ライフサイエンスコーパス: Escherichia coli

1 use model of colonization resistance against Escherichia coli.

2 200 mRNAs per cell for exponentially growing Escherichia coli.

3 mental characteristic of bacteria other than Escherichia coli.

4 ast to be segregated before cell division in Escherichia coli.

5 B Streptococcus, Staphylococcus aureus, and Escherichia coli.

6 l role of ribosome recycling factor (RRF) in Escherichia coli.

7 ions on antibiotic resistance development in Escherichia coli.

8 he transcription of a Fur-controlled gene in Escherichia coli.

9 processing of the 3' end of the 16S rRNA in Escherichia coli.

10 ylanase, Xyl10E, was cloned and expressed in Escherichia coli.

11 as low a level of in vivo mistakes in RNA as Escherichia coli.

12 enomes and functionally characterize them in Escherichia coli.

13 rillum rubrum and Extraintestinal Pathogenic Escherichia coli.

14 l data of DNA polymerase I diffusing in live Escherichia coli.

15 ndCDE from Salmonella enterica and IscS from Escherichia coli.

16 with competing strains of S. Typhimurium and Escherichia coli.

17 d to enhance the antimicrobial resistance of Escherichia coli.

18 with meropenem to treat carbapenem-resistant Escherichia coli.

19 achinery that controls flagellar motility in Escherichia coli.

20 gineering of Azotobacter vinelandii NifEN in Escherichia coli.

21 fA, suppresses protein synthesis by immature Escherichia coli 30S subunits.

22 ectron microscopy (cryo-EM) structure of the Escherichia coli 50S subunit at an average resolution of

23 To better understand how Escherichia coli acclimatizes to nutrient availability,

24 nesis in tobacco correlated with assembly in Escherichia coli advocating use of this bacterium to pre

25 munized camel and purified the antibody from Escherichia coli after refolding it from inclusion bodie

26 interest in the structure and specificity of Escherichia coli AlkB and its homologs, difficulties in

27 oea associated with typical enteropathogenic Escherichia coli among children aged 6-11 months was 2.0

28 usters between 15 diverse species (including Escherichia coli and 12 rhizobia) help identify the barr

29 from cheese rind microbiomes on 2 bacteria (Escherichia coli and a cheese-isolated Pseudomonas psych

30 proposed SEF-AuNI sensors for model bacteria Escherichia coli and Bacillus subtilis can go to 0.5119

31 esent BEs that cause C-to-A transversions in Escherichia coli and C-to-G transversions in mammalian c

32 psis thaliana, Schizosaccharomyces pombe and Escherichia coli and how it can be used to study RBP dyn

33 Using tREX, we test 243 candidate tRNAs in Escherichia coli and identify 71 orthogonal tRNAs, cover

34 Es to induce Cas9-independent deamination in Escherichia coli and in human cells.

35 stinct plasmids in communities consisting of Escherichia coli and Klebsiella pneumoniae once antibiot

36 Enterococcus spp., Escherichia coli and Klebsiella pneumoniae were the comm

37 A phenotype of Escherichia coli and Klebsiella pneumoniae, resistant to

38 zer or Trimo-San) on growth and viability of Escherichia coli and Lactobacillus crispatus.

39 eria strains (including carbapenem-resistant Escherichia coli and methicillin-resistant Staphylococcu

40 nce-specific killing of carbapenem-resistant Escherichia coli and methicillin-resistant Staphylococcu

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

42 rs of the family, the transporters AmtB from Escherichia coli and Rh50 from Nitrosomonas europaea.

43 d BSA [AcBSA], zymosan, mannan, and LPS from Escherichia coli and Salmonella as well as to the monosa

44 The human bacterial pathogens Escherichia coli and Salmonella enterica produce a biofi

45 Studies in Escherichia coli and Salmonella enterica showed that suc

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

47 factors and their target genes in pathogenic Escherichia coli and Salmonella revealed using chromatin

48 gle-cell lag times of populations of starved Escherichia coli and show that population growth after s

49 ines following heterologous stimulation with Escherichia coli and Streptococcus pneumoniae.

