ライフサイエンスコーパス: E. coli

1 E. coli ACPS is sufficiently different from the human fa

2 E. coli cells grown in rich medium that contained all am

3 E. coli grew from 56% (145/259) of the positive urine cu

4 E. coli infection stimulated proliferation of granulopoi

5 E. coli is a common human pathogen, but also a commensal

6 E. coli O157:H7 is an enterohemorrhagic bacteria respons

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

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

9 .coli O157:H7), a dangerous strain among 225 E. coli unique serotypes.

10 Of the 649 E. coli clinical isolates, 5 (0.8%) consistently produce

11 Both enzymes acylated E. coli lipid A, whereas only LpxL2 mediated K. pneumoni

12 e enterococci, fewer environmentally adapted E. coli strains were isolated on selective media contain

13 iability and growth; and (6) ethanol-adapted E. coli cells restore the majority of these reduced acti

14 of both ethanol-stressed and ethanol-adapted E. coli cells with computationally predicated ethanol-bi

15 than 73% against B. subtilis and 67% against E. coli as compared with that of control PVDF, while age

16 er zerumbone showed highest activity against E. coli, whereas its derivatives were least effective ag

17 in burn patients was more effective against E. coli than E. faecalis.

18 its derivatives were least effective against E. coli.

19 ills decreased disinfection efficacy against E. coli on heavy-duty tarp but does prevent splashing, w

20 MAIT cell effector responses against E. coli and C. albicans displayed differential MR1 depen

21 An E. coli expression system offers a mean for rapid, high

22 reduction in tetracycline accumulation in an E. coli strain expressing the tetracycline-specific effl

23 ue peptides were identified from 50 ng of an E. coli digest, and 2158 protein groups and 10005 peptid

24 he typical absence within STc648 of uidA, an E. coli-specific gene encoding beta-glucuronidase.

25 S. aureus and E. coli antigens were detected in immune-blotted HDM ext

26 HDM allergen molecules and to S. aureus and E. coli by IgE immunoblotting.

27 itol, with selective uptake in S. aureus and E. coli; and sorbitol, accumulating only in E. coli None

28 of serum-coated or -uncoated latex beads and E. coli However, consistent with previous studies, brefe

29 ed the abundance of FIB (Total coliforms and E. coli) and the Bacteroidales (HF183 marker) with bacte

30 of functional traits in N. meningitidis and E. coli Our study indicates that the expression of NMB04

31 samples in seven of 15 (46.7%) patients, and E. coli was found in both samples in three of 15 (20%) p

32 Eases tend to target modified DNA sites, and E. coli Mrr activity was previously shown to be elicited

33 In TDE and E. coli expressing MOSP with a PelB signal sequence (Pel

34 In compounds with vs without animals, E. coli was higher by 0.54 log10 in soil, 0.40 log10 in

35 anocomposite platform was modified with anti-E. coli O157:H7 monoclonal antibody.

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

37 In model bacteria, such as E. coli and B. subtilis, regulation of cell-cycle progre

38 that in the absence of chemical attractants E. coli exhibits a steady thermophilic response, the mag

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

40 0.6 J cm(-2) ) toward Gram-negative bacteria E. coli, making it a remarkably efficient optically medi

41 ugh activation by the Gram-negative bacteria E. coli, results in reduced NET production in FlnA-deple

42 impedimetric sensing of pathogenic bacteria E. coli O78:K80:H11.

43 two tractable genetic models, the bacterium E. coli and the nematode C. elegans, we performed three-

44 T4 in suppressing a model enteric bacterium (E. coli K-12) in mixtures with soil bacteria (Pseudomona

45 no acids using the transmembrane beta-barrel E. coli PagP as a scaffold protein.

46 ork identifies important differences between E. coli strains that cause persistent and transient mamm

47 expedite this method, we used bioluminescent E. coli in a simplified checkerboard assay to generate u

48 n rapidly and selectively differentiate both E. coli and S. aureus infections from sterile inflammati

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

50 In both E. coli and M. tuberculosis we find that four-gene LRCs

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

52 sm for substrate engagement and catalysis by E. coli Lnt.

