ライフサイエンスコーパス: bacterial cell

1 d a switchable interface for easy removal of bacterial cell.

2 a major barrier to foreign DNA entering the bacterial cell.

3 rily needed to maintain the integrity of the bacterial cell.

4 antibiotics and enterotoxin STII out of the bacterial cell.

5 to orchestrate replication initiation in the bacterial cell.

6 inked to its ability to penetrate within the bacterial cell.

7 ent of which could be observed from a single bacterial cell.

8 , thereby anchoring the cellulosome onto the bacterial cell.

9 ed consequences of these interactions in the bacterial cell.

10 eted spatial and intensity accuracy within a bacterial cell.

11 tRNA (>70%) appears to diffuse freely in the bacterial cell.

12 dynamics with single-molecule resolution in bacterial cells.

13 rganization of chromosomal DNA in individual bacterial cells.

14 o easier access of the essential oils to the bacterial cells.

15 r this interaction and transport activity in bacterial cells.

16 a steady supply of carbon to both plant and bacterial cells.

17 ue to the small size and nonflat geometry of bacterial cells.

18 differentiate between viable and non-viable bacterial cells.

19 roteins for super-resolution imaging in live bacterial cells.

20 the structural and mechanical properties of bacterial cells.

21 ocalize to highly specific subregions within bacterial cells.

22 oughput live-cell fluorescence microscopy of bacterial cells.

23 y characterize RNA structure and function in bacterial cells.

24 crofluidic devices, or localized within live bacterial cells.

25 g a "blocking effect" between humic acid and bacterial cells.

26 ction processes only PAA efficiently removed bacterial cells.

27 atial distribution of AMP-induced effects on bacterial cells.

28 jugative element (ICE) among individual live bacterial cells.

29 rivatized, biological specimen, i.e., intact bacterial cells.

30 rganization and dynamics of the replisome in bacterial cells.

31 bacterial adhesion to EPC cells from within bacterial cells.

32 f a beta-barrel protein inside mammalian and bacterial cells.

33 arch for compounds that can easily penetrate bacterial cells.

34 host various types of genetically engineered bacterial cells.

35 ch, in turn, conferred iron tolerance to the bacterial cells.

36 t CodY is a dimer at concentrations found in bacterial cells.

37 fluorescence in situ hybridization (FISH) of bacterial cells.

38 andom 4.5-kbp (1.5 mum) DNA segments between bacterial cells.

39 nt in reducing the systemic dissemination of bacterial cells.

40 knee joint fluid spiked with live pathogenic bacterial cells.

41 oduced virus-like particles in mammalian and bacterial cells.

42 f the macrophages that contained only 1 to 5 bacterial cells.

43 engineered myoglobin catalysts expressed in bacterial cells.

44 by the high abundance of ribosomal (r)RNA in bacterial cells.

45 mprehension of their interaction with target bacterial cells.

46 ed for rapid and selective detection of live bacterial cells.

47 beta-galactosidase (beta-gal) from the bound bacterial cells; (3) the release of beta-gal was detecte

48 short palindromic DNA sequences, protecting bacterial cells against bacteriophage infection by attac

49 deas that explain how the Psp response keeps bacterial cells alive.

50 th behavior and thereby confer the 'adapted' bacterial cells an enhanced ability to tolerate diverse

51 of antibiotic resistance mechanisms at both bacterial cell and community levels.

52 sion of PG is tightly coupled to growth of a bacterial cell and requires hydrolases to cleave the cro

53 ting antibiotic concentrations on individual bacterial cells and bacterial populations.

54 n (dMDA) to purified DNA templates, cultured bacterial cells and human microbiome samples in the virt

55 The results highlight the versatility of bacterial cells and illustrate possible evolutionary rou

56 trast was also observed for bla expressed in bacterial cells and mammalian cells.

57 The co-microencapsulation can deliver bacterial cells and omega-3 oil to human intestinal syst

58 ich facilitates easy release of the captured bacterial cells and subsequent regeneration of the CIP.

