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1 olecules capable of inducing luminescence in Vibrio harveyi.
2  the expression of the luminescence genes in Vibrio harveyi.
3 h the outer membrane of the marine bacterium Vibrio harveyi.
4 QS agonists than the natural ligand, DPD, in Vibrio harveyi.
5 A qrr4 in the model quorum-sensing bacterium Vibrio harveyi.
6 ing of the quorum-sensing receptor LuxN from Vibrio harveyi.
7 n the outer membrane of the marine bacterium Vibrio harveyi.
8 in was related to LuxP, the AI-2 receptor of Vibrio harveyi.
9 have been identified in the marine bacterium Vibrio harveyi.
10 hich catalyzes a light-producing reaction in Vibrio harveyi.
11 he closely related luminous marine bacterium Vibrio harveyi.
12  II (AI-2) of the signal system 2 pathway in Vibrio harveyi.
13 xpression of the promoterless luxAB genes of Vibrio harveyi.
14 roduction for the quorum-sensing system 2 in Vibrio harveyi.
15 ioluminescence (lux) in the marine bacterium Vibrio harveyi.
16                                              Vibrio harveyi, a Gram-negative bioluminescent marine ba
17                                              Vibrio harveyi, a marine pathogen, uses two parallel quo
18                 We report that expression of Vibrio harveyi acyl-ACP synthetase (AasS), a soluble cyt
19  different fatty acid activating enzyme, the Vibrio harveyi acyl-ACP synthetase, replaced RpfB in cou
20 ompetitively inhibits the interaction of the Vibrio harveyi AI-2 receptor (LuxP) with AI-2 from eithe
21  in E. coli W3110 chemostat cultures using a Vibrio harveyi AI-2 reporter assay.
22 onsible for production of autoinducer in the Vibrio harveyi and E. coli quorum-sensing systems is res
23 ar autoinducer concentrations in cultures of Vibrio harveyi and Escherichia coli were monitored by li
24 ues are more potent inhibitors of QS in both Vibrio harveyi and Salmonella typhimurium, the two organ
25 uated for the modulation of AI-2-based QS in Vibrio harveyi and Salmonella typhimurium.
26                                              Vibrio harveyi and Vibrio cholerae have quorum sensing p
27                                       In the Vibrio harveyi and Vibrio cholerae quorum-sensing circui
28    A screen for additional components of the Vibrio harveyi and Vibrio cholerae quorum-sensing circui
29 volved in quorum sensing with a focus on the Vibrio harveyi and Vibrio cholerae quorum-sensing system
30                                              Vibrio harveyi and Vibrio cholerae regulate their virule
31 g that operates at low cell density (LCD) in Vibrio harveyi and Vibrio cholerae.
32               We show that the P. mirabilis, Vibrio harveyi, and E. coli Crl homologs function simila
33  of autoinducer 2 (AI-2), which functions in Vibrio harveyi as a quorum-sensing signal that controls
34      Using the luxAB-encoded luciferase from Vibrio harveyi as a reporter (pMind-Lx), we observed a 4
35 e LuxS, which catalyzes the synthesis of the Vibrio harveyi autoinducer 2 (AI-2).
36                                The genome of Vibrio harveyi BAA-1116 contains a nonribosomal peptide
37                      Residues 257-291 of the Vibrio harveyi bacterial luciferase alpha subunit compri
38 i 35000HP produced AI-2 that functioned in a Vibrio harveyi-based reporter system.
39 addition of culture filtrates from wild-type Vibrio harveyi but exhibited no response to culture filt
40 mber of the master regulator protein LuxR in Vibrio harveyi can be determined in vivo by exploiting s
41  that unlike the other obg/cgtA GTPases, the Vibrio harveyi cgtAV is not essential.
42 increased at 24 h after pathogenic bacterium Vibrio harveyi challenge.
43                         The marine bacterium Vibrio harveyi controls its bioluminescence by a process
44          The bioluminescent marine bacterium Vibrio harveyi controls light production (lux) by an ela
45          The bioluminescent marine bacterium Vibrio harveyi controls light production using two paral
46 phenylalanine is present at this position in Vibrio harveyi CqsS and other homologues, suggesting tha
47 coding an inactive mutant alpha chain of the Vibrio harveyi enzyme.
48                 The quorum-sensing bacterium Vibrio harveyi exclusively detects the autoinducer N-((R
49 em, the NADPH-specific flavin reductase from Vibrio harveyi exhibits a uniquely high preference for N
50                                           In Vibrio harveyi, five homologous small RNAs (sRNAs) calle
51 A new crystal form of luciferase cloned from Vibrio harveyi has been grown under low-salt concentrati
52 t work, the enzyme from the marine bacterium Vibrio harveyi has been purified and characterized.
53                        Previous studies with Vibrio harveyi have shown that LuxR, the master quorum-s
54 ionarily closely related to the lux genes of Vibrio harveyi; (ii) the lux genes of two luminous strai
55 n of autoinducer-2 from Escherichia coli and Vibrio harveyi in proof-of-concept studies and was then
56                    Bacterial luciferase from Vibrio harveyi is a heterodimer composed of a catalytic
57 ch prediction by showing experimentally that Vibrio harveyi is capable of importing Autoinducer 2.
