ライフサイエンスコーパス: beta-glucan

1 l health benefits besides the soluble fibre (beta-glucan).

2 hased aqueous food system containing oil and beta-glucan.

3 ies of the concentrate containing 31% of oat beta-glucan.

4 ish the industrial application of acetylated beta-glucan.

5 arley flour and by 19.9%, 27.4% and 44.8% by beta-glucan.

6 flour but was not significantly affected by beta-glucan.

7 inked glucose units when compared with yeast beta-glucan.

8 mented with either wheat arabinoxylan or oat beta-glucan.

9 g) can be recommended as the best sources of beta-glucan.

10 ted the growth of B. thetaiotaomicron on 1,6-beta-glucan.

11 ood product containing soluble dietary fibre beta-glucan.

12 ciated molecular patterns (PAMPs), including beta-glucan.

13 mixture of trophic forms and cysts, or with beta-glucan.

14 NETosis early after binding fibronectin and beta-glucan.

15 odate the hook-like structure adopted by 1,6-beta-glucan.

16 and cell wall polysaccharide, mixed-linkage beta-glucan.

17 otential interaction between the protein and beta-glucan.

18 the hydroxyl radical mediated degradation of beta-glucan.

19 nd this related with a faster degradation of beta-glucan.

20 ifferent behaviors between mannoproteins and beta-glucans.

21 edicted to target mixed linked plant 1,3;1,4-beta-glucans.

22 due to their bioactive compounds, especially beta-glucans.

23 that this method is efficient for extracting beta-glucans.

24 tical for IL-1beta production in response to beta-glucans.

25 tform to target the side chains of decorated beta-glucans.

26 able to metabolize alpha-glucans rather than beta-glucans.

27 beta-glucosidase that targets primarily 1,6-beta-glucans.

28 hydrolase family 3 (GH3) members on diverse beta-glucans.

29 ly reflecting the pro-inflammatory cell wall beta-glucans.

30 coli, was active on a variety of xylans and beta-glucans.

31 ontaining barley flour (28%, 56% and 84%) or beta-glucan (1.5%, 3.0% and 4.5%) and their effect on st

32 iva) is an excellent source of mixed linkage beta-glucans ((1-->3)(1-->4)-beta-D-glucan), a dietary f

33 ) displayed 7.5-30.8% higher levels of total beta-glucan, 39.8-68.6% higher arabinoxylan content, 11.

34 Particulate beta-glucan (a DECTIN-1 agonist) induced mast cell degra

35 We report that the exposure of beta-glucan, a key pathogen-associated molecular pattern

36 ause some mediate the synthesis of (1,3;1,4)-beta-glucan, a polysaccharide characteristic of the evol

37 These studies suggest that beta-glucan-activated B lymphocytes have an important an

38 In this article, we demonstrate that beta-glucan-activated B lymphocytes upregulate proinflam

39 When compared with CpG (TLR9 agonist), beta-glucan-activated cells secreted significantly highe

40 Moreover, the influence of beta-glucan addition (BG, 0.5-3% w/v) on the gelation of

41 n the concentrated regime due to the size of beta-glucan aggregates formed.

42 ice from T1D as compared with treatment with beta-glucan alone.

43 Here we focus on beta-glucan, an immunogenic cell-wall polysaccharide who

44 sensitization and can be reconstituted with beta-glucan and abrogated by neutralization of IL-17A.

45 ies as well as signs of (incipient) protein, beta-glucan and arabinoxylan breakdown.

46 The soluble beta-glucan and arabinoxylan content of cultivars ranged

47 ural motifs at the cleavage sites of starch, beta-glucan and arabinoxylan fragments were identified,

48 ates and released NETs in response to fungal beta-glucan and Candida albicans hyphae when presented w

49 estingly, loss of PerA increases exposure of beta-glucan and chitin content on the hyphal cell surfac

50 lysaccharides of the fungal wall include 1,3-beta-glucan and chitin, which are synthesized by membran

51 The locus is up-regulated by 1,6-beta-glucan and encodes two enzymes, a surface endo-1,6-

52 for 28.9% and 37.6% of the variation in the beta-glucan and extract fractions of malt.

53 rated in the starchy endosperm (e.g. starch, beta-glucan and fructan) and the dietary fibre component

54 the hydroxyl radical-mediated degradation of beta-glucan and identified the intermediate species invo

55 of beta-glucan in aqueous food systems where beta-glucan and lipids co-exist.

