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1 e enzyme was induced after colonization with Bacteroides thetaiotaomicron.
2 ic mucin O-glycans by the human gut symbiont Bacteroides thetaiotaomicron.
3 drolyzing GTP in the gut commensal bacterium Bacteroides thetaiotaomicron.
4 m diverse gut Bacteroidales overexpressed in Bacteroides thetaiotaomicron.
5  in vivo and in vitro in the human commensal Bacteroides thetaiotaomicron.
6 bility of the next-generation biotherapeutic Bacteroides thetaiotaomicron.
7 different capsules of the human gut symbiont Bacteroides thetaiotaomicron.
8 hat infect the prevalent human gut bacterium Bacteroides thetaiotaomicron.
9 anno-heptose 1alpha-GDP pathway operative in Bacteroides thetaiotaomicron.
10 at controls the fructan utilization locus in Bacteroides thetaiotaomicron.
11 entified in the prominent human gut symbiont Bacteroides thetaiotaomicron.
12 glycosaminoglycan metabolism in the organism Bacteroides thetaiotaomicron.
13 hutchinsonii, and from an obligate anaerobe, Bacteroides thetaiotaomicron.
14 of BAM complexes from the human gut symbiont Bacteroides thetaiotaomicron (3.3 angstrom) and the huma
15 CTnDOT on expression of chromosomal genes in Bacteroides thetaiotaomicron 5482 (BT4001).
16 -specific integration into the chromosome of Bacteroides thetaiotaomicron 5482.
17 er baseflow conditions for Escherichia coli, Bacteroides thetaiotaomicron (a human source-tracking ma
18  used a gnotobiotic mouse model to show that Bacteroides thetaiotaomicron, a component of the intesti
19          Colonization of germ-free mice with Bacteroides thetaiotaomicron, a component of this flora,
20 enome sequence of the Gram-negative anaerobe Bacteroides thetaiotaomicron, a dominant member of our n
21     The genome of the Gram-negative symbiont Bacteroides thetaiotaomicron, a dominant member of the h
22  food source for the Gram-negative bacterium Bacteroides thetaiotaomicron, a dominant member of the m
23                             The abundance of Bacteroides thetaiotaomicron, a glutamate-fermenting com
24                                              Bacteroides thetaiotaomicron, a gram-negative colonic an
25                                              Bacteroides thetaiotaomicron, a gram-negative obligate a
26                                              Bacteroides thetaiotaomicron, a gram-negative obligate a
27                                           In Bacteroides thetaiotaomicron, a human colonic bacterium,
28 erized the proteins encoded by this locus in Bacteroides thetaiotaomicron, a member of the human gut
29 ic mice with a sialidase-deficient mutant of Bacteroides thetaiotaomicron, a model gut symbiont, redu
30                Ang4 expression is induced by Bacteroides thetaiotaomicron, a predominant member of th
31 omplex polysaccharides comes from studies of Bacteroides thetaiotaomicron, a prominent and geneticall
32             We colonized germ-free mice with Bacteroides thetaiotaomicron, a prominent component of t
33 tion of glucosinolates to isothiocyanates by Bacteroides thetaiotaomicron, a prominent gut commensal
34 ninvasive relative Listeria innocua, or with Bacteroides thetaiotaomicron, a prominent gut symbiont.
35                               The ability of Bacteroides thetaiotaomicron, a prominent human gut symb
36 ted from conventionally raised mice, or with Bacteroides thetaiotaomicron, a prominent inhabitant of
37 ate (HS) are high-priority carbohydrates for Bacteroides thetaiotaomicron, a prominent member of the
38 of gnotobiotic Fut2(+) and Fut2(-) mice with Bacteroides thetaiotaomicron, a prominent member of the
39 n this report, we examine the adaptations of Bacteroides thetaiotaomicron, a prominent member of the
40 in gnotobiotic mice that do or do not harbor Bacteroides thetaiotaomicron, a prominent saccharolytic
41       Here, we report that the gut commensal Bacteroides thetaiotaomicron acquires iron and sustains
42 coccus aureus, Streptococcus pneumoniae, and Bacteroides thetaiotaomicron all have potent protective
43 false discovery rate [FDR] = 0.025), and gut Bacteroides thetaiotaomicron (amplicon sequence variant
44 ive health, we colonized germ-free mice with Bacteroides thetaiotaomicron, an adaptive bacterial fora
45 abilities of colonic mucus degraders such as Bacteroides thetaiotaomicron and Akkermansia muciniphila
46 imilar to that of P. gingivalis are those of Bacteroides thetaiotaomicron and B. fragilis.