53 ating even the most serious of infections by E. coli "superbugs".

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

55 Chaperonin and cochaperonin, represented by E. coli GroEL and GroES, are essential molecular chapero

56 s are a class of cell-surface factor used by E. coli for adherence.

57 oach for de novo sequencing using whole cell E. coli lysate.

58 usceptibility of metabolically active cells (E. coli, B. subtilis, Enterococcus, P. aeruginosa and Sa

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

60 In this coculture, E. coli and R. palustris resemble an anaerobic food web

61 branes were tested against Escherichia coli (E. coli) and Bacillus subtilis (B. subtilis) by bacteria

62 l indicator bacteria (FIB) Escherichia coli (E. coli) and Enterococcus spp. were enumerated using cul

63 connected network motifs, Escherichia coli (E. coli) appears to favor crosstalk wherein at least one

64 -derived systemic neonatal Escherichia coli (E. coli) K1 infection.

65 cus aureus (S. aureus) and Escherichia coli (E. coli) species are abundant bacteria within the HDM mi

66 loped for the detection of Escherichia coli (E. coli) using the T7 bacteriophages engineered with lac

67 n in aerobically respiring Escherichia coli (E. coli).

68 ns with each other and with total coliforms, E. coli, enterococci, and biochemical oxygen demand (Ken

69 Using a DeltasdhE E. coli strain, we show that the requirement for the ass

70 tudies demonstrated that sialidase-dependent E. coli growth on mucin is enabled by Bacteroides EstA,

71 Subsequently, utilizing the RF1-depleted E. coli strain C321.DeltaA, we could produce mammalian s

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

73 he prepared sensor has the ability to detect E. coli with a recovery of 81-97% in e.g. river water.

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

75 ognition and statistical tools, to determine E. coli susceptibility within a few minutes to different

76 high selectivity and was able to distinguish E. coli when present together with competing bacterial s

77 adaptive responses by attaching and effacing E. coli.

78 interspecies competition and PEf1 eliminated E. coli faster than T4 (36 vs 42 h).

79 Indeed, Ccp enabled E. coli to grow on a nonfermentable carbon source when H

80 ELS-stimulated folding, using the endogenous E. coli metalloprotease PepQ.

81 n yield between three genetically engineered E. coli strains was successfully evaluated using SERS an

82 veral pathogens, including enterohemorrhagic E. coli The mechanisms that allow pathogens to target th

83 gregative Escherichia coli, enteropathogenic E. coli, and enterotoxigenic E. coli), 137 (94.5%) follo

84 f phenotypic variability in enteropathogenic E. coli (EPEC), an important human pathogen, both in vir

85 een norovirus GII + typical enteropathogenic E. coli (OR = 0.09, 95% CI: 0.01, 0.95).

86 nteropathogenic E. coli, and enterotoxigenic E. coli), 137 (94.5%) follow-up tests and 101 (95.3%) pa

87 We applied this strategy to two essential E. coli enzymes: the branched-chain aminotransferase BCA

88 s with alkynyl side chains display excellent E. coli DNA topoisomerase I inhibition properties with I

89 e developed methodology was then applied for E. coli quantification in water samples using nanomateri

90 ed the minimum inhibitory concentrations for E. coli under acidic conditions.

91 and three real growth phenotype datasets for E. coli, proteobacteria and yeast.

92 ave important physiological implications for E. coli and significantly expand the self-regulating cap

93 Same detection limit for E. coli was achieved for real sample analysis with a lit

94 hought to be a major source of nutrients for E. coli in the gut.

95 s first demonstrated for a community of four E. coli double auxotrophic mutants and is then applied t

96 or the labelling of the tagged amplicon from E. coli and Salmonella.

