ライフサイエンスコーパス: fischeri

1 or the inhibition of biofilm formation by V. fischeri.

2 urring, non-bioluminescent strains of Vibrio fischeri.

3 ated to promote symbiotic colonization by V. fischeri.

4 rum sensing proteins LuxR and LuxI of Vibrio fischeri.

5 n OMV production and biofilm formation by V. fischeri.

6 a scolopes and the luminous bacterium Vibrio fischeri.

7 opes and the bioluminescent bacterium Vibrio fischeri.

8 a second anthranilate-activating NRPS in N. fischeri.

9 rahaemolyticus, Vibrio vulnificus and Vibrio fischeri.

10 milar to that triggered by infection with V. fischeri.

11 ted to RscS-mediated biofilm formation in V. fischeri.

12 ironment to regulate biofilm formation by V. fischeri.

13 e loci contribute to biofilm formation in V. fischeri.

14 omonas aeruginosa; the model symbiont Vibrio fischeri.

15 for two CsrA-regulating small RNAs in Vibrio fischeri.

16 clic di-GMP in the control of motility of V. fischeri.

17 quorum sensing signaling pathway from Vibrio fischeri.

18 inally studied in the marine symbiont Vibrio fischeri.

19 modulating other symbiotic functions, in V. fischeri.

20 promoting colonization of E. scolopes by V. fischeri.

21 ls relative to that achieved by wild-type V. fischeri.

22 factor similar to the LuxR protein of Vibrio fischeri.

23 high density by the marine bacterium Vibrio fischeri.

24 Euprymna scolopes, the symbiotic host of V. fischeri.

25 and characterized a glnD:mTn5Cm mutant of V. fischeri.

26 an elevated bacterial toxicity to Aliivibrio fischeri.

27 ortant insights into biofilm dispersal by V. fischeri.

28 tes the aphrodisiac-like activity of live V. fischeri.

29 on the acute toxicity of OSPW toward Vibrio fischeri.

30 CRP, may help control cAMP-CRP activity in V.fischeri.

31 ts specific, bioluminescent symbiont, Vibrio fischeri.

32 positively control bioluminescence in Vibrio fischeri.

33 Previously, we identified in Vibrio fischeri a putative sensor kinase, RscS, required for in

34 Vibrio fischeri, a bioluminescent marine bacterium, exists in a

35 Vibrio fischeri, a luminescent marine bacterium, specifically c

36 d Eisenia fetida, the marine bacteria Vibrio fischeri, a suite of ten prokaryotic species, and a euka

37 First, animals inoculated with V. fischeri aboard the space shuttle showed effective colon

38 ted intracellular citrate levels in a Vibrio fischeri aconitase mutant correlate with activation of t

39 ould establish symbiosis, suggesting that V. fischeri acquires nutrients related to this compound wit

40 We have investigated the impact of the V. fischeri acyl-HSL synthase AinS on both luminescence and

41 st that the two quorum-sensing systems in V. fischeri, ain and lux, sequentially induce the expressio

42 ful colonization of E. scolopes, i.e. the V. fischeri ainS mutant failed to persist in the squid ligh

43 Here, we report that Vibrio fischeri also releases TCT, which acts in synergy with l

44 Using Vibrio fischeri , an acute bacterial toxicity was found for COF

45 his system include the genome sequence of V. fischeri, an expressed sequence tagged library for E. sc

46 HPTLC) in direct combination with Aliivibrio fischeri and Bacillus subtilis bioassays.

47 tant insight into the interaction between V. fischeri and E. scolopes.

48 s important for symbiotic colonization by V. fischeri and establishes a paradigm for evaluating two-c

49 The association of Vibrio fischeri and Euprymna scolopes provides insights into tr

50 f the symbiosis between the bacterium Vibrio fischeri and its squid host, which can be observed direc

51 The bioluminescent bacterium Vibrio fischeri and juveniles of the squid Euprymna scolopes sp

52 and bioluminescent (luxCDABE from Aliivibrio fischeri and Photorhabdus luminescens, NanoLuc) reporter

53 utualism between the marine bacterium Vibrio fischeri and the Hawaiian bobtail squid, we characterize

54 between the bioluminescent bacterium Vibrio fischeri and the Hawaiian bobtail squid.

55 athed flagellum in both the mutualist Vibrio fischeri and the pathogen Vibrio cholerae promotes relea

56 n the symbiosis between the bacterium Vibrio fischeri and the squid Euprymna scolopes, which proceeds

57 in the light-organ symbiosis between Vibrio fischeri and the squid Euprymna scolopes.

