ライフサイエンスコーパス: autoinducer

1 apabilities in the presence or absence of an autoinducer.

2 in the complex still retained tightly bound autoinducer.

3 ze the cell response to an exogenously added autoinducer.

4 AI-2 sensor protein, LuxP, in a complex with autoinducer.

5 ter the ability of the bacteria to access an autoinducer.

6 blages supplemented with exogenous, purified autoinducer.

7 on-wide detection of signal molecules called autoinducers.

8 n and detection of secreted molecules called autoinducers.

9 nse to extracellular signal molecules called autoinducers.

10 unicate via secreted signal molecules called autoinducers.

11 of extracellular signalling molecules called autoinducers.

12 receptors for acyl-homoserine lactone (AHL) autoinducers.

13 from a microorganism that also produces AHL autoinducers.

14 tection of small signalling molecules called autoinducers.

15 n of low-molecular-weight molecules known as autoinducers.

16 by means of chemical signal molecules called autoinducers.

17 and detection of signalling molecules called autoinducers.

18 ecrete hormone-like compounds referred to as autoinducers.

19 mediated by small molecule signals known as autoinducers.

20 e with extracellular signal molecules called autoinducers.

21 using extracellular signal molecules termed autoinducers.

22 using extracellular signal molecules called autoinducers.

23 g, and responding to signal molecules called autoinducers.

24 up-wide detection of signal molecules called autoinducers.

25 exchange of chemical signal molecules called autoinducers.

26 nother by exchanging chemical signals called autoinducers.

27 of extracellular signaling molecules called autoinducers.

28 s no resemblance to previously characterized autoinducers.

29 of extracellular signalling molecules called autoinducers.

30 cteria secrete hormone-like compounds called autoinducers.

31 e required for competence are quorum-sensing autoinducers.

32 oduce and detect diffusible molecules called autoinducers.

33 ion of extracellular signal molecules called autoinducers.

34 nse to extracellular signal molecules called autoinducers.

35 that are regulated by imported oligopeptide autoinducers.

36 the most rapid to respond to quorum-sensing autoinducers.

37 diated by small signaling molecules known as autoinducers.

38 hanging diffusible signal molecules known as autoinducers.

39 to express the autoinducer molecule cholera autoinducer 1 (CAI-1) (shown previously to prevent virul

40 yme involved in the biosynthesis of cholerae autoinducer-1 (CAI-1), the major Vibrio cholerae autoind

41 atio of signal to cell number for V. harveyi autoinducer-1 and E. coli autoinducer-2 varied as the cu

42 sis of polyamines, N-acylhomoserine lactone (autoinducer-1), and production of vitamins and other bio

43 The bacterial quorum-sensing autoinducer 2 (AI-2) has received intense interest becau

44 ne, which encodes an enzyme that synthesizes autoinducer 2 (AI-2) in other gram-negative bacteria.

45 y network for the uptake of Escherichia coli autoinducer 2 (AI-2) is comprised of a transporter compl

46 Bacterial autoinducer 2 (AI-2) is proposed to be an interspecies m

47 Autoinducer 2 (AI-2) is required for the growth of Aggre

48 Autoinducer 2 (AI-2) produced by the oral pathogen Actin

49 Mutation of luxS, a determinant of the autoinducer 2 (AI-2) quorum signal pathway, increases NT

50 Interestingly, while LuxS/autoinducer 2 (AI-2) regulated biofilms on both HREC and

51 tein interacts with cognate and heterologous autoinducer 2 (AI-2) signals and suggested that the rbsD

52 resent in many bacterial genera, encodes the autoinducer 2 (AI-2) synthase.

53 The QS system used by EHEC is the LuxS/autoinducer 2 (AI-2) system extensively involved in inte

54 Four signals, autoinducer 2 (AI-2), AI-3, and the human hormones epine

55 of the LuxS-associated quorum sensing signal autoinducer 2 (AI-2), it was demonstrated that this orth

56 cross-species bacterial communication signal autoinducer 2 (AI-2), produced by the purified enzymes P

57 furanosyl borate diester (BAI-2) subclass of autoinducer 2 (AI-2), QS molecules.

58 LuxS is responsible for the production of autoinducer 2 (AI-2), which functions in Vibrio harveyi

59 the precursor of the quorum-sensing molecule autoinducer 2 (AI-2).

60 for production of the quorum-sensing signal autoinducer 2 (AI-2).

