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1 em originally studied in the marine symbiont Vibrio fischeri.
2 iption factor similar to the LuxR protein of Vibrio fischeri.
3 ed to a high density by the marine bacterium Vibrio fischeri.
4 or quorum-sensing control of luminescence in Vibrio fischeri.
5 trations, VAI, the closely related signal of Vibrio fischeri.
6 thase and the LuxR transcription factor from Vibrio fischeri.
7 ), from the luminescent light organ symbiont Vibrio fischeri.
8  is directed by homologs of the luxi gene of Vibrio fischeri.
9 ht organ by the symbiotic luminous bacterium Vibrio fischeri.
10 a scolopes and the marine luminous bacterium Vibrio fischeri.
11 riptional activator of luminescence genes in Vibrio fischeri.
12  harbors a culture of the luminous bacterium Vibrio fischeri.
13  effect on the acute toxicity of OSPW toward Vibrio fischeri.
14 s and its specific, bioluminescent symbiont, Vibrio fischeri.
15 /AinR, positively control bioluminescence in Vibrio fischeri.
16 lly occurring, non-bioluminescent strains of Vibrio fischeri.
17 the quorum sensing proteins LuxR and LuxI of Vibrio fischeri.
18 Euprymna scolopes and the luminous bacterium Vibrio fischeri.
19 na scolopes and the bioluminescent bacterium Vibrio fischeri.
20 brio parahaemolyticus, Vibrio vulnificus and Vibrio fischeri.
21 d Pseudomonas aeruginosa; the model symbiont Vibrio fischeri.
22 ctions for two CsrA-regulating small RNAs in Vibrio fischeri.
23 sgenic quorum sensing signaling pathway from Vibrio fischeri.
24                 Previously, we identified in Vibrio fischeri a putative sensor kinase, RscS, required
25                                              Vibrio fischeri, a bioluminescent marine bacterium, exis
26                                              Vibrio fischeri, a luminescent marine bacterium, specifi
27 nosa and Eisenia fetida, the marine bacteria Vibrio fischeri, a suite of ten prokaryotic species, and
28 t elevated intracellular citrate levels in a Vibrio fischeri aconitase mutant correlate with activati
29                         Here, we report that Vibrio fischeri also releases TCT, which acts in synergy
30                                        Using Vibrio fischeri , an acute bacterial toxicity was found
31  homoserine lactone, freely diffuses through Vibrio fischeri and Escherichia coli cells has led to th
32                           The association of Vibrio fischeri and Euprymna scolopes provides insights
33 ation of the symbiosis between the bacterium Vibrio fischeri and its squid host, which can be observe
34                 The bioluminescent bacterium Vibrio fischeri and juveniles of the squid Euprymna scol
35 model mutualism between the marine bacterium Vibrio fischeri and the Hawaiian bobtail squid, we chara
36 mbiosis between the bioluminescent bacterium Vibrio fischeri and the Hawaiian bobtail squid.
37 the sheathed flagellum in both the mutualist Vibrio fischeri and the pathogen Vibrio cholerae promote
38 e association between the luminous bacterium Vibrio fischeri and the sepiolid squid Euprymna scolopes
39 mple, in the symbiosis between the bacterium Vibrio fischeri and the squid Euprymna scolopes, which p
40 al role in the light-organ symbiosis between Vibrio fischeri and the squid Euprymna scolopes.
41             The inhibition effect of OSPW on Vibrio fischeri and the toxicity effect on goldfish prim
42 acylhomoserine lactone synthase gene luxI of Vibrio fischeri and three genes that resemble the acylho
43 erial quorum sensing systems such as LuxR of Vibrio fischeri and TraR of Agrobacterium tumefaciens, t
44 ins related to the LuxR and LuxI proteins of Vibrio fischeri, and by a diffusible pheromone called an
45 , Magnetococcus marinus, Pseudomonas putida, Vibrio fischeri, and Escherichia coli) in microfluidic e
46 phic mutants of the bioluminescent bacterium Vibrio fischeri, and have demonstrated that the host squ
47 m Haemophilus influenzae, Proteus mirabilis, Vibrio fischeri, and Pasteurella multocida are all cleav
48 n NADH/NADPH-utilizing flavin reductase from Vibrio fischeri are quite similar to that of the wild-ty
49 rymna scolopes and its luminescent bacterium Vibrio fischeri as a model system.
50 rgan symbiosis between Euprymna scolopes and Vibrio fischeri As the juvenile host matures, it develop
51                             Synthesis of the Vibrio fischeri autoinducer, a signal involved in the ce
52 a scolopes squid is colonized exclusively by Vibrio fischeri bacteria.
53                                              Vibrio fischeri belongs to the Vibrionaceae, a large fam
54 inS/R- and LuxI/R-controlled branches of the Vibrio fischeri bioluminescence pathway.