58 The inhibition effect of OSPW on Vibrio fischeri and the toxicity effect on goldfish primary kid

59 oserine lactone synthase gene luxI of Vibrio fischeri and three genes that resemble the acylhomoserin

60 uorum sensing systems such as LuxR of Vibrio fischeri and TraR of Agrobacterium tumefaciens, there is

61 otein necessary for biofilm maturation by V. fischeri and, based on the conservation of bmp, potentia

62 ction between the Lux and Syp pathways in V. fischeri, and furthers our understanding of how the Lux

63 philus influenzae, Proteus mirabilis, Vibrio fischeri, and Pasteurella multocida are all cleaved by R

64 ADase activity in culture supernatants of V. fischeri, and this mutant initiated the light organ symb

65 a scolopes forms a natural symbiosis with V. fischeri, and utilizes the symbiont-derived bioluminesce

66 These results indicate a role for V. fischeri AOX in aerobic respiration during NO stress.

67 l regulation of TMAO reductase operons in V. fischeri appears to differ from that in previously studi

68 NADPH-utilizing flavin reductase from Vibrio fischeri are quite similar to that of the wild-type FRP(

69 This study lays the foundation for using V. fischeri as a model system for studying TMAO reductases

70 colopes and its luminescent bacterium Vibrio fischeri as a model system.

71 These updates further advance V. fischeri as an important model for understanding interce

72 mbiosis between Euprymna scolopes and Vibrio fischeri As the juvenile host matures, it develops compl

73 work suggests that the tissue with which V. fischeri associates not only can detect bioluminescence

74 wed coumarin to be active against Aliivibrio fischeri bacteria down to 100ng/band.

75 pes squid is colonized exclusively by Vibrio fischeri bacteria.

76 Vibrio fischeri belongs to the Vibrionaceae, a large family of

77 DPPH( *) reagent and luminescent Aliivibrio fischeri bioassay.

78 accharide, however, little is known about V. fischeri biofilm matrix components.

79 Here, we asked whether OMVs are part of V. fischeri biofilms.

80 factor CysB is shown to be necessary for V. fischeri both to grow on several sulfur sources in vitro

81 ecologically distinct bioluminescent Vibrio fischeri by colonization and growth within the light org

82 strate that SypE controls biofilms in Vibrio fischeri by regulating the activity of SypA, a STAS (sul

83 popolysaccharide (LPS) or free lipid A of V. fischeri can trigger morphological changes in the juveni

84 ggregation, suggest a two-step process of V. fischeri cell engagement: association with host cilia fo

85 ctly and in real time, approximately five V. fischeri cells aggregate along the mucociliary membranes

86 rrounding mucus, the environment in which V. fischeri cells aggregate before migration into the organ

87 h inocula demonstrated that environmental V. fischeri cells aggregate during a 3 h period in host-she

88 wing first exposure, only approximately 5 V. fischeri cells aggregated on the organ surface.

89 Vibrio fischeri cells are the sole colonists of a specialized l

90 -Seq dataset representing host-associated V. fischeri cells from colonized juvenile E. scolopes, as w

91 glycerol/tryptone-based medium, wild-type V. fischeri cells initially excrete acetate but, in a metab

92 ght-organ crypts, where the population of V. fischeri cells resides.

93 cent strains exhibit monophyly within the V. fischeri clade.

94 p, influence aggregate size and, thereby, V. fischeri colonization efficiency.

95 In a screen for V. fischeri colonization mutants, we identified a strain th

96 a galactose-utilization mutant (galK) of V. fischeri colonized juvenile squid to wild-type levels, i

97 V. fischeri colonizes the crypts of a host organ that is us

98 by SypE is a critical mechanism by which V. fischeri controls biofilm development and symbiotic colo

99 thus reveals a novel group of genes that V. fischeri controls through a sigma54-dependent response r

100 We found that His-tagged V. fischeri CRP could bind sequences upstream of both luxR

101 V. fischeri culture media have lower osmolarities than are

102 y demonstrated that oxygen consumption by V. fischeri CydAB quinol oxidase is inhibited by NO treatme

103 imitation or (ii) a mutation that renders V. fischeri defective in the synthesis of a homolog of the

104 id Euprymna scolopes by the bacterium Vibrio fischeri depends on bacterial biofilm formation on the s

105 Robust biofilm formation by Vibrio fischeri depends upon activation of the symbiosis polysa

106 llar biogenesis and hence motility of Vibrio fischeri depends upon the presence of magnesium.