56 FT-IR analyses indicate the presence of beta-glucan and ovotransferrin in both precipitate and s

57 a signaling pattern recognition receptor for beta-glucan and represent the first direct evidence of s

58 site flours contained up to three-times more beta-glucan and significantly more total phenolics inclu

59 slowly digestible starch (SDS) and insoluble beta-glucan and total arabinoxylan content was observed.

60 ed the effectiveness of barley mixed linkage beta-glucan and wheat arabinoxylan in retarding the tran

61 charides (xyloglucan, mannans, mixed-linkage beta-glucan and xylans); however, no transglycanases wer

62 In the CBMs that recognize beta-glucans and beta-mannans, differences in the confor

63 ins encoded by PUL1,6-beta-glucan target 1,6-beta-glucans and comprise a surface glycan-binding prote

64 Studies using beta-glucans and other Dectin-1 binding components have

65 ork evaluated the humid extraction of barley beta-glucans and partially characterized them.

66 ced by surface exposure of immunostimulatory beta-glucans and was mediated by activation of the Decti

67 o utilize certain hemicelluloses, especially beta-glucans and xyloglucan, for growth that was confirm

68 Epicor also contained both pro-inflammatory (beta-glucans) and anti-inflammatory components.

69 hat CLEC18 preferentially binds to fucoidan, beta-glucans, and galactans.

70 e canonical NLRP3 inflammasome, in mediating beta-glucan- and C. albicans-induced innate responses in

71 In addition, the presence of beta-glucan appeared to retard the hexanal production in

72 Wall proteins, galactomannan, chitin, and beta-glucan are not the relevant hyphal components; inst

73 Health effects of beta-glucan are typically related to dose, size and visc

74 Beta-glucans are a heterologous group of fibrous glucose

75 Beta-glucans are an important component of mold spores a

76 beta-Glucans are carbohydrates present in the cell wall

77 Fungal beta-glucans are comprised of d-glucose homopolymers con

78 Both beta-glucans are cross-linked, forming a huge alkali-ins

79 Beer wort beta-glucans are high-molecular-weight non-starch polysa

80 beta-Glucans are major components of fungal cell walls t

81 Pneumocystis carinii (Pc) beta-glucans are major components of the organism cell w

82 beta-Glucans are naturally occurring polysaccharides in

83 res have a high beta-glucan content, but the beta-glucans are not available on the surface of live sp

84 ontributor to the development of asthma, and beta-glucans are often used as a surrogate for mold expo

85 lpy of gelatinisation (DeltaHgel), similarly beta-glucan at 1.5% increased the DeltaHgel.

86 For added beta-glucan at levels >1%, the lower the concentration a

87 ough at least two mechanisms: concealment of beta-glucans beneath alpha-glucans and enzymatic removal

88 s and characterization of grafted poly(1-->4-beta-glucan) (beta-glu) strands on alumina.

89 usly unidentified CBM families that targeted beta-glucans, beta-mannans, and the pectic polysaccharid

90 ningitis without fungal diagnosis, for (1,3)-beta-glucan (BG).

91 present the first direct evidence of soluble beta-glucan binding and affecting a signaling-competent

92 odel system to study molecular regulation of beta-glucan biosynthesis as well as possible links betwe

93 of the mutant as well as regulate cell wall beta-glucan biosynthetic genes.

94 ulosolvens endoglucanase, bind to a range of beta-glucans but, uniquely, display significant preferen

95 istoplasma capsulatum minimizes detection of beta-glucan by host cells through at least two mechanism

96 fungal pathogen-associated molecular pattern beta-glucan by human neutrophils causes rapid (</= 30 mi

97 The (1,3)-beta-glucan callose is a major component of cell wall th

98 and in contrast to other CBMs that recognize beta-glucans, CBM65A utilizes different polar residues t

99 The deposition of the (1,3)-beta-glucan cell wall polymer callose at sites of attemp

100 e data to test models for packing of (1-->4)-beta-glucan chains in cellulose microfibrils.

101 CBMs that bind beta-glucan chains often display broad specificity recog

102 mechanism triggered by the fungal mimic and beta-glucan-containing stimulus zymosan, which produces

103 ponent or control vaccine confirmed that the beta-glucan-containing vaccine exerted its enhanced acti

104 Dectin-1 signal transduction pathway by the beta-glucan-containing vaccine.

105 an increased- and four lines with a reduced beta-glucan content for further study.

106 in untreated mice correlated with increased beta-glucan content in the lungs.