55 The light organ symbiont of Euprymna spp. is Vibrio fischeri, but until now, the light organ symbiont
56 evolved ecologically distinct bioluminescent Vibrio fischeri by colonization and growth within the li
57 e demonstrate that SypE controls biofilms in Vibrio fischeri by regulating the activity of SypA, a ST
58                                              Vibrio fischeri cells are the sole colonists of a specia
59 the squid Euprymna scolopes by the bacterium Vibrio fischeri depends on bacterial biofilm formation o
60                  Robust biofilm formation by Vibrio fischeri depends upon activation of the symbiosis
61   Flagellar biogenesis and hence motility of Vibrio fischeri depends upon the presence of magnesium.
62 how that cAMP-CRP is active and important in Vibrio fischeri during colonization of its host squid Eu
63 uid-vibrio symbiosis, the bacterial symbiont Vibrio fischeri encounters host-derived NO, which has be
64                                    LuxI is a Vibrio fischeri enzyme that catalyzes the synthesis of N
65                           Bioluminescence in Vibrio fischeri ES114 is activated by autoinducer pherom
66 ree culture fluids from the marine bacterium Vibrio fischeri ES114 prevent the growth of other vibrio
67       HvnA and HvnB are proteins secreted by Vibrio fischeri ES114, an extracellular light organ symb
68                                              Vibrio fischeri ES114, an isolate from the Euprymna scol
69            Building on the genome project of Vibrio fischeri ES114, we used a comparative approach to
70 (1)(,)(2)(,)(3) The bioluminescent bacterium Vibrio fischeri establishes a light-emitting symbiosis w
71                         The marine bacterium Vibrio fischeri establishes a mutualistic symbiosis with
72    Luminescent bacteria inhibition test with Vibrio fischeri exhibited that the TPs irgarol sulfoxide
73                                              Vibrio fischeri exists in a symbiotic relationship with
74             Magnesium-dependent induction of Vibrio fischeri flagellar (Mif) biogenesis depends upon
75  both: (i) selection of the specific partner Vibrio fischeri from the bacterioplankton during symbios
76 of Euprymna scolopes squid by bioluminescent Vibrio fischeri from the North Pacific Ocean.
77  decomposition in a 1 mM bulk solution above Vibrio fischeri (gamma-Protebacteria-Vibrionaceae) bacte
78 e gene, katA, of the sepiolid squid symbiont Vibrio fischeri has been cloned and sequenced.
79 regulation of the lux operon (luxICDABEG) of Vibrio fischeri has been intensively studied as a model
80 a scolopes, and the bioluminescent bacterium Vibrio fischeri has been studied as a model system for u
81                                              Vibrio fischeri has the capacity to produce at least two
82 minescence Y1 strain of the marine bacterium Vibrio fischeri have been purified and characterized wit
83 a scolopes, and the bioluminescent bacterium Vibrio fischeri have permitted a detailed understanding
84 minescence inhibition of the marine bacteria Vibrio fischeri, have been used.
85 hereas the LO has a binary relationship with Vibrio fischeri, housed in extracellular crypt spaces as
86  identity with the Escherichia coli (Ec) and Vibrio fischeri htpG.
87 transformed with a truncated lux operon from Vibrio fischeri, in the presence of 1-100 nM exogenous a
88 itously discovered that the marine bacterium Vibrio fischeri induces sexual reproduction in one of th
89 , we investigated how the bacterial symbiont Vibrio fischeri initially colonizes the light organ of t
90                 The bioluminescent bacterium Vibrio fischeri initiates a specific, persistent symbios
91                                              Vibrio fischeri is a bioluminescent bacterium that colon
92                                              Vibrio fischeri is a bioluminescent bacterium that enter
93                         Biofilm formation by Vibrio fischeri is a complex process involving multiple
94                         Biofilm formation by Vibrio fischeri is a complex process that requires multi
95 dent regulation of the luminescence genes in Vibrio fischeri is a model for quorum sensing in Gram-ne
96 luminescence emitted by the marine bacterium Vibrio fischeri is a particularly striking result of ind
97               Flagellum-mediated motility of Vibrio fischeri is an essential factor in the bacterium'
98 sity-dependent expression of luminescence in Vibrio fischeri is controlled by the autoinducer N-3-oxo
99 eron (luxICDABEG) of the symbiotic bacterium Vibrio fischeri is regulated by the transcriptional acti
100                                              Vibrio fischeri is the bacterial symbiont within the lig
101                                              Vibrio fischeri is the exclusive symbiont residing in th
102                         The marine bacterium Vibrio fischeri is the monospecific symbiont of the Hawa
103                                              Vibrio fischeri is the sole species colonizing the light
104                         The motile bacterium Vibrio fischeri is the specific bacterial symbiont of th
105                                              Vibrio fischeri isolates from Euprymna scolopes are dim
106 for cell density-dependent activation of the Vibrio fischeri luminescence (lux) genes.
107                                          The Vibrio fischeri luminescence (lux) operon is regulated b
108                                          The Vibrio fischeri luminescence genes are activated by the
109  in the cell density-dependent activation of Vibrio fischeri luminescence is directed by luxI.
110 icity profiles determined from inhibition of Vibrio fischeri luminescence.
111  OP2) that are similar to each other and the Vibrio fischeri lux operator.
112 -dependent transcriptional activation of the Vibrio fischeri lux operon during quorum sensing.
