ライフサイエンスコーパス: coli

1 (blank broth, Staphylococcus aureus, and E. coli).

2 st 5' to 3' RNA exonuclease identified in E. coli.

3 chors and Z-ring regulators described for E. coli.

4 ibutes to mutagenesis of S (p)-Me-PTEs in E. coli.

5 by which spacer orientation is defined in E. coli.

6 Azotobacter vinelandii NifEN in Escherichia coli.

7 ion-coupled repair in a manner similar to E. coli.

8 or mechanism of translational coupling in E. coli.

9 fecal shedding of ciprofloxacin-resistant E. coli.

10 colonization resistance against Escherichia coli.

11 antibacterial activity against wild-type E. coli.

12 r cell for exponentially growing Escherichia coli.

13 , by recombinantly expressing variants in E. coli.

14 as an alternative receptor when infecting E. coli.

15 cteristic of bacteria other than Escherichia coli.

16 gregated before cell division in Escherichia coli.

17 ycoside bacteriostasis and bactericide in E. coli.

18 cal prevalence of ciprofloxacin-resistant E. coli.

19 ibosome recycling on protein synthesis in E. coli.

20 e knob-into-hole and WT IgG4 molecules in E. coli.

21 the antimicrobial resistance of Escherichia coli.

22 em to treat carbapenem-resistant Escherichia coli.

23 t controls flagellar motility in Escherichia coli.

24 Results indicated the recovery of E. coli 13457 from four MacConkey agar manufacturers was re

25 es protein synthesis by immature Escherichia coli 30S subunits.

26 scopy (cryo-EM) structure of the Escherichia coli 50S subunit at an average resolution of 2.2 angstro

27 samples were frequently contaminated with E. coli (69%), and E. coli levels were the highest during t

28 l and purified the antibody from Escherichia coli after refolding it from inclusion bodies.

29 as nonlytic toxins leave large patches of E. coli alive.

30 ates a multitude of sequence ions for the E. coli ammonia channel (AmtB), provides improved localizat

31 ed with typical enteropathogenic Escherichia coli among children aged 6-11 months was 2.08 (95% CI 1.

32 en 15 diverse species (including Escherichia coli and 12 rhizobia) help identify the barriers that mu

33 a, Schizosaccharomyces pombe and Escherichia coli and how it can be used to study RBP dynamics.

34 , we test 243 candidate tRNAs in Escherichia coli and identify 71 orthogonal tRNAs, covering 16 isoac

35 an fragments (tri-diaminopimelic acid) in E. coli and in C. trachomatis These findings suggest that C

36 A phenotype of Escherichia coli and Klebsiella pneumoniae, resistant to piperacilli

37 treatment of ceftriaxone non-susceptible E. coli and Klebsiella.

38 defines an antifolate stress response in E. coli and links its associated metabolites to a major imm

39 showed increased killing of phagocytosed E. coli and M. smegmatis Polyphosphate inhibited phagosome

40 (including carbapenem-resistant Escherichia coli and methicillin-resistant Staphylococcus aureus).

41 the fatty acid synthase (FAS) of Escherichia coli and paired that model with a fully reconstituted in

42 ions, and chlorhexidine solutions against E. coli and S. aureus.

43 ], zymosan, mannan, and LPS from Escherichia coli and Salmonella as well as to the monosaccharides l-

44 Studies in Escherichia coli and Salmonella enterica showed that such sRNAs are

45 ct an eCRISPR based redox conduit in both E. coli and Salmonella enterica.

46 Our previous work in Escherichia coli and Salmonella identified a mechanism of translatio

47 ng heterologous stimulation with Escherichia coli and Streptococcus pneumoniae.

48 s were produced recombinantly in Escherichia coli and used as antigens in phage display selections us

49 saturation of lipids in Escherichia coli (E. coli) and Acinetobacter baumannii (A. baumannii).