50 luble chemical, 1-octanol, were evaluated in Escherichia coli and Synechocystis sp. PCC 6803.

51 wo live bacterial strains: the Gram-negative Escherichia coli and the Gram-positive Bacillus subtilis

52 hese proteins were produced recombinantly in Escherichia coli and used as antigens in phage display s

53 -encoding plasmid was present in K. oxytoca, Escherichia coli, and Enterobacter cloacae isolates from

54 ium tuberculosis, Staphylococcus aureus, and Escherichia coli, and identify thousands of MGEs, includ

55 n of the sensor surface with polyclonal anti-Escherichia coli antibody allow to obtain high detection

56 es of the compounds against efflux-deficient Escherichia coli are mediated by LpxA inhibition.

57 nity peptide probe for "OFF-ON" detection of Escherichia coli as a model endotoxin.

58 positive Bacillus subtilis and Gram-negative Escherichia coli as model organisms to monitor bacterial

59 e (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacterial pathogens as well as with he

60 The stability of the Escherichia coli beta-clamp, a homodimer, is particularl

61 tenot et al. now show that Fur purified from Escherichia coli binds an all-Cys-coordinated [2Fe-2S] c

62 The M. smegmatis Tam functionally replaced Escherichia coli BioC both in vivo and in vitro.

63 Four candidate genes were overexpressed in Escherichia coli BL21(DE3), refolded, and purified.

64 In Escherichia coli, Braun's lipoprotein (Lpp) forms the on

65 demonstrated Gram-negative activity against Escherichia coli BW25113, which is the first reported fo

66 dly, myristoylation efficiency of MA(NOS) in Escherichia coli by co-expressed mammalian NMT was reduc

67 in diameter) in the industrial microorganism Escherichia coli by expressing a set of carboxysome prot

68 on with the enteric pathogen enterotoxigenic Escherichia coli by maternal natural IgG antibodies agai

69 at its depletion attenuates the virulence of Escherichia coli by reducing levels of LPS and outer mem

70 We apply the approach to Escherichia coli by successively adapting it to defined

71 e that coordination is indirect, mediated in Escherichia coli by the alarmone (p)ppGpp.

72 Escherichia coli can carry the pathogenicity island pks,

73 ation factor antigen I (CFA/I) fimbriae from Escherichia coli can inhibit autoimmune diseases in muri

74 Escherichia coli can utilize citrate under anaerobic con

75 Mutant Escherichia coli carrying this mutation are viable and h

76 is class include M.EcoGII and M.EcoP15I from Escherichia coli, Caulobacter crescentus cell cycle-regu

77 Global N-acetylome profiling of Escherichia coli cells expressing AtNAA50 revealed conse

78 cally active recombinant hGFAT2 (rhGFAT2) in Escherichia coli cells fused or not to a HisTag at the C

79 Escherichia coli cells have a reversible rotary motor at

80 m of genetically modified Rosetta-gami B DE3 Escherichia coli cells, facilitating high-yield producti

81 ngle-cell measurements, we find that in live Escherichia coli cells, Zur's unbinding rate from DNA is

82 how these lesions impact DNA replication in Escherichia coli cells.

83 We examine two novel members of the Escherichia coli chaperone holdase family, RidA and CnoX

84 Phosphorylation of Escherichia coli CheY protein transduces chemoreceptor s

85 m (VREfc/VREfm), and ciprofloxacin-resistant Escherichia coli (CipREc) colonization.

86 and regulation, primarily for the human and Escherichia coli class Ia enzymes.

