コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 prominent loose-fitting structure called the exosporium.
2 o examine the distribution of Alr within the exosporium.
3 o material from the spore's core and not the exosporium.
4 prominent loose-fitting structure called the exosporium.
5 s required for the attachment of BclA to the exosporium.
6 in the outer spore coat and absent from the exosporium.
7 y a prominent loose fitting layer called the exosporium.
8 ther surrounded by a glycoprotein-containing exosporium.
9 loose-fitting, balloon-like layer called the exosporium.
10 n-like protein, BclB, is also present in the exosporium.
11 an important role in the construction of the exosporium.
12 hat is sufficient for incorporation into the exosporium.
13 nt for proper incorporation of BclA onto the exosporium.
14 NTD being sufficient to deliver BxpB to the exosporium.
15 lays a critical role in the formation of the exosporium.
16 roduce spores containing an outer layer, the exosporium.
17 hich is normally tightly associated with the exosporium.
18 l as a more interior location underneath the exosporium.
19 ar compatible with a protective role for the exosporium.
20 eveloping bacilli within the confines of the exosporium.
21 icated by previous proteomic analyses of the exosporium.
24 rected toward BclA, a major component of the exosporium, although other components were also distingu
25 B. anthracis: it guides the assembly of the exosporium, an outer structure encasing B. anthracis but
27 n N-terminal sequence that targets it to the exosporium and is similar in sequence to a cognate targe
29 tures of bacterial endospores, including the exosporium and spore coats of four Bacillus species in a
30 bclB mutant spores, the distance between the exosporium and the coat, the interspace, is reduced.
31 macrophage-mediated killing of nonsonicated (exosporium+) and sonicated (exosporium-) Sterne 34F2 spo
32 or probing the structure and function of the exosporium, and in the analysis of the life cycle of B.
37 during sporulation and the only part of the exosporium assembled in a DeltaexsY mutant strain of B.
38 or cap, corresponds to the first part of the exosporium assembled within the mother cell during sporu
39 sults provide the first direct evidence that exosporium assembly is a non-uniform process and suggest
44 ore than 20 proteins have been identified as exosporium-associated, their abundance, relationship to
46 of the protein at the site of the developing exosporium basal layer and stable incorporation which in
47 protein is a major structural protein of the exosporium basal layer of B. cereus family spores and th
54 mutant spores were encased by a double-layer exosporium, both layers of which were composed of a basa
55 red over approximately three-quarters of the exosporium but not in a cap-like region at one end of th
56 hich BclA and BetA are incorporated into the exosporium by a mechanism that depends on their similar
59 res of Bacillus anthracis are enclosed by an exosporium composed of a basal layer and an external hai
60 f anthrax, are enclosed by a loosely fitting exosporium composed of a basal layer and an external hai
61 res of Bacillus anthracis are enclosed by an exosporium composed of a basal layer and an external hai
62 Bacillus anthracis spores are enclosed by an exosporium comprised of a basal layer and an external ha
63 the Bacillus anthracis spore consists of an exosporium comprised of an outer hair-like nap layer and
64 the Bacillus anthracis spore consists of an exosporium comprised of two distinct layers, an outer ha
65 res, which cause anthrax, are enclosed by an exosporium consisting of a basal layer and an external h
67 ded by the densely packed endospore coat and exosporium, containing amyloid or amyloid-like proteins.
68 eltabxpB spores, which lack BxpB, contain an exosporium devoid of hair-like nap even though the Delta
69 Their findings may have implications for exosporium formation in other spore forming bacteria, in
75 at the chemokine was located internal to the exosporium in association primarily with the spore coat
80 rulent in animal models, indicating that the exosporium is dispensable for infection, at least in the
85 ost structure of the B. anthracis spore, the exosporium, is a shell composed of approximately 20 prot
86 t layer of the Bacillus anthracis spore, the exosporium, is composed of a paracrystalline basal layer
87 fic location of this glycoprotein within the exosporium layer and its role in the biology of the spor
89 s found to possess structural defects in the exosporium layer of the spore (visualized by electron mi
90 the incorporation of these proteins into the exosporium layer of the spore and used these targeting d
92 spore is not immunologically inert, (ii) the exosporium masks epitopes recognized by the Mphi, (iii)
93 on these data, we propose a revised model of exosporium maturation and assembly and suggest a novel r
94 the spore form of B. anthracis and that the exosporium may play a role in the protection of spores f
96 ng sporulation, as it enhances levels of the exosporium morphogenetic protein CdeC in a sigma(K) -dep
97 explained by differences in their shape and exosporium morphology, which may result in differences i
98 l location of structural proteins within the exosporium, namely a description of its three-dimensiona
104 characterized crystalline fragments from the exosporium of Bacillus cereus, B. thuringiensis and B. a
105 ted to incorporate foreign proteins into the exosporium of inactivated, spores resulting in the surfa
111 ative agent of anthrax, whose immunodominant exosporium protein BclA contains collagen-like repeat se
113 ing a visible exosporium were devoid of most exosporium proteins but, surprisingly, retained the puta
115 t in bclB mutant spores, the distribution of exosporium proteins CotY and BxpB is altered, suggesting
116 ic form in close association with many other exosporium proteins in high-molecular weight complexes.
117 that BetA is a member of a growing family of exosporium proteins that assemble under the control of t
121 oclonal antibodies, raised against spores or exosporium, reacted with the CTD, consistent with its ex
123 hment of essentially all BclA trimers to the exosporium requires the basal layer protein BxpB, and bo
125 the outgrowing cell always escapes from its exosporium shell by popping through the cap, suggesting
126 ation of purified DeltaexsY spores devoid of exosporium showed that they lacked detectable levels of
128 than wild-type spores, which had an extended exosporium (spore length for the wt, 2.40 +/- 0.56 micro
132 er proteins that have been identified in the exosporium such as GroEL, immune inhibitor A and arginas
137 lB is located principally in a region of the exosporium that excludes a short arc on one side of the
138 s partly due to the extreme stability of the exosporium that has proven to be refractive to existing
139 ess a loosely fitting outer layer called the exosporium that is composed of a basal layer and an exte
140 escence, and flow cytometry) resulting in an exosporium that is more fragile than that of a wild-type
141 le composition of the endospore coat and the exosporium that makes staining methodologies for endospo
142 stalline flexible yet resistant layer called exosporium that plays a major role in spore adhesion and
143 e to synthesize ExsB produced spores with an exosporium that was readily sloughed, indicating that Ex
145 rine Bacillus spores oxidize Mn(II) on their exosporium, the outermost layer of the spore, encrusting
146 of anthracis) is a major constituent of the exosporium, the outermost surface of B. anthracis spores
149 purified DeltaexsB spores lacking a visible exosporium were devoid of most exosporium proteins but,
150 layer of the Bacillus anthracis spore is the exosporium, which is composed of a paracrystalline basal
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。