ライフサイエンスコーパス: bacterial strain

1 e glucose tolerant than those fed the parent bacterial strain.

2 erved for HD5(ox) against this Gram-positive bacterial strain.

3 largest plasmid arrays sequenced in a single bacterial strain.

4 s depend on the route of inoculation and the bacterial strain.

5 ype III effector proteins carried by a given bacterial strain.

6 tely half of the worms are dominated by each bacterial strain.

7 elium was monitored using a copper biosensor bacterial strain.

8 chnologies and tested against drug-resistant bacterial strains.

9 exhibit potent inhibition of the enzyme and bacterial strains.

10 control of further resistance development of bacterial strains.

11 inst two Gram-positive and two Gram-negative bacterial strains.

12 ases expressed by other clinically prevalent bacterial strains.

13 vers granzymes into bacteria to kill diverse bacterial strains.

14 ficient platelets do not aggregate to 4 of 5 bacterial strains.

15 y and deposition-transport behavior of these bacterial strains.

16 ilamentous phage using different vectors and bacterial strains.

17 ives that are equally potent against several bacterial strains.

18 ial physiology and for the classification of bacterial strains.

19 eased antibiotics were potent against tested bacterial strains.

20 ched live bacteria for three different model bacterial strains.

21 Escherichia coli and Salmonella typhimurium) bacterial strains.

22 tinguish between F'-positive and F'-negative bacterial strains.

23 lined because of the appearance of resistant bacterial strains.

24 ombination with 7 other commensal intestinal bacterial strains.

25 f aqueous green tea leaf extract on selected bacterial strains.

26 ity for Mtb over a panel of other pathogenic bacterial strains.

27 xonomically related and/or distantly related bacterial strains.

28 antimicrobial-resistant versus -susceptible bacterial strains.

29 al activity, in particular for gram-positive bacterial strains.

30 found to be present in at least 70 different bacterial strains.

31 vity of CD27L against C. difficile and other bacterial strains.

32 inst a number of Gram-negative and -positive bacterial strains.

33 re used to assess genetic similarity between bacterial strains.

34 ate and the emergence of multidrug-resistant bacterial strains.

35 nished intestinal colonization with the same bacterial strains.

36 aureus (MRSA) and fluoroquinoline-resistant bacterial strains.

37 nced antimicrobial activity against specific bacterial strains.

38 l methods for phylogenomic classification of bacterial strains.

39 ssion in normal and riboflavin-overproducing bacterial strains.

40 inger even for the most widely characterized bacterial strains.

41 ficantly diminished activity against several bacterial strains.

42 h antibiotic resistance genes spread between bacterial strains.

43 ificant activity against medically important bacterial strains.

44 that are associated with acquisition of new bacterial strains.

45 romised cells after 24 h of exposure of both bacterial strains.

46 n up in both gram-positive and gram-negative bacterial strains.

47 pplying a MASTERMIND approach using purified bacterial strains.

48 ltrated with different immunity inducers and bacterial strains.

49 potential for application to all culturable bacterial strains.

50 icant nephrotoxicity and polymyxin-resistant bacterial strains.

51 ties against various sensitive and resistant bacterial strains.

52 mosGCTLs facilitate colonization by multiple bacterial strains.

53 sure to radiation had selected for resistant bacterial strains.

54 or clonal expansion of preexisting resistant bacterial strains.

55 The recently isolated bacterial strain 80/3 represents one of the most abundan

56 ifferent experimental conditions, models and bacterial strains according to their metabolic response

57 20-400 nm) on the lipids and proteins of two bacterial strains ( Acinetobacter sp. strain PT5I1.2G an

58 A taxonomically unique bacterial strain, Acinetobacter sp. A47, has been recove

59 nverting CO2 into biosuccinic acid using the bacterial strain Actinobacillus succinogenes 130 Z, and

60 rst inoculated into mice, followed by (live) bacterial strain administration, an in vivo role for Nap

61 TICR) MS to discriminate clinically relevant bacterial strains after species identification performed

62 Newly isolated Enterococci faecalis bacterial strains AIM06 (DSM100702) and SR14 (DSM100701)

63 The isolated bacterial strains all showed far better growth on buffer

64 atabolic operon in Acinetobacter and related bacterial strains, allowing utilization of hydroxycinnam

65 ic condition were very different because the bacterial strain alone degraded phenanthrene with sigmoi

66 utant of this regulatory gene in the nonfood bacterial strain altered its secondary metabolite profil

67 method for discrimination of highly adaptive bacterial strains among the populations present in a giv

68 severity of disease varied according to the bacterial strain and age, but not sex, of the host.