107 ation process gave a better yield and higher beta-glucan content than did traditional isolation metho

108 dosporium cladosporioides spores have a high beta-glucan content, but the beta-glucans are not availa

109 bility of beta-glucans rather than the total beta-glucan content.

110 Many wild growing species present high beta-glucan contents, especially Bracket fungi.

111 ld growing mushrooms were analysed for their beta-glucan contents.

112 Total beta-glucan correlated negatively (r=-0.846, p<0.05) wit

113 beta-Glucan decreased in IAC responding to therapy and i

114 (up to 105% and 65%), whereas incorporating beta-glucan decreased the PV and FV by 20.3% and 20.6%,

115 However, the presence of ovotransferrin in beta-glucan decreased the viscosity of the solution, whi

116 pothesise the mechanism of the inhibition of beta-glucan degradation by superoxide dismutase.

117 showed that while lipid oxidation proceeded, beta-glucan degradation occurred.

118 peroxide value and hexanal production while beta-glucan degradation was evaluated by viscosity and m

119 rocessing methods, glycopeptide-enriched and beta-glucan-depleted products were each prepared from Br

120 l role of the endo-1,6-beta-glucanase in 1,6-beta-glucan depolymerization by deleting bt3312, which p

121 donor substrates (cellulose or mixed-linkage beta-glucan) differ qualitatively from its acceptor subs

122 vitamins and minerals, fruit polyphenolics, beta-glucan, docosahexaenoic acid) appropriate for decon

123 We show here that PUL1,6-beta-glucan does not orchestrate the degradation of a pl

124 microscopy to explore the fine structure of beta-glucan exposed on C. albicans cell walls before and

125 Upon Ag presentation, beta-glucan-exposed dendritic cells induced a significan

126 lled Aspergillus conidia, which have minimal beta-glucan expression on their cell surface.

127 usly described in bacteria but resembling ML beta-glucans found in plants and lichens.

128 ated CpG motifs, found in bacterial DNA, and beta-glucans, found in the cell wall of fungi, both indu

129 In this study, we show that the beta-glucan from Saccharomyces cerevisiae induces the ex

130 erences, qualitative differences between the beta-glucans from the different lines were found.

131 e a similar role as Eng1 in removing exposed beta-glucans from the yeast cell surface.

132 The beta-glucan gel showed a reduction in hardness and adhes

133 ter-soluble cellulose acetate, mixed-linkage beta-glucan, glucomannan and arabinoxylan).

134 results showed that each extraction step of beta-glucan had a significant effects on its chemical pr

135 Fibers of beta-glucan have been added to foods for their thickenin

136 epresenting interesting sources of bioactive beta-glucans have been widely studied.

137 beta-Glucans, homopolymers of glucose, are widespread in

138 potential of curdlan, a naturally occurring beta-glucan immunomodulator, against visceral leishmania

139 ipid oxidation may induce the degradation of beta-glucan in aqueous food systems where beta-glucan an

140 or velB results in elevated accumulation of beta-glucan in asexual spores.

141 able one to obtain interesting parameters of beta-glucan in beer wort, such as the molecular weight a

142 at by controlling the structural features of beta-glucan in mixtures with sodium caseinate, informed

143 gnificant fibre fractions in rye flakes, and beta-glucan in oat flakes, cellulose and resistant starc

144 of soluble arabinoxylan in wholemeals and of beta-glucan in semolina.

145 The presence of iron(II) in beta-glucan in solution causes the formation of hydroxyl

146 At equivalent hydrodynamic volume of beta-glucan in the mixtures, samples varying in molecula

147 The presence of greater levels of beta-glucan in whole barley flour and bran of high altit

148 rminations of all glucans, alpha-glucans and beta-glucans in 39 mushrooms species were performed, lea

149 was developed to determine and characterize beta-glucans in beer wort using size exclusion chromatog

150 o determine whether altering the exposure of beta-glucans in C cladosporioides through heat killing c

151 Thus, beta-glucans in Pneumocystis cysts are largely masked, w

152 ies support a significant role for cell wall beta-glucans in stimulating inflammatory responses.

153 r dietary fibre components, arabinoxylan and beta-glucan, in semolina and wholemeal flour of old and

154 acts both on cellulose and on non-cellulose beta-glucans, including cellodextrins and xyloglucan.