59 sity, morphology and spatial distribution of bacterial cells and the pools of microbial metabolites i

60 y mediated by the SFE difference between the bacterial cells and the solid substratum.

61 enrichment steps to magnetically concentrate bacterial cells and their DNA with a 500-fold reduction

62 that P450 21A2 thermal stability assessed in bacterial cells and with purified enzymes differed among

63 es: magainin 2 amide (which is selective for bacterial cells) and melittin (which targets both mammal

64 the basic units of the response system in a bacterial cell, and each consists of a set of transcript

65 y visualized the effect of these peptides on bacterial cells, and confocal microscopy confirmed their

66 ; however, the routes by which it enters the bacterial cell are largely unknown.

67 Bacterial cells are fortified against osmotic lysis by a

68 ctrical conductance of evaporating droplets, bacterial cells are identified within a few minutes comp

69 The bacterial cells are introduced into the channel in the p

70 Most bacterial cells are stressed, and as a result, some beco

71 Most bacterial cells are surrounded by a peptidoglycan cell w

72 Bacterial cells are surrounded by a polymer known as pep

73 of 3D-printing hydrogel inks with programed bacterial cells as responsive components into large-scal

74 cteria at the mug/mL level and killed static bacterial cells at polymer concentrations of tens of ng/

75 the transcription machinery and DNA in live bacterial cells, at both the single-molecule and the pop

76 ial and disrupts membrane integrity, causing bacterial cell autolysis and DNA release.

77 This problem is particularly acute in bacterial cells because of their small sizes.

78 Within bacterial cells, BMCs are metabolic modules that can be

79 Antibiotics are effluxed out of the bacterial cell by a tripartite efflux pump, a complex ma

80 EPSs can lead to spontaneous aggregation of bacterial cells by a depletion attraction and thereby ge

81 tates the delivery of OMV-associated iron to bacterial cells by engaging the Fe(III)-pyochelin recept

82 H2O2 diffusion into biofilms and bacterial cells can be increased by damaging the biofilm

83 iments show that social interactions between bacterial cells can drive evolutionary change at the pop

84 Quorum sensing is a process of bacterial cell-cell communication that relies on the pro

85 to determine carbapenem susceptibility from bacterial cell characteristics in an international K. pn

86 er, resulting in enlarged and densely packed bacterial cell-clusters (microcolonies).

87 rent phenomena, such as in neuropathologies, bacterial cell colonies, social systems and semiconducto

88 have made snapshot and time-lapse imaging of bacterial cells commonplace, yet fundamental challenges

89 quence of samples containing low or variable bacterial cell concentrations.

90 vealed that nanoplexes efficiently transfect bacterial cells, consistently with biological efficacy o

91 on the advantages of DNA PT modification to bacterial cells coping with environmental stresses.

92 archical adaptors that drive the Caulobacter bacterial cell cycle and the quality control adaptor Ssp

93 simple and robust method of controlling the bacterial cell cycle is a useful asset for synthetic bio

94 e develop a novel system for controlling the bacterial cell cycle, based on binding of CRISPR/dCas9 t

95 es drives destruction of proteins during the bacterial cell cycle.

96 NFS1 provokes bacterial cell death and early nodule senescence in an a

97 With increasing bacterial cell densities, Cfree of solvent-spiked PAHs d

98 We found that bacterial cell density-dependent gene expression termed

99 whole genome sequencing revealed that edited bacterial cells did not harbour chromosomal abnormalitie

100 We capture bacterial cells directly from samples with low bacterial

101 r modeling of intracellular Min gradients in bacterial cell division as well as, more generally, for

102 zes to form a discontinuous ring that drives bacterial cell division by directing local cell wall syn

103 Bacterial cell division involves the dynamic assembly of

104 Bacterial cell division is driven by the divisome, a rin

105 The bacterial cell division regulators MinD and MinE togethe

106 Here, we combined a fluorescent reporter of bacterial cell division with single-cell RNA-sequencing

107 The central player in bacterial cell division, FtsZ, is essential in almost al

108 tubulin-like protein FtsZ is key for proper bacterial cell division.

