ライフサイエンスコーパス: Vibrio fischeri

1 s and its specific, bioluminescent 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 /AinR, positively control bioluminescence in Vibrio fischeri.

14 lly occurring, non-bioluminescent strains of Vibrio fischeri.

15 the quorum sensing proteins LuxR and LuxI of Vibrio fischeri.

16 Euprymna scolopes and the luminous bacterium Vibrio fischeri.

17 na scolopes and the bioluminescent bacterium Vibrio fischeri.

18 effect on the acute toxicity of OSPW toward Vibrio fischeri.

19 brio parahaemolyticus, Vibrio vulnificus and Vibrio fischeri.

20 d Pseudomonas aeruginosa; the model symbiont Vibrio fischeri.

21 ctions for two CsrA-regulating small RNAs in Vibrio fischeri.

22 sgenic quorum sensing signaling pathway from Vibrio fischeri.

23 em originally studied in the marine symbiont 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 the sheathed flagellum in both the mutualist Vibrio fischeri and the pathogen Vibrio cholerae promote

36 e association between the luminous bacterium Vibrio fischeri and the sepiolid squid Euprymna scolopes

37 mple, in the symbiosis between the bacterium Vibrio fischeri and the squid Euprymna scolopes, which p

38 The inhibition effect of OSPW on Vibrio fischeri and the toxicity effect on goldfish prim

39 acylhomoserine lactone synthase gene luxI of Vibrio fischeri and three genes that resemble the acylho

40 erial quorum sensing systems such as LuxR of Vibrio fischeri and TraR of Agrobacterium tumefaciens, t

41 ins related to the LuxR and LuxI proteins of Vibrio fischeri, and by a diffusible pheromone called an

42 phic mutants of the bioluminescent bacterium Vibrio fischeri, and have demonstrated that the host squ

43 m Haemophilus influenzae, Proteus mirabilis, Vibrio fischeri, and Pasteurella multocida are all cleav

44 n NADH/NADPH-utilizing flavin reductase from Vibrio fischeri are quite similar to that of the wild-ty

45 rymna scolopes and its luminescent bacterium Vibrio fischeri as a model system.

46 Synthesis of the Vibrio fischeri autoinducer, a signal involved in the ce

47 a scolopes squid is colonized exclusively by Vibrio fischeri bacteria.

48 Vibrio fischeri belongs to the Vibrionaceae, a large fam

49 The light organ symbiont of Euprymna spp. is Vibrio fischeri, but until now, the light organ symbiont

50 evolved ecologically distinct bioluminescent Vibrio fischeri by colonization and growth within the li

51 e demonstrate that SypE controls biofilms in Vibrio fischeri by regulating the activity of SypA, a ST

52 Vibrio fischeri cells are the sole colonists of a specia

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

54 Flagellar biogenesis and hence motility of Vibrio fischeri depends upon the presence of magnesium.

55 how that cAMP-CRP is active and important in Vibrio fischeri during colonization of its host squid Eu

56 uid-vibrio symbiosis, the bacterial symbiont Vibrio fischeri encounters host-derived NO, which has be

57 LuxI is a Vibrio fischeri enzyme that catalyzes the synthesis of N

58 Bioluminescence in Vibrio fischeri ES114 is activated by autoinducer pherom

59 HvnA and HvnB are proteins secreted by Vibrio fischeri ES114, an extracellular light organ symb

60 Vibrio fischeri ES114, an isolate from the Euprymna scol

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

62 The marine bacterium Vibrio fischeri establishes a mutualistic symbiosis with

63 Luminescent bacteria inhibition test with Vibrio fischeri exhibited that the TPs irgarol sulfoxide

64 Vibrio fischeri exists in a symbiotic relationship with

65 Magnesium-dependent induction of Vibrio fischeri flagellar (Mif) biogenesis depends upon

66 both: (i) selection of the specific partner Vibrio fischeri from the bacterioplankton during symbios

67 of Euprymna scolopes squid by bioluminescent Vibrio fischeri from the North Pacific Ocean.

68 decomposition in a 1 mM bulk solution above Vibrio fischeri (gamma-Protebacteria-Vibrionaceae) bacte

69 e gene, katA, of the sepiolid squid symbiont Vibrio fischeri has been cloned and sequenced.

70 regulation of the lux operon (luxICDABEG) of Vibrio fischeri has been intensively studied as a model

71 Vibrio fischeri has the capacity to produce at least two

72 minescence Y1 strain of the marine bacterium Vibrio fischeri have been purified and characterized wit

73 minescence inhibition of the marine bacteria Vibrio fischeri, have been used.

74 identity with the Escherichia coli (Ec) and Vibrio fischeri htpG.

75 transformed with a truncated lux operon from Vibrio fischeri, in the presence of 1-100 nM exogenous a

76 itously discovered that the marine bacterium Vibrio fischeri induces sexual reproduction in one of th

77 The bioluminescent bacterium Vibrio fischeri initiates a specific, persistent symbios

78 Vibrio fischeri is a bioluminescent bacterium that enter

79 Biofilm formation by Vibrio fischeri is a complex process involving multiple

80 Biofilm formation by Vibrio fischeri is a complex process that requires multi

81 dent regulation of the luminescence genes in Vibrio fischeri is a model for quorum sensing in Gram-ne

82 luminescence emitted by the marine bacterium Vibrio fischeri is a particularly striking result of ind

83 Flagellum-mediated motility of Vibrio fischeri is an essential factor in the bacterium'

84 sity-dependent expression of luminescence in Vibrio fischeri is controlled by the autoinducer N-3-oxo

85 eron (luxICDABEG) of the symbiotic bacterium Vibrio fischeri is regulated by the transcriptional acti

86 Vibrio fischeri is the bacterial symbiont within the lig

87 Vibrio fischeri is the exclusive symbiont residing in th

88 The marine bacterium Vibrio fischeri is the monospecific symbiont of the Hawa

89 Vibrio fischeri is the sole species colonizing the light

90 The motile bacterium Vibrio fischeri is the specific bacterial symbiont of th

91 Vibrio fischeri isolates from Euprymna scolopes are dim

92 for cell density-dependent activation of the Vibrio fischeri luminescence (lux) genes.