155 microscopy were characteristic of commercial beta-glucans, indicating that this method is efficient f

156 d the hydroxyl radical driven-degradation of beta-glucan induced by iron(II) or ascorbic acid/iron(II

157 t time investigated oxidative degradation of beta-glucan induced by lipid oxidation using an oil-in-w

158 proapoptotic protease caspase-8 in promoting beta-glucan-induced cell death and NLRP3 inflammasome-de

159 dectin-1 play a crucial role in coordinating beta-glucan-induced IL-1beta processing as well as a cel

160 Conversely, trophic forms suppress beta-glucan-induced proinflammatory responses in vitro,

161 by the Dectin-1 receptor, but the effects of beta-glucan-induced type I IFNs have not been defined.

162 Alone, immobilized beta-glucan induces reactive oxygen species (ROS) produc

163 Beta-glucan is a polysaccharide widely accepted and used

164 starch retrogradation index, indicating that beta-glucan is associated with starch retrogradation.

165 ron bgsBA required for production of this ML beta-glucan is conserved among several genera within the

166 rently a pharmaceutical grade preparation of beta-glucan is in several clinical trials with an anti-c

167 However, beta-glucan is readily degraded in aqueous systems in pr

168 e innate immune response induced by low-dose beta-glucan is regulatory in nature and can be exploited

169 NET release to Fn with beta-glucan is robust, accounting for 17.2 +/- 3.4% of t

170 We also noted that PUL1,6-beta-glucan is syntenic to many PULs from other Bacteroi

171 tilization of yeast and fungal cell wall 1,6-beta-glucans is a widespread adaptation within the human

172 Binding to the backbone chains of beta-glucans is mediated primarily by five aromatic resi

173 One important source of beta-glucans is the cell wall of yeasts, especially that

174 es C of mixtures of sodium caseinate and oat beta-glucan isolates varying in molecular weight (MW) wa

175 nd the network melting temperature, with the beta-glucan itself giving the strongest network.

176 ines and identified ten lines that displayed beta-glucan levels above 6.7% and 10 below 3.6%.The extr

177 Laminarin, a beta-glucan ligand of Dectin-1, was incorporated into th

178 The high and low beta-glucan lines will now be used as a model system to

179 In contrast, trophic forms suppressed beta-glucan-, LTA-, and LPS-induced IL-1beta, IL-6, and

180 Exposure to lactate induces beta-glucan masking in C. albicans via a signalling path

181 f cell-wall-related genes that contribute to beta-glucan masking.

182 these data indicate that molecules targeting beta-glucan may provide a mechanism for treatment of fun

183 d that the physical presentation geometry of beta-glucan might determine whether it can be recognized

184 High beta-glucan mutant barley, mother barley and oat beta-gl

185 In particular the barley high beta-glucan mutant proved to exhibit a unique block stru

186 -glucan/sodium caseinate system increases as beta-glucan MW decreases.

187 linkage (1 --> 3)(1 --> 4)-beta-D-glucan (ML beta-glucan), not previously described in bacteria but r

188 e based on a diet containing >/=3 g/d of oat beta-glucan (OBG).

189 The cyst cell wall beta-glucans of Pneumocystis have been shown to stimulat

190 tal, insoluble and soluble dietary fiber and beta-glucans of sorghum flour samples were all negativel

191 Emulsions containing beta-glucan, oil and ferrous ion showed significant visc

192 al epithelial cell PRR that binds to exposed beta-glucans on the surface of the fungal pathogen Candi

193 C cladosporioides spores effectively exposed beta-glucans on the surface of the spores and increased

194 ector functions in response to either fungal beta-glucan or C. albicans hyphae and fibronectin, with

195 ils are exposed either to immobilized fungal beta-glucan or to C. albicans hyphae without ECM.

196 Administration of soluble beta-glucans or a SYK inhibitor reduced visceral hyperse

197 ced by administration of fungicides, soluble beta-glucans, or a SYK inhibitor.

198 lorimetry provided evidence for existence of beta-glucan ordered domains in the mixed gel structures

199 In contrast, beta-glucan partially reverses the LPS-induced tolerance

200 The S. meliloti ML beta-glucan participates in bacterial aggregation and bi

201 FNs regulate CD8 T cell activation by fungal beta-glucan particle-stimulated DCs.

202 Yeast-derived whole beta-glucan particles (WGP; a ligand to engage and activ

203 adjuvant aqueous formulation) and Dectin-1 (beta-glucan peptide) acted synergistically in newborns a

204 romoted the recovery of total dietary fiber, beta-glucans, phenolic acids and anthocyanins in the bra

205 rface proteins in Pneumocystis and what role beta-glucans play in Pneumocystis-associated inflammatio

206 , the innate immune receptor that recognizes beta-glucan, plays an important role in immunity against

207 Furthermore, systemic coadministration of beta-glucan plus pancreatic beta cell Ag resulted in an

208 gal attack is deposition of callose, a (1,3)-beta-glucan polymer, in the form of cell wall thickening

209 hich suggests co-synthesis of chitin and 1,3-beta-glucan polysaccharides at sites of exocytosis.