109 rization of a positive regulatory process of bacterial cell division.

110 The Min proteins from E.coli position the bacterial cell-division machinery through pole-to-pole o

111 impse of how the molecular components of the bacterial cell envelope interact with each other to medi

112 Bacterial cell envelope protein (CEP) complexes mediate

113 After blocking the bacterial cell envelope sulfhydryl sites using a qBBr tr

114 ainst P. acnes, and complete breaches in the bacterial cell envelope were observed.

115 Lipoproteins serve essential roles in the bacterial cell envelope.

116 If antibiotics cross bacterial cell envelopes slowly to reach their target, t

117 inant FMDV subunit proteins in mammalian and bacterial cells expressing P1-3C transgenes and retained

118 Applying two optimized LC methods to bacterial cell extracts detected more than 200 metabolit

119 Our data suggest a mechanism for bacterial cell filamentation during infection under anae

120 in-mediated dynamic pump assembly allows the bacterial cell for efficient efflux upon cellular demand

121 detection limits of 10(0), 10(2), and 10(2) bacterial cells for H. pylori detection and two differen

122 echanisms to degrade C3b and thus to protect bacterial cells from the complement response of the host

123 oli as few as 10CFUmL(-1) and capture 98% of bacterial cells from their very high concentrated soluti

124 modeling and quantitative imaging to analyze bacterial cell growth and division.

125 VI secretion system delivers toxins between bacterial cells has broadened our understanding of how b

126 e fundamental question is whether individual bacterial cells have an increased tolerance to stress if

127 Bacterial cells have developed sophisticated systems to

128 me (i-t) curves corresponds to the number of bacterial cells (i.e., Escherichia coli) on the UME surf

129 that the QDs can be tailored to kill 92% of bacterial cells in a monoculture, and in a co-culture of

130 proach can be used for specific detection of bacterial cells in aqueous samples.

131 o carry electronic information to engineered bacterial cells in order to control transcription from a

132 In general, at higher bubble velocities bacterial cells in the corners of the geometry are less

133 ipient's biology are routinely attributed to bacterial cells in the donor feces (~1011 per gram of hu

134 Our findings suggest that bacterial cells in/on the particles and colloids could h

135 lectron microscopy confirmed the presence of bacterial cells in/on the subvisible particles and collo

136 t constriction in a variety of Gram-negative bacterial cells, including Proteus mirabilis and Cauloba

137 of built-in capabilities for characterizing bacterial cells, including the identification of cell di

138 The number of collision events involving the bacterial cells indicated in current-time (i-t) curves c

139 d melittin (which targets both mammalian and bacterial cells indiscriminately).

140 that Tmm is present in approximately 20% of bacterial cells inhabiting marine surface waters, partic

141 of water can facilitate entry of additional bacterial cells into the apoplast.

142 ormula: see text] Here, lysis of an infected bacterial cell is orchestrated by the expression and acc

143 Their potency and uptake into bacterial cells is directly modulated by the length of t

144 Cam export from bacterial cells is one of the mechanisms by which pathog

145 tween the PSA/AgNP cryogel interface and the bacterial cells is required to accomplish disinfection.

146 pproach to eliminating confinement errors in bacterial cells is to analyze molecule displacements onl

147 Originally developed for bacterial cells, it has also been adapted for eukaryotic

148 Protein captured from a crude bacterial cell lysate could also be deuterated without t

149 applied for the extraction of DNA from crude bacterial cell lysate spiked with 1 pg mL(-1) template D

150 xtraction and purification of DNA from crude bacterial cell lysate with subsequent quantification by

151 (Irbb12) analogue, which is not taken up by bacterial cells, maintained only a surface-bound associa

152 this is the first report of Cam uptake into bacterial cells mediated by a specific transporter prote

153 onfirmed that both peptides permeabilize the bacterial cell membrane but suggested slightly different

154 Localization of IRGB10 to the bacterial cell membrane compromised bacterial structural

155 k, a stress effect not captured by measuring bacterial cell membrane integrity.