61 which synthesizes the quorum-sensing signal autoinducer 2 (AI-2).

62 homocysteine, spontaneously cyclizes to form autoinducer 2 (AI-2).

63 uce a class of pheromones collectively named autoinducer 2 (AI-2).

64 esis of an extracellular signaling molecule, autoinducer 2 (AI-2).

65 atalyzes the synthesis of the Vibrio harveyi autoinducer 2 (AI-2).

66 nd increased intracellular concentrations of autoinducer 2 (AI-2); hence, YdgG enhances transport of

67 The gene expression data also suggested that autoinducer 2 uptake was repressed upon exposure to epin

68 hen present with another signaling molecule, autoinducer 2, at high concentrations) and determined th

69 dihydroxy-2,3-pentanedione, the precursor of autoinducer 2.

70 that Vibrio harveyi is capable of importing Autoinducer 2.

71 The quorum-sensing (QS) signal autoinducer-2 (AI-2) has been proposed to promote inters

72 Autoinducer-2 (AI-2) is a QS signaling molecule that is

73 Autoinducer-2 (AI-2) is a Quorum Sensing (QS) molecule u

74 The universal bacterial signal molecule autoinducer-2 (AI-2) is derived from 4,5-dihydroxy-2,3-p

75 via a family of molecules generically termed autoinducer-2 (AI-2) is essential for many phenotypes.

76 Autoinducer-2 (AI-2) is required for biofilm formation a

77 Importantly, autoinducer-2 (AI-2) is synthesized via the enzyme LuxS

78 The extracellular signaling molecule autoinducer-2 (AI-2) mediates quorum-sensing communicati

79 Our prior work shows that production of autoinducer-2 (AI-2) promotes biofilm development and pe

80 The autoinducer-2 (AI-2) quorum-sensing system has been link

81 ene product is an integral component of LuxS/autoinducer-2 (AI-2) quorum-sensing systems in bacteria.

82 The quorum sensing signal autoinducer-2 (AI-2) regulates important bacterial behav

83 . cholerae colonization, that R. obeum luxS (autoinducer-2 (AI-2) synthase) expression and AI-2 produ

84 Autoinducer-2 (AI-2), a class of QS signaling molecules

85 Autoinducer-2 (AI-2), a class of QS signals derived from

86 Autoinducer-2 (AI-2), a secreted signaling molecule orig

87 hile most autoinducers are species specific, autoinducer-2 (AI-2), first identified in the marine bac

88 scores of bacteria, and its signal molecule, autoinducer-2 (AI-2), is synthesized as a product of 1-c

89 O157:H7 as well as E. coli K-12 produces the autoinducer-2 (AI-2), which is synthesized by the produc

90 strate that these spirochetes utilize a LuxS/autoinducer-2 (AI-2)-based quorum-sensing mechanism to r

91 cter actinomycetemcomitans is dependent upon autoinducer-2 (AI-2)-mediated quorum sensing.

92 roduces the universal quorum-sensing signal, autoinducer-2 (AI-2).

93 sis of the quorum-sensing signaling molecule autoinducer-2 (AI-2).

94 synthesizes 4,5-dihydroxy-2,3-pentanedione (autoinducer-2 [AI-2]) and responds to AI-2 by measurably

95 e salvage pathway, the SAM radical pathways, autoinducer-2 biosynthesis, and menaquinone biosynthesis

96 These data indicate that V. harveyi uses autoinducer-2 for quorum sensing, while the other molecu

97 ensitive measurement of the concentration of autoinducer-2 from a variety of sources.

98 is technique was applied to the detection of autoinducer-2 from Escherichia coli and Vibrio harveyi i

99 However, the direct detection of autoinducer-2 has been difficult, leaving the in vivo re

100 for bacterial colonization or infection, and autoinducer-2 has been proposed as a universal interspec

101 r outer membrane protein; luxS, encoding the autoinducer-2 synthase; nadE, encoding an essential NAD

102 Although V. harveyi was able to keep the autoinducer-2 to cell number ratio constant, the ratio o

103 ber for V. harveyi autoinducer-1 and E. coli autoinducer-2 varied as the cultures grew.

104 abolic pathways and limits the production of autoinducer-2, a molecule proposed to play a central rol

105 ed by a quorum sensing (QS) signal molecule, autoinducer-2, to express surface-displayed fusions cons

106 ion were regulated by quorum sensing through autoinducer-2, which is synthesized by the product of th

107 and norepinephrine, and bacterially produced autoinducer 3 (AI-3), through two-component systems.

