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1                                              B. thetaiotaomicron adapts to E. rectale by up-regulatin
2                                              B. thetaiotaomicron contains a large number of glycoside
3                                              B. thetaiotaomicron had larger first order rate constant
4                                              B. thetaiotaomicron produces TLR4-stimulatory lipid A be
5                                              B. thetaiotaomicron strains that expressed an antistimul
6                                              B. thetaiotaomicron was then harvested from the ceca of
7                                              B. thetaiotaomicron-M. smithii cocolonization produces a
8 is the first molecular characterization of a B. thetaiotaomicron outer membrane protein involved in m
9 The products afforded by chondroitinase ABC (B. thetaiotaomicron) and chondroitinase ACII (A. auresce
10                                    Acapsular B. thetaiotaomicron, which lacks all B. thetaiotaomicron
11 s H2 O2 formation was much higher in aerated B. thetaiotaomicron than in Escherichia coli.
12   Previous analyses established that aerated B. thetaiotaomicron loses some enzyme activities due to
13 domas disclosed that this IgA did not affect B. thetaiotaomicron population density or suppress 260.8
14 suggesting that the identified strategy aids B. thetaiotaomicron in the competitive gut environment.
15 apsular B. thetaiotaomicron, which lacks all B. thetaiotaomicron CPSs, stimulated BthetaOM T cells mo
16                                  E. coli and B. thetaiotaomicron were routinely detected in sampled r
17 nical isolates, Bacteroides fragilis ERL and B. thetaiotaomicron DOT.
18                 Comparisons of germ-free and B. thetaiotaomicron-colonized transgenic mice lacking Pa
19                              B. infantis and B. thetaiotaomicron differentially affected stool metabo
20  the separateness of the unknown species and B. thetaiotaomicron.
21  secreted by mucin-foraging bacteria such as B. thetaiotaomicron, inhabiting the same niche, may affe
22 teins that are the primary interface between B. thetaiotaomicron and its environment.
23                                Although both B. thetaiotaomicron and P. gingivalis synthesize lipopol
24 of approximately 1.6 kb was produced in both B. thetaiotaomicron and E. coli gdhA+ transformants.
25         The different strategies employed by B. thetaiotaomicron when faced with multiple polysacchar
26 es showed that metabolism of yeast mannan by B. thetaiotaomicron presents a 'selfish' model for the c
27                      In the absence of CPSs, B. thetaiotaomicron escapes bacteriophage predation by a
28 tained at these two time points using custom B. thetaiotaomicron GeneChips.
29 t wild-type, but not sphingolipid-deficient, B. thetaiotaomicron is sufficient to induce NLRP6-depend
30 ed that, unlike D. piger, M. smithii directs B. thetaiotaomicron to focus on fermentation of dietary
31 genic B. fragilis isolates or B. distasonis, B. thetaiotaomicron, B. uniformis, B. ovatus, Escherichi
32 lular beta2-6 endo-fructanase, distinguishes B. thetaiotaomicron genetically and functionally, and en
33 remains intact in the presence of engineered B. thetaiotaomicron.
34 ory and prostimulatory single CPS-expressing B. thetaiotaomicron strains regulated the activation of
35                    All single CPS-expressing B. thetaiotaomicron strains stimulated the innate immune
36 OM Ag expression, many single CPS-expressing B. thetaiotaomicron strains were antistimulatory and wea
37  and a complete set of single CPS-expressing B. thetaiotaomicron strains, we ask whether CPSs can mod
38  biofilm formation could be key features for B. thetaiotaomicron stress resistance and gut colonizati
39 hore utilization as a critical mechanism for B. thetaiotaomicron to sustain colonization during infla
40 rsified sensor domains may be one reason for B. thetaiotaomicron's success in our intestinal ecosyste
41 D4(+) T cell, BthetaOM, that is specific for B. thetaiotaomicron and a complete set of single CPS-exp
42 body that recognizes an epitope specific for B. thetaiotaomicron isolates in a large panel of hospita
43  and patients, T cell responses specific for B. thetaiotaomicron or B. fragilis were associated with
44 ediated eDNA degradation is required to form B. thetaiotaomicron biofilm in the presence of bile.