50 vation of Gram-negative Escherichia coli (E. coli) and Gram-positive Enterococcus durans (E. durans)

51 ion zone method against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), which decre

52 DIP) Human, Drosophila, Escherichia coli (E. coli), and Caenorhabditis elegans (C. elegan) datasets.

53 lopment of high-accumulating compounds in E. coli, and a general blueprint for the conversion of Gram

54 asmid was present in K. oxytoca, Escherichia coli, and Enterobacter cloacae isolates from unlinked pa

55 sor surface with polyclonal anti-Escherichia coli antibody allow to obtain high detection sensitivity

56 RC tumorigenesis in an adenomatous polyposis coli (APC(Delta14/+)) mouse model.

57 The adenomatous polyposis coli (APC) tumor suppressor protein is associated with t

58 Adenomatous polyposis coli (APC), a protein with both tumor suppressor and cyt

59 over-proliferation in Adenomatous polyposis coli (APC)-mutated intestine.

60 versely, in a vaginal colonization model, E. coli are detected inside vaginal cells and the urinary t

61 mpounds against efflux-deficient Escherichia coli are mediated by LpxA inhibition.

62 ntification and quantitative detection of E. coli are of great importance for bovine mastitis control

63 illus subtilis and Gram-negative Escherichia coli as model organisms to monitor bacterial concentrati

64 m-positive (S. aureus) and gram-negative (E. coli) bacteria on solid and porous surfaces.

65 The stability of the Escherichia coli beta-clamp, a homodimer, is particularly remarkable

66 now show that Fur purified from Escherichia coli binds an all-Cys-coordinated [2Fe-2S] cluster.

67 es, the M. tuberculosis Tam also replaced E. coli BioC both in vivo and in vitro and complemented bio

68 date genes were overexpressed in Escherichia coli BL21(DE3), refolded, and purified.

69 esults were interpreted according to CLSI E. coli breakpoints, with 49.0 to 85.8% considered suscepti

70 ppressed growth and colonisation by focal E. coli but also prevented it from evolving antibiotic resi

71 ly characterize gene repression in living E. coli by a collection of individual TALED loops with syst

72 enteric pathogen enterotoxigenic Escherichia coli by maternal natural IgG antibodies against the mate

73 Shedding of mcr-1 E. coli by small gull flocks followed a lognormal curve and

74 We apply the approach to Escherichia coli by successively adapting it to defined glucose medi

75 tion of C. difficile vaccine candidate in E. coli by using restricted DO growth.

76 Escherichia coli can carry the pathogenicity island pks, which encod

77 antigen I (CFA/I) fimbriae from Escherichia coli can inhibit autoimmune diseases in murine models by

78 ulating petroleum-polluted sediments with E. coli carrying the vector pSF-OXB15-p450camfusion showed

79 Multidrug-resistance among E.coli causing device- and procedure-related HAIs has incr

80 of any redox indicators, allowed a single E. coli cell detection and from 1 to 4 x 10(4) CFU mL(-1) E

81 starved bacteria as a biological probe of E. coli cell function during nitrogen starvation, we demons

82 phate buffered saline (PBS) and spiked in E. coli cell lysate.

83 membrane lipid cardiolipin accumulate in E. coli cells cultivated at high osmotic pressure.

84 r pSF-OXB15-p450camfusion showed that the E. coli cells died after five days but a variety of bacteri

85 Global N-acetylome profiling of Escherichia coli cells expressing AtNAA50 revealed conservation of N

86 Escherichia coli cells have a reversible rotary motor at the base of

87 ally modified Rosetta-gami B DE3 Escherichia coli cells, facilitating high-yield production.

88 removes the [2Fe-2S] cluster from Fur in E. coli cells, suggesting that Fur senses the intracellular

89 asurements, we find that in live Escherichia coli cells, Zur's unbinding rate from DNA is sensitive t

90 re replaced by alanine is highly toxic to E. coli cells.

91 utant cells and is decreased to ~4% in WT E. coli cells.

