the middle of the beta barrel of the Escherichia coli OMPs OmpLA and EspP creates an energy b

205 e contribution of CsrA to gene expression in Escherichia coli on a global scale.

206 Here, we performed a genetic screen in Escherichia coli on the LCFA, oleate, and compared our r

207 al microorganisms are not close relatives of Escherichia coli or other model organisms and have elude

208 ly transformed by the same DNA propagated in Escherichia coli or produced with PCR.

209 nce of Topoisomerase and RNase H activity in Escherichia coli or Saccharomyces cerevisiae caused R-lo

210 with or without heat-labile toxin (LT) from Escherichia coli or subcutaneously with aluminum hydroxi

211 When inactivated along with ExoI in Escherichia coli, or Sae2 in eukaryotes, palindromic amp

212 receptor binding and the penetration of the Escherichia coli outer membrane.

213 egative bacteria (Pseudomonas aeruginosa and Escherichia coli) over time through lag and log growth p

214 upported the phagocytic uptake of bacterial (Escherichia coli) particles by (i) capturing along the f

215 he present study quantifies the transport of Escherichia coli pathogenic O157:H7 and nonpathogenic K1

216 amine the effects of membrane thickness, the Escherichia coli periplasmic chaperones Skp and SurA, an

217 is based on the C-terminal D4 domain of the Escherichia coli polysaccharide transporter Wza.

218 We modelled this scenario using Escherichia coli populations producing colicins, an anti

219 two multi MCE domain-containing proteins in Escherichia coli, PqiB and YebT, the latter of which is

220 metagenomic library that, when expressed in Escherichia coli, produce halos on LB agar supplemented

221 Enterotoxigenic Escherichia coli produces a long type 4 pilus called Lon

222 Using available data for Escherichia coli protein solubility in a cell-free expre

223 The pathway controlling chemotaxis of Escherichia coli provides one example where posttranslat

224 requires a posttranslational modification in Escherichia coli, Pseudomonas aeruginosa, and Bacillus s

225 report the crystal structures of full length Escherichia coli RapZ at 3.40 A and 3.25 A, and its isol

226 Here, we show that Escherichia coli RecQ, a central DNA recombination and r

227 -term (9 month) efficacy for particulate and Escherichia coli removal under simulated real-world usag

228 ed proteins in the bacterial cytoplasm of an Escherichia coli reporter strain.

229 aureus (OR, 2.80; 95% CI, 1.65-4.74) and in Escherichia coli-resistant infections (OR, 2.28; 95% CI,

230 s identified Arg-213 as a crucial residue on Escherichia coli RF2 for discriminating guanine in the t

231 e of a quaternary complex of the translating Escherichia coli ribosome, the SRP-SR in the 'activated'

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

233 The Escherichia coli RNA polymerase (RNAP) is a multisubunit

234 Here, we present the structure of Escherichia coli RNA polymerase complexed with NusG.

235 horyl transfer or proofreading hydrolysis by Escherichia coli RNAP.

236 e of diverse targets, including latex beads, Escherichia coli, Salmonella typhimurium, and Mycobacter

237 -blood assays and an in vivo baboon model of Escherichia coli sepsis.

238 The Escherichia coli sequence type 648 complex (STc648) is a

239 s as the primary biosynthetic determinant of Escherichia coli size and present evidence supporting a

240 etained within the in vivo environment of an Escherichia coli SSO, their development was based on str

241 operties on tester strains (Bacillus cereus, Escherichia coli, Staphylococcus aureus and Pseudomonas

242 sfully sensitize high-density populations of Escherichia coli, Staphylococcus aureus, and Mycobacteri

243 ance, particularly for Shiga toxin-producing Escherichia coli (STEC) and Salmonella" The document say

244 detection to identify Shiga toxin-producing Escherichia coli (STEC) in preserved stool specimens.

245 patients infected with Shiga toxin-producing Escherichia coli (STEC) remain unclear.

246 determine whether OMVs from a uropathogenic Escherichia coli strain can induce cardiac dysfunction,

247 esistance on the antibiotic cefotaxime in an Escherichia coli strain with a high mistranslation rate.

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

249 ae pathway enzymes in a specially engineered Escherichia coli strain.

250 on was achieved using a cysteine auxotrophic Escherichia coli strain.