45 , but they can be differentiated easily from B. thetaiotaomicron by virtue of not utilizing trehalose
46 a pullulanase, and an alpha-glucosidase from B. thetaiotaomicron had been purified and characterized
47 micron, if the primary integration site from B. thetaiotaomicron, BT1-1, was provided on a plasmid in
48  properties and crystal structure of the GH2 B. thetaiotaomicron enzyme BtMan2A.
49 n in vivo indicated that in the suckling gut B. thetaiotaomicron prefers host-derived polysaccharides
50 fatases than anticipated and establishes how B. thetaiotaomicron, and other major human commensal bac
51                   Using RNA-seq, we identify B. thetaiotaomicron genes that were upregulated during S
52  NrtR family transcription factor (BT0354 in B. thetaiotaomicron, BtAraR) as a novel regulator contro
53                             These changes in B. thetaiotaomicron gene expression were only evident in
54 of the starch-degrading activity detected in B. thetaiotaomicron cell extracts.
55     Only one of these genes was expressed in B. thetaiotaomicron, the homolog of linA, a lincomycin r
56 e discover an ENGase from the GH18 family in B. thetaiotaomicron, BT1285, encoded in a distinct PUL w
57 s lower than the frequency of integration in B. thetaiotaomicron.
58 ethods to combine them, have been limited in B. thetaiotaomicron(2-5).
59 r, essential for exogenous DNA metabolism in B. thetaiotaomicron.
60 ron required for glucosinolate metabolism in B. thetaiotaomicron.
61               Whereas integration of NBU1 in B. thetaiotaomicron is site specific, integration of NBU
62  microbiome likely exceeds those observed in B. thetaiotaomicron by an order of magnitude.
63 egrates preferentially into a single site in B. thetaiotaomicron 5482.
64 Integration occurred in two primary sites in B. thetaiotaomicron.
65 t increasing the number of copies of susR in B. thetaiotaomicron increased the rate of growth on star
66 egration was much less site specific than in B. thetaiotaomicron.
67  and regulator compete for the intermediate, B. thetaiotaomicron tunes transcription of CS utilizatio
68 described species closest to both of them is B. thetaiotaomicron (approximately 94% sequence similari
69 fructans with different glycosidic linkages: B. thetaiotaomicron ferments levan with beta2-6 linkages
70 e, triggers the formation of biofilm in many B. thetaiotaomicron isolates and common gut Bacteroidale
71                      During growth in mucin, B. thetaiotaomicron contributes to EHEC virulence by cle
72 aride synthesis and conserved among multiple B. thetaiotaomicron isolates, that is required for 260.8
73 whereas swapping the fermentation ability of B. thetaiotaomicron to inulin confers increased consumpt
74 iduals, including the decreased abundance of B. thetaiotaomicron and the elevated serum glutamate con
75 f RelA and the anti-inflammatory activity of B. thetaiotaomicron.
76                            Administration of B. thetaiotaomicron to mice, but not an SPT-deficient st
77 r of DNA contributes to the aerotolerance of B. thetaiotaomicron.
78 at disruption of NQR reduces the capacity of B. thetaiotaomicron to induce IL-10 by impairing biogene
79 bited significantly higher concentrations of B. thetaiotaomicron.
80 n, little is known about the determinants of B. thetaiotaomicron biofilm formation.
81 leting bt3312, which prevented the growth of B. thetaiotaomicron on 1,6-beta-glucan.
82          Characterization of the lipidome of B. thetaiotaomicron OMVs revealed enrichment of dihydroc
83 level analysis identifying the preference of B. thetaiotaomicron and B. intestinalis in FVP degradati
84    Whole-genome transcriptional profiling of B. thetaiotaomicron, combined with mass spectrometry, re
85 starch-associated outer membrane proteins of B. thetaiotaomicron that have no starch-degrading activi
86 aerobic excellence and oxygen sensitivity of B. thetaiotaomicron are two sides of the same coin.
87 strate that the starch utilization system of B. thetaiotaomicron is controlled on at least two levels
88 s show that the starch utilization system of B. thetaiotaomicron is quite complex and contains a numb
89 ting for 22.4% expansion of the known TRN of B. thetaiotaomicron.