107 Here, we show that the repressor NagC of V. fischeri directly regulates several chitin- and N-acetyl

108 t cAMP-CRP is active and important in Vibrio fischeri during colonization of its host squid Euprymna

109 Lipid A from V. fischeri, E. coli, or S. flexneri induced apoptosis.

110 o the already considerable utility of the V. fischeri-E. scolopes model system.

111 Although V. fischeri encodes two putative large adhesins, LapI (near

112 rio symbiosis, the bacterial symbiont Vibrio fischeri encounters host-derived NO, which has been hypo

113 Comparison of the V. fischeri ES114 genome with that of conspecific strain MJ

114 Bioluminescence in Vibrio fischeri ES114 is activated by autoinducer pheromones, a

115 s model, we found that bioluminescence in V. fischeri ES114 is modulated by glucose and stimulated by

116 ble for this phenomenon, the lipid A from V. fischeri ES114 LPS was isolated and characterized by mul

117 In contrast, V. fischeri ES114 mutants incapable of aerobactin productio

118 ture fluids from the marine bacterium Vibrio fischeri ES114 prevent the growth of other vibrio specie

119 conditions, aerobactin production allows V. fischeri ES114 to competitively exclude Vibrio harveyi,

120 t known relatives, flrA mutant strains of V. fischeri ES114 were completely abolished in swimming cap

121 vnA and HvnB are proteins secreted by Vibrio fischeri ES114, an extracellular light organ symbiont of

122 Vibrio fischeri ES114, an isolate from the Euprymna scolopes li

123 In the squid symbiont V. fischeri ES114, RscS controls light-organ colonization b

124 Building on the genome project of Vibrio fischeri ES114, we used a comparative approach to identi

125 Here we report the genome sequence of V. fischeri ES114, which enters into a mutualistic symbiosi

126 The marine bacterium Vibrio fischeri establishes a mutualistic symbiosis within the

127 nescent bacteria inhibition test with Vibrio fischeri exhibited that the TPs irgarol sulfoxide and te

128 Vibrio fischeri exists in a symbiotic relationship with the Haw

129 Like other gram-negative organisms, V. fischeri expresses lipopolysaccharide (LPS) on its cell

130 Magnesium-dependent induction of Vibrio fischeri flagellar (Mif) biogenesis depends upon two dig

131 Hmp protects V. fischeri from NO inhibition of aerobic respiration, and

132 (i) selection of the specific partner Vibrio fischeri from the bacterioplankton during symbiosis onse

133 ymna scolopes squid by bioluminescent Vibrio fischeri from the North Pacific Ocean.

134 that are produced by the squid to select V. fischeri from the ocean microbiota.

135 osition in a 1 mM bulk solution above Vibrio fischeri (gamma-Protebacteria-Vibrionaceae) bacterial bi

136 etween E. coli Pgm and the product of the V. fischeri gene, which was therefore designated pgm.

137 -Mbp genome sequence represents the first V. fischeri genome from an S. robusta symbiont and the firs

138 Analysis of the V. fischeri genome revealed the presence of a putative thir

139 nt response regulators encoded within the V. fischeri genome.

140 edicted, in the presence of NO, wild-type V. fischeri grew more slowly on hemin than a hnoX deletion

141 g symbiosis onset and, (ii) modulation of V. fischeri growth in symbiotic maintenance.

142 Importantly, the acs mutant of V. fischeri has a competitive defect when colonizing the sq

143 ion of the lux operon (luxICDABEG) of Vibrio fischeri has been intensively studied as a model for quo

144 V. fischeri has six flagellin genes that are uniquely arran

145 Vibrio fischeri has the capacity to produce at least two distin

146 the luminescence (lux) genes of symbiotic V. fischeri have been shown to be highly induced within the

147 nce inhibition of the marine bacteria Vibrio fischeri, have been used.

148 V. fischeri hnoX encodes a heme NO/oxygen-binding (H-NOX) p

149 The study of V. fischeri HnoX permits us to understand not only host-ass

150 n colonizing the light organ of the model V. fischeri host, the Hawaiian bobtail squid Euprymna scolo

151 id not compromise symbiotic competence of V. fischeri; however, levels of colonization of an ainS lux

152 reduced the inhibition of luminescence to V. fischeri, i.e., were beneficial for the bacteria, with P

153 ignificantly decreased the growth rate of V. fischeri in culture.

