ライフサイエンスコーパス: mannan

1 ong with low acetylation levels in xylan and mannan.

2 ffinities for C. albicans yeast and purified mannan.

3 years, possess an elaborate cell wall alpha-mannan.

4 ies of glycoside hydrolases that can degrade mannan.

5 mpletely blocked by the addition of EGTA and mannan.

6 SLA enzyme to produce glucomannan instead of mannan.

7 ch showed it to be a phosphorylated branched mannan.

8 ent and GtfB-mediated binding to C. albicans mannan.

9 of preserving the carbohydrate structure of mannan.

10 lf of the phosphomannan attached to N-linked mannans.

11 eta1,6-branched beta1,3-d-glucan and free of mannans.

12 though further studies ruled out cytoplasmic mannans.

13 ed or if mannose receptors were blocked with mannans.

14 cytes mainly via recognition of cell-surface mannans.

15 for the observed accommodation of decorated mannans.

16 esses two loci conferring metabolism of beta-mannans.

17 ans, galactans, arabinogalactan proteins and mannans.

18 tivities of an LM glycan backbone, alpha(1-6)mannans.

19 aginella, pine, spruce, rice and poplar were mannan 2-O- and 3-O-acetyltransferases, whereas the two

20 6 was observed, which was inhibited by yeast mannan (a known CD206 ligand), free mannose, and a block

21 by anti-DC-SIGN mAb and soluble DC-SIGN, and mannan, a natural ligand for DC-SIGN.

22 benefits of commensal fungi are mediated by mannans, a highly conserved component of fungal cell wal

23 A previous study has shown that mannan acetylation in Arabidopsis and konjac is mediated

24 o glycan-binding proteins, confirmed by beta-mannan affinity electrophoresis.

25 gh titers of Ab recognizing C. albicans beta-mannan Ag.

26 e is little to no information on how exactly mannan alignment, including the number of mannose units

27 to synthesize these glycoconjugates and beta-mannan, although at reduced levels.

28 endomannanases) catalyse degradation of beta-mannans, an abundant class of plant polysaccharides.

29 n of FMS contains mainly the backbone of 1,4-mannan and 1,6-alpha-galactan and through the Fucalpha1-

30 In addition, the DC-SIGN ligand mannan and an anti-DC-SIGN antibody did not inhibit DC-m

31 Mannan and anti-CD206 antibody significantly decreased t

32 -7 in macrophages stimulated with zymosan or mannan and ATP.

33 te to the EPS matrix structure, while fungal mannan and beta-glucan provide sites for GtfB binding an

34 We detected no binding to mannan and BSA.

35 tically with Man5B in the hydrolysis of beta-mannan and carboxymethyl cellulose.

36 phobicity and substantial amounts of exposed mannan and chitin at the surface.

37 ng to loss of hydrophobicity and exposure of mannan and chitin polysaccharides.

38 njugate was useful in generation of MOS from mannan and enrichment of fruit juices.

39 Thus, differential surface expression of mannan and glucan may influence recognition of C. albica

40 We show here the distinct effects of mannan and glucan on complement activation and opsonopha

41 rphogenesis and cell wall components such as mannan and glucan were also upregulated, indicating enha

42 ), and Populus trichocarpa catalyze beta-1,4-mannan and glucomannan synthase reactions in vitro.

43 nsect cells, and each CslA protein catalyzed mannan and glucomannan synthase reactions in vitro.

44 al MOS is being derived from yeast cell wall mannan and is widely used as prebiotic in feed supplemen

45 Mannan and xylan concentrations were low in P. zonale an

46 important for understanding many aspects of mannan and xyloglucan biosynthesis.

47 multiple membrane spans, and their products (mannan and xyloglucan) accumulate in the Golgi lumen.

48 tion by Ig was inhibited by coapplication of mannan and, thus, likely to be mediated by C-type lectin

49 mechanism for binding of dectin-2 to fungal mannans and also to bacterial lipopolysaccharides, capsu

50 ex cell wall consisting of an outer layer of mannans and an inner layer of beta-glucans and chitin.

51 as a sugar-rich cell wall mainly composed of mannans and glucans.

52 ris and identifies critical roles for fungal mannans and mannoproteins.

53 bind Manalpha1-2Man in internal positions in mannans and other polysaccharides.

54 s as immunodominant epitopes in (1-->2)-beta-mannans and to the viability of a glycoconjugate vaccine

55 beta-mannans and xylans are important components of the plant

56 ayer enriched in mannosylated glycoproteins (mannan) and an inner layer enriched in beta-(1,3)-glucan

57 ve ligands (acetylated BSA [AcBSA], zymosan, mannan, and LPS from Escherichia coli and Salmonella as

58 eins showed similar or lower solubility than mannan, and they exhibited a Newtonian behaviour.

