ライフサイエンスコーパス: proteobacterium

1 nsfer and are probably derived from an alpha-proteobacterium.

2 It appears to be a typical gamma proteobacterium.

3 ity is from an uncultured, unsequenced gamma-proteobacterium.

4 autotrophic, sulfur-compound-oxidizing, beta-proteobacterium.

5 tal gene transfer of thymidine kinase from a proteobacterium.

6 (HOT2C01) originated from a planktonic alpha-proteobacterium.

7 dobacter sphaeroides, a photosynthetic alpha-proteobacterium, a transcriptional response to the react

8 the crystal structure of DddY from the gamma-proteobacterium Acinetobacter bereziniae originally isol

9 The delta-proteobacterium Actinobacillus pleuropneumoniae encodes

10 grown Sterolibacterium denitrificans, a beta-proteobacterium, adopts an oxygenase-independent pathway

11 The alpha-Proteobacterium Agrobacterium tumefaciens has proteins h

12 coded in the genome of an uncultivated gamma-proteobacterium and shared highest amino acid sequence s

13 tid (a cyanobacterium), the mitochondrion (a proteobacterium), and its host (an archaeon)--and carrie

14 ter asiaticus" (CLas), an unculturable alpha-proteobacterium associated with citrus Huanglongbing (HL

15 degradation of 3-methylbenzoate in the beta-proteobacterium Azoarcus sp. CIB.

16 d two-component system (HTCS), from the beta-proteobacterium Azoarcus sp. strain CIB that degrades c-

17 he expression of the box cluster in the beta-proteobacterium Azoarcus sp., their cognate transcriptio

18 has previously been reported that the alpha-proteobacterium Azospirillum brasilense undergoes methyl

19 proceed through this mechanism in the alpha-proteobacterium Azospirillum brasilense.

20 isease is caused by infection with the alpha-proteobacterium Bartonella bacilliformis.

21 and nitrogen-fixing life styles of the alpha-proteobacterium Bradyrhizobium japonicum.

22 itional symbiotic association with the gamma-proteobacterium Buchnera aphidicola.

23 microsporus (Rm, Mucoromycotina) and a beta-proteobacterium Burkholderia, which controls host asexua

24 Fusion proteins from marine alpha-proteobacterium Candidatus Pelagibacter ubique, actinoba

25 e Lissoclinum patella with a symbiotic alpha-proteobacterium, Candidatus Endolissoclinum faulkneri, a

26 larization module from the free living alpha-proteobacterium Caulobacter crescentus and an orthologou

27 ria and we found that sigma32 from the alpha-proteobacterium Caulobacter crescentus does not need the

28 g one-piece tmRNAs have been lost, the alpha-proteobacterium Caulobacter crescentus produces a functi

29 The alpha-proteobacterium Caulobacter crescentus produces a motile

30 typical two-protein bacteriocin in the alpha-proteobacterium Caulobacter crescentus that is retained

31 In the alpha-proteobacterium Caulobacter crescentus, cell cycle-regul

32 In the alpha-proteobacterium Caulobacter crescentus, regulated protei

33 f an RNA degradosome assembly from the alpha-proteobacterium Caulobacter crescentus, which is a model

34 ome assembly has been described in the alpha-proteobacterium Caulobacter crescentus, with the interac

35 The chromosome of the alpha-proteobacterium, Caulobacter crescentus, encodes eight P

36 Strain CJ2 is a beta proteobacterium closely related to Polaromonas vacuolata

37 species Chloroherpeton thalassium, and beta-proteobacterium D. acidovorans each produce a different

38 amine putrescine by fusion enzymes from beta-proteobacterium Delftia acidovorans and delta-proteobact

39 ng genome fragment from a Monterey Bay gamma-proteobacterium (EBAC31A08).

40 In the gamma-proteobacterium Erwinia carotovora, genes common to phos

41 enchmark datasets for the well-studied gamma-proteobacterium Escherichia coli showed that it outperfo

42 The gamma-proteobacterium Francisella tularensis is one of the mos

43 2 plasmid is distinct from that of the alpha proteobacterium genomic replicon origins but is conserve

44 microbial community, dominated by the gamma-proteobacterium Halomonas sulfidaeris, was detected in s

45 mplete genome sequence of the deep-sea gamma-proteobacterium, Idiomarina loihiensis, isolated recentl

46 ter crescentus, a Gram-negative alpha-purple proteobacterium, is an oligotroph that lives in aquatic

47 er asiaticus" (CLas), a non-culturable alpha-proteobacterium, is associated with citrus Huanglongbing

48 Pseudomonas aeruginosa, a gamma-proteobacterium, is motile by means of a single polar fl

49 ular, tick-transmitted, gram-negative, alpha-proteobacterium, is the primary etiologic agent of globa

50 Colwellia psychrerythraea 34H, a gamma-proteobacterium isolated from subzero Arctic marine sedi

51 ve agent of Legionnaires' disease, the gamma-proteobacterium Legionella pneumophila, resides and repl

52 omes evolved from the chromosome of an alpha-proteobacterium-like ancestor and developed during evolu

53 The methylotrophic proteobacterium Methylobacterium extorquens AM1 possesse

54 one-carbon (C1) compounds, the aerobic alpha-proteobacterium Methylobacterium extorquens AM1 synthesi

55 or a sterol biosynthetic pathway were in the proteobacterium, Methylococcus capsulatus, in which ster

56 glutamate pathway in the methylotrophic beta-proteobacterium Methyloversatilis universalis FAM5.