92 Phosphorylation of Escherichia coli CheY protein transduces chemoreceptor stimulation t

93 fm), and ciprofloxacin-resistant Escherichia coli (CipREc) colonization.

94 e of transcripts that are Np(4)-capped in E. coli, clear evidence for Np(4) cap acquisition by Np(4)N

95 penem activity against an NDM-1-producing E. coli clinical strain.

96 encoding aggregative adherence fimbriae, E. coli common pilus, flagellin and EAEC heat-stable entero

97 blished examples of multi-strain Escherichia coli communities with increasing complexity: uni-, bi-,

98 In Escherichia coli, conditional lethality of the yggS and glyA (encodi

99 say was performed on Ab-modified MBs, and E. coli could be quantified in tap water and milk.

100 sume 3.6-4.9 log(10) most probable number E. coli/day.

101 Here we show that Escherichia coli DeltabipA cells grown at suboptimal temperature acc

102 E. coli DeltaL YA constitutively co-expressing alpha-L-fuco

103 Escherichia coli DeltaL YA, in which lacZ is deleted and lacY is ret

104 ted that 2,7-anhydro-Neu5Ac catabolism in E. coli depended on YjhC and on the predicted sialic acid t

105 In addition, deletion of TrkA in Escherichia coli depolarizes the cell, suggesting that the TrkH-TrkA

106 f an RNA-guided Cas9 nickase, an Escherichia coli-derived uracil DNA N-glycosylase (eUNG) and a rat A

107 edge, this level of sensitivity for whole E. coli detection is unprecedented in label-free biosensing

108 plied the Stabilized Peptide Evolution by E. coli Display technique to develop disrupters of the ther

109 d how frameshift-inducing stem-loops from E. coli dnaX mRNA and the gag-pol transcript of Human Immun

110 tes of unsaturation of lipids in Escherichia coli (E. coli) and Acinetobacter baumannii (A. baumannii

111 he inactivation of Gram-negative Escherichia coli (E. coli) and Gram-positive Enterococcus durans (E.

112 e inhibition zone method against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), wh

113 entified 711 proteoforms from an Escherichia coli (E. coli) proteome consuming only nanograms of prot

114 Most Escherichia coli (E. coli) strains do not cause disease, naturally l

115 Protein (DIP) Human, Drosophila, Escherichia coli (E. coli), and Caenorhabditis elegans (C. elegan) d

116 Enteroaggregative E. coli (EAEC) are a major cause of diarrhoea worldwide.

117 Enteroaggregative Escherichia coli (EAEC) is an E. coli pathotype associated with diar

118 eginning treatment, cultured for Escherichia coli (EC) and DNA extracted.

119 In enterohemorrhagic Escherichia coli (EHEC) O157:H7, EutR responds to ethanolamine to ac

120 servations were analogous to how Escherichia coli encountering cell stress and nutrient deprivation c

121 s these challenges, we show that Escherichia coli Endonuclease V (eEndoV), an inosine-cleaving enzyme

122 Enterotoxigenic Escherichia coli (ETEC) is a leading diarrheagenic bacterial pathoge

123 tosis, thereby facilitating resolution of E. coli-evoked lung injury.

124 Extraintestinal pathogenic Escherichia coli (ExPEC) is the leading cause in humans of urinary t

125 ch as Neisseria meningitidis and Escherichia coli express acidic capsules.

126 porin (omp)-deficient strain of Escherichia coli expressing heterologous VcChiP could grow on M9 min

127 ent expression of the designed vaccine in E. coli expression system.

128 lex with the elongating KSs from Escherichia coli, FabF and FabB, in order to better understand the s

129 Escherichia coli FadR is a transcription factor regulated by acyl-Co

130 Here, we use the Escherichia coli FAS AT, FabD, and its cognate ACP, AcpP, to interro

131 constrained by a large set of single-cell E. coli flagellar synthesis data from different strains and

132 eta-estradiol (E) for seven days, 50 ng/ml E.coli flagellin (F) for 12 h, or 4 nM 17beta-estradiol pl

133 structure of the BAM complex of Escherichia coli folding BamA itself.