87 microscopy (cryo-EM) structures of an intact Escherichia coli class-II CAP-dependent transcription ac

88 ined high-resolution structures of wild-type Escherichia coli ClpAP undergoing active substrate unfol

89 to three published examples of multi-strain Escherichia coli communities with increasing complexity:

90 In Escherichia coli, conditional lethality of the yggS and

91 Enteropathogenic and enterohemorrhagic Escherichia coli contain a well-defined T3SS but in addi

92 he remaining microimplants were incubated in Escherichia coli culture.

93 'gold-standard' is represented by infecting Escherichia coli cultures, followed by precipitation wit

94 Here we show that Escherichia coli DeltabipA cells grown at suboptimal tem

95 Escherichia coli DeltaL YA, in which lacZ is deleted and

96 gulation of gene expression by small RNAs in Escherichia coli depends on RNA binding proteins Hfq and

97 In addition, deletion of TrkA in Escherichia coli depolarizes the cell, suggesting that t

98 , consists of an RNA-guided Cas9 nickase, an Escherichia coli-derived uracil DNA N-glycosylase (eUNG)

99 Here, we show that Pal accumulation at Escherichia coli division sites is a consequence of thre

100 hering of a protein of interest (POI) to the Escherichia coli DNA adenine methyltransferase (Dam).

101 entapeptide motif toward the beta subunit of Escherichia coli DNA polymerase III holoenzyme by mutati

102 Several functions have been proposed for the Escherichia coli DNA polymerase IV (pol IV).

103 We present the NMR solution structure for Escherichia coli DolP, which is composed of two BON doma

104 and DNA gap repair typically involve growing Escherichia coli (E coli) containing plasmids, followed

105 ofiles of sites of unsaturation of lipids in Escherichia coli (E. coli) and Acinetobacter baumannii (

106 vestigated the inactivation of Gram-negative Escherichia coli (E. coli) and Gram-positive Enterococcu

107 sed using the inhibition zone method against Escherichia coli (E. coli) and Staphylococcus aureus (S.

108 an in vivo assessment platform comprised of Escherichia coli (E. coli) and transgenic zebrafish embr

109 demonstrate rapid, sensitive and label-free Escherichia coli (E. coli) detection utilizing interfero

110 IEF-MS/MS identified 711 proteoforms from an Escherichia coli (E. coli) proteome consuming only nanog

111 Most Escherichia coli (E. coli) strains do not cause disease,

112 Escherichia coli (E. coli) was engineered to catalyse th

113 Interacting Protein (DIP) Human, Drosophila, Escherichia coli (E. coli), and Caenorhabditis elegans (

114 xides that in the dark inactivate planktonic Escherichia coli (E. coli).

115 modelling (FBA, pFBA, FVA and MOMA) and the Escherichia coli (E.coli) core stoichiometric model to i

116 Enteroaggregative Escherichia coli (EAEC) is an E. coli pathotype associat

117 ith the diarrheal pathogen enteroaggregative Escherichia coli (EAEC) is associated with growth falter

118 days after beginning treatment, cultured for Escherichia coli (EC) and DNA extracted.

119 otypic multidrug (Mdr) transporter MdfA from Escherichia coli efflux chemically- dissimilar substrate

120 In enterohemorrhagic Escherichia coli (EHEC) O157:H7, EutR responds to ethano

121 These observations were analogous to how Escherichia coli encountering cell stress and nutrient d

122 To address these challenges, we show that Escherichia coli Endonuclease V (eEndoV), an inosine-cle

123 Diarrheagenic Escherichia coli (enteroaggretative, enteropathogenic),

124 d analysis of the three most common species, Escherichia coli, Enterococcus faecalis and Bacteroides

125 Enterotoxigenic Escherichia coli (ETEC) cause acute secretory diarrhoea

126 Enterotoxigenic Escherichia coli (ETEC) is a leading diarrheagenic bacte

127 Recent efforts to develop an enterotoxigenic Escherichia coli (ETEC) vaccine have focused on the anti

128 Extraintestinal pathogenic Escherichia coli (ExPEC) is the leading cause in humans

129 pathogens such as Neisseria meningitidis and Escherichia coli express acidic capsules.