251 es of genomic DNA from lambda bacteriophage, Escherichia coli (strain K12, MG1655) and Mus musculus (

252 Although industrial Escherichia coli strains efficiently use glucose, their

253 Here we have assembled a large panel of 696 Escherichia coli strains, which we have genotyped and me

254 up to eight times more of soluble protein in Escherichia coli than fusions with several conventional

255 ms culminated in the creation of a strain of Escherichia coli that, by virtue of a nucleoside triphos

256 terminus in cultured cells and purified from Escherichia coli The alpha-helical motif was not require

257 In some cases (e.g., Escherichia coli) the gene is not located within a bioti

258 Here, to produce hFGF21 efficiently in Escherichia coli, the expression and solubility of hFGF2

259 In bacteria such as Escherichia coli, the outer membrane is a unique asymmet

260 When applied to Escherichia coli, the regulation network constructed by

261 s heat resistance 100-fold when expressed in Escherichia coli This qualifies ClpG as a potential pers

262 xtracellular SrtA expression was achieved in Escherichia coli through molecular engineering, includin

263 rocin PDI inhibits a diversity of pathogenic Escherichia coli through the action of an effector prote

264 of of concept we exposed growing colonies of Escherichia coli to a virulent mutant of phage P1.

265 We subjected Escherichia coli to an antibiotic to obtain motile cells

266 he combined IS treatment enabled a commensal Escherichia coli to flourish, and dramatically increased

267 icroscopy structure of full-length ZntB from Escherichia coli together with the results of isothermal

268 tion candidates within the flexible loops of Escherichia coli transketolase (TK).

269 ation function of suppressor tRNA species in Escherichia coli; tRNAs with 8/4 or 9/3 structures effic

270 Here we show that the Escherichia coli UbiD enzyme, which is implicated in ubi

271 ct infections (UTIs) caused by uropathogenic Escherichia coli (UPEC) affect 150 million people annual

272 ECs) that expels intracellular uropathogenic Escherichia coli (UPEC) from their intracellular niche.

273 Uropathogenic Escherichia coli (UPEC), the predominant cause of urinar

274 elevated during UTI caused by uropathogenic Escherichia coli (UPEC).

275 hetic pathway (11.9 kb encoding 10 genes) in Escherichia coli using a highly error-prone microchip-sy

276 ols biofilm formation in the model bacterium Escherichia coli using computational network analysis, a

277 fect of growth rate on flagellar assembly in Escherichia coli using steady-state chemostat cultures w

278 ways for production of alpha-methyl acids in Escherichia coli using these enzymes allows the construc

279 Bacteriophage T4 infects the bacterial host (Escherichia coli) using an efficient genomic delivery ma

280 lution in twelve experimental populations of Escherichia coli, using whole-genome metagenomic sequenc

281 pendencies mediated by amino acid leakage in Escherichia coli vary across 189 amino acid pairs.

282 SY based solution NMR study showing that the Escherichia coli version of Hsp70, DnaK, binds to as man

283 e function against Klebsiella pneumoniae and Escherichia coli; vi) MAIT cell hyperactivation and aner

284 MS2 infects Escherichia coli via the host 'sex pilus' (F-pilus); it

285 Green fluorescent protein (GFP)-expressing Escherichia coli was cultured onto PAR4-AP-modified tita

286 l blood mononuclear cell (PBMC) responses to Escherichia coli was employed.

287 In this work, the Cu-ATPase CopA from Escherichia coli was expressed and purified in fully fun

288 The quantification of Escherichia coli was investigated with standard and nano

289 system reconstituting bilin biosynthesis in Escherichia coli was modified to utilize HY2 from the st

290 monella enterica, Klebsiella pneumoniae, and Escherichia coli We compare patterns of selection operat

291 lcholine-phosphatidylserine [PCPS]) vs LD100 Escherichia coli We found that, albeit with different ti

292 al characterization of the MsrQ protein from Escherichia coli We optimized conditions for the overexp

293 Pfs25 was codon harmonized for expression in Escherichia coli We produced a rPfs25-PfMSP8 fusion prot

294 rough case studies using Cryptosporidium and Escherichia coli, we show that failure to consider bipha

295 Using a chemical genomics screen in Escherichia coli, we uncover a mode of action for DTPs-t

296 Densities of Escherichia coli were also comparable during wet versus

297 o a tight complex that can also be formed in Escherichia coli when it is co-expressed with genes enco

298 of functional PfVIT in the inner membrane of Escherichia coli which, in turn, conferred iron toleranc

299 We demonstrate the technique on strains of Escherichia coli with various tolerance levels.

300 mammalian system, such as has been done with Escherichia coli, yeast, and mammalian HSP90.