90 t adiposity compared with monoassociated, or B. thetaiotaomicron-D. piger biassociated, animals.
91  by polysaccharides, and its absence reduces B. thetaiotaomicron fitness in polysaccharide-rich diet-
92 pe integrity and that loss of BT4193 reduces B. thetaiotaomicron fitness during in vitro growth withi
93 egrading extracellular DNA (eDNA) in several B. thetaiotaomicron strains.
94                                   Similarly, B. thetaiotaomicron colonization results in sphingolipid
95  to the current paradigm, we discovered that B. thetaiotaomicron possesses an authentic GAG endosulfa
96                         Our data reveal that B. thetaiotaomicron stimulates production of the cytokin
97                             (2020) show that B. thetaiotaomicron can also extract the monosaccharide
98 he most significantly upregulated across the B. thetaiotaomicron transcriptome in response to gut col
99 lipid A phosphate positions observed for the B. thetaiotaomicron and P. gingivalis LPS contributes to
100 sed screen, we identified a key role for the B. thetaiotaomicron-encoded NADH:ubiquinone oxidoreducta
101                     Within Fut2(-) mice, the B. thetaiotaomicron fucose catabolic pathway was markedl
102 port the sequencing of a 7-kbp region of the B. thetaiotaomicron chromosome that lies immediately dow
103 ween these mechanisms, the components of the B. thetaiotaomicron Hep/HS degrading apparatus were anal
104 resented here is the atomic structure of the B. thetaiotaomicron protein BT1043, an outer membrane li
105 ity, BT1043 is a structural homologue of the B. thetaiotaomicron starch-binding protein SusD.
106 ch led to disruption of the gdhA gene on the B. thetaiotaomicron chromosome indicated that gdhA mutan
107                We previously showed that the B. thetaiotaomicron reference strain VPI-5482 is a poor
108 emonstrate that the binding of starch to the B. thetaiotaomicron surface involves at least four outer
109                         E. rectale adapts to B. thetaiotaomicron by decreasing production of its glyc
110 leocytoplasmic redistribution in response to B. thetaiotaomicron.
111 thetaOM T cells more strongly than wild-type B. thetaiotaomicron Despite similar levels of BthetaOM A
112 encing by these sugars outcompeted wild-type B. thetaiotaomicron in mice fed a diet rich in glucose a
113 terol sulfate (Ch-S) compared with wild-type B. thetaiotaomicron-colonized mice.
114 he role of HTCS in nutrient sensing, we used B. thetaiotaomicron GeneChips to characterize their expr
115                                        Using B. thetaiotaomicron strains that express defined subsets
116 uced a unique gene expression profile versus B. thetaiotaomicron.
117                               After weaning, B. thetaiotaomicron expands its metabolism to exploit ab
118 yR stress response to H2 O2 was induced when B. thetaiotaomicron was aerated, and in that circumstanc
119 e HTCS BT0366 is phosphorylated in vivo when B. thetaiotaomicron experiences the BT0366 inducer arabi
120 tion of dietary fructans to acetate, whereas B. thetaiotaomicron-derived formate is used by M. smithi
121 M. loti GmhB prefer the beta-anomer, whereas B. thetaiotaomicron GmhB is selective for the alpha-anom
122  only evident in mice fed a PD diet, wherein B. thetaiotaomicron relies on host mucus consumption.
123 lactosidase from family GH43; however, while B. thetaiotaomicron grows on larch wood arabinogalactan,
124 to the fermentable ones: mice colonized with B. thetaiotaomicron consume more inulin diet, while mice
125                      Genomic comparison with B. thetaiotaomicron in conjunction with cell culture stu
126                    Consistently, gavage with B. thetaiotaomicron reduced plasma glutamate concentrati
127 ific T cells compared with pups gavaged with B. thetaiotaomicron.
128          Colonization of germ-free mice with B. thetaiotaomicron has shown how this anaerobe modifies
129  70-fold, to a value close to that seen with B. thetaiotaomicron, if the primary integration site fro

 
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