130 ter-membrane porin (omp)-deficient strain of Escherichia coli expressing heterologous VcChiP could gr

131 Unexpectedly, strains of Escherichia coli expressing this artificial protein spec

132 ACPs in complex with the elongating KSs from Escherichia coli, FabF and FabB, in order to better unde

133 Escherichia coli FadR is a transcription factor regulate

134 Here, we use the Escherichia coli FAS AT, FabD, and its cognate ACP, AcpP

135 Here we show that damage-induced Escherichia coli filaments divide asymmetrically, produc

136 prisingly, recent single-cell experiments in Escherichia coli flagellar synthesis showed that flagell

137 e report the structure of the BAM complex of Escherichia coli folding BamA itself.

138 ost well-studied of organisms, the bacterium Escherichia coli, for ~65% of promoters we remain ignora

139 ic diversity of colistin-resistant commensal Escherichia coli from broiler chickens.

140 no acid sequence identity, were expressed in Escherichia coli Functional characterization of the puri

141 Purified prodigiosin and ShlA from Escherichia coli further supported the role of these fac

142 In this work, we express the Escherichia coli gene mreB inside vesicles with bilayers

143 fied evolutionarily conserved rare codons in Escherichia coli genes and associated such codons with c

144 aureus, 456 Pseudomonas aeruginosa, and 1588 Escherichia coli genomes.

145 Cytomegalovirus, Escherichia coli, group B Streptococcus, and other infec

146 , DNA-wrapping domain of the GyrA subunit of Escherichia coli gyrase (the 'CTD').

147 he authors describe an elegant strategy that Escherichia coli has evolved to minimize metabolic stres

148 ol-Pal components to the cytokinetic ring in Escherichia coli has led to the proposal that the primar

149 ed from intestinal bacteria and expressed in Escherichia coli, has become commercially available.

150 ble for recycling peptidoglycan fragments in Escherichia coli, has not been annotated for most intrac

151 ere, we present the crystal structure of the Escherichia coli Hfq Core bound to a 30 bp DNA, containi

152 ine that the high-persister mutant strain of Escherichia coli, HipQ, is associated with the phenotype

153 itro impair P2 OLD-mediated killing of recBC-Escherichia coli hosts, indicating that both the ATPase

154 haride (LPS) and the Gram-negative bacterium Escherichia coli However, the physiological roles of TCP

155 microfluidic device to study thermotaxis of Escherichia coli in a broad range of thermal gradients w

156 tress, and contributes to gene expression in Escherichia coli In addition, Q8 was proposed to confer

157 th the prevalence of ciprofloxacin-resistant Escherichia coli in cattle and to determine if removal o

158 In 2015, the mcr-1 gene was discovered in Escherichia coli in domestic swine in China that conferr

159 ull-length human FMRP, FXR1P, and FXR2P from Escherichia coli in high yields, free of protein and nuc

160 Overexpression of BPSS2242 in Escherichia coli increased bacterial survival upon expos

161 We used a preclinical model of uropathogenic Escherichia coli-induced acute pyelonephritis to determi

162 Escherichia coli is a pathogen commonly encountered in c

163 MdfA from Escherichia coli is a prototypical H(+) -dependent multi

164 Enterohemorrhagic Escherichia coli is a significant human pathogen that ca

165 Escherichia coli is an important model organism in micro

166 factor of human pathogenic enterohemorrhagic Escherichia coli is Shiga toxin (Stx).

167 Escherichia coli is the leading cause of urinary tract i

168 hesis machinery responsible for rod shape in Escherichia coli is the processive 'Rod complex'.

169 ded-spectrum beta-lactamase (ESBL)-producing Escherichia coli is worrisome.

170 hat is present in mycobacteria but absent in Escherichia coli, is required for the EsxA:B separation.