59 , the degree of acetylation of xylan, (gluco)mannan, and xyloglucan as well as overall cell wall acet

60 olysaccharides and the hemicelluloses xylan, mannan, and xyloglucan.

61 enzymes on four substrates: lichenan, xylan, mannan, and xyloglucan.

62 rhamnogalacturonan I), xyloglucans, xylans, mannans, and glucans.

63 BM families that targeted beta-glucans, beta-mannans, and the pectic polysaccharide homogalacturonan.

64 Mannan/anti-mannan immunoglobulin G, beta-D-glucan (BDG)

65 ing cells by human neutrophils requires anti-mannan antibody, whereas ingestion of glucan-displaying

66 ion with homology modeling of the bound beta-mannan antigen suggested an optimum oligosaccharide for

67 a surface-associated phosphorylated branched mannan (APS) indicated that this locus is also downregul

68 The MW for glycogen and mannan are 604+/-0.002 kDa and 54+/-0.002 kDa, respectiv

69 ell wall components chitin and outer chain N-mannans are absent, based on genome content and experime

70 Mannans are also present in chloronemal and caulonemal f

71 Mannans are an abundant cell wall polysaccharide in bryo

72 Mannans are hemicellulosic polysaccharides that have a s

73 Mannans are hemicellulosic polysaccharides that have pre

74 (AcXEs); however, the enzymes deacetylating mannans are less understood.

75 beta-Mannans are plant cell wall polysaccharides that are com

76 array analysis of Arabidopsis indicated that mannans are present throughout the plant and are especia

77 beta-mannans are widely present in human and animal diets as

78 In addition, we discuss the use of fungal mannan as a diagnostic marker of fungal disease.

79 LM and the number of arabinan chains on the mannan backbone in LAM remain.

80 ansferase involved in extending the alpha1-6-mannan backbone of LM intermediates.

81 ays a critical role in the elongation of the mannan backbone of mycobacterial and corynebacterial LM,

82 Galactomannans comprise a beta-1,4-mannan backbone substituted with alpha-1,6-galactosyl re

83 arides composed of a (1 --> 4)-linked beta-D-mannan backbone substituted with single-unit (1 --> 6)-a

84 tus, this polysaccharide is made of a linear mannan backbone with side chains of galactofuran and is

85 a-mannanase catalyzes endo-hydrolysis of the mannan backbone, a major constituent of woody biomass.

86 addition to alpha(1-->2)Man branching on the mannan backbones of LM and LAM, confirming the involveme

87 of alpha(1-->2)-linked Man branching on the mannan backbones of LM and LAM.

88 evalence of dual specificity for glucan- and mannan-based substrates in the GH5 family.

89 members of the healthy microbiota using beta-mannan-based therapeutic interventions.

90 Prior blocking with anti-HAF antibody or mannan before coculture impaired viral trans-infection.

91 ajor polysaccharide constituents being alpha-mannan, beta-1,6 glucan, and beta-1,3 glucan.

92 Appending a mannan binding CBM27 to CjCE2C potentiated its activity

93 The data show that cellulose and mannan binding CBMs have the greatest impact on the remo

94 Measurement of mannan binding lectin (MBL) antigenic level and activity

95 Mannan binding lectin (MBL) is an innate immune mediator

96 nt, the pattern recognition molecules (PRMs) mannan-binding lectin (MBL) and ficolins complexed with

97 C1q and mannan-binding lectin (MBL) are not only recognition com

98 In teleost fish, the immune functions of mannan-binding lectin (MBL) associated protein (MAP) and

99 Mannan-binding lectin (MBL) is a component of the innate

100 Mannan-binding lectin (MBL) is an important protein of t

101 b, CR1 was reported to interact with C1q and mannan-binding lectin (MBL) likely through its C-termina

102 It is activated upon binding of mannan-binding lectin (MBL) or ficolins (H-, L-, and M-f

103 ght to occur via recognition of pathogens by mannan-binding lectin (MBL) or ficolins in complex with

104 t the soluble pattern recognition molecules, mannan-binding lectin (MBL), L-ficolin, and M-ficolin, w

105 The pattern recognition molecule, mannan-binding lectin (MBL), plays an important role in

106 ction of an endogenous complement inhibitor, mannan-binding lectin (MBL)-associated protein (MAp)44,

107 Mannan-binding lectin (MBL)-associated serine proteases,

108 found that the C7 rs6876739 CC genotypes and mannan-binding lectin (MBL2) gene polymorphisms of liver

109 Also, the mannan-binding lectin (MBL2), an innate immune lectin th

110 way and absence of the LP complement protein mannan-binding lectin abrogates elastase-induced AAA.