134 died of organisms, the bacterium Escherichia coli, for ~65% of promoters we remain ignorant of their

135 of colistin-resistant commensal Escherichia coli from broiler chickens.

136 ucibility and detection of potential ESBL E. coli from poultry cecal (n = 30) and water (n = 30) samp

137 ence identity, were expressed in Escherichia coli Functional characterization of the purified recombi

138 GEM that has been developed to date: the E. coli GEM.

139 In this work, we express the Escherichia coli gene mreB inside vesicles with bilayers made of lip

140 onarily conserved rare codons in Escherichia coli genes and associated such codons with cotranslation

141 Cytomegalovirus, Escherichia coli, group B Streptococcus, and other infections contri

142 compared to control in both germ-free or E. coli gut microbiota states was used to quantitate pathwa

143 We show that B. subtilis and E. coli gyrases are proficient DNA-stimulated ATPases and e

144 escribe an elegant strategy that Escherichia coli has evolved to minimize metabolic stress that resul

145 stinal bacteria and expressed in Escherichia coli, has become commercially available.

146 d, because MK and DMK are also present in E. coli Here, we established that UQ(9) is the major quinon

147 ent the crystal structure of the Escherichia coli Hfq Core bound to a 30 bp DNA, containing three 6 b

148 es not confer antimicrobial resistance in E. coli, highlighting the importance of verifying protein p

149 t in eukaryotic enzymes but absent in the E. coli homolog.

150 p)-tagged AR plasmid (pRP4-gfp) within an E. coli host (EcoFJ1) in the liquid phase and biofilms in b

151 Our findings implicate the E. coli host 3'-5' exonucleases DnaQ and ExoT in spacer ada

152 P2 OLD-mediated killing of recBC-Escherichia coli hosts, indicating that both the ATPase and nuclease

153 and the Gram-negative bacterium Escherichia coli However, the physiological roles of TCP96 in contro

154 ontributes to gene expression in Escherichia coli In addition, Q8 was proposed to confer bacterial os

155 lence of ciprofloxacin-resistant Escherichia coli in cattle and to determine if removal of invasive b

156 gy to help reduce ciprofloxacin-resistant E. coli in cattle within the United States.

157 the mcr-1 gene was discovered in Escherichia coli in domestic swine in China that conferred resistanc

158 uman FMRP, FXR1P, and FXR2P from Escherichia coli in high yields, free of protein and nucleic acid co

159 K. michiganensis generally outcompeted E. coli in vitro, but in vivo administration of galactitol-

160 e-examined the experimental parameters of E. coli in-cell NMR and found that the detectability and re

161 Acidosis is associated with E. coli induced pyelonephritis but whether bacterial cell w

162 eclinical model of uropathogenic Escherichia coli-induced acute pyelonephritis to determine the contr

163 ted that adenosine or ATPgammaS mitigates E. coli-induced ALI in mice and may be useful as an adjuvan

164 effectiveness of antibiotic treatment in E. coli-induced myositis and a clinically relevant S. aureu

165 ce demonstrated baseline translocation of E. coli into the liver and spleen and were more susceptible

166 Mice were inoculated with live E. coli intratracheally (i.t.) with or without adenosine or

167 Escherichia coli is a pathogen commonly encountered in clinical labo

168 MdfA from Escherichia coli is a prototypical H(+) -dependent multidrug transpo

169 Enterohemorrhagic Escherichia coli is a significant human pathogen that causes disease

170 Escherichia coli is the leading cause of urinary tract infection, on

171 ery responsible for rod shape in Escherichia coli is the processive 'Rod complex'.

172 beta-lactamase (ESBL)-producing Escherichia coli is worrisome.

173 nt in mycobacteria but absent in Escherichia coli, is required for the EsxA:B separation.

