ライフサイエンスコーパス: Bacteroides thetaiotaomicron

1 anno-heptose 1alpha-GDP pathway operative in Bacteroides thetaiotaomicron.

2 at controls the fructan utilization locus in Bacteroides thetaiotaomicron.

3 entified in the prominent human gut symbiont Bacteroides thetaiotaomicron.

4 hutchinsonii, and from an obligate anaerobe, Bacteroides thetaiotaomicron.

5 different capsules of the human gut symbiont Bacteroides thetaiotaomicron.

6 e enzyme was induced after colonization with Bacteroides thetaiotaomicron.

7 CTnDOT on expression of chromosomal genes in Bacteroides thetaiotaomicron 5482 (BT4001).

8 -specific integration into the chromosome of Bacteroides thetaiotaomicron 5482.

9 er baseflow conditions for Escherichia coli, Bacteroides thetaiotaomicron (a human source-tracking ma

10 used a gnotobiotic mouse model to show that Bacteroides thetaiotaomicron, a component of the intesti

11 Colonization of germ-free mice with Bacteroides thetaiotaomicron, a component of this flora,

12 enome sequence of the Gram-negative anaerobe Bacteroides thetaiotaomicron, a dominant member of our n

13 food source for the Gram-negative bacterium Bacteroides thetaiotaomicron, a dominant member of the m

14 The abundance of Bacteroides thetaiotaomicron, a glutamate-fermenting com

15 Bacteroides thetaiotaomicron, a gram-negative colonic an

16 Bacteroides thetaiotaomicron, a gram-negative obligate a

17 Bacteroides thetaiotaomicron, a gram-negative obligate a

18 In Bacteroides thetaiotaomicron, a human colonic bacterium,

19 erized the proteins encoded by this locus in Bacteroides thetaiotaomicron, a member of the human gut

20 ic mice with a sialidase-deficient mutant of Bacteroides thetaiotaomicron, a model gut symbiont, redu

21 Ang4 expression is induced by Bacteroides thetaiotaomicron, a predominant member of th

22 omplex polysaccharides comes from studies of Bacteroides thetaiotaomicron, a prominent and geneticall

23 We colonized germ-free mice with Bacteroides thetaiotaomicron, a prominent component of t

24 ninvasive relative Listeria innocua, or with Bacteroides thetaiotaomicron, a prominent gut symbiont.

25 The ability of Bacteroides thetaiotaomicron, a prominent human gut symb

26 ted from conventionally raised mice, or with Bacteroides thetaiotaomicron, a prominent inhabitant of

27 ate (HS) are high-priority carbohydrates for Bacteroides thetaiotaomicron, a prominent member of the

28 of gnotobiotic Fut2(+) and Fut2(-) mice with Bacteroides thetaiotaomicron, a prominent member of the

29 n this report, we examine the adaptations of Bacteroides thetaiotaomicron, a prominent member of the

30 in gnotobiotic mice that do or do not harbor Bacteroides thetaiotaomicron, a prominent saccharolytic

31 ive health, we colonized germ-free mice with Bacteroides thetaiotaomicron, an adaptive bacterial fora

32 imilar to that of P. gingivalis are those of Bacteroides thetaiotaomicron and B. fragilis.

33 ch are colonized with two bacterial species, Bacteroides thetaiotaomicron and Bifidobacterium longum.

34 nally distinct SusCD complexes purified from Bacteroides thetaiotaomicron and derive a general model

35 gh intraspecies variability was observed for Bacteroides thetaiotaomicron and Fusobacterium nucleatum

36 ted LPS, from the mucosa-associated bacteria Bacteroides thetaiotaomicron and Prevotella intermedia,

37 included the outer membrane proteins SusC of Bacteroides thetaiotaomicron and RagA of Porphyromonas g

38 bial community: the saccharolytic bacterium, Bacteroides thetaiotaomicron and the methanogenic archae

39 Hickey et al. (2015) show that sulfatases of Bacteroides thetaiotaomicron are required for its outer

40 Using Bacteroides thetaiotaomicron as a model, we have created

41 spontaneous, fulminant colitis, triggered by Bacteroides thetaiotaomicron (B. theta), we investigated

42 ourse of predicting operons in the genome of Bacteroides thetaiotaomicron (B.theta), a common anaerob

43 haga hutchinsonii) and apparently nonmotile (Bacteroides thetaiotaomicron, Bacteroides fragilis, Tann

44 get aspartyl residue, we show that RimO from Bacteroides thetaiotaomicron (Bt) catalyzes abstraction

45 Bacteroides thetaiotaomicron (Bt) is a human colonic sym

46 A predominant member of the microbiota, Bacteroides thetaiotaomicron (Bt), is resident at EHEC a

47 acillus acidophilus [LA]), or the commensal, Bacteroides thetaiotaomicron (BT).