111 in pathway (LP) showed that both ficolin and mannan-binding lectin can activate the LP through natura

112 MASP1 encodes mannan-binding lectin serine protease 1.

113 etic deficiency in early complement, IgM, or mannan-binding lectin were characterized in a mesenteric

114 to ischemic Ag providing a binding site for mannan-binding lectin which subsequently leads to activa

115 he lectin activation pathway upon binding of mannan-binding lectin, ficolins, or collectin kidney 1 (

116 and factor H in the alternative pathway and mannan-binding lectin, mannan-binding lectin-associated

117 substrate complex consisting of glycan-bound mannan-binding lectin, MASP-2, and C4 is discussed.

118 to the same areas that stain positively for mannan-binding lectin, which suggests that the complemen

119 Mannan-binding lectin-associated serine protease 2 (MASP

120 n pathway deficiency, a mouse strain lacking mannan-binding lectin-associated serine protease-2 (MASP

121 mediated by direct cleavage of native C3 by mannan-binding lectin-associated serine protease-2 bound

122 Lectin pathway effector enzyme mannan-binding lectin-associated serine protease-2 can a

123 C2 bypass route is dependent on LP-specific mannan-binding lectin-associated serine protease-2.

124 We found that the complex bound to mannan-binding lectin-associated serine proteases (MASPs

125 lecules leading to the activation of zymogen mannan-binding lectin-associated serine proteases (MASPs

126 H-ficolin is found in plasma associated with mannan-binding lectin-associated serine proteases (MASPs

127 ternative pathway and mannan-binding lectin, mannan-binding lectin-associated serine proteases 1 and

128 In serum, CL-L1 was found in complexes with mannan-binding lectin-associated serine proteases, sugge

129 anism, which is conserved in C1r and also in mannan-binding lectin-associated serine proteases, the s

130 Mannan-binding lectin-associated serine proteinase 2 (MA

131 ution of blistering had a similar pattern in mannan-binding lectin-deficient and control mice and was

132 ys in this model, we injected C1q-deficient, mannan-binding lectin-deficient, and factor B-deficient

133 nd has ligand specificity similar to that of mannan-binding lectin.

134 ly reported for the lectin homologs SP-D and mannan-binding lectin.

135 Lectins like mannan-binding protein are part of the innate immune sys

136 Results also implicate the mannan-binding receptor Dectin-2 in regulating cPLA(2)al

137 hat C. albicans engages both beta-glucan and mannan-binding receptors on macrophages that act with My

138 cans where inactivation of genes involved in mannan biosynthesis has usually been linked to an attenu

139 This review focuses on O- and N-linked mannan biosynthesis in the fungal pathogen Candida albic

140 t NCgl1505 was involved in core alpha(1-->6) mannan biosynthesis of Cg-LM-A and Cg-LM-B, extending Ac

141 nclude that the MSR protein is important for mannan biosynthesis, and offer some ideas about its role

142 Because this protein is involved in mannan biosynthesis, we named it 'mannan synthesis-relat

143 CaMnt4 and CaMnt5 participated in N-mannan branching.

144 s with antibody specific for DC-SIGN or with mannan but not antibody specific for xCT, a cystine/glut

145 Next, removal of the surface-displayed mannan by acid treatment of periodate-borohydride cells

146 ring studies showed that metabolism of yeast mannan by B. thetaiotaomicron presents a 'selfish' model

147 es and that the masking of primary cell wall mannan by pectin is a potential mechanism for controllin

148 In addition, although purified mannans cannot solely mediate the priming, the presence

149 i-encoded proteins that are involved in beta-mannan capturing, importation, de-branching and degradat

150 f the GH130_1 subfamily would be involved in mannan catabolism, whereas the enzymes belonging to the

151 anched mannosyl residues, the alpha-6-linked mannan chain is terminated with an alpha-mannopyranose a

152 in N-glycosylated proteins that have shorter mannan chains.