174 2S] cluster in Fur protein is ~31% in the E. coli iscA/sufA mutant cells and is decreased to ~4% in W

175 also found that 12.8% of broiler chicken E. coli isolates and 7.61% of layer chicken isolates carrie

176 Up to 48 presumptive Escherichia coli isolates were collected from each stool sample (n =

177 genotypes observed among the investigated E. coli isolates.

178 nt manner has been discovered recently in E. coli Its physiological relevance is not yet understood,

179 c carbon source, pointing to S. elongatus-E. coli K-12 as the most active community.

180 cus elongatus with heterotrophic Escherichia coli K-12, Escherichia coli W, Yarrowia lipolytica, or B

181 wall, and eventually growth inhibition of E. coli K-12.

182 enzymes (almA, xylE, p450cam) in Escherichia coli led to degradation of 60-99% of target hydrocarbon

183 ntly contaminated with E. coli (69%), and E. coli levels were the highest during the wet season.

184 tor-alpha (TNF-alpha), IL-1beta, Escherichia coli lipopolysaccharide (Ec-LPS) and Porphyromonas gingi

185 We studied Escherichia coli LPS in patients with biopsy-proven NAFLD, 25 simple

186 In NAFLD, Escherichia coli LPS may increase liver damage by inducing macrophag

187 arrow-derived dendritic cells compared to E. coli LPS.

188 RNA and is structurally unrelated to the E. coli McrB DNA-binding domain.

189 ographic studies have shown that Escherichia coli McrB uses a base-flipping mechanism to recognize th

190 In the Gram-negative bacterium Escherichia coli, membrane-bound sensor CusS and its response regula

191 determine cryo-EM structures of Escherichia coli MlaFEDB in an apo state and bound to phospholipid,

192 ions of proteomes extracted from Escherichia coli, mouse embryonic fibroblast cell cultures, and Arab

193 ored for C. crescentus MreB over Escherichia coli MreB because of a closer match in the degree of ope

194 nslation initiation step of many Escherichia coli mRNAs, particularly those with weak Shine-Dalgarno

195 Finally, using E. coli mutants and complementation growth assays, we demon

196 Klebsiella pneumoniae (n = 236), Escherichia coli (n = 22), Enterobacter cloacae (n = 23), Klebsiella

197 The genome of Escherichia coli O157:H7 bacteriophage vB_EcoM_CBA120 encodes four d

198 ze new niches, interrogation of sequenced E. coli O157:H7 genomes showed a high level of CycA conserv

199 is imported passively across the Escherichia coli OM through OmpF.

200 a with costained nucleoids and membranes (E. coli) on surfaces with nanopillars.

201 sical bacteriophages that infect Escherichia coli or Salmonella, yet, less is known about the packagi

202 and puncture or bacteremia with Escherichia coli or Streptococcus pneumoniae infection).

203 ion and puncture or infection by Escherichia coli or Streptococcus pneumoniae) and endotoxaemia.

204 ) and outside (extraintestinal pathogenic E. coli, or ExPEC).

205 trating CD45(+) cells in the prostates of E. coli- or phosphate-buffered saline-treated mice.

206 terobacteriaceae (p = 0.002) and Escherichia coli (p = 0.033).

207 aggregative Escherichia coli (EAEC) is an E. coli pathotype associated with diarrhea and growth falte

208 ycan precursors and fragments by Escherichia coli PBP1B, allowing us to (a) identify recognition elem

209 mpounds directly for stimulating Escherichia coli persister cell resuscitation, we identified that 2-

210 viously characterized viruses of Escherichia coli (phages T6, T2, T4, and T7).

211 trand-breaks in purified DNA from Eschericia coli, phosphorothioate epigenetics in Salmonella enteric

212 uggesting a recalcitrant mismatch between E. coli physiology and growth on citrate.

213 n citrate (Cit(+)) evolved in an Escherichia coli population during adaptation to a minimal glucose m

214 The DBeQ-induced loss of E. coli proliferation was exacerbated by heat shock but was

215 pair resolution dissection of more than a E. coli promoters in 12 growth conditions.

