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1 scriptomic and proteomic data collected from Desulfovibrio vulgaris.
2 nctional urea transporter from the bacterium Desulfovibrio vulgaris.
3 rom the anaerobic sulfate-reducing bacterium Desulfovibrio vulgaris.
4 el for flavin binding to the flavodoxin from Desulfovibrio vulgaris.
5 MN) and riboflavin to the apoflavodoxin from Desulfovibrio vulgaris.
6 s on recombinant two-iron SOR (2Fe-SOR) from Desulfovibrio vulgaris.
7 lavodoxins from Clostridium beijerinckii and Desulfovibrio vulgaris.
8 ssed from a gene-fusion with flavodoxin from Desulfovibrio vulgaris (2C9/FLD).
9 in this work by examination of an engineered Desulfovibrio vulgaris 2Fe-SOR variant, C13S, in which o
10 re present in the sulfate-reducing bacterium Desulfovibrio vulgaris, although it grows only poorly on
11 Most of these operons were also conserved in Desulfovibrio vulgaris, an additional metal reducing org
12 ant versions of Desulfovibrio desulfuricans, Desulfovibrio vulgaris and Methanosarcina barkeri AhbA/B
13 cerevisiae to environmental microbes such as Desulfovibrio vulgaris and Shewanella oneidensis.
14 ndent pairings (cocultures) of the bacterium Desulfovibrio vulgaris and the archaeon Methanococcus ma
15 ostridium pasteurianum, Desulfovibrio gigas, Desulfovibrio vulgaris, and Pyrococcus furiosus.
16                                        Using Desulfovibrio vulgaris as a model SRB organism, we compa
17 br(red) from the sulfate reducing bacterium, Desulfovibrio vulgaris, as well as its azide adduct (Rbr
18 on and protein abundance data collected from Desulfovibrio vulgaris by DNA microarray and liquid chro
19 operties of the soluble C-terminal domain of Desulfovibrio vulgaris CcmE, dvCcmE'.
20 roquinones for one-electron reduction in the Desulfovibrio vulgaris ( D. vulgaris) flavodoxin ( E sq/
21 bane cluster in HdrB from a non-methanogenic Desulfovibrio vulgaris (Dv) Hildenborough organism.
22 revious work revealed how a sulfate reducer (Desulfovibrio vulgaris, Dv) and a methanogen (Methanococ
23 (1.50-2.48 angstrom resolution) of CODH from Desulfovibrio vulgaris (DvCODH) heterologously expressed
24 e trinuclear center, bacterial ferritin from Desulfovibrio vulgaris (DvFtn) and its E130A variant was
25 brio desulfuricans, Desulfovibrio gigas, and Desulfovibrio vulgaris, exhibited significantly relaxed
26                        Cytochrome c-553 from Desulfovibrio vulgaris exhibits a highly exposed heme an
27                           Two mutants of the Desulfovibrio vulgaris flavodoxin, T12H and N14H, were g
28                                       In the Desulfovibrio vulgaris flavodoxin, the elimination of th
29 used at the genetic level to flavodoxin from Desulfovibrio vulgaris (FLD) to create the chimeric CYP2
30 nse regulators (RR) were identified from the Desulfovibrio vulgaris genome.
31 microarray and proteomic data collected from Desulfovibrio vulgaris grown under three different condi
32 lavodoxin from the sulfate-reducing bacteria Desulfovibrio vulgaris has been proposed, based on elect
33 s for two syntrophic cocultures, Dhc195 with Desulfovibrio vulgaris Hildenborough (-13.0 +/- 2.0 per
34 lms of sulfate-reducing bacterium (SRB) like Desulfovibrio vulgaris Hildenborough (DvH) can facilitat
35 le, most abundant multi-protein complexes in Desulfovibrio vulgaris Hildenborough (DvH) that are larg
36 pecific transcripts, causing a population of Desulfovibrio vulgaris Hildenborough (DvH) to collapse a
37 , we couple formate dehydrogenase (FDH) from Desulfovibrio vulgaris Hildenborough (DvH) to metal oxid
38 ogical, proteomic and biochemical studies of Desulfovibrio vulgaris Hildenborough and mutants affecte
39 hic co-culture containing lactate-fermenting Desulfovibrio vulgaris Hildenborough and solvent-dechlor
40                                              Desulfovibrio vulgaris Hildenborough belongs to a class
41 ytochrome c from Rhodobacter sphaeroides and Desulfovibrio vulgaris Hildenborough cytochrome c(3)).