48 eriplasmic GH115 from the human gut symbiont Bacteroides thetaiotaomicron, BtGH115A, hydrolyzes termi

49 In the presence of the gut symbiont Bacteroides thetaiotaomicron, C. difficile induces a pat

50 ith eight health-relevant bacterial species (Bacteroides thetaiotaomicron, Campylobacter jejuni, Ente

51 cus of NBU1 site-specific integration in the Bacteroides thetaiotaomicron chromosome, attBT1-1, conta

52 BT3082, a nonspecific beta-fructosidase from Bacteroides thetaiotaomicron, confers exolevanase activi

53 me of a prominent human intestinal symbiont, Bacteroides thetaiotaomicron, contains an elaborate envi

54 lfatase or the sulfatase-producing commensal Bacteroides thetaiotaomicron decreased binding of E. col

55 report that the prominent human gut symbiont Bacteroides thetaiotaomicron employs three functional, h

56 in dietary polysaccharides, the model member Bacteroides thetaiotaomicron exhibits only limited coope

57 recombinant lyases, chondroitinase ABC from Bacteroides thetaiotaomicron (expressed in Escherichia c

58 The structure of a putative protease from Bacteroides thetaiotaomicron features an unprecedented b

59 and/or a prominent human gut Bacteroidetes, Bacteroides thetaiotaomicron, followed by whole-genome t

60 s with an organism also found in human guts, Bacteroides thetaiotaomicron, followed by whole-genome t

61 ging enzymes that might protect the anaerobe Bacteroides thetaiotaomicron from the H2 O2 that would b

62 Initial analysis of the archetypal Bacteroides thetaiotaomicron genome identified 172 glyco

63 One such gene, BT1713, from the Bacteroides thetaiotaomicron genome was recently found t

64 Recent studies of a gut commensal, Bacteroides thetaiotaomicron, has revealed a novel signa

65 In the human gut symbiont Bacteroides thetaiotaomicron, hybrid two-component syste

66 Bacteroides thetaiotaomicron is a human gut symbiotic ba

67 Bacteroides thetaiotaomicron is a prominent member of ou

68 sulphate (CS) in the mammalian gut symbiont Bacteroides thetaiotaomicron is activated by an intermed

69 Bacteroides thetaiotaomicron is an opportunistic pathoge

70 n early step in the utilization of starch by Bacteroides thetaiotaomicron is the binding of starch to

71 The human gut bacterium Bacteroides thetaiotaomicron is well endowed with the ab

72 Bacteroides thetaiotaomicron mutants that fail to remove

73 The anaerobic isolates included Bacteroides thetaiotaomicron (n = 1), Propionibacterium

74 D660, was transferred from E. coli donors to Bacteroides thetaiotaomicron or Bacteroides ovatus recip

75 Bacteroides thetaiotaomicron produces multiple fucosidas

76 The human symbiont Bacteroides thetaiotaomicron promotes intestinal functio

77 We report the construction and analysis of a Bacteroides thetaiotaomicron recA disruption mutant and

78 sal and prevalent human gut bacteria such as Bacteroides thetaiotaomicron remain mostly unknown.

79 tives of each of these domains: BT_3511 from Bacteroides thetaiotaomicron (strain VPI-5482) [PDB:3KZT

80 charide Utilization Loci in the gut symbiont Bacteroides thetaiotaomicron, suggesting their involveme

81 ally, isolation of oxygen-enabled mutants of Bacteroides thetaiotaomicron suggests that Oxe may media

82 These points are illustrated by the human-Bacteroides thetaiotaomicron symbiosis.

83 Bacteroides thetaiotaomicron targets transcriptionally a

84 bed putative protease from the gut bacterium Bacteroides thetaiotaomicron (termed ppBat) exhibits two

85 cloning and sequencing of susC, a gene from Bacteroides thetaiotaomicron that encoded a 115-kDa oute

86 of hypothetical proteins encoded by genes of Bacteroides thetaiotaomicron that were up-regulated by a

87 n common with that of the colonic prokaryote Bacteroides thetaiotaomicron, the genome of C. japonicus

88 In the gut symbiont Bacteroides thetaiotaomicron, the sensor kinase and resp

89 ria lymphocytes from mice monocolonized with Bacteroides thetaiotaomicron to a myeloma fusion partner

90 BU1 could be transferred by conjugation from Bacteroides thetaiotaomicron to Escherichia coli.

91 tation of a major human commensal bacterium, Bacteroides thetaiotaomicron, to its host.

92 The intestinal symbiont Bacteroides thetaiotaomicron uses five outer membrane pr

93 Bacteroides thetaiotaomicron uses starch as a source of

94 Here we show that the gut bacterium Bacteroides thetaiotaomicron uses the most structurally

95 BT2127 (Uniprot accession code Q8A5 V9) from Bacteroides thetaiotaomicron using an integrated bioinfo

96 lts from previous studies had suggested that Bacteroides thetaiotaomicron utilizes starch by binding

97 the hexose phosphate phosphatase BT4131 from Bacteroides thetaiotaomicron VPI-5482 (HPP) determined a

98 The BT4131 gene from the bacterium Bacteroides thetaiotaomicron VPI-5482 has been cloned an

99 BT_1012 from Bacteroides thetaiotaomicron VPI-5482 is a protein of un

100 train but absent in strains 638R, YCH46, and Bacteroides thetaiotaomicron VPI-5482.

101 quences of Bacteroides fragilis NCTC9343 and Bacteroides thetaiotaomicron VPI5482.

102 t the first step in utilization of starch by Bacteroides thetaiotaomicron was binding of the polysacc

103 -dependent glutamate dehydrogenase (gdhA) in Bacteroides thetaiotaomicron was cloned and expressed in

104 rom their nearest validly described species, Bacteroides thetaiotaomicron, were characterized by phen

105 ived from the human gut microbiota bacterium Bacteroides thetaiotaomicron, which are up-regulated in

106 systems (HTCSs) from the human gut symbiont Bacteroides thetaiotaomicron, which harbor both the SK a

107 The human colonic bacterium Bacteroides thetaiotaomicron, which plays an important r