97 Highly purified minicells derived from E. coli strains containing gene circuits for biosensing

98 ormed between sigma(70) RNAP holoenzyme from E. coli and the T7A1 promoter, as well as to observe the

99 Finally, a homologue of lymphostatin from E. coli O157:H7 (ToxB; L7095) was also found to possess

100 In summary, the GCSF-Fc purified from E. coli was not as efficient as PEG-GCSF in treating neu

101 and optimisation of HBc particle yield from E. coli is required to improve laboratory-scale producti

102 etic features of bla KPC emergence in global E. coli, 2008-2013, using both long- and short-read whol

103 mples are incubated with beta-glucuronidase (E. coli K12) and then analyzed by liquid chromatography-

104 e food contaminant Escherichia coli O157:H7 (E. coli O157:H7) in complex food products due to the rec

105 5 gal, and 2 gal filters, respectively, had E. coli concentrations of <1 colony-forming unit/100 mL.

106 However, disease-associated hybrid E. coli, containing unique combinations of multiple cano

107 n microbiology, were mostly able to identify E. coli and negative cultures.

108 In E. coli, activity of AasC was sensitive to triacsin C an

109 In E. coli, the lipid II transporter candidate FtsW is thou

110 Importantly, this fusion is active in E. coli live-cell protein synthesis allowing peptidyl tr

111 e glutamate is the major monovalent anion in E. coli, these results suggest that SSB likely binds to

112 gene (oxyBAC) present in this gene array in E. coli resulted in formation of BDMA from BACs at a rat

113 n synthesis although this is not the case in E. coli.

114 Moreover, the accumulation of Cd in E. coli (147 +/- 25 mg/L) at 1 h of exposure to 25 mg/L

115 a typhimurium InvA gene sequences (cloned in E. coli and after 30-cycle PCR) with SYBR((R)) Green I f

116 and Phe, respectively) but not conserved in E. coli OtsA (His, Leu, and Asp, respectively), providin

117 1295 treatment reduced plasma LPS content in E. coli-challenged baboons, implying reduced complement-

118 Phosphorus depletion in E. coli after reaction with AMZ, together with evidence

119 strand mismatches occurs bi-directionally in E. coli and that, while all MutS-recognized mismatches h

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

121 allysine precursor is genetically encoded in E. coli.

122 te favorable properties as potential EPIs in E. coli cells including the ability to penetrate the out

123 show that the CopA chaperone is expressed in E. coli from the same gene that encodes the transporter.

124 drolysis activity of an amidase expressed in E. coli with three different substrates.

125 ded a 64.9 kDa protein that was expressed in E. coli, and purified with Ni-NTA agarose affinity chrom

126 man protein fragments have been expressed in E. coli.

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

128 play a significant role in motor function in E. coli.

129 rexpressing Escherichia coli pxpABC genes in E. coli increased 5-oxoprolinase activity in lysates >/=

130 e orthogonal and highly inducible by 3-HP in E. coli (12.3- and 23.3-fold, respectively) and Cupriavi

131 igated proteome-wide protein interactions in E. coli and HeLa cell lysates, respectively, identifying

132 Predictive cysteine cross-linking in E. coli membranes and PELDOR measurements along the tran

133 acts with palmitoleic acid, a major lipid in E. coli Last, in Salmonella enterica, ubiK was required

134 enzymatic lysine acetylation modification in E. coli.

135 Zinc ribbon motifs in E. coli TopoI-CTD are involved in the interaction with R

136 E. coli; and sorbitol, accumulating only in E. coli None accumulated in mammalian cells or heat-kill

137 the entire T. denticola LicCA-Cpt pathway in E. coli resulted in phosphatidylcholine biosynthesis.

138 AMPs induce membrane permeability in E. coli spheroplasts or giant unilamellar vesicles (GUVs

139 e various oxidative stress combat players in E. coli, ubiquinone acts as the cell's first line of def

140 port-related, folding pathway not present in E. coli.

141 sylated RSV G protein ectodomain produced in E. coli (in presence and absence of oil-in-water adjuvan

142 vacuolar SlCAT2 was cloned, over-produced in E. coli and reconstituted in proteoliposomes.

143 of macrocyclic peptide libraries produced in E. coli cells.

144 In this study, RAC and PAC were produced in E. coli, and chromatographically purified, then chemical

145 hlorinated coumarin "non-natural" product in E. coli.

