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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.
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
14 ndent pairings (cocultures) of the bacterium Desulfovibrio vulgaris and the archaeon Methanococcus ma
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
20 roquinones for one-electron reduction in the Desulfovibrio vulgaris ( D. vulgaris) flavodoxin ( E sq/
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
29 used at the genetic level to flavodoxin from Desulfovibrio vulgaris (FLD) to create the chimeric CYP2
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
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
45 of the anaerobic, sulfate-reducing organism Desulfovibrio vulgaris Hildenborough to low-oxygen expos
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
52 5' RNA sequencing to identify transcripts in Desulfovibrio vulgaris Hildenborough, a model sulfate-re
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
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
63 om the anaerobic sulfate-reducing bacterium, Desulfovibrio vulgaris (Hildenborough), has a hemerythri
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
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
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
81 angstrom resolution cryo-EM structure of the Desulfovibrio vulgaris type I-C Cascade, revealing the m
83 nd corrosive Desulfovibrio desulfuricans and Desulfovibrio vulgaris were identified within the biofil