69 ion of heme analogs using a widely available bacterial strain and offers an attractive alternative to

70 ing capable of differentiating Gram-negative bacterial strain and species, for many important applica

71 t are dependent on both the virulence of the bacterial strain and the genetic background of the host.

72 al Collection (miBC), a public repository of bacterial strains and associated genomes from the mouse

73 very sensitive technique for differentiating bacterial strains and can be applied to any of the sever

74 highly conserved in phylogenetically diverse bacterial strains and contains an unusual hybrid polyket

75 mation and failure behavior for two separate bacterial strains and develop a simplified but nonlinear

76 framework for studies of the inheritance of bacterial strains and discuss the advantages and disadva

77 el simulates the growth of a large number of bacterial strains and incorporates variation in microbio

78 ane integrity, and ultrastructure of various bacterial strains and Leishmania species.

79 ntire procedure will depend on the number of bacterial strains and mice included in the study.

80 Lead fragments were also cocultured with the bacterial strains and RAW M.

81 ly flexible, allowing the study of different bacterial strains and species of uropathogens in a broad

82 F, and has been shown to accurately identify bacterial strains and species.

83 e increasing numbers of antibiotic-resistant bacterial strains and the limited success of currently a

84 Communication between different bacterial strains and with the environment is achieved v

85 ed with diverse microbes, including numerous bacterial strains and yeasts, but not viral pathogens.

86 ociated with the emergence of new pathogenic bacterial strains and/or serotypes, there is a dearth of

87 allelic variants, genetic background of the bacterial strain, and control of expression by phase var

88 CDI toxin delivery and activity to the same bacterial strain, and that CDI system proteins can media

89 udied their bacteriostatic effect on several bacterial strains, and examined their conformational cha

90 amental studies of microorganisms, screening bacterial strains, and toxicity detection in water.

91 against both gram-positive and gram-negative bacterial strains; and (3) their hemolytic activity.

92 Respiratory tract bacterial strains are becoming increasingly resistant to

93 s due to clonal expansion of highly virulent bacterial strains are clear and present threats to human

94 Clonally arrayed sequenced collections of bacterial strains are constructed from representative do

95 sively drug-resistant, and pandrug-resistant bacterial strains are now frequently encountered.

96 es in the battle against multidrug-resistant bacterial strains are urgently needed, and one obvious a

97 We screened a panel of 41 bacterial strains as a platform to determine how differe

98 es selective detection of LPS from different bacterial strains as well as LPS on the membrane of livi

99 cability for the discrimination of different bacterial strains, as achieved with typing based on gene

100 all known antibiotics is isolated from these bacterial strains, as well as a variety of other drugs s

101 antimicrobial efficacy against a variety of bacterial strains associated with cystic fibrosis and ch

102 hat allow simultaneous detection of multiple bacterial strains at multiple spatial scales.

103 of 2,400 transposon mutants in two different bacterial strain backgrounds for H. pylori genetic loci

104 Four model bacterial strains bearing various classes of beta-lactam

105 Bacterial strain Burkholderia contaminans MS14 was isola

106 B-Glc-Ent probe is sensitive not only to the bacterial strain but also to the iron condition in the e

107 bacterial sensors (inducible or constitutive bacterial strains) but with a different conservation mod

108 ld difference in virulence was found between bacterial strains, but no significant differences betwee

109 unbiased view of structural variation of gut bacterial strains by measuring them in their natural hab

110 A) showed that three different Gram-negative bacterial strains can be clearly differentiated.

111 lysaccharides (LPS) isolated from particular bacterial strains can bias innate immune responses towar