146 -selective photo-cross-linking reactivity in E. coli when placed at an appropriate site at the protei

147 tant component of robust shape regulation in E. coli.

148 eved a minimum of 5.9 and 3.1 log removal in E. coli and Phi6, respectively.

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

150 co-expression of CP and the RNAi scaffold in E. coli.

151 proposed that in fact the majority of TCR in E. coli is catalyzed by a second pathway ("backtracking-

152 e that UvrD and ppGpp play no role in TCR in E. coli.

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

154 6-R254I, respectively, and expressed them in E. coli.

155 ous proteins interacting with thioredoxin in E. coli cells, allowing for mass spectrometric identific

156 systems support conjugative DNA transfer in E. coli and trigger P. aeruginosa T6SS killing, but not

157 te colicin sensitivity and iron transport in E. coli Numerous sRNA interactions were also identified

158 tracer of LPS biosynthesis and transport in E. coli We propose that our findings will be helpful for

159 casei, Lactobacillus johnsonii and increased E. coli.

160 ota, which leads to overgrowth of indigenous E. coli and facilitates colonization by opportunistic pa

161 T4 was more effective than PEf1 in infecting E. coli K-12 in pure cultures, PEf1 was 20-fold more eff

162 the wca operon caused a persistent-infection E. coli strain to become sensitive to complement-mediate

163 ophages killed Escherichia coli and ingested E. coli BioParticles better.

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

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

166 C D-amino acids for their incorporation into E. coli in culture, we identified D-methionine as a prob

167 The first is E. coli PI-7, a virulent and antibiotic-resistant strain

168 sults show that chicken cathelicidin-2 kills E. coli by permeabilizing the bacterial inner membrane a

169 d invasion compared to strains lacking known E. coli virulence factors.

170 Amongst 43/45 successfully sequenced bla KPC-E. coli strains, we identified substantial strain divers

171 sbA increases the colistin MIC of laboratory E. coli.

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

173 rsion of the polycation was observed to make E. coli cells more susceptible to other quaternary ammon

174 nstructed directed assemblies of the 4.6 Mb E. coli genome, 48.5 kb lambda genome, and a representa

175 e comparative gene expression profile of MDR E. coli 381 and the reference human strain E. coli ATCC

176 al information about the highly virulent MDR E. coli strain of poultry origin and warrant further inv

177 g samples with 10(3), 10(4) and 10(5) CFU/mL E. coli O157:H7 were 106.98, 96.52 and 102.65 (in yogurt

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

179 ernal perturbation in a dense bath of motile E. coli bacteria.

180 Soil had >120000 mean MPN E. coli per gram.

181 ith differences in clustering between native E. coli receptors, with the TM sequence of better-cluste

182 NFs inhibited growth of model Gram-negative (E. coli) and Gram-positive (S. aureus) bacteria to a gre

183 Among them, nine E. coli strains possess an epidemic pCSZ4-like IncX4 pla

184 In experiments on nonmotile E. coli exposed to polymyxin B, cell-generated frequency

185 y inhibit macrophage activation by nonviable E. coli In total, this study shows that cathelicidins do

186 it of detection (LOD) down to 10CFUmL(-1) of E. coli and Salmonella.

187 sensor was developed based on the ability of E. coli O157:H7 proteases to change the optical response

188 ) also inhibit RNA topoisomerase activity of E. coli DNA topoisomerase I.

189 ation of the large conductance MS channel of E. coli, (MscL), in DHBs.

190 e-determining step in the catalytic cycle of E. coli dihydrofolate reductase is tetrahydrofolate (THF

191 By following the changes in density of E. coli in liquid and embedded in glucose-limited soft a

192 mical immunosensor for specific detection of E. coli O157:H7 contamination with the use of sandwich a

193 The detection of E. coli O157:H7 in foods has held the attention of many

194 ensitive and 99.3% specific for detection of E. coli serotype O:157.

195 cholera toxin, or heat-stable enterotoxin of E. coli (STa toxin), with IC50 down to approximately 5 n

196 these findings suggest that the frequency of E. coli lineages in invasive disease is driven by negati

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

198 ced in rats by intratracheal instillation of E. coli (1.5-2 x 10 CFU/kg).