108 ly with a bacterial quorum sensing molecule, autoinducer 3 (AI-3), to affect bacterial virulence and

109 inducing (Ti) plasmid in the presence of the autoinducer 3-oxooctanoyl-homoserine lactone (OOHL).

110 produced by the intestinal microbial flora, autoinducer-3 (AI-3), and the host hormones epinephrine

111 als from the microbiota or the host, such as autoinducer-3 (AI-3), epinephrine (Epi), and norepinephr

112 The autoinducer-3 (AI-3)/epinephrine (Epi)/norepinephrine (N

113 of coral cell-free culture fluid (CFCF) and autoinducer (a quorum sensing signaling molecule) on cor

114 nsing regulator TraR and its inducing ligand autoinducer (AAI) are soluble in Escherichia coli, where

115 System 2 consists of the LuxS-dependent autoinducer AI-2 and the AI-2 detector, LuxPQ.

116 ommunication; however, a recently discovered autoinducer AI-2 has been proposed to serve as a 'univer

117 The autoinducer AI-2 is a furanosyl borate diester whose syn

118 The LuxS-dependent autoinducer AI-2 is proposed to function in interspecies

119 e positively regulated by the quorum-sensing autoinducer AI-2, which in turn activates a two-componen

120 facilitated by the production and sensing of autoinducer (AI) molecules via quorum sensing.

121 this association: bacterial luminescence or autoinducer (AI) production.

122 p in the biosynthetic pathway of the type II autoinducer (AI-2) in both Gram-positive and Gram-negati

123 r species of bacteria, a recently discovered autoinducer (AI-2) is produced by a large number of bact

124 ne (DPD), the precursor of type II bacterial autoinducer (AI-2).

125 HEC produces another, previously undescribed autoinducer (AI-3) whose synthesis depends on the presen

126 light production in response to two distinct autoinducers (AI-1 and AI-2).

127 hat antagonize the action of the "universal" autoinducer, AI-2, have been reported.

128 One autoinducer, AI-2, is proposed to promote interspecies b

129 via the family of related homoserine lactone autoinducers, AI-2 is a unique, 'universal' signal that

130 hich is regulated by signal molecules called autoinducers (AIs) can protect V. cholerae against preda

131 ibrio harveyi produces and responds to three autoinducers (AIs), and this sensory information converg

132 which extracellular signal molecules, called autoinducers (AIs), are released, accumulate, and are sy

133 secretion and detection of molecules called autoinducers (AIs).

134 ion of extracellular signal molecules called autoinducers (AIs).

135 e with extracellular signal molecules called autoinducers (AIs).

136 ria respond to hormone-like molecules called autoinducers (AIs).

137 nals that elicit new gene expression include autoinducers, amino acids, peptides, proteins, and carbo

138 etection of a diffusible signaling molecule (autoinducer) among a multicellular group, it is consider

139 nce leads to a tradeoff between accessing an autoinducer and accessing nutrients, which determines th

140 ioluminescent even after treatment with both autoinducer and aldehyde, substrate additions that typic

141 the permeability of the cell membrane to the autoinducer and the symmetry of autoinducer diffusion) w

142 onment through a trade-off between retaining autoinducers and accessing nutrients.

143 ested for induction by a set of 33 synthetic autoinducers and analogues, and was most strongly induce

144 substrate analogues also limits synthesis of autoinducers and hence causes reduction in biofilm forma

145 sease has led to the elucidation of numerous autoinducers and their corresponding QS signaling pathwa

146 on (P </= 0.05) in response to the exogenous autoinducers and were classified as QS regulated.

147 hi or other populations for members that use autoinducers and/or other mechanisms to limit colonizati

148 ranslocated to the nucleus in the absence of autoinducer, and truncated LasR-based proteins functione

149 bacteria use acylated homoserine lactones as autoinducers, and Gram-positive bacteria use processed o

150 mmunicate via the secretion and detection of autoinducers, and in V. cholerae, QS represses biofilm f

151 nhibitor (QSI) - a N-acyl homoserine lactone autoinducer antagonist - and then dosed onto healthy tes

152 Detection of and response to the V.harveyi autoinducers are accomplished through two two-component

153 lyses suggested that the observed effects of autoinducers are mediated in part through the quorum sen

154 scriminates between conditions in which both autoinducers are present and all other conditions.