154 rmed with a truncated lux operon from Vibrio fischeri, in the presence of 1-100 nM exogenous acyl-hom

155 discovered that the marine bacterium Vibrio fischeri induces sexual reproduction in one of the close

156 s, this work reveals a mechanism by which V. fischeri inhibits cellulose-dependent biofilm formation

157 The bioluminescent bacterium Vibrio fischeri initiates a specific, persistent symbiosis in t

158 lay a role in the normal process by which V. fischeri initiates its colonization of the nascent light

159 ing alterations in membrane physiology as V. fischeri initiates its symbiotic program.

160 A Deltahmp mutant of V. fischeri initiates squid colonization less effectively t

161 Vibrio fischeri is a bioluminescent bacterium that colonizes an

162 Vibrio fischeri is a bioluminescent bacterium that enters into

163 Biofilm formation by Vibrio fischeri is a complex process involving multiple regulat

164 Biofilm formation by Vibrio fischeri is a complex process that requires multiple reg

165 these results show that the flagellum of V. fischeri is a complex structure consisting of multiple f

166 cence emitted by the marine bacterium Vibrio fischeri is a particularly striking result of individual

167 Flagellum-mediated motility of Vibrio fischeri is an essential factor in the bacterium's abili

168 During the early stages of colonization, V. fischeri is exposed to host-derived nitric oxide (NO).

169 uxICDABEG) of the symbiotic bacterium Vibrio fischeri is regulated by the transcriptional activator L

170 Genetic arrangement of the flrA locus in V. fischeri is similar to motility master-regulator operons

171 Vibrio fischeri is the bacterial symbiont within the light-emit

172 Vibrio fischeri is the exclusive symbiont residing in the light

173 The marine bacterium Vibrio fischeri is the monospecific symbiont of the Hawaiian bo

174 Vibrio fischeri is the sole species colonizing the light-emitti

175 The motile bacterium Vibrio fischeri is the specific bacterial symbiont of the Hawai

176 fied TMAO reductase activity in symbiotic V. fischeri isolates associated with the light organs of ad

177 Vibrio fischeri isolates from Euprymna scolopes are dim in cult

178 combination with L(H) or luciferase from V. fischeri (L(F)).

179 it is possible that these features of the V. fischeri lipid A may underlie the ability of E. scolopes

180 ne transferase for the lipid-A portion of V. fischeri lipopolysaccharide.

181 ild-type and waaL strains showed that the V. fischeri LPS has a single O-antigen repeat composed of y

182 Purified V. fischeri LPS, as well as the LPS of V. cholerae, Haemoph

183 The Vibrio fischeri luminescence (lux) operon is regulated by a quo

184 , we identified three novel regulators of V. fischeri luminescence and seven regulators that altered

185 rofiles determined from inhibition of Vibrio fischeri luminescence.

186 ent transcriptional activation of the Vibrio fischeri lux operon during quorum sensing.

187 With the Vibrio fischeri lux quorum sensing circuit, the hypoxia-respons

188 Bioluminescence generated by the Vibrio fischeri Lux system consumes oxygen and reducing power,

189 The V. fischeri luxI mutant does not express detectable light l

190 The Vibrio fischeri LuxR protein is the founding member of a family

191 ein and a number of other homologs of Vibrio fischeri LuxR that function as receptors for N-acylhomos

192 Taken together, these data indicate that V. fischeri LuxS affects both luminescence regulation and c

193 this study, we investigated the impact of V. fischeri LuxS on luminescence and colonization competenc

194 e closely related sexual species Neosartorya fischeri, many of which may have roles in the pathogenic

195 The results suggest that V. fischeri may help modulate the host stress responses und

196 We used a recently developed V. fischeri microarray to identify genes that are controlle

197 new subgroup of PTase genes from Neosartorya fischeri, Microsporum canis, and Trichophyton tonsurans

198 a chemoattractant gradient that promotes V. fischeri migration into host tissues.

199 ly identified several non-Lux proteins in V. fischeri MJ-100 whose expression was dependent on LuxR a

200 ablishing that there is a LuxR regulon in V. fischeri MJ-100 whose genes are coordinately expressed d

201 re fully characterize the LuxR regulon in V. fischeri MJ-100, real-time reverse transcription-PCR was

202 mbionts, is absent from the fish symbiont V. fischeri MJ11.