153 onal antibody 3F8 inhibited C3 deposition on mannan-coated plates in MBL2 KI, but not wild-type, mice

154 n vitro, MBL/MASP complexes were captured on mannan-coated plates, and cleavage of a chromogenic thro

155 significant increase in sensitivity to both mannan competition and endoglycosidase H digestion compa

156 ebound to 2G12 was 10-fold more sensitive to mannan competition than gp120 that was not prebound in a

157 This work suggests that Con A-mannan complex could be potentially utilized for insulin

158 Treatment with mannan considerably reduced infection of feline monocyte

159 softwoods, such as conifers and cycads, are mannans consisting of a 1,4-linked beta-mannopyranosyl m

160 ta, a molecular mechanism for utilization of mannan-containing nutrients by C. polysaccharolyticus is

161 akes them a resource for depolymerization of mannan-containing polysaccharides in the biofuel industr

162 MYB46 resulted in a significant increase in mannan content.

163 abinan chain attached near the middle of the mannan core is present in mature LAM and allow for an up

164 s of the number of arabinans attached to the mannan core of LM in two other mutants (DeltaembC and De

165 ages of the biosynthesis of the alpha(1-->6) mannan core of LM.

166 the addition of alpha(1-->2) branches to the mannan core of LM/LAM and that arrest of this branching

167 d exactly one arabinosyl substitution of the mannan core suggestive of the arabinosylation of a linea

168 the LM glycans that consist of an alpha(1,6) mannan core, with and without the complete alpha(1,2) ma

169 omposed of only the phosphatidylinositol and mannan core.

170 T Rv2181 in the dual role of Man capping and mannan-core branching, and in the process generated a ra

171 f mannose receptor (MR) activity on MDM with mannan decreased the association of F. novicida and opso

172 anscriptome sequencing to gain insights into mannan degradation by the thermophilic anaerobic bacteri

173 ring seed germination and suggest a role for mannan degradation in tobacco.

174 in N-glycan maturation and microbiotal yeast mannan degradation, respectively.

175 gulation of glycoside hydrolases involved in mannan degradation.

176 The present study shows that this mannan-dependent resistance can be overcome by periodate

177 he CBMs that recognize beta-glucans and beta-mannans, differences in the conformation of conserved ar

178 Additionally, we found that, like mannan, different airborne allergens can effectively dow

179 Finally, ingestion of mannan-displaying cells by human neutrophils requires an

180 (zymosan and sheep erythrocytes coated with mannan (E(Man))) revealed that the convertases (ZymM1,C4

181 In secondary cell walls, mannan esterification can prevent probe recognition of e

182 The most highly up-regulated genes during mannan fermentation occur in a cluster containing severa

183 a phosphatidylinositol anchor followed by a mannan followed by an arabinan that may be capped with v

184 oteins, which synthesize beta-(1-->4)-linked mannans found in the walls of many plant species, and CS

185 Indeed, we found that phosphatidylinositol mannan from M. tuberculosis inhibits macrophage response

186 lar weights (MW) of glycogen from Oyster and mannan from Saccharomyces cerevisiae are determined by s

187 A single i.p. exposure to mannan from Saccharomyces cerevisiae induced an acute in

188 s have the greatest impact on the removal of mannan from tobacco and Physcomitrella cell walls, respe

189 Structural analysis of mannans from moss and Selaginella showed they were compo

190 an synthases and support the hypothesis that mannans function in metabolic networks devoted to other

191 wed that longer chain of synthetic alpha(1-6)mannans gain better lectin's binding affinity.

192 ohydrate-binding module directed against the mannan group of hemicellulose cell wall polysaccharides,

193 m covalent C-O-Fe bonds through beta-(1,4)-d-mannan groups.

194 The recalcitrant mannan, however, was fully accessible to the GH26 mannan

195 Multi-scale characterization of mannan hydrolysate was done using FTIR and (13)C NMR whi

196 several genes encoding enzymes for efficient mannan hydrolysis as well as a solute-binding protein (C

197 l glycone binding site more efficiently than mannan-hydrolyzing glycoside hydrolases in related enzym

198 spectra of trehalose, glycogen, glucose, and mannan, i.e., the major carbohydrates present in S. cere

199 Mannan/anti-mannan immunoglobulin G, beta-D-glucan (BDG) and polymer

200 gus was inhibited by beta-glucans but not by mannans, implicating a lectin-like activity in recogniti

201 tions identify an inhibitory role for intact mannan in complement activation.

202 o, only CjCE2C was active against acetylated mannan in Physcomitrella.

203 y reduced level of the virulence factor beta-mannan in the glucose transporter null mutants compared

204 lactan and with reduced amounts of xylan and mannan in the outer S2 (S2L) region of tracheids.