155 Quorum-sensing autoinducers are small molecules that ordinarily regulat

156 Autoinducers are small signaling molecules that mediate

157 While most autoinducers are species specific, autoinducer-2 (AI-2),

158 ododecanoyl homoserine lactone (3OC(12)-HSL) autoinducer as a signaling molecule to coordinate the ex

159 to generate a cyclic lactone, that it is an autoinducer as well as a cross-inhibitor, and that all o

160 AttM) that hydrolyzes acylhomoserine lactone autoinducers, as well as two putative dehydrogenases (At

161 a narrow agar lane and introduced exogenous autoinducer at one terminus of the lane.

162 ention such that other previously identified autoinducers be reevaluated for additional biological fu

163 The deduced AvhR protein has characteristic autoinducer binding and DNA binding domains and is uniqu

164 AvsR possesses characteristic autoinducer binding and helix-turn-helix DNA binding dom

165 ich are predicted to play important roles in autoinducer binding in TraR.

166 Autoinducer binding inactivates the receptors' kinase ac

167 eness to autoinducer required the N-terminal autoinducer-binding domains of LasR and RhlR.

168 inhibit quorum sensing via antagonism of the autoinducer-binding receptors, LasR and RhlR.

169 CviI synthesizes the autoinducer C(10)-homoserine lactone (C(10)-HSL), and Cv

170 V. cholerae is made up of the CqsA-dependent autoinducer CAI-1 and a sensor called CqsS.

171 At 10 microM, the cholera-autoinducer CAI-1 stimulates activity 4.8-fold.

172 nd bacteria were supplemented with exogenous autoinducers CAI-1 or AI-2 produced by recombinant strai

173 A novel autoinducer called AI-2, originally discovered in the qu

174 promote intraspecies communication, but one autoinducer, called AI-2, is produced and detected by a

175 We show that increased access to an autoinducer can enhance cooperation, but can also reduce

176 ired for synthesis of the biofilm dispersion autoinducer cis-2-decenoic acid in the human pathogen Ps

177 ex with the centrally important oligopeptide autoinducer competence and sporulation factor (CSF, also

178 ducer LuxS, low pH induced another potential autoinducer component, the LuxH homolog RibB.

179 Extracellular autoinducer concentrations in cultures of Vibrio harveyi

180 Calculations of autoinducer concentrations showed that expression was si

181 in high local bacterial densities with high autoinducer concentrations.

182 f AHLs, and the gene was designated as aidP (autoinducer degrading gene from Planococcus sp.).

183 orter as a function of space and time as the autoinducer diffused along the lane.

184 brane to the autoinducer and the symmetry of autoinducer diffusion) we construct the solution of the

185 ed by high concentrations of three different autoinducers, each having six-carbon acyl chains.

186 mproved by using enrichment media containing autoinducers either expressed from cloned synthase genes

187 Most autoinducers enable intraspecies communication; however,

188 Population-wide detection of autoinducers enables bacteria to orchestrate collective

189 inducer-1 (CAI-1), the major Vibrio cholerae autoinducer engaged in quorum sensing.

190 acterium tumefaciens, there is no endogenous autoinducer for SdiA in E.coli: the E.coli genome does n

191 uorum sensing, bacteria use chemicals called autoinducers for cell-cell communication.

192 that phagocyte-derived oxidants target these autoinducers for inactivation as an innate defense mecha

193 e also capable of acting as a folding-switch autoinducers for SdiA.

194 System 1 consists of the LuxM-dependent autoinducer HAI-1 and the HAI-1 sensor, LuxN.

195 Proteins capable of degrading these autoinducers have been called "quorum-quenching" enzymes

196 een shown to secrete a signal related to the autoinducer II (AI-2) of the signal system 2 pathway in

197 The autoinducer II (AI-2) pathway has recently been shown to

198 Autoinducer inactivator A (AiiA) is a metal-dependent N-

199 e full-length LuxR has not been purified, an autoinducer-independent N-terminally truncated form of L

200 esigned to precisely translate extracellular autoinducer information into internal changes in gene ex

201 on reaching a threshold concentration, these autoinducers interact with transcription factors to regu

202 oretical model, cells synthesize and secrete autoinducers into the environment, up-regulate their pro

203 thesized AI-2 we showed that AI-2 is not the autoinducer involved in the bacterial signaling.