47 ch are colonized with two bacterial species, Bacteroides thetaiotaomicron and Bifidobacterium longum.
48 nally distinct SusCD complexes purified from Bacteroides thetaiotaomicron and derive a general model
49 gh intraspecies variability was observed for Bacteroides thetaiotaomicron and Fusobacterium nucleatum
50 ted LPS, from the mucosa-associated bacteria Bacteroides thetaiotaomicron and Prevotella intermedia,
51 included the outer membrane proteins SusC of Bacteroides thetaiotaomicron and RagA of Porphyromonas g
52 bial community: the saccharolytic bacterium, Bacteroides thetaiotaomicron and the methanogenic archae
53 terium prausnitzii, Eubacterium eligens, and Bacteroides thetaiotaomicron) and inversely associated w
54 en intragenic invertons in the gut commensal Bacteroides thetaiotaomicron, and experimentally charact
55 Hickey et al. (2015) show that sulfatases of Bacteroides thetaiotaomicron are required for its outer
56                                        Using Bacteroides thetaiotaomicron as a model, we have created
57  were functional and supported the growth of Bacteroides thetaiotaomicron (B. theta) and short-chain
58              The prominent human gut microbe Bacteroides thetaiotaomicron (B. theta) is a versatile a
59  In this study, we used genetically barcoded Bacteroides thetaiotaomicron (B. theta) strains to quant
60 spontaneous, fulminant colitis, triggered by Bacteroides thetaiotaomicron (B. theta), we investigated
61 ourse of predicting operons in the genome of Bacteroides thetaiotaomicron (B.theta), a common anaerob
62 haga hutchinsonii) and apparently nonmotile (Bacteroides thetaiotaomicron, Bacteroides fragilis, Tann
63 monstrate that a model community composed of Bacteroides thetaiotaomicron (Bt) and Bacteroides fragil
64 pecies that associate with the gut commensal Bacteroides thetaiotaomicron (Bt) and with insulin sensi
65 , we have shown that the human gut bacterium Bacteroides thetaiotaomicron (Bt) can depolymerize the m
66 get aspartyl residue, we show that RimO from Bacteroides thetaiotaomicron (Bt) catalyzes abstraction
67 ic techniques reveal the pathway employed by Bacteroides thetaiotaomicron (Bt) for CNG degradation.
68                                              Bacteroides thetaiotaomicron (Bt) is a human colonic sym
69 e that the auxiliary [4Fe-4S](2+) cluster in Bacteroides thetaiotaomicron (Bt) MiaB is converted to a
70  Recently, the prominent human gut bacterium Bacteroides thetaiotaomicron (BT) was reported to produc
71                                              Bacteroides thetaiotaomicron (Bt), a prominent member of
72 (1,3)-glucan utilization loci (1,3GULs) from Bacteroides thetaiotaomicron (Bt), Bacteroides uniformis
73      A predominant member of the microbiota, Bacteroides thetaiotaomicron (Bt), is resident at EHEC a
74 we engineer a human commensal gut bacterium, Bacteroides thetaiotaomicron (Bt), to detoxify MeHg by h
75 red for OMV biogenesis and its regulation in Bacteroides thetaiotaomicron (Bt).
76 es colonic GVHD in mice via the expansion of Bacteroides thetaiotaomicron (BT).
77 acillus acidophilus [LA]), or the commensal, Bacteroides thetaiotaomicron (BT).
