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1 creased the proportion of chitin attached to beta(1-6)glucan.
2 ry chitin chains from chitin synthase III to beta(1-6)glucan.
3 and in the lateral wall, attached in part to beta(1-6)glucan.
4 the remainder attached to beta(1-3)glucan or beta(1-6)glucan.
5 nase activity was induced in the presence of beta-1,6-glucans.
6 ly implicated in cross-linking beta-1,3- and beta-1,6-glucans.
7 ailable acceptor sites for the attachment of beta-1,6-glucans.
8 eotypic receptors proliferate in response to beta-(1,6)-glucan.
9 20% chitosan, 5% beta-(1,3)-glucan, and 70% beta-(1,6)-glucan.
10 ecific interaction between the collectin and beta(1-->6)-glucan.
11 ressing stereotypic BCRs highly specific for beta-(1,6)-glucan, a major antigenic determinant of yeas
13 r by a decline in beta-1,3-glucan-associated beta-1, 6-glucans and, within several generations, a fiv
14 n provides a characteristic "fingerprint" of beta-1,6-glucan and the fine structure of the oligosacch
18 E6 and KRE1, two other genes involved in the beta-1,6-glucan biosynthetic pathway, disappear in the a
19 ich are large molecules composed of a linear beta-(1,6)-glucan chains with beta-(1,3)-glucosyl side c
20 wth phenotype and 75% reduction in cell wall beta-1,6-glucan, characteristic of the cwh41Deltakre1Del
21 onents of the cell wall, beta(1-->3)-glucan, beta(1-->6)-glucan, chitin, and mannoprotein are linked
22 otein incorporation, whereas the beta(1-->3)-beta(1-->6)glucan complex was synthesized at almost norm
23 t the cell cortex, the area where the chitin-beta(1-6)glucan complex is found, was greatly enhanced a
27 kre6Deltaskn1Delta contained less cell wall beta-1,6-glucan, grew slowly with an aberrant morphology
29 a gene involved in the assembly of cell wall beta-1,6-glucan, has recently been shown to be the struc
30 d that cross-reactive proteins are linked by beta 1,6-glucan in the cell wall of each non-albicans Ca
33 mline configuration reduced the affinity for beta-(1,6)-glucan, indicating that these BCRs are indeed
34 ogether, these observations demonstrate that beta(1-->6)-glucan is an important fungal ligand for SP-
37 s-links, we have found that chitin linked to beta(1-6)glucan is diminished in mutants of the CRH1 or
39 I (Cwh41p) in the biosynthesis of cell wall beta-1,6-glucan is indirect and that dolichol-P-glucose
40 ngs on the linkage between mannoproteins and beta(1-->6)-glucan, it is concluded that the latter poly
42 es and motifs consistent with linkage to the beta-1, 6-glucan of C. albicans cell walls have provided
43 other organisms support important roles for beta-1,6 glucans, predominantly in mediating host cellul
45 ne receptor protein than cyclic beta-(1-->3),beta-(1-->6)-glucans produced by wild-type B. japonicum.
46 atographic pattern of endoglucanase digested beta-1,6-glucan provides a characteristic "fingerprint"
47 It contains wild-type levels of cell wall beta-1,6-glucan, shows moderate underglycosylation of N-
48 ion of a functional P. carinii kre6 (Pckre6) beta-1,6 glucan synthase in Pneumocystis that, when expr
50 a new gene (ndvC) involved in beta-(1--> 3), beta-(1-->6)-glucan synthesis and in nodule development.
51 ate that KRE5, KRE6 and SKN1 are involved in beta-1,6-glucan synthesis, maintenance of cell wall inte
53 out 100 kDa in apparent size, is attached to beta(1-->6)-glucan through a remnant of a glycosylphosph
55 direct role of Cwh41p in the biosynthesis of beta-1,6-glucan, we constructed a double mutant, alg5Del
57 roteins act by transferring chitin chains to beta(1-6)glucan, with a newly observed high activity in
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