171 ned priority AMR phenotypes and genotypes of Escherichia coli isolated from the gastrointestinal trac

172 Up to 48 presumptive Escherichia coli isolates were collected from each stool

173 ached the genome-scale in the widely studied Escherichia coli K-12 MG1655 strain.

174 g Synechococcus elongatus with heterotrophic Escherichia coli K-12, Escherichia coli W, Yarrowia lipo

175 zed 48 RIBO-Seq samples from nine studies of Escherichia coli K12 grown in lysogeny broth medium and

176 odification genes in model organisms such as Escherichia coli K12.

177 reference for transcriptional regulation in Escherichia coli K12.

178 mon alkylating agents to growing cultures of Escherichia coli leads to the accumulation of several ad

179 ssing three enzymes (almA, xylE, p450cam) in Escherichia coli led to degradation of 60-99% of target

180 necrosis factor-alpha (TNF-alpha), IL-1beta, Escherichia coli lipopolysaccharide (Ec-LPS) and Porphyr

181 vitro antimicrobial activity of CAR against Escherichia coli, Listeria monocytogenes, Salmonella ent

182 We studied Escherichia coli LPS in patients with biopsy-proven NAFL

183 In NAFLD, Escherichia coli LPS may increase liver damage by induci

184 ous crystallographic studies have shown that Escherichia coli McrB uses a base-flipping mechanism to

185 In the Gram-negative bacterium Escherichia coli, membrane-bound sensor CusS and its res

186 Injection of non-uropathogenic Escherichia coli (MG1655 strain) or phosphate-buffered s

187 Here we determine cryo-EM structures of Escherichia coli MlaFEDB in an apo state and bound to ph

188 ution digestions of proteomes extracted from Escherichia coli, mouse embryonic fibroblast cell cultur

189 ction is favored for C. crescentus MreB over Escherichia coli MreB because of a closer match in the d

190 s in the translation initiation step of many Escherichia coli mRNAs, particularly those with weak Shi

191 -R assay in Klebsiella pneumoniae (n = 236), Escherichia coli (n = 22), Enterobacter cloacae (n = 23)

192 o difference in the prevalence of pathogenic Escherichia coli, norovirus, or Giardia genes in the dom

193 ct substrate is especially difficult for the Escherichia coli Nudix hydrolase RppH, which triggers 5'

194 The genome of Escherichia coli O157:H7 bacteriophage vB_EcoM_CBA120 en

195 aT2 toxin from a toxin-antitoxin system from Escherichia coli O157:H7.

196 iocin ColE9 is imported passively across the Escherichia coli OM through OmpF.

197 , breakpoints have been established only for Escherichia coli or Enterobacterales per the Clinical an

198 ally in classical bacteriophages that infect Escherichia coli or Salmonella, yet, less is known about

199 cal ligation and puncture or bacteremia with Escherichia coli or Streptococcus pneumoniae infection).

200 caecal ligation and puncture or infection by Escherichia coli or Streptococcus pneumoniae) and endoto

201 The Escherichia coli outer membrane receptor FepA transports

202 he family Enterobacteriaceae (p = 0.002) and Escherichia coli (p = 0.033).

203 ve peptidoglycan precursors and fragments by Escherichia coli PBP1B, allowing us to (a) identify reco

204 19)F-(19)F nuclear Overhauser effects in the Escherichia coli peptidyl-prolyl cis/trans-isomerase B f

205 erminal domain is toxic when targeted to the Escherichia coli periplasm and that it depolarizes the c

206 r, we made the surprising discovery that the Escherichia coli periplasmic glycerol-3-phosphate (G3P)-

207 ng 10,000 compounds directly for stimulating Escherichia coli persister cell resuscitation, we identi

208 characterize host dependencies of two novel Escherichia coli phages, the T1-like siphophage LL5 and

209 tors for previously characterized viruses of Escherichia coli (phages T6, T2, T4, and T7).