42    We therefore tested a deposited strain of Desulfovibrio vulgaris Hildenborough for its capacity to
43  desulfothioredoxin (Dtrx) from the anaerobe Desulfovibrio vulgaris Hildenborough has been identified
44                                              Desulfovibrio vulgaris Hildenborough is a model organism
45  of the anaerobic, sulfate-reducing organism Desulfovibrio vulgaris Hildenborough to low-oxygen expos
46        The response of exponentially growing Desulfovibrio vulgaris Hildenborough to pH 10 stress was
47                               The ability of Desulfovibrio vulgaris Hildenborough to reduce, and ther
48 ctivation of modA and modBC genes by TunR in Desulfovibrio vulgaris Hildenborough was confirmed in vi
49 istribution in central metabolic pathways of Desulfovibrio vulgaris Hildenborough was examined using
50           For the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, 347 of the 3634 ge
51                                           In Desulfovibrio vulgaris Hildenborough, a model bacterium
52 5' RNA sequencing to identify transcripts in Desulfovibrio vulgaris Hildenborough, a model sulfate-re
53                                              Desulfovibrio vulgaris Hildenborough, a sulfate-reducing
54 gene in the model sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, but two copies in
55 o plays a role during fermentative growth of Desulfovibrio vulgaris Hildenborough, by studying two st
56           Sulfate-reducing microbes, such as Desulfovibrio vulgaris Hildenborough, cause "souring" of
57  reductase, formate dehydrogenase (FDH) from Desulfovibrio vulgaris Hildenborough, is interfaced with
58 nalysis of a model sulfate-reducing microbe, Desulfovibrio vulgaris Hildenborough, suggested the use
59        In the model sulfate-reducing microbe Desulfovibrio vulgaris Hildenborough, the gene DVU_0916
60          In this work, we studied FlxABCD of Desulfovibrio vulgaris Hildenborough.
61 ion of cationic metabolites in the bacterium Desulfovibrio vulgaris Hildenborough.
62  a biomass hydrolysate of the soil bacterium Desulfovibrio vulgaris Hildenborough.
63 om the anaerobic sulfate-reducing bacterium, Desulfovibrio vulgaris (Hildenborough), has a hemerythri
64 on protein of unknown function isolated from Desulfovibrio vulgaris (Hildenborough).
65               The periplasmic hydrogenase of Desulfovibrio vulgaris (Hildenbourough) is an all Fe-con
66 2+) complex with the [NiFe]-hydrogenase from Desulfovibrio vulgaris immobilized on a functionalized e
67 owth of the model sulfate-reducing bacterium Desulfovibrio vulgaris in the absence of sulfate or a sy
68                              Flavodoxin from Desulfovibrio vulgaris is a low molecular weight (15 000
69          Cytochrome c(553) (cyt c(553)) from Desulfovibrio vulgaris is a small helical heme protein t
70 e (57)Fe-labelled fully reduced Ni-R form of Desulfovibrio vulgaris Miyazaki F [NiFe]-hydrogenase.
71 rmations using two genomes from each domain: Desulfovibrio vulgaris, Pseudomonas aeruginosa, Archaeog
72                    Antibodies raised against Desulfovibrio vulgaris Rbr reacted with both native and
73 Phascolopsis gouldii hemerythrin (Pg-Hr) and Desulfovibrio vulgaris rubrerythrin (Dv-Rr), have been e
74  mixed-valent (Fe(2+),Fe(3+)) diiron site of Desulfovibrio vulgaris rubrerythrin (Rbr(mv)) were deter
75   The X-ray crystal structure of recombinant Desulfovibrio vulgaris rubrerythrin (Rbr) that was subje
76 asurement on a similar protein isolated from Desulfovibrio vulgaris showed that the protein contains
77 s of Desulfovibrio alaskensis strain G20 and Desulfovibrio vulgaris strain Hildenborough growing synt
78 -catalase oxidative stress defense system in Desulfovibrio vulgaris (strain Hildenborough).
79                              The capacity of Desulfovibrio vulgaris to reduce U(VI) was studied previ
80                   Stopped-flow mixing of the Desulfovibrio vulgaris two-iron superoxide reductase (2F
81 angstrom resolution cryo-EM structure of the Desulfovibrio vulgaris type I-C Cascade, revealing the m
82 tion, the properties of a beta-class CA from Desulfovibrio vulgaris were dramatically enhanced.
83 nd corrosive Desulfovibrio desulfuricans and Desulfovibrio vulgaris were identified within the biofil