204 The major V. cholerae autoinducer is (S)-3-hydroxytridecan-4-one (CAI-1).

205 ation density increases, the accumulation of autoinducers leads to co-ordinated changes in gene expre

206 ich are transcribed when quorum sensing (QS) autoinducer levels are low.

207 ermore propose LuxO and LuxR interact at all autoinducer levels via an unknown mechanism.

208 roteins were only activated by their cognate autoinducer ligand and not by N-butyryl-L-homoserine lac

209 In addition to the autoinducer LuxS, low pH induced another potential autoi

210 AI-2 is an autoinducer made by many bacteria.

211 s can enter mammalian cells and suggest that autoinducers may influence gene expression in host cells

212 On the basis of our findings, quorum sensing autoinducers merit further investigation as biomarkers f

213 e presence of an acylated homoserine lactone autoinducer molecule [N-(3-oxohexanoyl) homoserine lacto

214 hia coli Nissle 1917 (Nissle) to express the autoinducer molecule cholera autoinducer 1 (CAI-1) (show

215 In the three-dimensional structure, the autoinducer molecule is sequestered in a deep pocket in

216 In this process, autoinducer molecules are detected by membrane-bound sen

217 In vitro experiments suggest that autoinducer molecules are signals used to coordinate coo

218 The vibrio autoinducer molecules bind to transmembrane receptors of

219 These data provide evidence that autoinducer molecules from human pathogens can enter mam

220 ed in response to the concentration of small autoinducer molecules that are also released by the bact

221 e biosynthesis of one or more quorum sensing autoinducer molecules.

222 oup-wide secretion and detection of specific autoinducer molecules.

223 o the plant invasion defect displayed by the autoinducer mutant.

224 erium Vibrio harveyi exclusively detects the autoinducer N-((R)-3-hydroxybutanoyl)-L-homoserine lacto

225 TraR requires its cognate autoinducer N-3-oxooctanoyl-homoserine lactone (OOHL) fo

226 ein SdiA of Escherichia coli and a candidate autoinducer N-octanoyl-L-homoserine lactone (C8-HSL) has

227 as cultured with and without added exogenous autoinducers [N-(3-oxododecanoyl) homoserine lactone and

228 d by quorum sensing via TraR and its cognate autoinducer, N-(3-oxo-octanoyl)-L-homoserine lactone.

229 The Pseudomonas autoinducer, N-3-oxododecanoyl homoserine lactone (3-O-C

230 eudomonas aeruginosa, along with its cognate autoinducer, N-butyryl homoserine lactone (C(4)-HSL), re

231 Here we show that two P. aeruginosa autoinducers, N-3-oxododecanoyl-homoserine lactone and N

232 These results indicate that TDA acts as an autoinducer of its own synthesis and suggest that roseob

233 lar and intercellular communication, both as autoinducers of their own production.

234 endent of the lux promoter and unaffected by autoinducers or the level of lux expression, but the add

235 TraR activity requires the autoinducer pheromone N-3-oxooctanoyl-l-homoserine lacto

236 nce in Vibrio fischeri ES114 is activated by autoinducer pheromones, and this regulation serves as a

237 Inactivation of the autoinducer prevented both the up-regulation of virulenc

238 The autoinducer produced by one pherotype activates its coen

239 of sigma 38 and dgt leads to a model for how autoinducer production is controlled under changing phys

240 Elucidating the mechanisms that control autoinducer production is, thus, pertinent to understand

241 Most quorum-sensing autoinducers promote intraspecies communication, but one

242 The autoinducers promoted nuclear localization of chimeric p

243 ce of the native acylated homoserine lactone autoinducer, provided that they stabilize a closed confo

244 hat at high cell density (in the presence of autoinducers), quorum sensing represses TTS in V. harvey

245 e polymorphism for the identification of agr autoinducer receptor specificity groups within a populat

246 species show high intraspecific diversity of autoinducer-receptor alleles, called pherotypes.