112 udy shows how competition between coevolving bacterial strains can generate antibiotic resistance and

113 effective as a number of standard laboratory bacterial strains can serve as sources for SLiCE extract

114 minobacter sp. MSH1 and ASI1, the only known bacterial strains capable of mineralizing BAM-was large,

115 Furthermore, identification of the bacterial strains capable of suppressing sensory neuron

116 Bacterial strains carrying nonsense suppressor tRNA gene

117 he extent of apoptosis induced by individual bacterial strains, caspase-3 activity was measured as a

118 labeling of marker proteins derived from two bacterial strains cocultured in media supplemented with

119 ces, coupled with the availability of unique bacterial strain collections, have facilitated a systems

120 All bacterial strains colonized the intestines, reaching lev

121 cultured isolates, was used to characterize bacterial strain composition in the fecal microbiota of

122 We here demonstrate for eight bacterial strains comprising four species, that bacteria

123 e were able to study the behavior of LacI in bacterial strains containing the natural copy numbers (

124 Moreover, we found that lead exposed bacterial strains could be successfully discriminated fr

125 ed young germ-free mice with a consortium of bacterial strains cultured from the fecal microbiota of

126 g samples of human liver with metastases and bacterial strains, cultured on solid medium, belonging t

127 The disease in mice was Stx2 and bacterial strain dependent.

128 rdia and that flies injected with cyanogenic bacterial strains die more rapidly than those injected w

129 tial, and tracked them over time to evaluate bacterial strain dispersal among infants.

130 This bacterial strain displays potent antimicrobial activitie

131 Studying how bacterial strains diverge over space and time and how di

132 rmative environments suggests that resistant bacterial strains do not evolve because a lethal mutatio

133 bendazole (TBZ) at 100 mug L(-1)) and two AR bacterial strains (E. coli and E. faecalis, at 10(5) CFU

134 on strategy that relies on co-culture of two bacterial strains, each expressing a half-antibody.

135 SRA-dependent and -independent gram-negative bacterial strains elicit SRA-dependent increased cytokin

136 Pathogenic bacterial strains emerge largely due to transfer of viru

137 The bacterial strains employed in this study had equivalent

138 e door to develop an array of methanotrophic bacterial strain-engineering strategies currently employ

139 to assay cellobiohydrolase activity on model bacterial strains (Escherichia coli and Bacillus subtili

140 The alarming spread of bacterial strains exhibiting resistance to current antib

141 In experiments on the same bacterial strain exposed to ampicillin, frequency noise

142 Live attenuated bacterial strains expressing heterologous antigens repre

143 Bacterial strains expressing mDHFR fusions with the solu

144 Methods to select bacterial strains for drug discovery have historically b

145 on efficiency, and it is not uncommon that a bacterial strain forms functional (Fix(+)) nodules on on

146 roducts, current changes are specific to the bacterial strain from which the PCR fragment is produced

147 harboring a consortium of sequenced cultured bacterial strains from the Bangladeshi donor's microbiot

148 ignals controlling swarming, we isolated two bacterial strains from the same red seaweed, Vibrio algi

149 dented detail about the molecular anatomy of bacterial strain genotype-patient phenotype relationship

150 Wolfe-Simon et al. reported that the bacterial strain GFAJ-1 can grow by using arsenic (As) i

151 Wolfe-Simon et al. reported that bacterial strain GFAJ-1 can substitute arsenic for phosp

152 t study described the isolation of a special bacterial strain, GFAJ-1, that could grow in medium cont

153 tion of neonatal airways with the pathogenic bacterial strains Haemophilus influenzae, Moraxella cata

154 pact on clinical outcomes and variation with bacterial strain has rarely been explored using integrat

155 Unfortunately, the development of resistant bacterial strains has compromised the effectiveness of m

156 complex of multidrug-resistant Gram-positive bacterial strains, has proven especially problematic in

157 Many heavy metal resistant bacterial strains have a high biosorption capacity and t

158 e of host factors, Shiga toxin 2 (Stx2), and bacterial strain in disease due to EHEC.