210 Escherichia coli/pMTLacZ containing the tetracycline-med

211 bic growth on citrate (Cit(+)) evolved in an Escherichia coli population during adaptation to a minim

212 he "escape time" required for drug-resistant Escherichia coli populations to eclipse a threshold dens

213 eveal that colonization with curli-producing Escherichia coli promotes alphaSyn pathology in the gut

214 Here, we identify the uncharacterized Escherichia coli protein YcaQ as an ICL repair glycosyla

215 ntional 'on-bead' approach, we reconstituted Escherichia coli proteins MsbA and MscS and find that pe

216 ive organisms, including the human pathogens Escherichia coli, Pseudomonas aeruginosa, and Vibrio cho

217 erable 'all-in-one' vector was functional in Escherichia coli, Pseudomonas syringae and Klebsiella pn

218 AAE genes, expressed them heterologously in Escherichia coli, purified the corresponding recombinant

219 ion sensitivity on various concentrations of Escherichia coli reaching 10(3) CFU/ml.

220 ositive blood cultures for P. aeruginosa and Escherichia coli, respectively.

221 tein HU and on the ParB partition protein in Escherichia coli, revealing partially reversible dissoci

222 The synthetic capability of the Escherichia coli ribosome has attracted efforts to repur

223 ilarly affect both the efficiency with which Escherichia coli RNA polymerase incorporates dinucleosid

224 to visualize seven intermediates containing Escherichia coli RNAP with the transcription factor TraR

225 , can stimulate translesion RNA synthesis by Escherichia coli RNAP without altering the fidelity of n

226 emical approach for halting transcription by Escherichia coli RNAP.

227 OPEX-guided exploration of Escherichia coli's populations exposed to biocide and an

228 Enterococcus spp., Escherichia coli, Salmonella enterica, Staphylococcus au

229 Escherichia coli, Salmonella enteritidis, Listeria innoc

230 one due to neutropenic sepsis and one due to Escherichia coli sepsis), each in the setting of progres

231 In Escherichia coli, septal PG synthesis and cell constrict

232 Escherichia coli serogroups O157, O26, O45, O103, O111,

233 ons of increased chromosome occupancy of the Escherichia coli SMC complex, MukBEF, the chromosome is

234 Colicins are Escherichia coli-specific bacteriocins that translocate

235 l inflammatory profile accounted for reduced Escherichia coli-specific responses in aged MAIT cells c

236 Here we show that the Escherichia coli SSB protein forms liquid-liquid phase-s

237 scent domains are inserted within the IDL of Escherichia coli SSB.

238 tibody (mAb) targeting the O25b O-antigen of Escherichia coli ST131.

239 Shiga-toxigenic Escherichia coli (STEC) infection causes severe bloody d

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

241 e finding that commensal bacteria, including Escherichia coli, stimulated HDAC activity through metab

242 When expressed in an Escherichia coli strain deficient in sulfite assimilatio

243 Here we introduce an Escherichia coli strain that forms small minicells posse

244 rowth of the C. elegans dynamin mutant on an Escherichia coli strain with low vitamin B12 also strong

245 of febrile UTI is often caused by a virulent Escherichia coli strain, whereas recurrent infections an

246 e double-stranded DNA phages using two model Escherichia coli strains (K-12 and BL21) with known sequ

247 in vivo k (cat)s using metabolic specialist Escherichia coli strains that resulted from gene knockou

248 A library of recombinant non-pathogenic Escherichia coli strains was engineered to express seven

249 ation-enabled large-scale experiment wherein Escherichia coli strains were evolved in parallel after

250 rmine the antibiotic dose-response curves of Escherichia coli strains, and previous observations on a

251 Cross-feeding Escherichia coli strains, where one strain feeds on a ca

252 t of adhesive type 1 pili from uropathogenic Escherichia coli strains.

253 sate consisting of heat-killed Gram-negative Escherichia coli Symbio and Gram-positive Enterococcus f

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

255 fitness effects of missense mutations in the Escherichia coli TEM-1 beta-lactamase antibiotic resista

256 a high-flux diffusive pathway for PL flow in Escherichia coli that is modulated by YhdP.