199 ted most significantly by measured levels of E. coli(log MPN/100 mL) (chi(2) > 8.7; p < 0.003).

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

201 esource for future computational modeling of E. coli gene regulation, transcription, and translation.

202 nome-scale metabolic reconstructed models of E. coli, calculating essential genes and comparing with

203 rect evidence for Min oscillation outside of E. coli and have broader implications for Min-system fun

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

205 as not the dominant reason for prevalence of E. coli lineages in this population.

206 ly predicted and modeled for the proteome of E. coli.

207 amate residue in the transmembrane region of E. coli TatC, which when modified by DCCD interferes wit

208 tive to the concrete BSFs for the removal of E. coli and turbidity from drinking water.

209 A) cycle resulted in increased resistance of E. coli to PGRP killing.

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

211 magnifying the imbalance of redox status of E. coli O157:H7.

212 We present cryo-EM structures of E. coli RNAP core bound to the small ribosomal 30S subun

213 Subpopulations of E. coli PI-7 expressed genes related to dormancy and per

214 a systematic 11-yr hospital-based survey of E. coli associated with bacteremia using isolates collec

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

216 Simulated transport of E. coli in a beach aquifer is complex and does not corre

217 wt % led to a reduction in the transport of E. coli O157:H7 and K12 from 98 to 10% and from 95 to 70

218 we analyse the impact of MCR-1 expression on E. coli morphology, fitness, competitiveness, immune sti

219 te the antibacterial effect of gentamicin on E. coli growth.

220 In our performance tests on E. coli, A. thaliana and Maylandia zebra data sets, HALC

221 t, in animals colonized at P2 but not at P9, E. coli K1 bacteria gain access to the enterocyte surfac

222 l processes in bacterial cells, particularly E. coli and Salmonella enterica Typhimurium.

223 nderstanding of how commensal and pathogenic E. coli colonise their environments.

224 ialic acids by both commensal and pathogenic E. coli strains.

225 te almost completely retained the pathogenic E. coli in the subsurface, suggesting that utilizing san

226 he electrical properties once the pathogenic E. coli O157:H7 captured on the sensor surface.

227 terococcus) and two gram negative pathogens (E. coli and Salmonella).

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

229 samples than the blaNDM- and mcr-1-positive E. coli, indicating a substantial segment of unseen resi

230 tion with a commensal, potentially probiotic E. coli bacteriuria strain.

231 and oxidative stress, in which 3MST protects E. coli against oxidative stress via l-cysteine utilizat

232 Hinokiflavone also inhibited a purified, E. coli expressed SUMO protease, SENP1, in vitro, indica

233 tores colistin susceptibility of recombinant E. coli.

234 In vitro studies of reconstituted E. coli replisomes have attributed this remarkable proce

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

236 0.001] times more likely to harbor resistant E. coli strains than layer farms.

237 cin was performed on 649 multidrug-resistant E. coli clinical isolates collected between 2011 and 201

238 n of omega and its role in assembly of RNAP, E. coli mutants lacking rpoZ (codes for omega) are viabl

239 /stromal cells reduce the severity of rodent E. coli-induced acute respiratory distress syndrome.

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

241 e method is gram negative pathogenic species E. coli O157:H7.

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

243 e DNA polymerase III holoenzyme in a stalled E. coli replisome can directly bypass a single cyclobuta

244 R E. coli 381 and the reference human strain E. coli ATCC 25922 was completed with Illumina HiSeq.

245 4 was slightly more effective in suppressing E. coli in these planktonic mixed cultures, even though

246 f1 was 20-fold more effective in suppressing E. coli under simulated multispecies biofilm conditions

247 loped a suitable bacterial selection system (E. coli strain BW5Delta).

248 S has a prophylactic effect against systemic E. coli K1 infection in neonates.

249 ould enhance neonatal resistance to systemic E. coli K1 infection via promoting maturation of neonata

250 eruginosa BioH is more highly expressed than E. coli BioH.