159 must be rescued by the presence of the same bacterial strain in the egg for normal development to pr

160 and evaluated in several clinically relevant bacterial strains in cultures and in living mice.

161 Administration of bacterial strains in drinking water was used, respective

162 ethods for predicting resistance profiles of bacterial strains in hospital microbiology and public he

163 more suitable for analyzing large numbers of bacterial strains in human populations.

164 e detection and discrimination of the tested bacterial strains in less than 10 h from an initial bact

165 Identifying bacterial strains in metagenome and microbiome samples u

166 cement in cells with WT CFTR using all three bacterial strains in one cell line, whereas in the other

167 periments were conducted with selected fecal bacterial strains in pure culture.

168 eficiency to an enrichment of H2O2-producing bacterial strains in the gut.

169 f Escherichia coli and Klebsiella pneumoniae bacterial strains in urinary tract infections are resist

170 AIT cells are activated by a wide variety of bacterial strains in vitro, but their role in defense ag

171 clear antimicrobial activity against several bacterial strains in vitro.

172 is induced by AvrA-deficient and -sufficient bacterial strains in vivo.

173 es demonstrating the attenuated virulence of bacterial strains in which modified carbohydrate biosynt

174 zolid-resistant MRSA and other Gram-positive bacterial strains, in vivo efficacy in a mouse model of

175 th a detection limit of 10(2)CFU/mL for four bacterial strains including Escherichia coli (E. coli),

176 at show improved whole cell activity against bacterial strains including methicillin-resistant Staphy

177 olium and imidazole-derived PDA with various bacterial strains including MRSA (methicillin-resistant

178 ctivity observed against clinically relevant bacterial strains including MRSA and VRE.

179 This method was tested on four bacterial strains, including both Gram-negative and Gram

180 ated against Gram-positive and Gram-negative bacterial strains, including drug-resistant pathogens, r

181 effectively killed a panel of representative bacterial strains, including multidrug-resistant hospita

182 Most bacterial strains, including those extracted from cecal

183 Certain bacterial strains increased viral co-infection of mammal

184 Neither bacterial strain induced inflammation in wild-type mice,

185 hylogenetically diverse, sequenced human gut bacterial strains introduced into adult gnotobiotic mice

186 lism by human gut microbiota and to identify bacterial strains involved.

187 encing of pooled samples of large numbers of bacterial strains is a robust, rapid and cost-efficient

188 The analysis of metabolic differences in bacterial strains is a useful tool for the development o

189 nt monitoring for the emergence of resistant bacterial strains is essential.

190 ividuality, so identification of conspecific bacterial strains is imperative for improved understandi

191 rr) /J mice albeit the damage caused by both bacterial strains is more severe in these transgenic mic

192 and selection of highly antibiotic-resistant bacterial strains is of major concern, the clinical rele

193 artificial mineralization of a polyresistant bacterial strain isolated from an acidic, oligotrophic l

194 The ability of Bacillus sp. 3B6, a bacterial strain isolated from cloudwaters, to biotransf

195 xtent of mutually positive interaction among bacterial strains isolated from a common aquatic environ

196 present a detailed polyphasic analysis of 10 bacterial strains isolated from three coastal lichens Li

197 osystem Therapeutic (MET-1) consisting of 33 bacterial strains, isolated from human stool and previou

198 umor cell lines as well as some of the worst bacterial strains known to humanity, including methicill

199 Here we test DNA looping in bacterial strains lacking the nucleoid proteins HU, IHF

200 A screen of bacterial strains led to the discovery of a two-componen

201 ion of 16S rRNA analytes of three pathogenic bacterial strains: Legionella pneumophila, Pseudomonas a

202 P can dramatically reduce binding, and thus, bacterial strains may employ such modifications to evade

203 we describe the mechanism by which a single bacterial strain, Methylocella silvestris, can use metha

204 In reference and wild bacterial strains, minimal inhibitory concentrations (MI

205 antibiotic resistance in clinically relevant bacterial strains necessitates the development and refin

206 s revealed several HCM-like enzymes in other bacterial strains not related to MTBE degradation, indic

207 Two bacterial strains, o-17 and DF-1, that link their growth

208 hat proliferation of a series of recombinant bacterial strains occurred over the past few decades.