216 olonization with curli-producing Escherichia coli promotes alphaSyn pathology in the gut and the brai

217 the discrimination between RNA ligands by E. coli ProQ and Hfq depends both on positive determinants

218 bead' approach, we reconstituted Escherichia coli proteins MsbA and MscS and find that peptidiscs sta

219 Two other E. coli proteins that contain SecA-like MBDs, YecA and YchJ

220 711 proteoforms from an Escherichia coli (E. coli) proteome consuming only nanograms of proteins.

221 s, including the human pathogens Escherichia coli, Pseudomonas aeruginosa, and Vibrio cholerae, and t

222 in-one' vector was functional in Escherichia coli, Pseudomonas syringae and Klebsiella pneumoniae, an

223 ection and from 1 to 4 x 10(4) CFU mL(-1) E. coli quantification.

224 ity on various concentrations of Escherichia coli reaching 10(3) CFU/ml.

225 In this system, an E. coli recording strain is exposed to a microbial sample a

226 t both the efficiency with which Escherichia coli RNA polymerase incorporates dinucleoside polyphosph

227 e seven intermediates containing Escherichia coli RNAP with the transcription factor TraR en route to

228 ate translesion RNA synthesis by Escherichia coli RNAP without altering the fidelity of nucleotide in

229 ach for halting transcription by Escherichia coli RNAP.

230 Instead, serine alters E. coli's 1C-metabolism, reduces the provision of nucleotid

231 he highest antimicrobial activity against E. coli, S. aureus, and S. typhi in in vitro antimicrobial

232 Enterococcus spp., Escherichia coli, Salmonella enterica, Staphylococcus aureus and Str

233 Escherichia coli, Salmonella enteritidis, Listeria innocua, Pseudomo

234 ased chromosome occupancy of the Escherichia coli SMC complex, MukBEF, the chromosome is organized as

235 Colicins are Escherichia coli-specific bacteriocins that translocate across the o

236 ry profile accounted for reduced Escherichia coli-specific responses in aged MAIT cells compared with

237 Here we show that the Escherichia coli SSB protein forms liquid-liquid phase-separated con

238 targeting the O25b O-antigen of Escherichia coli ST131.

239 Shiga-toxigenic Escherichia coli (STEC) infection causes severe bloody diarrhea, ren

240 tbreaks of Shiga toxin-producing Escherichia coli (STEC) were first identified in 1991.

241 at commensal bacteria, including Escherichia coli, stimulated HDAC activity through metabolism of phy

242 When expressed in an Escherichia coli strain deficient in sulfite assimilation, pssm2-Fd

243 TI is often caused by a virulent Escherichia coli strain, whereas recurrent infections and asymptomat

244 was nearly eliminated in a ClpB-deficient E. coli strain, which demonstrates a significant selectivit

245 control strains and (ii) 288 human-source E. coli strains classified by PCR as ExPEC and non-ExPEC.

246 ry of recombinant non-pathogenic Escherichia coli strains was engineered to express seven potential C

247 tibiotic dose-response curves of Escherichia coli strains, and previous observations on antibiotic re

248 not) distinguish UTI- from ASB-associated E. coli strains.

249 pparent for each manufacturer for control E. coli strains.

250 Most Escherichia coli (E. coli) strains do not cause disease, naturally living in

251 ance capacity of K. michiganensis against E. coli, supporting the idea that nutrient competition is t

252 ata show that endogenous DNA gap repair in E coli supports efficient multiplex site-directed mutagene

253 The ATR system is important for E. coli survival in the mouse intestine and for production

254 lus subtilis) and Gram-negative (Escherichia coli) targets.

255 gradients with narrow temperature ranges, E. coli tended to aggregate near a sidewall of the gradient

256 microbial community with three strains of E. coli that cyclically interact through (i) the inhibition

257 By exposing E. coli that do not perform lysis to the DNase colicin, we

258 n derived from enterohemorrhagic Escherichia coli that is tolerant to a wide range of glycoforms.