203 To understand environmental influences on V. fischeri motility, we investigated migration of this org

204 A V. fischeri mutant defective in chitin catabolism was able

205 The V. fischeri mutant grew poorly with galactose as a sole car

206 A V. fischeri mutant unable to produce PepN is significantly

207 Through phenotypic studies of V. fischeri mutants we have found that the AinS-signal is t

208 nt bacteria (in the Euprymna scolopes-Vibrio fischeri mutualism) is discussed.

209 scence reactions using FRP(H) and the Vibrio fischeri NAD(P)H-utilizing flavin reductase G (FRG(F)) i

210 ganisms and toxicity end points using Vibrio fischeri (nonspecific), specific fish macrophage antimic

211 Our data suggest that V. fischeri normally senses a host-generated NO signal thro

212 acetylaszonalenin synthetase of Neosartorya fischeri NRRL 181 activates anthranilate to anthranilyl-

213 These studies indicate that the unusual V. fischeri O-antigen sugars play a role in the early phase

214 ent with that activity, introduction into V. fischeri of medium-copy plasmids carrying these genes in

215 We report the presence in V. fischeri of ompU, a gene encoding a 32.5-kDa protein hom

216 a scolopes and the luminous bacterium Vibrio fischeri offers the opportunity to decipher the hour-by-

217 A null mutation introduced into the V. fischeri ompU resulted in the loss of an OMP with an est

218 The expression of the V. fischeri OmpU was not significantly affected by either (

219 lation and to contribute to the growth of V. fischeri on cystine, which is the oxidized form of cyste

220 n of 4 in Escherichia coli expressing the N. fischeri pcPTase gene.

221 ut may also use this light to monitor the V. fischeri population.

222 to be differentially expressed among the V. fischeri populations occupying the various colonization

223 these results suggest the biogeography of V. fischeri populations within the squid light organ impact

224 Vibrio fischeri possesses two acyl-homoserine lactone quorum-se

225 Vibrio fischeri possesses two quorum-sensing systems, ain and l

226 Vibrio fischeri produces a specific biofilm to promote coloniza

227 lar Microbiology, Dunn et al. report that V. fischeri produces an NO-inducible and NO-resistant alter

228 e here that the flavohaemoglobin, Hmp, of V. fischeri protects against NO, both in culture and during

229 Here, we show that a single V. fischeri protein, the previously uncharacterized EroS, f

230 h a recently developed metabolic model of V. fischeri provides us with a clearer picture of the metab

231 Finally, we show that V. fischeri, purified EroS, and other bacterial chondroitin

232 V. fischeri qsrP and ribB mutants exhibited no distinct phe

233 This demonstrates that V. fischeri quorum sensing regulates a substantial number o

234 enes, we examined the protein patterns of V. fischeri quorum-sensing mutants defective in luxI, ainS,

235 The Vibrio fischeri quorum-sensing signal N-3-oxohexanoyl-l-homoser

236 the ainS promoter depended on whether the V. fischeri regulatory gene litR was also introduced.

237 The light-organ symbiont Vibrio fischeri releases N-acetylglucosaminyl-1,6-anhydro-N-ace

238 The bacterium Vibrio fischeri requires bacterial motility to initiate coloniz

239 ymna scolopes by the marine bacterium Vibrio fischeri requires the symbiosis polysaccharide (syp) gen

240 ilm formation by the marine bacterium Vibrio fischeri requires the Syp polysaccharide, but the involv

241 whether the net release of PG monomers by V. fischeri resulted from lytic transglycosylase activity o

242 gions of a number of flagellar operons in V. fischeri revealed apparent sigma(54) recognition motifs,

243 The genome sequence of Vibrio fischeri revealed three putative TMAO reductase operons,

244 Overexpression of the Vibrio fischeri sensor kinase RscS induces expression of the sy

245 omonas shigelloides, Vibrio cholerae, Vibrio fischeri, Shewanella putrefaciens, and Pseudomonas aerug

246 Finally, a single mutation in V. fischeri-specifically, deletion of the lux operon, which

247 arly stage of symbiotic initiation in the V. fischeri-squid model symbiosis, and more broadly it adds

248 describe the draft genome sequence of Vibrio fischeri SR5, a squid symbiotic isolate from Sepiola rob

249 tivity associated with whole cells of Vibrio fischeri strain ES114 was identified as the product of a

250 ation of juvenile E. scolopes; however, a V. fischeri strain lacking TMAO reductase activity displays

251 When grown in culture, cells of V. fischeri strain PMF8, in which litR was insertionally in

252 prone to later superinfection by a second V. fischeri strain.