209 n-vitro CAP detection is performed using the bacterial strain of Haemophilus influenza.

210 ever, current strategies require specialised bacterial strains or laborious protocols.

211 the bacterial test strains from either other bacterial strains or plants (in our laboratory we use ei

212 ombination among 55 metabolisms of different bacterial strains or species, and show that their novel

213 n applied to differentiate amongst different bacterial strains or the same strain under different gro

214 ific biological entities, such as particular bacterial strains or viruses, remains a largely unsolved

215 e than 10000 single-cell Raman spectra of 34 bacterial strains out of 13 different species was built

216 Selectivity for this pathogenic bacterial strain over a common lab strain (E. coli DH5al

217 The secreted pyocyanin levels from two bacterial strains, PA11 and PA14, were measured to have

218 ith an increased antibiotic activity against bacterial strains possessing high level vancomycin resis

219 This bacterial strain produces purified minicircles in a time

220 ion, neither patients' CD4(+) cell count nor bacterial strain properties necessarily predicted the cl

221 e to the type III secretion system-deficient bacterial strain Pseudomonas syringae pv tomato (Pst) DC

222 haracterized gram-positive and gram-negative bacterial strains published by ARLG investigators.

223 reen tea have been studied, its role against bacterial strains related to skin infections and mechani

224 components mapping to 906 T6SSs found in 498 bacterial strains representing 240 species, as well as a

225 Most current clinical methods that identify bacterial strains require time-consuming culture of the

226 The increase in the number of bacterial strains resistant to known antibiotics is alar

227 The rapid emergence of bacterial strains resistant to multiple antibiotics is p

228 ble to tackle the continuous outbreak of new bacterial strains resistant to traditional antibiotics.

229 me, direct tracking of a single plasmid in a bacterial strain responsible for an outbreak is possible

230 Mining the microbiota for bacterial strains responsible for shaping the structure

231 Whole genome analysis of this bacterial strain revealed the presence of an N-acyl homo

232 ctivity studies performed on three nontarget bacterial strains revealed that the immunomagnetic beads

233 Here, we show that the bacterial strain Rhodococcus jostii RHA1 can biotransfor

234 ls, which grow more rapidly on nutrient-rich bacterial strains, rictor mutants display even slower gr

235 growth inhibition assay with three different bacterial strains showed significant activity of several

236 cal isolates of Zygomycetes, with 33% of the bacterial strains showing 87% identity to Burkholderia 1

237 on of initial illness, toxicity of infecting bacterial strain, smoking, mucosal markers of inflammati

238 We isolated and identified 101 distinct bacterial strains spanning 6 phyla including (1) novel s

239 erefore, facilitated the characterization of bacterial strains, species, and Gram type.

240 icate that DOM effects on Hg methylation are bacterial strain specific, depend on the DOM:Hg ratio or

241 eumolysin contributes to cardiac damage in a bacterial strain-specific manner, and pneumolysin kills

242 outer membrane vesicles combine to produce a bacterial strain-specific response that is distinct from

243 s enantiomers of alpha-HCH using two aerobic bacterial strains: Sphingobium indicum strain B90A and S

244 his bubble-driven detachment process for the bacterial strain Staphylococcus aureus.

245 atensimycin and platencin, isolated from the bacterial strain Streptomyces platensis, represent a nov

246 One bacterial strain (Streptomyces sp. CLI2509) from the bra

247 key role in shaping the host response to the bacterial strains studied herein.