247 oth environmental factors and quorum sensing autoinducers regulate the metabolism and/or processing o

248 Genetic screens designed to discover autoinducer-regulated targets in V. harveyi have reveale

249 Responsiveness to autoinducer required the N-terminal autoinducer-binding

250 Incubation with autoinducer resulted in complete tissue loss in all cora

251 Here we demonstrate that the Vibrio cholerae autoinducer (S)-3-hydroxytridecan-4-one, termed CAI-1, i

252 orum-sensing circuits, each consisting of an autoinducer-sensor pair, to control the expression of ge

253 nsing circuit of V. cholerae consists of two autoinducer/sensor systems, CAI-1/CqsS and AI-2/LuxPQ, a

254 A mutant unable to produce autoinducer signal molecules (sinI) is deficient in its

255 acteria recognize two different forms of the autoinducer signal, both derived from 4,5-dihydroxy-2,3-

256 sion that develop in response to a diffusing autoinducer signal.

257 hat bacterial quorum sensing signals, called autoinducers, signal to eukaryotic cells, mimicking horm

258 es on production, detection, and response to autoinducer signaling molecules.

259 cterial cells through converging pathways to autoinducer signaling.

260 at played a dual role as nutrient source and autoinducer sink.

261 e also describe several mutants with altered autoinducer specificity.

262 luxS mutant, unable to produce the bacterial autoinducer, still responds to a eukaryotic cell signal

263 the genes encoding an additional V. cholerae autoinducer synthase and its cognate sensor.

264 r synthases and was predicted to be the only autoinducer synthase encoded by A. baumannii.

265 Disruption of the autoinducer synthase gene, sinI, abolished EPS II produc

266 e shown a heterogeneous promoter activity of autoinducer synthase genes, suggesting that some of the

267 CspD, polysaccharide transporter RfbX3, and autoinducer synthase PhzI.

268 nd we also found that ainS, which encodes an autoinducer synthase, mediates repression of luminescenc

269 production of AI-2 is dependent on the LuxS autoinducer synthase.

270 was similar to members of the LuxI family of autoinducer synthases and was predicted to be the only a

271 CqsA, one of two known autoinducer synthases in V. cholerae, acts through HapR

272 atY), the RpoS growth phase regulon, and the autoinducer synthesis protein LuxS.

273 Although the nature of the autoinducer synthesized by LuxS cannot be deduced from t

274 ontain a gene analogous to the LuxI and TraI autoinducer synthetases.

275 ation also affects the synthesis of the AI-3 autoinducer that activates enterohemorrhagic Escherichia

276 ion of extracellular signal molecules called autoinducers that elicit population-wide changes in gene

277 and release chemical signal molecules called autoinducers that increase in concentration as a functio

278 ports indicate that the signaling molecules (autoinducers) that mediate QS in Pseudomonas aeruginosa

279 tein and of the signal molecule, a bacterial autoinducer, that is involved.

280 non-thermal plasma to modify and degrade AHL autoinducers thereby attenuating QS-dependent virulence

281 h their own production and the production of autoinducers, thereby establishing internal and external

282 marine bacterium, Vibrio harveyi, uses three autoinducers to achieve intra-species, intra-genera and

283 nicate with chemical signal molecules called autoinducers to control collective behaviors.

284 teria communicate via small molecules called autoinducers to coordinate collective behaviors.

285 detection of extracellular chemicals called autoinducers to monitor cell population density.

286 ilizes hormone-like compounds referred to as autoinducers to regulate bacterial gene expression.

287 ous environmental factors and quorum sensing autoinducers to regulate the metabolism of various nucle

288 cluding Vibrio cholerae, the accumulation of autoinducers triggers repression of genes responsible fo

289 in the complex, together with the variety of autoinducer-type molecules that can apparently act as fo

290 The detection of these autoinducers ultimately leads to the production of LuxR,

291 An important class of autoinducers used by Gram-negative bacteria is the famil

292 ll density in the presence of quorum-sensing autoinducers, V. cholerae represses these behaviours at

293 ally represent the external concentration of autoinducers via the level of monitor proteins.

294 nt groups of signalling molecules, including autoinducers, virulence factors and morphogenic substanc

295 gene rhlI and the production of the C(4)-HSL autoinducer were increased in the ptxR mutant, while the

296 isogenic cells in a population might produce autoinducers, whereas others might not.

297 nase that acts as the receptor for the CAI-1 autoinducer which is produced by the CqsA synthase.

298 e bacteria use acyl-homoserine lactone (AHL) autoinducers, which are detected by one of two receptor

299 Unlike other autoinducers, which are specific to a particular species

300 rial community contained in extracellular QS autoinducers with the intracellular environmental inform