ライフサイエンスコーパス: Desulfovibrio vulgaris

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 br(red) from the sulfate reducing bacterium, Desulfovibrio vulgaris, as well as its azide adduct (Rbr

17 on and protein abundance data collected from Desulfovibrio vulgaris by DNA microarray and liquid chro

18 operties of the soluble C-terminal domain of Desulfovibrio vulgaris CcmE, dvCcmE'.

19 roquinones for one-electron reduction in the Desulfovibrio vulgaris ( D. vulgaris) flavodoxin ( E sq/

20 e trinuclear center, bacterial ferritin from Desulfovibrio vulgaris (DvFtn) and its E130A variant was

21 brio desulfuricans, Desulfovibrio gigas, and Desulfovibrio vulgaris, exhibited significantly relaxed

22 Cytochrome c-553 from Desulfovibrio vulgaris exhibits a highly exposed heme an

23 Two mutants of the Desulfovibrio vulgaris flavodoxin, T12H and N14H, were g

24 In the Desulfovibrio vulgaris flavodoxin, the elimination of th

25 used at the genetic level to flavodoxin from Desulfovibrio vulgaris (FLD) to create the chimeric CYP2

26 nse regulators (RR) were identified from the Desulfovibrio vulgaris genome.

27 microarray and proteomic data collected from Desulfovibrio vulgaris grown under three different condi

28 lavodoxin from the sulfate-reducing bacteria Desulfovibrio vulgaris has been proposed, based on elect

29 s for two syntrophic cocultures, Dhc195 with Desulfovibrio vulgaris Hildenborough (-13.0 +/- 2.0 per

30 le, most abundant multi-protein complexes in Desulfovibrio vulgaris Hildenborough (DvH) that are larg

31 pecific transcripts, causing a population of Desulfovibrio vulgaris Hildenborough (DvH) to collapse a

32 Desulfovibrio vulgaris Hildenborough belongs to a class

33 desulfothioredoxin (Dtrx) from the anaerobe Desulfovibrio vulgaris Hildenborough has been identified

34 Desulfovibrio vulgaris Hildenborough is a model organism

35 of the anaerobic, sulfate-reducing organism Desulfovibrio vulgaris Hildenborough to low-oxygen expos

36 The response of exponentially growing Desulfovibrio vulgaris Hildenborough to pH 10 stress was

37 The ability of Desulfovibrio vulgaris Hildenborough to reduce, and ther

38 ctivation of modA and modBC genes by TunR in Desulfovibrio vulgaris Hildenborough was confirmed in vi

39 istribution in central metabolic pathways of Desulfovibrio vulgaris Hildenborough was examined using

40 For the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, 347 of the 3634 ge

41 5' RNA sequencing to identify transcripts in Desulfovibrio vulgaris Hildenborough, a model sulfate-re

42 Desulfovibrio vulgaris Hildenborough, a sulfate-reducing

43 gene in the model sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, but two copies in

44 Sulfate-reducing microbes, such as Desulfovibrio vulgaris Hildenborough, cause "souring" of

45 nalysis of a model sulfate-reducing microbe, Desulfovibrio vulgaris Hildenborough, suggested the use

46 In the model sulfate-reducing microbe Desulfovibrio vulgaris Hildenborough, the gene DVU_0916

47 ion of cationic metabolites in the bacterium Desulfovibrio vulgaris Hildenborough.

48 a biomass hydrolysate of the soil bacterium Desulfovibrio vulgaris Hildenborough.

49 In this work, we studied FlxABCD of Desulfovibrio vulgaris Hildenborough.

50 om the anaerobic sulfate-reducing bacterium, Desulfovibrio vulgaris (Hildenborough), has a hemerythri

51 on protein of unknown function isolated from Desulfovibrio vulgaris (Hildenborough).

52 The periplasmic hydrogenase of Desulfovibrio vulgaris (Hildenbourough) is an all Fe-con

53 2+) complex with the [NiFe]-hydrogenase from Desulfovibrio vulgaris immobilized on a functionalized e

54 owth of the model sulfate-reducing bacterium Desulfovibrio vulgaris in the absence of sulfate or a sy

55 Flavodoxin from Desulfovibrio vulgaris is a low molecular weight (15 000

56 Cytochrome c(553) (cyt c(553)) from Desulfovibrio vulgaris is a small helical heme protein t

57 e (57)Fe-labelled fully reduced Ni-R form of Desulfovibrio vulgaris Miyazaki F [NiFe]-hydrogenase.

58 rmations using two genomes from each domain: Desulfovibrio vulgaris, Pseudomonas aeruginosa, Archaeog

59 Antibodies raised against Desulfovibrio vulgaris Rbr reacted with both native and

60 Phascolopsis gouldii hemerythrin (Pg-Hr) and Desulfovibrio vulgaris rubrerythrin (Dv-Rr), have been e

61 mixed-valent (Fe(2+),Fe(3+)) diiron site of Desulfovibrio vulgaris rubrerythrin (Rbr(mv)) were deter

62 The X-ray crystal structure of recombinant Desulfovibrio vulgaris rubrerythrin (Rbr) that was subje

63 asurement on a similar protein isolated from Desulfovibrio vulgaris showed that the protein contains

64 s of Desulfovibrio alaskensis strain G20 and Desulfovibrio vulgaris strain Hildenborough growing synt

65 -catalase oxidative stress defense system in Desulfovibrio vulgaris (strain Hildenborough).

66 The capacity of Desulfovibrio vulgaris to reduce U(VI) was studied previ

67 Stopped-flow mixing of the Desulfovibrio vulgaris two-iron superoxide reductase (2F

68 tion, the properties of a beta-class CA from Desulfovibrio vulgaris were dramatically enhanced.