156 Studies of zeta potential at the bacterial cell membrane suggested that both peptides acc

157 e among the most prominent structures in the bacterial cell membrane, and they play important functio

158 ient last-resort antibiotic that targets the bacterial cell membrane.

159 action that often involves disruption of the bacterial cell membrane.

160 ria within 20 minutes without disrupting the bacterial cell membrane.

161 nZVI accumulated on and penetrated into the bacterial cell membrane.

162 es selectively interacted with and disrupted bacterial cell membranes and caused secondary gene-regul

163 Bacterial cell membranes contain several protein pumps t

164 the separated hydrophobic domain, mimicking bacterial cell membranes, by using dialysis and chromato

165 tic related to daptomycin that permeabilizes bacterial cell membranes.

166 Bacterial cells modulate transcription in response to ch

167 In addition, bacterial cell morphology is adaptable to changes in env

168 es that are homogeneously distributed in the bacterial cell, mRNAs that encode inner-membrane protein

169 study evaluates the impact of intravascular bacterial cell numbers (ie, the level of bacteremia), in

170 It could be shown that even very low bacterial cell numbers (minimum 500 cell ml(-1)) could b

171 d both bacterial and nematode abundance, but bacterial cell numbers also declined under warming, demo

172 ate how temperature variability affects soil bacterial cell numbers, and abundance and traits of soil

173 o fluorescently label the mature PG in whole bacterial cells of Bacillus subtilis.

174 order to determine and model the effects of bacterial cells on metal cycling and metal bioavailabili

175 We detected single living bacterial cells on ultramicroelectrode (UME) using a sin

176 pillary method, in which zoospores mobilized bacterial cells only when they were exposed to a zoospor

177 i with the nanopillars can kill only growing bacterial cells or also dormant spores that are harder t

178 toxic, but the underlying mechanism by which bacterial cells overcome this toxicity during curli asse

179 nation process on physiological processes in bacterial cells, particularly E. coli and Salmonella ent

180 proteins to subcellular microdomains within bacterial cells, particularly to the poles.

181 over novel mechanisms involved in regulating bacterial cell polarity.

182 rays of FMDV-like particles in mammalian and bacterial cells, potentially providing a practical metho

183 DNA in bacterial cells primarily exists in a negatively superco

184 However, a minor fraction of bacterial cells, probably transient phase variants of Ga

185 In bacterial cells, processing of double-stranded DNA break

186 nown about the third most abundant cation in bacterial cells, putrescine2+, and how RNA folding might

187 In order to isolate the bacterial cells, pyoverdine was immobilized covalently o

188 During amino acid starvation, bacterial cells rapidly synthesize the nucleotides (p)pp

189 nism underlying mutagenesis in RER-deficient bacterial cells remains unknown.

190 o degrade pGpG and prevent its accumulation, bacterial cells require an additional nuclease, the iden

191 Thus, the bacterial cell responds to lowered levels of acetyl-CoA

192 Strikingly, the bacterial cell response exhibits Fur-dependent, switch-l

193 uridylation of stop codons in eukaryotic and bacterial cells results in stop-codon read through.

194 ibacter containing vacuoles (LCVs), in which bacterial cells seem to propagate.

195 l wall is an integral organelle critical for bacterial cell shape and stability.

196 Bacterial cell shape is a genetically encoded and inheri

197 ptidases (CPs) are important determinants of bacterial cell shape.

198 cal processes is involved in determining the bacterial cell shape.

199 ability to understand the molecular basis of bacterial cell size control.

200 In particular, we show that the increase of bacterial cell size during Lenski's long-term evolution

201 owth rates, the authors provide insight into bacterial cell size regulation and propose that a thresh

202 nmental perturbations can lead to changes in bacterial cell size that are not predicted by current mo

203 Together, our data indicate that small bacterial cell size, which is signified by the absence o

204 k provides new insights into the dynamics of bacterial cell-size regulation with implications for the

205 ased on chemically aggressive destruction of bacterial cell structures can promote a residual microbi

206 ilamentous appendages that protrude from the bacterial cell surface and facilitate host adhesion.