210 glucans and enzymatic removal of any exposed beta-glucan polysaccharides by the secreted glucanase En

211 Fungal cell walls contain beta-glucan polysaccharides that stimulate immune respon

212 The extracted beta-glucans presented a higher apparent viscosity than

213 on a linear mixed-linkage (1 --> 3)(1 --> 4)-beta-glucan produced by a bacterium.

214 roscopy was investigated to characterise the beta-glucan profiles of several commercial health supple

215 PS matrix structure, while fungal mannan and beta-glucan provide sites for GtfB binding and activity.

216 In addition, beta-glucan quality parameters like molecular weight and

217 The results showed that concentrations of beta-glucan range from 2.40 to 7.42g/100g.

218 The degree of substitution of the acetylated beta-glucans ranged from 0.03 to 0.12, suitable for use

219 is dependent on the surface availability of beta-glucans rather than the total beta-glucan content.

220 shown that lung responses generated via the beta-glucan receptor Dectin-1 are required for lung defe

221 tivity are dependent on CD18, but not on the beta-glucan receptor dectin-1.

222 s not reduce detection of yeasts by the host beta-glucan receptor Dectin-1.

223 Dectin-1, a beta-glucan receptor, contributes to host anti-fungal de

224 Release is dependent on beta-glucan recognition by complement receptor 3 (CD11b/

225 albicans hyphae was also found to depend on beta-glucan recognition by complement receptor 3, requir

226 d -deficient mice to investigate the role of beta-glucan recognition in the immunity against pulmonar

227 Insect beta-glucan recognition protein (betaGRP), a pathogen re

228 hese findings establish a novel link between beta-glucan recognition receptors and the inflammatory p

229 0 and C-trim30, which have about 20% and 30% beta-glucan, respectively, exhibited more fluid-like beh

230 nd C-trim95, which contain about 50% and 95% beta-glucan, respectively, showed solid viscoelastic pro

231 78.3% upon incorporation of barley flour and beta-glucan, respectively.

232 atment of prediabetic NOD mice with low-dose beta-glucan resulted in a profound delay in hyperglycemi

233 The beta-glucan-rich polysaccharides (GE) from P. sajor-caju

234 NMR studies with xyloglucans, i.e., branched beta-glucans, showed an extended binding surface compare

235 rams indicated that the compatibility of the beta-glucan/sodium caseinate system increases as beta-gl

236 orbate/iron(II) induced hydroxyl radicals in beta-glucan solutions.

237 This report reveals the mechanism by which beta-glucan-specific CBMs can distinguish between linear

238 study demonstrated that bacterial and fungal beta-glucans stimulate IFN-beta production by dendritic

239 eotide (CpG), and study the participation of beta-glucan-stimulated B cells in the innate immune resp

240 ver, we observed that conditioned media from beta-glucan-stimulated B lymphocytes elicited neutrophil

241 pathway via TLR9 receptor to induced MMP-7, beta-glucan-stimulated cells were mTOR-independent and u

242 and IFN-gamma and granzyme B production) by beta-glucan-stimulated DCs in vitro and in vivo due to a

243 We demonstrate that beta-glucan-stimulated DCs induce CD8 T cell proliferati

244 n of IL-12 p70, IL-2, IL-6, and TNF-alpha by beta-glucan-stimulated DCs.

245 ms and cytokine profiles generated following beta-glucan stimulation of B lymphocytes, compared with

246 viscosity associated with a high content of beta-glucan suggests that they are good sources of fibre

247 Accordingly, beta-glucan surface exposure during Aspergillus fumigatu

248 which human neutrophils first detect nearby beta-glucan surfaces as c/j0 approximately 0.0044 s/mum.

249 less Sid2p/Mob1p and Clp1p phosphatase, and beta-glucan synthase Bgs1p accumulated slowly at the cle

250 s to involve allosteric activation of the ML beta-glucan synthase BgsA by c-di-GMP binding to its C-t

251 and VosA bind to the promoter region of the beta-glucan synthase gene fksA in asexual spores.

