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1 umazine protein and riboflavin synthase from Photobacterium.
2 om nature and which represent 11 Aliivibrio, Photobacterium, and Vibrio species, were screened for in
3 f CqsA-CqsS pairs, here, we characterize the Photobacterium angustum CqsA/S system.
4 io isolates, two Listonella species, and two Photobacterium angustum isolates produced acetone in the
5  recombinant alpha2-6 sialyltransferase from Photobacterium damsela (Pd2,6ST) exhibits unique regiose
6 ida alpha2-3-sialyltransferase M144D mutant, Photobacterium damsela alpha2-6-sialyltransferase, and H
7  A bacterial alpha2-6-sialyltransferase from Photobacterium damselae (Pd2,6ST) exhibited unexpected a
8 elated ICE derived from a Spanish isolate of Photobacterium damselae subsp. piscicida, the causative
9                                              Photobacterium damselae was identified as the most proba
10  (iii) the lux genes of a luminous strain of Photobacterium damselae, BT-6, were closely related to t
11                             In contrast, the Photobacterium fischeri NAD(P)H-FMN oxidoreductase FRG s
12                                     When the Photobacterium fischeri NADH:FMN oxidoreductase was subs
13 rs of the Streptococcus, Erysipelothrix, and Photobacterium genera are additionally described from di
14       We report here that certain strains of Photobacterium leiognathi carry multiple phylogeneticall
15 tacts and feeds on the luminescent bacterium Photobacterium leiognathi starts to glow, and demonstrat
16 sults are observed using rec-luciferase from Photobacterium leiognathi to produce the donor.
17 ur knowledge) for CuZnSOD from a prokaryote, Photobacterium leiognathi, a luminescent symbiont of Lei
18 ts the growth of the bioluminescent symbiont Photobacterium leiognathi.
19 erties to those of the lumazine protein from Photobacterium leiognathi.
20 to the lux genes of the lux-rib(2) operon of Photobacterium leiognathi; and (iv) a strain of the lumi
21 her than the rate previously observed in the Photobacterium luciferase hydroxyflavin-lumazine protein
22                                 The Siphamia-Photobacterium mandapamensis symbiosis is a binary, gut-
23  and (iv) a strain of the luminous bacterium Photobacterium mandapamensis was found to be merodiploid
24 enna) proteins, lumazine protein (LumP) from Photobacterium or the yellow fluorescence proteins (YFP)
25 mphenicol, has previously been identified in Photobacterium piscicida and Salmonella enterica serovar
26 8% amino acid sequence identity) and OmpL of Photobacterium profundum (45.5% identity).
27  the sialic acid TRAP transporter SiaQM from Photobacterium profundum at 2.97 angstrom resolution.
28                                              Photobacterium profundum SS9 is a Gram-negative bacteriu
29  library derived from the deep-sea bacterium Photobacterium profundum SS9 was conjugally delivered in
30 oson mutagenesis with the deep-sea bacterium Photobacterium profundum strain SS9 to isolate dozens of
31 chrotolerant, piezophilic deep-sea bacterium Photobacterium profundum strain SS9 was characterized an
32 the role of ToxR-mediated gene regulation in Photobacterium profundum strain SS9.
33 ing peptide linker from the PUFA synthase of Photobacterium profundum.
34 ssed and purified the Orf6 thioesterase from Photobacterium profundum.
35 al toxR gene sequences from seven Vibrio and Photobacterium species and subspecies, demonstrating tha
36 of gene expression in the deep-sea bacterium Photobacterium species strain SS9.
37 te the ompL gene from the deep-sea bacterium Photobacterium species strain SS9.
38 seful tool for the distinction of Vibrio and Photobacterium species.
39 the chromosome and is transmissible to other Photobacterium strains, as well as to Escherichia coli,
40 pidly progressive necrotizing fasciitis from Photobacterium (Vibrio) damsela infection and ensuing mu
41  of saving the lives of patients affected by Photobacterium (Vibrio) damsela.
42 icus (12 strains), V. cholerae (30 strains), Photobacterium (Vibrio) damselae (10 strains), V. fluvia