207 c interaction between the negatively charged bacterial cell surface and the positively charged polyme

208 ell adhesion: adsorption of zinc ions to the bacterial cell surface increases cell wall cohesion and

209 me measurements of antibiotic effects on the bacterial cell surface LPS, which is shown to correlate

210 ification that can be found in gram-positive bacterial cell surface proteins, has previously been use

211 e discuss deviations in composition, through bacterial cell surface remodeling, and alternative modal

212 Type IV pili (T4P) are ubiquitous bacterial cell surface structures, involved in processes

213 Binding of OligoG CF-5/20 to the bacterial cell surface was demonstrated in Gram-negative

214 ly promote adhesion to carbohydrates and the bacterial cell surface.

215 haride intercellular adhesin (PIA), with the bacterial cell surface.

216 ting showed that IFN-beta interacts with the bacterial cell surface.

217 Types 1 and P pili are prototypical bacterial cell-surface appendages playing essential role

218 rdingly, unraveling the sugar composition of bacterial cell surfaces can shed light on bacterial grow

219 ncorporation of exogenous D-amino acids onto bacterial cell surfaces with vast promiscuity for the si

220 (P:G ratios) are greater in actively growing bacterial cells than in resting cells.

221 ersisters are dormant phenotypic variants of bacterial cells that are tolerant to killing by antibiot

222 e the device to monitor the growth of single bacterial cells that undergo symmetric (Bacillus subtili

223 Recent studies strongly suggest that in bacterial cells the order of genes along the chromosomal

224 nstantaneous turgor pressure within cultured bacterial cells; the first time this has been performed

225 at vancomycin treatment sequesters zinc from bacterial cells thereby triggering a Zur-dependent zinc

226 These components exit the bacterial cell through the ComE pore through which the N

227 , matrix production enables biofilm-dwelling bacterial cells to establish an osmotic pressure differe

228 s a genetically programmed response enabling bacterial cells to exit the biofilm in response to parti

229 ription factor that regulates the ability of bacterial cells to uptake and metabolize lactose.

230 Quorum quenching (QQ) is the disruption of bacterial cell-to-cell communication (known as quorum se

231 Since its discovery 22 years ago, the bacterial cell-to-cell communication system, termed quor

232 our recent pioneering developments in single bacterial cell transcriptomic analysis technology, we ge

233 Nearly all motile bacterial cells use a highly sensitive and adaptable sen

234 enabled electromechanical lysis mechanism of bacterial cells using electroconvective vortices near io

235 grobacterium nutrients and imported into the bacterial cell via periplasmic-binding proteins (PBPs) a

236 nd that a Cu(2+) complex readily crosses the bacterial cell wall and inhibits SlyD, which is a molecu

237 ) are a major component of the Gram-negative bacterial cell wall and play an important role in mediat

238 ables the tail tube to penetrate through the bacterial cell wall and serve as a channel for the trans

239 ocesses, to address fundamental questions of bacterial cell wall biogenesis.

240 PG cross-link cleavage and its regulation in bacterial cell wall biogenesis.

241 his report, we exploited one key difference, bacterial cell wall biosynthesis, to detect living bacte

242 , a mechanism utilized by S. aureus to block bacterial cell wall breakdown, limits the induction of p

243 estigated the structural modification of the bacterial cell wall by OligoG CF-5/20 and its effect on

244 ed the effects of muramyl dipeptide (MDP), a bacterial cell wall component that activates NOD2, on HC

245 discomfort, and lipopolysaccharide (LPS), a bacterial cell wall component that induces inflammation,

246 enous structure (MARCO), which recognize the bacterial cell wall component trehalose 6,6'-dimycolate

247 Since MDP is a bacterial cell wall component, ongoing microbial exposur

248 Bacterial cell wall degrading enzyme antimicrobials can

249 The bacterial cell wall is a highly conserved essential comp

250 ozyme containing serum, the integrity of the bacterial cell wall is affected and the cells detach fro

251 The bacterial cell wall is critical for maintenance of cell

252 n channels are associated with the export of bacterial cell wall lipids outside of vacuole.