78 o-oligosaccharide (FOS) importing SusCD from Bacteroides thetaiotaomicron (Bt1762-Bt1763) to shed lig
79 eriplasmic GH115 from the human gut symbiont Bacteroides thetaiotaomicron, BtGH115A, hydrolyzes termi
80          In the presence of the gut symbiont Bacteroides thetaiotaomicron, C. difficile induces a pat
81 ith eight health-relevant bacterial species (Bacteroides thetaiotaomicron, Campylobacter jejuni, Ente
82                       Most notably the RA of Bacteroides thetaiotaomicron, Chlamydia thrachomatis, Pa
83 cus of NBU1 site-specific integration in the Bacteroides thetaiotaomicron chromosome, attBT1-1, conta
84                          Ablation of RbpB in Bacteroides thetaiotaomicron compromises colonization in
85 BT3082, a nonspecific beta-fructosidase from Bacteroides thetaiotaomicron, confers exolevanase activi
86 me of a prominent human intestinal symbiont, Bacteroides thetaiotaomicron, contains an elaborate envi
87 s efficiently metabolize exogenous DNA, with Bacteroides thetaiotaomicron converting it into the deam
88 lfatase or the sulfatase-producing commensal Bacteroides thetaiotaomicron decreased binding of E. col
89            Germ-free mice monocolonized with Bacteroides thetaiotaomicron DeltaBT0416 exhibited reduc
90               Curiously, the human commensal Bacteroides thetaiotaomicron does not produce siderophor
91 ted colon cells for 8 h with four strains of Bacteroides thetaiotaomicron, each engineered to detect
92 report that the prominent human gut symbiont Bacteroides thetaiotaomicron employs three functional, h
93 lycan glyco-polypeptides in the gut symbiont Bacteroides thetaiotaomicron, encoding a surface endo-be
94  biomass of three microorganism populations: Bacteroides thetaiotaomicron, Eubacterium rectale, and M
95 he mechanisms through which the gut symbiont Bacteroides thetaiotaomicron exerts its immunomodulatory
96 in dietary polysaccharides, the model member Bacteroides thetaiotaomicron exhibits only limited coope
97  recombinant lyases, chondroitinase ABC from Bacteroides thetaiotaomicron (expressed in Escherichia c
98                  The human colonic commensal Bacteroides thetaiotaomicron expresses a consortium of 2
99    The structure of a putative protease from Bacteroides thetaiotaomicron features an unprecedented b
100  and/or a prominent human gut Bacteroidetes, Bacteroides thetaiotaomicron, followed by whole-genome t
101 s with an organism also found in human guts, Bacteroides thetaiotaomicron, followed by whole-genome t
102  (CRISPRi) in the abundant microbiota member Bacteroides thetaiotaomicron for genome-wide sRNA screen
103 Here we show that the BtuB transporters from Bacteroides thetaiotaomicron form stable, pedal bin-like
104 ches, we discover that the human gut microbe Bacteroides thetaiotaomicron forms distinct sub-populati
105 ging enzymes that might protect the anaerobe Bacteroides thetaiotaomicron from the H2 O2 that would b
106           Initial analysis of the archetypal Bacteroides thetaiotaomicron genome identified 172 glyco
107              One such gene, BT1713, from the Bacteroides thetaiotaomicron genome was recently found t
108           Recent studies of a gut commensal, Bacteroides thetaiotaomicron, has revealed a novel signa
109                    In the human gut symbiont Bacteroides thetaiotaomicron, hybrid two-component syste
110 tant libraries of Parabacteroides merdae and Bacteroides thetaiotaomicron implicated genes involved i
111 tal structure of the ENGase EndoBT-3987 from Bacteroides thetaiotaomicron in complex with a hybrid-ty
112 cteroides-phage interactions, we isolated 71 Bacteroides thetaiotaomicron-infecting bacteriophages fr
113                                              Bacteroides thetaiotaomicron is a gut symbiont that inha
114                                              Bacteroides thetaiotaomicron is a human gut symbiotic ba
115                                              Bacteroides thetaiotaomicron is a human-associated bacte
116                                              Bacteroides thetaiotaomicron is a prominent member of ou
117  sulphate (CS) in the mammalian gut symbiont Bacteroides thetaiotaomicron is activated by an intermed
118                                              Bacteroides thetaiotaomicron is an opportunistic pathoge
119                   BT4244(E575A) derived from Bacteroides thetaiotaomicron is selective for truncated,
120 n early step in the utilization of starch by Bacteroides thetaiotaomicron is the binding of starch to
121                      The human gut bacterium Bacteroides thetaiotaomicron is well endowed with the ab
122                      Mice monocolonized with Bacteroides thetaiotaomicron lacking Bt_0416 showed alte
123                                 The anaerobe Bacteroides thetaiotaomicron, like E. coli, uses iron.
124                                              Bacteroides thetaiotaomicron mutants that fail to remove
125              The anaerobic isolates included Bacteroides thetaiotaomicron (n = 1), Propionibacterium
126 temporarily reduce the absolute abundance of Bacteroides thetaiotaomicron or B. cellulosilyticus by 1
127 D660, was transferred from E. coli donors to Bacteroides thetaiotaomicron or Bacteroides ovatus recip
128                              Measurements of Bacteroides thetaiotaomicron population dynamics within
129 ression in the human gut commensal bacterium Bacteroides thetaiotaomicron, prevented escape from thym
130                                              Bacteroides thetaiotaomicron produces multiple fucosidas
131                           The human symbiont Bacteroides thetaiotaomicron promotes intestinal functio
132 We report the construction and analysis of a Bacteroides thetaiotaomicron recA disruption mutant and
133 sal and prevalent human gut bacteria such as Bacteroides thetaiotaomicron remain mostly unknown.