58              The luxS gene of quorum-sensing Vibrio harveyi is required for type 2 autoinducer produc
59 y discovered in the quorum-sensing bacterium Vibrio harveyi, is made by many species of Gram-negative
60 2), first identified in the marine bacterium Vibrio harveyi, is produced and detected by many Gram-ne
61 xN, a nine-transmembrane domain protein from Vibrio harveyi, is the founding example of membrane-boun
62                           Both the wild-type Vibrio harveyi luciferase and a catalytically active alp
63 g essential residues on the alpha subunit of Vibrio harveyi luciferase and elucidating their function
64                                              Vibrio harveyi luciferase and flavin reductase FRP are,
65 crystal structure of the beta 2 homodimer of Vibrio harveyi luciferase has been determined to 2.5 A r
66                                              Vibrio harveyi luciferase is an alphabeta heterodimer co
67 of the His44 residue of the alpha subunit of Vibrio harveyi luciferase to an alanine was known to red
68 ions of the essential alpha His45 residue of Vibrio harveyi luciferase, especially with respect to th
69                   In this study, we used the Vibrio harveyi luminescence bioassay to determine whethe
70 mine whether B. anthracis produces AI-2, the Vibrio harveyi luminescence bioassay was used.
71                                     When the Vibrio harveyi luxA gene is expressed in Escherichia col
72  in which cyanobacterial promoters drive the Vibrio harveyi luxAB genes and produce an oscillation of
73 ut it does show sequence similarity with the Vibrio harveyi LuxM protein.
74  respond to C8-AHL and, based on homology to Vibrio harveyi LuxN, to mediate the repression of a Qrr
75                           Here, we show that Vibrio harveyi LuxP associates with LuxQ in both the pre
76                          Previously, OpaR, a Vibrio harveyi LuxR homolog, was shown to activate expre
77 ed regulator proteins: Vibrio cholerae HapR, Vibrio harveyi LuxR, Vibrio parahaemolyticus OpaR and Vi
78 lonies and that opacity is controlled by the Vibrio harveyi LuxR-type transcriptional activator OpaR.
79                                          The Vibrio harveyi NADPH-FMN oxidoreductase (FRP) and the lu
80                                              Vibrio harveyi NADPH-FMN oxidoreductase (FRP) catalyzes
81 cates a direct flavin cofactor transfer from Vibrio harveyi NADPH-preferring flavin reductase P (FRP(
82                                          The Vibrio harveyi NADPH-specific flavin reductase FRP follo
83  flavin mononucleotide (FMNH(2)) cofactor of Vibrio harveyi NADPH:FMN oxidoreductase (FRP) to lucifer
84                                              Vibrio harveyi NADPH:FMN oxidoreductase P (FRP(Vh)) is a
85             We identify and characterize two Vibrio harveyi negative feedback loops that facilitate p
86 nstrate here that flavinylation of truncated Vibrio harveyi NqrC at Thr-229 in Escherichia coli cells
87 odovirus), bacteria (Aeromonas hydrophila or Vibrio harveyi) or heavy metals (cadmium or lead) signif
88 o hypothetical proteobacterial proteins, and Vibrio harveyi phage VHML ORF 19.
89                         The marine bacterium Vibrio harveyi possesses two quorum sensing systems (Sys
90 3-hydroxytridecan-4-one (C10-CAI-1), whereas Vibrio harveyi produces and detects a distinct but simil
91                 The quorum-sensing bacterium Vibrio harveyi produces and responds to three autoinduce
92 s), called the Qrr1-5 sRNAs, function in the Vibrio harveyi quorum-sensing cascade to drive its opera
93                                       In the Vibrio harveyi quorum-sensing circuit, two master transc
94 mental analyses of the Bacillus subtilis and Vibrio harveyi quorum-sensing networks to show that accu
95 d by LuxO and sigma54, demonstrating that in Vibrio harveyi, quorum sensing controls multiple process
96                                              Vibrio harveyi regulates the expression of bioluminescen
97 dentified in studies of the marine bacterium Vibrio harveyi, regulates quorum-sensing responses and a
98       In the bioluminescent marine bacterium Vibrio harveyi, sensory information from three independe
99 tein synthetase (AasS) of the bioluminescent Vibrio harveyi strain B392 has been isolated by expressi
100 l sensing system for AI-2, which is based on Vibrio harveyi strain BB170.
101 ction of organisms, including the prokaryote Vibrio harveyi, the eukaryotic malarial parasite Plasmod
102                                           In Vibrio harveyi, the master quorum-sensing transcription
103       In the bioluminescent marine bacterium Vibrio harveyi, two different auto inducers (AI-1 and AI
104          The bioluminescent marine bacterium Vibrio harveyi uses a cell-to-cell communication process
105                        The marine bacterium, Vibrio harveyi, uses three autoinducers to achieve intra
106 crystal structure of flavin reductase P from Vibrio harveyi was solved by multiple isomorphous replac
107 which was previously linked to QS systems in Vibrio harveyi) was affected by LsrR.
108           Genes for the luciferase enzyme of Vibrio harveyi were isolated in Escherichia coli by a ge
109  Rv1625c by the quorum-sensing receptor from Vibrio harveyi which has an identical 6TM design and obt

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