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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 was then harvested from the ceca of
6 B. thetaiotaomicron-M. smithii cocolonization produces a
7 is the first molecular characterization of a B. thetaiotaomicron outer membrane protein involved in m
8 The products afforded by chondroitinase ABC (B. thetaiotaomicron) and chondroitinase ACII (A. auresce
10 domas disclosed that this IgA did not affect B. thetaiotaomicron population density or suppress 260.8
11 suggesting that the identified strategy aids B. thetaiotaomicron in the competitive gut environment.
16 secreted by mucin-foraging bacteria such as B. thetaiotaomicron, inhabiting the same niche, may affe
19 of approximately 1.6 kb was produced in both B. thetaiotaomicron and E. coli gdhA+ transformants.
21 es showed that metabolism of yeast mannan by B. thetaiotaomicron presents a 'selfish' model for the c
23 ed that, unlike D. piger, M. smithii directs B. thetaiotaomicron to focus on fermentation of dietary
24 genic B. fragilis isolates or B. distasonis, B. thetaiotaomicron, B. uniformis, B. ovatus, Escherichi
25 lular beta2-6 endo-fructanase, distinguishes B. thetaiotaomicron genetically and functionally, and en
26 rsified sensor domains may be one reason for B. thetaiotaomicron's success in our intestinal ecosyste
27 body that recognizes an epitope specific for B. thetaiotaomicron isolates in a large panel of hospita
28 and patients, T cell responses specific for B. thetaiotaomicron or B. fragilis were associated with
29 , but they can be differentiated easily from B. thetaiotaomicron by virtue of not utilizing trehalose
30 a pullulanase, and an alpha-glucosidase from B. thetaiotaomicron had been purified and characterized
31 micron, if the primary integration site from B. thetaiotaomicron, BT1-1, was provided on a plasmid in
33 n in vivo indicated that in the suckling gut B. thetaiotaomicron prefers host-derived polysaccharides
34 fatases than anticipated and establishes how B. thetaiotaomicron, and other major human commensal bac
35 NrtR family transcription factor (BT0354 in B. thetaiotaomicron, BtAraR) as a novel regulator contro
38 Only one of these genes was expressed in B. thetaiotaomicron, the homolog of linA, a lincomycin r
44 t increasing the number of copies of susR in B. thetaiotaomicron increased the rate of growth on star
46 and regulator compete for the intermediate, B. thetaiotaomicron tunes transcription of CS utilizatio
47 described species closest to both of them is B. thetaiotaomicron (approximately 94% sequence similari
49 aride synthesis and conserved among multiple B. thetaiotaomicron isolates, that is required for 260.8
50 iduals, including the decreased abundance of B. thetaiotaomicron and the elevated serum glutamate con
55 Whole-genome transcriptional profiling of B. thetaiotaomicron, combined with mass spectrometry, re
56 starch-associated outer membrane proteins of B. thetaiotaomicron that have no starch-degrading activi
57 strate that the starch utilization system of B. thetaiotaomicron is controlled on at least two levels
58 s show that the starch utilization system of B. thetaiotaomicron is quite complex and contains a numb
60 by polysaccharides, and its absence reduces B. thetaiotaomicron fitness in polysaccharide-rich diet-
61 to the current paradigm, we discovered that B. thetaiotaomicron possesses an authentic GAG endosulfa
62 lipid A phosphate positions observed for the B. thetaiotaomicron and P. gingivalis LPS contributes to
64 port the sequencing of a 7-kbp region of the B. thetaiotaomicron chromosome that lies immediately dow
65 ween these mechanisms, the components of the B. thetaiotaomicron Hep/HS degrading apparatus were anal
66 resented here is the atomic structure of the B. thetaiotaomicron protein BT1043, an outer membrane li
68 ch led to disruption of the gdhA gene on the B. thetaiotaomicron chromosome indicated that gdhA mutan
69 emonstrate that the binding of starch to the B. thetaiotaomicron surface involves at least four outer
72 he role of HTCS in nutrient sensing, we used B. thetaiotaomicron GeneChips to characterize their expr
74 yR stress response to H2 O2 was induced when B. thetaiotaomicron was aerated, and in that circumstanc
75 e HTCS BT0366 is phosphorylated in vivo when B. thetaiotaomicron experiences the BT0366 inducer arabi
76 tion of dietary fructans to acetate, whereas B. thetaiotaomicron-derived formate is used by M. smithi
77 M. loti GmhB prefer the beta-anomer, whereas B. thetaiotaomicron GmhB is selective for the alpha-anom
78 only evident in mice fed a PD diet, wherein B. thetaiotaomicron relies on host mucus consumption.
79 lactosidase from family GH43; however, while B. thetaiotaomicron grows on larch wood arabinogalactan,
83 70-fold, to a value close to that seen with B. thetaiotaomicron, if the primary integration site fro
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