248 died the effect of Sphingomonas capsulata, a bacterial strain that carries both NKT cell and TLR liga

249 were transformed into EL350, a DH10B-derived bacterial strain that expresses Cre recombinase under th

250 een raised about the possible emergence of a bacterial strain that is untreatable by US Food and Drug

251 ylase LigM from Sphingomonas paucimobilis, a bacterial strain that metabolizes lignin-derived aromati

252 ve been introduced into the environment, and bacterial strains that are able to grow on them are idea

253 herichia coli and Enterococcus faecalis, two bacterial strains that are commonly encountered in urina

254 poultry microbiota was assembled, including bacterial strains that are not typically retrieved from

255 ould be particularly useful for detection of bacterial strains that are slow growing, e.g., Mycobacte

256 he marine bacterium Marinomonas and from two bacterial strains that associate with higher plants, the

257 might someday be able to mine for intestinal bacterial strains that can be used in the diagnosis or t

258 Importantly, bacterial strains that induced viral co-infection facili

259 Here, we report stable, engineered bacterial strains that maintain their function for 6 mon

260 Collectively, this screen identifies bacterial strains that may use ZPSs to interact with the

261 lysins were able to lyse only Gram-positive bacterial strains that possess PG with D-Ala(4)-->D-Asx-

262 ytic anti-cancer therapies employ attenuated bacterial strains that selectively proliferate within tu

263 ernatants from wild type and isogenic mutant bacterial strains that the Major Facilitator Superfamily

264 One bacterial strain (the donor) of each pair to be introduc

265 For both bacterial strains, the long-range interactions we observ

266 ut they restrain the virulence of pathogenic bacterial strains, thereby preventing infections caused

267 mice across a range of conditions (mouse and bacterial strain, time post infection) and was validated

268 r of cumulative recoding changes in a single bacterial strain to date.

269 onses can be exploited to construct reporter bacterial strains to probe the temporal and spatial envi

270 WGS (n = 206) revealed diverse bacterial strain type (STs).

271 icrobial engineering applications, including bacterial strain typing, immunization of cultures, autoi

272 es (MbetaL) are enzymes naturally evolved by bacterial strains under the evolutionary pressure of bet

273 alse-negative results were observed among 90 bacterial strains used to evaluate assay specificity.

274 quencing now brings finer resolution to both bacterial strain variation and the host genetic state th

275 Bacterial strains vary in their colonization efficiency

276 ransformation of chloroanilines by these two bacterial strains via dissimilar dehalogenation pathways

277 e pathogen detection, a mixture of all three bacterial strains was isolated and identified within the

278 r against Bacillus subtilis, a Gram-positive bacterial strain, was measured to be 4.1 x 10(-5) M, whi

279 In contrast, the representative bacterial strains we studied were able to acquire iron f

280 o neutrally competing, fluorescently labeled bacterial strains, we observe stochastically driven bimo

281 Using 24 model compounds and 4 different bacterial strains, we optimized the screening technology

282 neither all humans nor mice harbor the same bacterial strains, we posited that more prevalent factor

283 Using seven bacterial strains, we show that SMALR yields significant

284 d is suitable for screening large numbers of bacterial strains, whereas the Arabidopsis model provide

285 protegrin against several common pathogenic bacterial strains, whereas the hexafluoroleucine-substit

286 E. coli when present together with competing bacterial strains which are known to have similar shape.

287 to C. burnetii NMII infection and that this bacterial strain, which activates the immune deficiency

288 istical model was validated with independent bacterial strains, which were grown in ascitic fluid.

289 Moreover, a mixture of 20 bacterial strains, which were selected and isolated from

290 The particles were tested with several bacterial strains, while biocompatibility was verified w

291 antibacterial activity against Gram positive bacterial strains, while their evaluation against wild-t

292 Using bacterial strains whose individual loops have been remov

293 of cell-surface interaction forces for seven bacterial strains with a wide range of cell morphology,

294 otein in order to survive, we have generated bacterial strains with enhanced periplasmic folding capa

295 f Pi is crucial in stimulating the growth of bacterial strains with high RNA contents and thus faster

296 Bacterial strains with industrial and therapeutic releva

297 The use of bacterial strains with regulated uppS expression and inh

298 ing cells is examined herein for a number of bacterial strains with well-defined flagellar geometries

299 o low density mock communities of 11 diverse bacterial strains (with and without human DNA supplement

300 t show any bacterial capture for these other bacterial strains within a 15 min incubation period.