113 al activator that controls expression of the Vibrio fischeri lux operon in response to an acylhomoser
114                                     With the Vibrio fischeri lux quorum sensing circuit, the hypoxia-
115             Bioluminescence generated by the Vibrio fischeri Lux system consumes oxygen and reducing
116                                          The Vibrio fischeri LuxR protein is the founding member of a
117 iR protein and a number of other homologs of Vibrio fischeri LuxR that function as receptors for N-ac
118 minescent bacteria (in the Euprymna scolopes-Vibrio fischeri mutualism) is discussed.
119  luminescence reactions using FRP(H) and the Vibrio fischeri NAD(P)H-utilizing flavin reductase G (FR
120 n of organisms and toxicity end points using Vibrio fischeri (nonspecific), specific fish macrophage
121 Euprymna scolopes and the luminous bacterium Vibrio fischeri offers the opportunity to decipher the h
122                                              Vibrio fischeri possesses two acyl-homoserine lactone qu
123                                              Vibrio fischeri possesses two quorum-sensing systems, ai
124                                              Vibrio fischeri produces a specific biofilm to promote c
125                                          The Vibrio fischeri quorum-sensing signal N-3-oxohexanoyl-l-
126                     The light-organ symbiont Vibrio fischeri releases N-acetylglucosaminyl-1,6-anhydr
127                                The bacterium Vibrio fischeri requires bacterial motility to initiate
128 id Euprymna scolopes by the marine bacterium Vibrio fischeri requires the symbiosis polysaccharide (s
129    Biofilm formation by the marine bacterium Vibrio fischeri requires the Syp polysaccharide, but the
130                       The genome sequence of Vibrio fischeri revealed three putative TMAO reductase o
131                        Overexpression of the Vibrio fischeri sensor kinase RscS induces expression of
132 g Plesiomonas shigelloides, Vibrio cholerae, Vibrio fischeri, Shewanella putrefaciens, and Pseudomona
133 re, we describe the draft genome sequence of Vibrio fischeri SR5, a squid symbiotic isolate from Sepi
134 ease activity associated with whole cells of Vibrio fischeri strain ES114 was identified as the produ
135  proteins (YFP) having FMN or Rf bound, from Vibrio fischeri strain Y1.
136 ex involved in the yellow bioluminescence of Vibrio fischeri, strain Y1.
137                 The Hawaiian bobtail squid's Vibrio fischeri symbionts use quorum sensing for both bi
138             We studied the Euprymna scolopes-Vibrio fischeri symbiosis to characterize, in vivo and i
139 olated TPs exhibited higher toxic effects on Vibrio fischeri than BP-4.
140 olopes is specifically colonized by cells of Vibrio fischeri that are obtained from the ambient seawa
141       For example, the C8-HSL AI produced by Vibrio fischeri that coexists with Aeromonads in aquatic
142  Euprymna scolopes and its bacterial partner Vibrio fischeri, the bacteria induce dramatic morphogene
143                     During quorum sensing in Vibrio fischeri, the luminescence, or lux, operon is reg
144                                              Vibrio fischeri, the symbiotic partner of the Hawaiian b
145 tion between the squid Euprymna scolopes and Vibrio fischeri to examine this process.
146 s polysaccharide locus, syp, is required for Vibrio fischeri to form a symbiotic association with the
147                   RscS is an SK required for Vibrio fischeri to initiate a symbiotic partnership with
148 scolopes and its luminous bacterial partner, Vibrio fischeri, to define the impact of colonization on
149                         The marine bacterium Vibrio fischeri uses a biofilm to promote colonization o
150                           The squid symbiont Vibrio fischeri uses an elaborate TCS phosphorelay conta
151                                              Vibrio fischeri uses the AinS/AinR pheromone-signaling s
152                         The marine bacterium Vibrio fischeri uses two acyl-homoserine lactone (acyl-H
153 ansferase secreted from the marine bacterium Vibrio fischeri (V. fischeri ADP-r) is described.
154 olopes and sensed by the bacterial symbiont, Vibrio fischeri, via the NO sensor HnoX.
155          Complete removal of toxicity toward Vibrio fischeri was achieved after ozonation followed by
156            The acute toxicity of OSPW toward Vibrio fischeri was reduced after the solar/chlorine tre
157 uprymna scolopes and its beneficial symbiont Vibrio fischeri was used as a model system under a simul
158 ng the genetic tractability of the bacterium Vibrio fischeri, we explore the regulation of aox expres
159  repression of LitR, the global regulator in Vibrio fischeri, we have performed a series of genetic a
160 accharide molecules released by the bacteria Vibrio fischeri when it rotates its flagella prompts its
161 es, we have focused on the LuxR protein from Vibrio fischeri, which activates gene transcription in r
162                     We studied the bacterium Vibrio fischeri, which establishes a mutualistic associa
163 ible for the marine bioluminescent bacterium Vibrio fischeri, which exists either in a free-living st
164 uprymna scolopes and its beneficial symbiont Vibrio fischeri, which form a highly specific binary mut
165 ation of the bioluminescent marine bacterium Vibrio fischeri with its animal host, the Hawaiian bobta

 
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