257 n-mucin stain derived from enterohemorrhagic Escherichia coli that is tolerant to a wide range of gly

258 MinD is a cell division ATPase in Escherichia coli that oscillates from pole to pole and r

259 It has been proposed that in Escherichia coli the component of cytochrome bd-I termin

260 ve bioprocess using metabolically engineered Escherichia coli The pretreatment step achieved an almos

261 In Escherichia coli, the CTT contains a structurally flexib

262 scharging is not known to occur in bacteria, Escherichia coli ThrRS also possesses robust cross-editi

263 Thymineless death in Escherichia coli thyA mutants growing in the absence of

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

265 n most studied species and R1-R2 octamers in Escherichia coli To better understand the distribution o

266 The attractant chemotaxis response of Escherichia coli to norepinephrine requires that it be c

267 d a two-color fluorescence reporter assay in Escherichia coli to overcome this problem.

268 By performing SEER in Escherichia coli to screen hundreds of putative SSAPs, w

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

270 ts of transcript, protein and flux levels of Escherichia coli under various growth conditions as well

271 TPS1 and with a heterologous TPS (OtsA) from Escherichia coli, under the control of the TPS1 promoter

272 es are caused by Gram-negative uropathogenic Escherichia coli (UPEC) or Gram-positive Enterococcus fa

273 remove established biofilms of uropathogenic Escherichia coli (UPEC), Pseudomonas aeruginosa, and Sta

274 t infections (rUTIs) linked to uropathogenic Escherichia coli (UPEC).

275 protein expressed in mammalian cells and in Escherichia coli using in vitro and in vivo methods.

276 The Escherichia coli Uup and RadD proteins function in diffe

277 . smegmatis, which possesses homologs of the Escherichia coli uvrA, uvrB, and uvrC genes, removes cyc

278 us with heterotrophic Escherichia coli K-12, Escherichia coli W, Yarrowia lipolytica, or Bacillus sub

279 Translocation of Escherichia coli was associated with the formation of co

280 Escherichia coli was detected as a model analyte.

281 charide synthesis, as has been suggested for Escherichia coli We find that ftsH interacts with divers

282 monas aeruginosa, Staphylococcus aureus, and Escherichia coli We have previously demonstrated that sp

283 genotypes in three distinct mRNA contexts in Escherichia coli We uncovered generic principles governi

284 tribution of the FinO-domain ProQ protein in Escherichia coli, we carried out RIL-seq to identify RNA

285 -canonical cross-links into the cell wall of Escherichia coli, we generated a bacterium where up to 3

286 tive guidelines for compound accumulation in Escherichia coli, we have converted the antibiotic Riboc

287 rary of the bla(ampC) beta-lactamase gene of Escherichia coli, we identified mutations that allow gro

288 monitoring of gene-copy-number mutations in Escherichia coli, we show that gene duplications and amp

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

290 By contrast, (ATP-dependent) PfkA of Escherichia coli, which does rely on transaldolase, had

291 veal an increased sensitivity also to LPS of Escherichia coli, which had no effect in WT mice.

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

293 ted, arsH1 and arsH2 genes were expressed in Escherichia coli, which has an endogenous arsRBC operon

294 into a Flux Balance Analysis (FBA) model of Escherichia coli, which quantitatively revealed potentia

295 anslocation of a gut-resident human pathogen Escherichia coli, which spreads systemically and caused

296 by the treatment of beta-lactamase-carrying Escherichia coli with cefotaxime.

297 We experimentally evolved populations of Escherichia coli with genetically perturbed TMs for 1,00

298 from a biochemical analysis of the purified Escherichia coli YecSC-FliY cysteine/cystine import syst

299 tive Shigella species are close relatives of Escherichia coli, yet relatively few previously describe

300 some profiling analysis of phage T4-infected Escherichia coli yielded protected mRNA fragments within