134                                          One Bacteroides thetaiotaomicron RUS variant is critical for
135 e cell populations of the human gut symbiont Bacteroides thetaiotaomicron separated by fluorescence a
136  synthesis pathways in gut-dominant symbiote Bacteroides thetaiotaomicron significantly decreases the
137  of these sugars, by the human gut commensal Bacteroides thetaiotaomicron Silencing by fructose and g
138 germ-free mice with a sphingolipid-deficient Bacteroides thetaiotaomicron strain.
139 tives of each of these domains: BT_3511 from Bacteroides thetaiotaomicron (strain VPI-5482) [PDB:3KZT
140 charide Utilization Loci in the gut symbiont Bacteroides thetaiotaomicron, suggesting their involveme
141 ally, isolation of oxygen-enabled mutants of Bacteroides thetaiotaomicron suggests that Oxe may media
142    These points are illustrated by the human-Bacteroides thetaiotaomicron symbiosis.
143                                              Bacteroides thetaiotaomicron targets transcriptionally a
144 bed putative protease from the gut bacterium Bacteroides thetaiotaomicron (termed ppBat) exhibits two
145 ntify serine hydrolases in the gut commensal Bacteroides thetaiotaomicron that are specific to the Ba
146  cloning and sequencing of susC, a gene from Bacteroides thetaiotaomicron that encoded a 115-kDa oute
147 of hypothetical proteins encoded by genes of Bacteroides thetaiotaomicron that were up-regulated by a
148 the levan and dextran utilization systems of Bacteroides thetaiotaomicron, the additional outer membr
149 n common with that of the colonic prokaryote Bacteroides thetaiotaomicron, the genome of C. japonicus
150                          In the gut symbiont Bacteroides thetaiotaomicron, the sensor kinase and resp
151 ria lymphocytes from mice monocolonized with Bacteroides thetaiotaomicron to a myeloma fusion partner
152 BU1 could be transferred by conjugation from Bacteroides thetaiotaomicron to Escherichia coli.
153 ventional RNA-seq to the model gut bacterium Bacteroides thetaiotaomicron to map transcriptional unit
154 nd charted the adaptation of a gut commensal Bacteroides thetaiotaomicron to micrometer-scale niches
155 acterial sphingolipids from the gut symbiont Bacteroides thetaiotaomicron to mouse colons and livers.
156 tation of a major human commensal bacterium, Bacteroides thetaiotaomicron, to its host.
157                      The intestinal symbiont Bacteroides thetaiotaomicron uses five outer membrane pr
158                                              Bacteroides thetaiotaomicron uses starch as a source of
159          Here we show that the gut bacterium Bacteroides thetaiotaomicron uses the most structurally
160 BT2127 (Uniprot accession code Q8A5 V9) from Bacteroides thetaiotaomicron using an integrated bioinfo
161 lts from previous studies had suggested that Bacteroides thetaiotaomicron utilizes starch by binding
162 the hexose phosphate phosphatase BT4131 from Bacteroides thetaiotaomicron VPI-5482 (HPP) determined a
163           The BT4131 gene from the bacterium Bacteroides thetaiotaomicron VPI-5482 has been cloned an
164                                              Bacteroides thetaiotaomicron VPI-5482 is a prominent hum
165                                 BT_1012 from Bacteroides thetaiotaomicron VPI-5482 is a protein of un
166 train but absent in strains 638R, YCH46, and Bacteroides thetaiotaomicron VPI-5482.
167 quences of Bacteroides fragilis NCTC9343 and Bacteroides thetaiotaomicron VPI5482.
168 t the first step in utilization of starch by Bacteroides thetaiotaomicron was binding of the polysacc
169 -dependent glutamate dehydrogenase (gdhA) in Bacteroides thetaiotaomicron was cloned and expressed in
170 ched in the stools of high responders, while Bacteroides thetaiotaomicron was enriched in low respond
171                                              Bacteroides thetaiotaomicron was examined to determine w
172                           Elevated levels of Bacteroides thetaiotaomicron were independently associat
173                    Bacteroides eggerthii and Bacteroides thetaiotaomicron were observed to be positiv
174 rom their nearest validly described species, Bacteroides thetaiotaomicron, were characterized by phen
175 ived from the human gut microbiota bacterium Bacteroides thetaiotaomicron, which are up-regulated in
176  systems (HTCSs) from the human gut symbiont Bacteroides thetaiotaomicron, which harbor both the SK a
177                  The human colonic bacterium Bacteroides thetaiotaomicron, which plays an important r
178 bacterales, but not with the major commensal Bacteroides thetaiotaomicron, which suggests that acetat

 
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