253 We find that bacterial cell wall peptidoglycan (CW), a universal PAMP

254 ne is an antibiotic which targets sequential bacterial cell wall peptidoglycan biosynthesis enzymes:

255 Degradation of Gram-positive bacterial cell wall peptidoglycan in macrophage and dend

256 ed Gram-positive bacteria via binding to the bacterial cell wall peptidoglycan.

257 osphate (C55-P) and inhibit formation of the bacterial cell wall precursor lipid II.

258 ing to S. aureusteichoic acids and increases bacterial cell wall rigidity.

259 Bacterial cell wall synthesis is the target for some of

260 zymes, which play key morphogenetic roles in bacterial cell wall synthesis.

261 te synthase (UppS) is an essential enzyme in bacterial cell wall synthesis.

262 f oxygen activates a pathway that causes the bacterial cell wall to break down, which, in turn, aids

263 mnipresent constituents of the Gram-positive bacterial cell wall where they fulfill a variety of vita

264 ysaccharide (LPS, the main component of G(-) bacterial cell wall) induced septic shock.

265 are enzymes involved in the assembly of the bacterial cell wall, a major target for antibiotics.

266 an essential stress-bearing component of the bacterial cell wall, is synthesised by penicillin bindin

267 at projects the rest of Aap outward from the bacterial cell wall, promoting intercellular adhesion be

268 Due to specific receptors of the bacterial cell wall, the iron loaded pyoverdine molecule

269 ity often found near the attachment point of bacterial cell wall-anchored proteins.

270 s uncharacterized protein was predicted as a bacterial cell wall-modifying enzyme (CWME) and shown to

271 arge, possibly by altering properties of the bacterial cell wall.

272 eractions that work in unison to disrupt the bacterial cell wall.

273 TG that may occur after self-assembly in the bacterial cell wall.

274 acyl-transferase FemXWv for synthesis of the bacterial cell wall.

275 rial peptidoglycan (PG), the coat woven into bacterial cell wall.

276 ilaments), both oriented tangentially to the bacterial cell wall.

277 have evolved over a billion years to degrade bacterial cell wall.

278 peptidoglycan, the major constituent of the bacterial cell wall.

279 ts its bactericidal effect by binding to the bacterial cell-wall precursor lipid II on the inner memb

280 Bacterial cell walls are composed of the large cross-lin

281 Bacterial cell walls are essential to bacteria, thus mak

282 l and immunologically relevant components of bacterial cell walls.

283 -called 'inner core' sugars of Gram-negative bacterial cell walls.

284 of 4-->3 cross-links in the peptidoglycan of bacterial cell walls.

285 tive and Gram-negative peptidoglycans on the bacterial cell walls.

286 orneal epithelial cells and Escherichia coli bacterial cells, was investigated.

287 or, lyophilised Lactobacillus delbruecki sp. bacterial cells were immobilised with polypyrrole on a p

288 At 2 weeks postinoculation, the bacterial cells were mostly trapped within the surface m

289 roduced at one end of the capillary, and the bacterial cells were suspended in the spacer electrolyte

290 are instead actively transported inside the bacterial cell where they bind and inactivate specific t

291 Results correlate with behavior of bacterial cells, which become resistant to antibiotics a

292 provide sensitive and specific detection of bacterial cells, which can be applied across multiple ap

293 Ribosomal RNA is naturally amplified in bacterial cells, which makes it a promising target for s

294 fective in rupturing and killing the growing bacterial cells, while wafers without nanopillars had no

295 ead-beating module for the disruption of the bacterial cell with the LOC-SERS device enables the appl

296 We observe direct interaction of the bacterial cells with Al NPs and elucidate the nanoshield

297 DNA and 10 colony-forming units (CFU)/ml of bacterial cells with dynamic ranges of 0-100ng/ml (R(2)=

298 Treatment of bacterial cells with high concentrations of these antibi

299 udies have described chromosomal dynamics in bacterial cells with more than two complete chromosome c

300 In particular, as phages can kill bacterial cells within <10 minutes, the associated endot