259 inD is a cell division ATPase in Escherichia coli that oscillates from pole to pole and regulates the

260 s using metabolically engineered Escherichia coli The pretreatment step achieved an almost 100% recov

261 are readily colonized with mcr-1 positive E. coli, their shedding patterns, transmission among conspe

262 tial adaptive response to N starvation in E. coli These results serve as a paradigm to demonstrate th

263 In E. coli, this is mediated by the proteins DsbC and DsbD.

264 bacteria could obtain these vectors from E. coli through several mechanisms of horizontal gene trans

265 We show utilization hierarchy of Escherichia coli to be ordered by the carbon-uptake flux rather than

266 ed species and R1-R2 octamers in Escherichia coli To better understand the distribution of different

267 Curli expression is required for E. coli to exacerbate alphaSyn-induced behavioral deficits,

268 facilitate transmission of mcr-1 positive E. coli to humans and livestock through fecal contamination

269 i have a role in the adaptive response of E. coli to long-term nitrogen starvation.

270 The binding of E. coli to the M13 phage on the cytosensor surface increase

271 nutrient that supports the growth of only E. coli-to bi-colonized gnotobiotic mice abolished the colo

272 ntly characterised a low-activity form of E. coli transketolase, TK(low), which also binds the cofact

273 emonstrates remarkable versatility of the E. coli translational machinery for initiation with ncAAs i

274 xidation-induced abasic sites in DNA from E. coli treated with a sublethal dose of hydrogen peroxide.

275 CGC, and CGA) are decoded by two Escherichia coli tRNA(Arg) isoacceptors.

276 h a heterologous TPS (OtsA) from Escherichia coli, under the control of the TPS1 promoter, and tested

277 d by Gram-negative uropathogenic Escherichia coli (UPEC) or Gram-positive Enterococcus faecalis, we u

278 (rUTIs) linked to uropathogenic Escherichia coli (UPEC).

279 We apply it to the detection of E.Coli using a faster and innovative functionalization met

280 ressed in mammalian cells and in Escherichia coli using in vitro and in vivo methods.

281 which possesses homologs of the Escherichia coli uvrA, uvrB, and uvrC genes, removes cyclobutane pyr

282 irulence genes were added to the existing E. coli VirulenceFinder database.

283 rotrophic Escherichia coli K-12, Escherichia coli W, Yarrowia lipolytica, or Bacillus subtilis.

284 nce of 3G-C and fluoroquinolone-resistant E. coli was 4% and 10%, respectively.

285 Escherichia coli was detected as a model analyte.

286 a were decreased in all 3 studies, whereas E coli was increased in 4 of 9 studies.

287 to in vivo metatranscriptomic data where E. coli was present at high abundances, and found that our

288 nosa, Staphylococcus aureus, and Escherichia coli We have previously demonstrated that sphingosine is

289 ross-links into the cell wall of Escherichia coli, we generated a bacterium where up to 31% of the ce

290 Among Gram-negative bacteria, Escherichia coli were predominant.

291 ngly, we find that in B. subtilis, unlike E. coli where multiple enzymes have a biochemical activity

292 lA potentiated carbapenem efficacy in CRE E. coli, whereas inhibition of the genes flhC and ygaC conf

293 eased sensitivity also to LPS of Escherichia coli, which had no effect in WT mice.

294 In Escherichia coli, which has a type I-E system, Cas1-Cas2 preferentia

295 ice using an engineered genetic circuit in E.coli, which responded to microgravity by changing the ex

296 ves multiplex editing by 5- to 10-fold in E. coli, while PapRecT enables efficient recombineering in

297 tment of beta-lactamase-carrying Escherichia coli with cefotaxime.

298 imentally evolved populations of Escherichia coli with genetically perturbed TMs for 1,000 generation

299 hemical analysis of the purified Escherichia coli YecSC-FliY cysteine/cystine import system.

300 a species are close relatives of Escherichia coli, yet relatively few previously described phages app