253 pared and analyzed the ain locus from two V. fischeri strains and a Vibrio salmonicida strain to expl

254 These 'dark' V. fischeri strains remained non-bioluminescent even after

255 nes) was absent in over 97% of these dark V. fischeri strains.

256 promotes successful squid colonization by V. fischeri, supporting its potential role in initiation of

257 tive during colonization, suggesting that V. fischeri symbionts are exposed to NO.

258 We studied the Euprymna scolopes-Vibrio fischeri symbiosis to characterize, in vivo and in real

259 TPs exhibited higher toxic effects on Vibrio fischeri than BP-4.

260 e less toxic toward the bacterium Aliivibrio fischeri than their parent compounds.

261 is specifically colonized by cells of Vibrio fischeri that are obtained from the ambient seawater.

262 606 bp open reading frame was cloned from V. fischeri that encoded a protein, which we named LitR, th

263 have cloned a gene, designated flrA, from V. fischeri that encodes a putative sigma(54)-dependent tra

264 o high density, we identified a mutant of V. fischeri that exhibited an apparent defect in symbiosis

265 ore synthesis and symbiosis competence in V. fischeri that involves the glnD gene.

266 na scolopes and its bacterial partner Vibrio fischeri, the bacteria induce dramatic morphogenesis of

267 During quorum sensing in Vibrio fischeri, the luminescence, or lux, operon is regulated

268 Vibrio fischeri, the symbiotic partner of the Hawaiian bobtail

269 derivatives (1-4) isolated from Neosartorya fischeri, three of which had significant antimicrobial a

270 We found the luminescence of V. fischeri to be correlated with external osmolarity both

271 e understanding of the matrix produced by V. fischeri to enhance cell-cell interactions and promote s

272 tween the squid Euprymna scolopes and Vibrio fischeri to examine this process.

273 accharide locus, syp, is required for Vibrio fischeri to form a symbiotic association with the squid

274 RscS is an SK required for Vibrio fischeri to initiate a symbiotic partnership with the Ha

275 ght organ, in which case, the response of V. fischeri to NO is of considerable interest.

276 host-like pH increased the resistance of V. fischeri to the cationic antimicrobial peptide polymixin

277 s and its luminous bacterial partner, Vibrio fischeri, to define the impact of colonization on transc

278 on mediated by the syp gene cluster helps V. fischeri transition from a dispersed planktonic lifestyl

279 his association, we searched a library of V. fischeri transposon insertion mutants for those that fai

280 r contributor to TMAO-dependent growth in V. fischeri under the conditions tested.

281 The marine bacterium Vibrio fischeri uses a biofilm to promote colonization of its e

282 a component of the host defense, and that V. fischeri uses a cytotoxin-like molecule to induce host d

283 The squid symbiont Vibrio fischeri uses an elaborate TCS phosphorelay containing a

284 Vibrio fischeri uses the AinS/AinR pheromone-signaling system t

285 The marine bacterium Vibrio fischeri uses two acyl-homoserine lactone (acyl-HSL) quo

286 -scale mutagenesis of a class of genes in V. fischeri using a genomic approach and emphasizes the imp

287 iofilm formation and host colonization by V. fischeri via its impact on transcription of the symbiosi

288 and sensed by the bacterial symbiont, Vibrio fischeri, via the NO sensor HnoX.

289 Our results show that the V. fischeri waaL mutant has a motility defect, is significa

290 Complete removal of toxicity toward Vibrio fischeri was achieved after ozonation followed by 28-day

291 The acute toxicity of OSPW toward Vibrio fischeri was reduced after the solar/chlorine treatment.

292 genetic tractability of the bacterium Vibrio fischeri, we explore the regulation of aox expression an

293 sion of LitR, the global regulator in Vibrio fischeri, we have performed a series of genetic and phen

294 Moreover, in V. fischeri, we observed ainR-dependent repression of a Pqr

295 other regulators of biofilm formation in V. fischeri, we screened a transposon library for mutants d

296 de molecules released by the bacteria Vibrio fischeri when it rotates its flagella prompts its host,

297 have focused on the LuxR protein from Vibrio fischeri, which activates gene transcription in response

298 r the marine bioluminescent bacterium Vibrio fischeri, which exists either in a free-living state or

299 scolopes and its beneficial symbiont Vibrio fischeri, which form a highly specific binary mutualism.

300 f the bioluminescent marine bacterium Vibrio fischeri with its animal host, the Hawaiian bobtail squi