252 U. maydis class VII chitin synthase and 1,3-beta-glucan synthase travel in Mcs1-containing vesicles,

253 ic for aspergilli by targeting cell wall 1,3-beta-glucan synthases.

254 ry unit tightly controlling proper levels of beta-glucan synthesis in asexual and sexual spores.

255 B play an inter-dependent role in repressing beta-glucan synthesis in asexual spores.

256 Here, we report that beta-glucan synthesis in both asexual and sexual spores

257 thetic genes including those associated with beta-glucan synthesis in both types of spores.

258 y, VosA is required for proper repression of beta-glucan synthesis in sexual spores.

259 ML beta-glucan synthesis is subjected to both transcription

260 the amounts and fine structures of (1,3;1,4)-beta-glucans synthesized.

261 d the transcription of the Pneumocystis gsc1 beta-glucan synthetase, confirming the activity of a Pc

262 The non-catalytic proteins encoded by PUL1,6-beta-glucan target 1,6-beta-glucans and comprise a surfa

263 for C-trim dispersions were dependent on the beta-glucan that C-trim contained.

264 Laminarin is a (1-->3, 1-->6)-beta-glucan that is widely reported to be a Dectin-1 ant

265 dy reveals that EphA2 functions as a PRR for beta-glucans that senses epithelial cell fungal burden a

266 al Bacteroides species contain a PUL, PUL1,6-beta-glucan, that was predicted to target mixed linked p

267 ation and the higher the molecular weight of beta-glucan, the weaker the gelling ability of the mixed

268 Immune cells recognize these beta-glucans through a cell surface pathogen recognition

269 , we sought to determine the contribution of beta-glucans to C. albicans-induced inflammasome respons

270 responsible for removal of exposed cell wall beta-glucans to minimize host detection of Histoplasma y

271 which is active toward cellulose and soluble beta-glucans, to study the enzyme-substrate interaction

272 d Spain) were analysed for their contents of beta-glucan, tocols and phenolic compounds (free and bou

273 tracts or particular oat components, such as beta-glucans, tocols (vitamin E), or avenanthramides.

274 h the Candida albicans cell wall constituent beta-glucan, together with a genome-wide transcriptome,

275 B presented the highest protein, lipid, ash, beta-glucan, total and insoluble dietary fiber contents;

276 The dietary fibre, beta-glucan, total phenolic, alkylresorcinol content and

277 beta-glucan training elicits an exclusive epigenetic sig

278 actanases, as well as yeast cell wall chitin/beta-glucan transglycosylases.

279 Importantly, ex vivo beta-glucan treatment of monocytes from volunteers with

280 evelopment represents a strategy for evading beta-glucan-triggered immunity.

281 Of interest, beta-glucan, unlike CpG, had no effect on B lymphocyte p

282 ch correlated positively with the content of beta-glucans (up to R=0.77) and arabinoxylans (up to R=0

283 Several processes for the isolation of beta-glucans, using alkali, acid or a combination of bot

284 s of seeds it was shown that localization of beta-glucan varied between the different lines.

285 Further, the binding of TLP8 to beta-glucan was dependent on redox.

286 ins and a YPE, a mannoprotein fraction and a beta-glucan were monitored by binding experiments, ITC a

287 content and composition of arabinoxylan and beta-glucan were more stable in the older than in the mo

288 genitor functions; and interestingly, fungal beta-glucans were also detected in serum.

289 The extracted beta-glucans were characterized by chemical and rheologi

290 -glucan mutant barley, mother barley and oat beta-glucans were large-scale extracted by comparable pr

291 As a result, beta-glucans were obtained in a yield of 18.0% of the or

292 fect on the ascorbate induced degradation of beta-glucan, whereas ovotransferrin completely inhibited

293 product composed principally of particulate beta-glucans, whereas inflammation in transgenic and wil

294 e D-CAR(+) T cells exhibited specificity for beta-glucan which led to damage and inhibition of hyphal

295 e but targets a fungal cell wall glycan, 1,6-beta-glucan, which is a growth substrate for the bacteri

296 to water avoidance stress were given soluble beta-glucans, which antagonize C-type lectin domain fami

297 beta-glucans, which can activate innate immune responses

298 industry, even though it is a main source of beta-glucans, which have important health benefits and a

299 These immunoadhesins bind beta-glucan with high affinity, and precoating the surfa

300 table cellulose-xyloglucan and mixed-linkage beta-glucan-xyloglucan covalent bonds, and may therefore