251 Importantly, it is also demonstrated that E. coli bacteremia initiated from translocation across t

252 Using a microfluidic approach, we find that E. coli cells respond to the gradient of chemoattractant

253 Using a metabolomics approach, we found that E. coli and other Enterobacteriaceae expressing the Yers

254 We further show that E. coli plasmid and PCR-derived DNA can efficiently tran

255 This study shows that E. coli OMVs induce cardiac injury in vitro and in vivo,

256 k, providing the molecular basis for how the E. coli replisome can maintain high processivity and yet

257 In the E. coli class 1a RNR the thiyl radical (C439(*)) is a tr

258 erial prion-like protein (RepA-WH1) into the E. coli releasing factor RF1 promotes its aggregation an

259 thway for cluster regeneration involving the E. coli protein IscU.

260 le proteins assemble on the 5' domain of the E. coli 16S rRNA.

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

262 ntity, respectively; de novo assembly of the E. coli genome from raw reads yielded a single contig co

263 perator site in the regulatory region of the E. coli GUS operon is identified, and structure-guided G

264 experiments show that the acidic tip of the E. coli Hfq CTD transiently binds the basic Sm core resi

265 mechanisms of covalent flavinylation of the E. coli QFR FrdA subunit.

266 scopy (CoSMoS) to follow the exchange of the E. coli replicative DNA polymerase Pol IIIcore with the

267 ting phage and the level of virulence of the E. coli strain.

268 We sequenced the genomes of the E. coli strains and report genes unique to the two pheno

269 randomly mutagenized by error-prone PCR the E. coli dsbB gene and selected dsbB mutants that confer

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

271 show that CsrA differentially regulates the E. coli K-12 and Salmonella nrf operons.

272 Ms are thinner hydrophobic bilayers than the E. coli OMs, which is expected from the difference in th

273 Together, our results demonstrate that the E. coli adhesin MAM(HS) facilitates retention of a gut c

274 Previous results had suggested that the E. coli replicase might play a role in lesion bypass, bu

275 We showed that over time, the E. coli population was only transiently disturbed by the

276 Our results support a model in which the E. coli clamp loader actively opens the beta-sliding cla

277 nsification of color was correlated with the E. coli O157:H7 concentration.

278 r intramuscularly or intramammarily with the E. coli P4 were submitted to a homologous mastitis chall

279 This E. coli CEP 'interactome' provides insights into the fun

280 Importantly, the inhibitory effects of 42 to E. coli betaG was reduced as the pH decreased due to the

281 how interspecies competition contributes to E. coli suppression without the confounding effects of r

282 mediate outcome in children after HUS due to E. coli O104:H4 have been lacking.

283 tissue resolution tone and host responses to E. coli infections.

284 h graphene based capacitors were specific to E. coli O157:H7 strain with a sensitivity as low as 10-1

285 Virulence functions unique to E. coli PI-7 were also upregulated.

286 The wild-type E. coli AlkB and its D135S mutant can remove most of m(1

287 gnotobiotic larvae inoculated with wild-type E. coli reduced midgut oxygen levels below 5%, whereas l

288 ediated immunity is the key to understanding E. coli vaccine-induced protection of the mammary gland.

289 ally increased colonization by uropathogenic E. coli strain 536.

290 essed in a clinically relevant uropathogenic E. coli strain.

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

292 is able to reduce total cell numbers, viable E. coli remained and expressed genes that enable surviva

293 to OMCCs from the A. tumefaciens VirB/VirD4, E. coli R388 Trw, and Bordetella pertussis Ptl systems s

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

295 chment, within catchment land-uses, and with E. coli concentration.

296 ing S. aureus and B. anthracis compared with E. coli Alveolar macrophages and CD14(+) cells were over

297 o decay and a longer half-life compared with E. coli DSM1103 (6.64 +/- 0.63 h and 2.85 +/- 0.46 min v

298 ted sensor was reduced after incubation with E. coli K-12 cultures, with the reduction level increase

299 els below 5%, whereas larvae inoculated with E. coli mutants defective for cytochrome bd oxidase did

300 nted in the cross-linked motifs found within E. coli.