ライフサイエンスコーパス: Escherichia

1 ysbiotic expansion of potentially pathogenic Escherichia and Salmonella by reducing the bioavailabili

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

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

4 3C2Tx modified membranes were tested against Escherichia coli (E. coli) and Bacillus subtilis (B. sub

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 Escherichia coli and Enterococcus species, both indicato

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

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

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

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

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

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

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

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

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

51 Escherichia coli and other Enterobacteriaceae are among

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

69 Urinary Escherichia coli antibiograms were compared between inst

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

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

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

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

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

75 Escherichia coli associated with urinary tract infection

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

77 biosensors for electrochemical detection of Escherichia coli B.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 Escherichia coli CNT family member NupC resembles hCNT1

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

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

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

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

101 Escherichia coli contains at least 36 putative toxin-ant

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

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

104 Escherichia coli CusCFBA is a complex efflux system, res

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

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

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

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

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

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

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

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

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

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

115 Escherichia coli have the genetic potential to use chiti

116 Using an Escherichia coli heterologous sterol expression system,

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

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

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

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

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

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

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

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

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

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

127 Escherichia coli is a commensal or pathogenic bacterium

128 Escherichia coli is a leading cause of bacterial mastiti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 We identified Escherichia coli mutants that demonstrated increased mem

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

185 horyl transfer or proofreading hydrolysis by Escherichia coli RNAP.

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

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

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

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

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

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

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

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

194 Although industrial Escherichia coli strains efficiently use glucose, their

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 Densities of Escherichia coli were also comparable during wet versus

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

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

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

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

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

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

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

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

232 In Escherichia coli, a proteolytic system comprising the pe

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

234 In Escherichia coli, about half of the transcription events

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

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

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

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

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

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

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

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

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

244 In Escherichia coli, CpxRA senses and responds to envelope

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

276 tumor necrosis factor and adherent-invasive Escherichia coli.

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

278 ylate antibiotic produced by some strains of Escherichia coli.

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

280 ription factor GreA inhibits break repair in Escherichia coli.

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

282 to investigate the thermotactic response of Escherichia coli.

283 naerobic to aerobic growth for the bacterium Escherichia coli.

284 a Proteus mirabilis and Antibiotic resistant Escherichia coli.

285 al species outside Actinobacteria, including Escherichia coli.

286 ngle compact RNA mechanism that functions in Escherichia coli.

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

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

289 he microbiota, characterized by expansion of Escherichia coli.

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

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

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

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

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

295 to an intimin derived from enterohemorrhagic Escherichia coli.

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

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

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

299 ed on 10 adaptively evolved pgi knockouts of Escherichia coliPgi catalyzes the first reaction in glyc

300 Despite its potential importance in Escherichia, Salmonella, Klebsiella, Shigella, and Yersi