57 ith an unusual nested arrangement: the gamma-proteobacterium Moranella endobia lives in the cytoplasm

58 The delta-proteobacterium Myxococcus xanthus coordinates its motil

59 In the delta-proteobacterium Myxococcus xanthus, TsaP is also importa

60 ant phenotype and gene function in the delta proteobacterium Myxococcus xanthus.

61 In the beta-proteobacterium Neisseria gonorrhoeae, the native PilQ s

62 ase in tested actinobacteria and in the beta-proteobacterium Nitrosomonas europaea.

63 rome c oxidase of Rhodobacter sphaeroides, a proteobacterium of the alpha subgroup, is structurally s

64 ment derived from an uncultured marine gamma-proteobacterium of the SAR86 group.

65 The eubacterial organism is either a proteobacterium, or a member of a larger photosynthetic

66 re of the intact ATP synthase from the alpha-proteobacterium Paracoccus denitrificans, inhibited by i

67 ng Gram-negative bacteria, mostly within the Proteobacterium Phylum.

68 ulates key iron metabolism genes in an alpha-proteobacterium, pointing to a departure from the canoni

69 An ancient endosymbiosis of an alpha-proteobacterium produced a diverse range of organelles i

70 s in their respiratory chains, and the gamma-proteobacterium Pseudomonas stutzeri.

71 ing soluble hydrogenase (SH) of aerobic beta-proteobacterium Ralstonia eutropha strain H16 to accompl

72 cleotidyltransferase, acquired from an alpha-proteobacterium, replaced the ancestral enzyme in Metazo

73 equence of Geobacter sulfurreducens, a delta-proteobacterium, reveals unsuspected capabilities, inclu

74 show that the red-type RbcL subunits in the proteobacterium Rhodobacter sphaeroides also fold with G

75 build a large-scale TRN model for the alpha-Proteobacterium Rhodobacter sphaeroides that comprises 1

76 he strategy used by the photosynthetic alpha-proteobacterium Rhodobacter sphaeroides to procure the c

77 In the facultatively phototrophic proteobacterium Rhodobacter sphaeroides, formation of th

78 Surf1p is encoded by the genome of the alpha-proteobacterium Rhodobacter sphaeroides, which synthesiz

79 second RpoH homolog, RpoH(II), in the alpha-proteobacterium Rhodobacter sphaeroides.

80 requirements for photosynthesis in the alpha-proteobacterium Rhodobacter sphaeroides.

81 on pathway much like that found in the alpha-proteobacterium Rhodobacter sphaeroides.

82 .6-Mb genome of the facultative phototrophic proteobacterium, Rhodobacter sphaeroides 2.4.1, was cust

83 tive (photoferrotrophic) growth by the alpha-proteobacterium Rhodopseudomonas palustris TIE-1.

84 In the purple photosynthetic alpha-proteobacterium Rhodopseudomonas palustris, two protein

85 Here we report that the alpha-proteobacterium Rhodospirillum centenum secretes cGMP wh

86 at a partner-switching system of the aquatic Proteobacterium Shewanella oneidensis regulates post-tra

87 The gamma-proteobacterium Shewanella oneidensis strain MR-1 is a m

88 ess gene function in the Gram negative gamma-proteobacterium Shewanella oneidensis strain MR-1.

89 oarray experiments were performed in a gamma-proteobacterium Shewanella oneidensis.

90 The soil-dwelling alpha-proteobacterium Sinorhizobium meliloti engages in a symb

91 The alpha-proteobacterium Sinorhizobium meliloti establishes a chr

92 anaerobic cholesterol metabolism in the beta-proteobacterium Sterolibacterium denitrificans is cataly

93 rse organisms, including a plant and a gamma-proteobacterium, suggest an ancient origin for this regu

94 PDH gene by lateral transfer from an epsilon-proteobacterium, suggesting that the parasite enzyme mig

95 roteobacterium Delftia acidovorans and delta-proteobacterium Syntrophus aciditrophicus, in a Deltaspe

96 eptides first reported from the marine alpha-proteobacterium Thalassospira sp. CNJ-328.

97 biovar viciae strain 3841 is a motile alpha-proteobacterium that can establish a nitrogen-fixing sym

98 lella fastidiosa (Xf), a xylem-limited gamma-proteobacterium that is responsible for several economic

99 knowledge, the first free-living alpha-class proteobacterium to be sequenced and will serve as a foun

100 a endobia lives in the cytoplasm of the beta-proteobacterium Tremblaya princeps These two bacteria, a

101 genomic sequence of the gram negative, gamma-Proteobacterium Vibrio cholerae El Tor N16961 to be 4,03

102 h are produced by a nearshore isolate, gamma Proteobacterium, Vibrio sp. R-10.

103 lobacter crescentus is an oligotrophic alpha-proteobacterium with a complex cell cycle involving sess

104 strain Walvis Bay is a Hg-methylating delta-proteobacterium with a sequenced genome and has unusual

105 ibly an ancestor of the cyanobacterium and a proteobacterium, with an archaeal eocyte (crenarchaea),

106 The maternally inherited alpha-proteobacterium Wolbachia has been proposed as a tool to

107 The alpha-proteobacterium Wolbachia is probably the most prevalent

108 terial blight of rice is caused by the gamma-proteobacterium Xanthomonas oryzae pv. oryzae, which uti