93 The Vibrio fischeri luminescence (lux) operon is regulated b

94 The Vibrio fischeri luminescence genes are activated by the

95 in the cell density-dependent activation of Vibrio fischeri luminescence is directed by luxI.

96 icity profiles determined from inhibition of Vibrio fischeri luminescence.

97 OP2) that are similar to each other and the Vibrio fischeri lux operator.

98 -dependent transcriptional activation of the Vibrio fischeri lux operon during quorum sensing.

99 al activator that controls expression of the Vibrio fischeri lux operon in response to an acylhomoser

100 With the Vibrio fischeri lux quorum sensing circuit, the hypoxia-

101 Bioluminescence generated by the Vibrio fischeri Lux system consumes oxygen and reducing

102 The Vibrio fischeri LuxR protein is the founding member of a

103 iR protein and a number of other homologs of Vibrio fischeri LuxR that function as receptors for N-ac

104 minescent bacteria (in the Euprymna scolopes-Vibrio fischeri mutualism) is discussed.

105 luminescence reactions using FRP(H) and the Vibrio fischeri NAD(P)H-utilizing flavin reductase G (FR

106 n of organisms and toxicity end points using Vibrio fischeri (nonspecific), specific fish macrophage

107 Euprymna scolopes and the luminous bacterium Vibrio fischeri offers the opportunity to decipher the h

108 Vibrio fischeri possesses two acyl-homoserine lactone qu

109 Vibrio fischeri possesses two quorum-sensing systems, ai

110 Vibrio fischeri produces a specific biofilm to promote c

111 The Vibrio fischeri quorum-sensing signal N-3-oxohexanoyl-l-

112 The light-organ symbiont Vibrio fischeri releases N-acetylglucosaminyl-1,6-anhydr

113 The bacterium Vibrio fischeri requires bacterial motility to initiate

114 id Euprymna scolopes by the marine bacterium Vibrio fischeri requires the symbiosis polysaccharide (s

115 Biofilm formation by the marine bacterium Vibrio fischeri requires the Syp polysaccharide, but the

116 The genome sequence of Vibrio fischeri revealed three putative TMAO reductase o

117 Overexpression of the Vibrio fischeri sensor kinase RscS induces expression of

118 re, we describe the draft genome sequence of Vibrio fischeri SR5, a squid symbiotic isolate from Sepi

119 ease activity associated with whole cells of Vibrio fischeri strain ES114 was identified as the produ

120 proteins (YFP) having FMN or Rf bound, from Vibrio fischeri strain Y1.

121 ex involved in the yellow bioluminescence of Vibrio fischeri, strain Y1.

122 We studied the Euprymna scolopes-Vibrio fischeri symbiosis to characterize, in vivo and i

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

124 olopes is specifically colonized by cells of Vibrio fischeri that are obtained from the ambient seawa

125 Euprymna scolopes and its bacterial partner Vibrio fischeri, the bacteria induce dramatic morphogene

126 During quorum sensing in Vibrio fischeri, the luminescence, or lux, operon is reg

127 Vibrio fischeri, the symbiotic partner of the Hawaiian b

128 tion between the squid Euprymna scolopes and Vibrio fischeri to examine this process.

129 s polysaccharide locus, syp, is required for Vibrio fischeri to form a symbiotic association with the

130 RscS is an SK required for Vibrio fischeri to initiate a symbiotic partnership with

131 The marine bacterium Vibrio fischeri uses a biofilm to promote colonization o

132 The squid symbiont Vibrio fischeri uses an elaborate TCS phosphorelay conta

133 Vibrio fischeri uses the AinS/AinR pheromone-signaling s

134 The marine bacterium Vibrio fischeri uses two acyl-homoserine lactone (acyl-H

135 ansferase secreted from the marine bacterium Vibrio fischeri (V. fischeri ADP-r) is described.

136 Complete removal of toxicity toward Vibrio fischeri was achieved after ozonation followed by

137 The acute toxicity of OSPW toward Vibrio fischeri was reduced after the solar/chlorine tre

138 ng the genetic tractability of the bacterium Vibrio fischeri, we explore the regulation of aox expres

139 repression of LitR, the global regulator in Vibrio fischeri, we have performed a series of genetic a

140 accharide molecules released by the bacteria Vibrio fischeri when it rotates its flagella prompts its

141 es, we have focused on the LuxR protein from Vibrio fischeri, which activates gene transcription in r

142 ible for the marine bioluminescent bacterium Vibrio fischeri, which exists either in a free-living st

143 uprymna scolopes and its beneficial symbiont Vibrio fischeri, which form a highly specific binary mut

144 ation of the bioluminescent marine bacterium Vibrio fischeri with its animal host, the Hawaiian bobta