205 mannanase was independent of the context of mannan in tobacco cell walls, a significant proportion o

206 e is known about the acetylation patterns of mannans in bryophytes and seedless vascular plants, and

207 nition of epitopes/ligands, and detection of mannans in primary cell walls can be effectively blocked

208 affects the structure of the fungal N-linked mannan, in line with their predicted functions, and this

209 cifically, high iron decreased the levels of mannans (including phosphomannans) and chitin; and incre

210 nted levels of the storage carbohydrate beta-mannan, increased cell size and increased growth as inse

211 he purified cell wall components zymosan and mannan induced caspase-1 activation and IL-1beta secreti

212 Hence, we propose that mannan-induced activation of macrophages leads to TNF-al

213 on of IL-17, but not TNF, prevented enhanced mannan-induced arthritis in LACC1 KO mice.

214 We investigated mannan-induced arthritis in SKG mice and how NADPH oxida

215 Similar results were obtained in a mannan-induced arthritis model.

216 ation constants for Con A-glycogen and Con A-mannan interactions are KA=3.93+/-0.7x10(6) M(-1)/KD=0.2

217 Mannan is a major cell wall component found in Candida s

218 Here we show that yeast alpha-mannan is a viable food source for the Gram-negative bac

219 By 28 DAP labeling of hetero-(1-->4)-beta-D-mannan is observed in the walls of the starchy endosperm

220 hestrate the depolymerization of yeast alpha-mannans, it is likely that the two enzymes target the be

221 -glucan to the immune system occurs when the mannan layer is altered or removed in a process called u

222 In wild-type C. albicans, the outer mannan layer of the wall masks the inner layer of beta(1

223 ated neutrophils with three soluble glucans, mannan, lipopolysaccharide, or a variety of cytokines re

224 nnobiose to 4-O-beta-d-mannosyl-d-glucose in mannan metabolism.

225 veral cell-wall polysaccharides (xyloglucan, mannans, mixed-linkage beta-glucan and xylans); however,

226 ition of a fungal cell wall component, alpha-mannan (Mn), an Mn (sugar) polymer, by the C-type lectin

227 N demonstrated the significance of alpha(1-6)mannan motif present in LM structure.

228 ion in Arabidopsis and konjac is mediated by mannan O-acetyltransferases belonging to the Domain of U

229 cular plants, and the evolutionary origin of mannan O-acetyltransferases in land plants has not yet b

230 es originated in algae, their recruitment as mannan O-acetyltransferases probably occurred in bryophy

231 ESI-MS/MS results showed that the isolated mannan oligomers, MOS-III, MOS-IV, MOS-V and MOS-VI cons

232 A self-consistent model of beta-mannan oligosaccharides bound to a monoclonal antibody,

233 rve, mannogen, which is composed of beta-1,2-mannan oligosaccharides.

234 , that multivalently and selectively bind to mannan on the C. albicans cell surface to form crosslink

235 The influence of yeast mannan on the ecology of the human microbiota is unknown

236 rt a model whereby limited cleavage of alpha-mannan on the surface generates large oligosaccharides t

237 We demonstrate that MR senses mannan on the surface of attenuated Blastomyces dermatit

238 Although intact yeast display mannan on the surface, glucan, typically located in the

239 Upon binding to mannan or DNA in the presence of MASP-2, the CL-L1-CL-K1

240 phagocytosis of C. albicans cells displaying mannan or glucan.

241 Upon treatment of DCs with mannan or LRP ligand alpha2-macroglobulin, we observed o

242 h alanine at this position failed to bind to mannan or maltose-substituted solid supports.

243 ficantly inhibited by the addition of either mannan or mannose.

244 narin (beta-1,3-glucan) but not sialic acid, mannan or pustulan mediated Hst 5 binding to C. albicans

245 e MTPs are structurally related to bacterial mannan phosphorylases, they constitute a distinct family

246 Polymerized allergoids conjugated to mannan (PM) are suitable vaccines for allergen-specific

247 rized grass pollen allergoids to nonoxidized mannan (PM) compared with glutaraldehyde-polymerized all

248 Mannan polysaccharides and homologs of CslA genes appear

249 Mannan polysaccharides are widespread among plants, wher

250 ily have previously been shown to synthesise mannan polysaccharides in vitro when heterologously expr

251 rides, we show that molecular recognition of mannan polysaccharides present in intact cell walls is s

252 BoMan26A primarily formed mannobiose from mannan polysaccharides.

253 erm tissue, showing higher levels of galacto-mannan precursors in fenugreek endosperm.

254 One example is the beta-mannan present in the phosphomannan glycoprotein of Cand

255 the glycoside hydrolases encoded by the beta-mannan PUL and involved in the beta-mannan utilization p

256 ne at 343 (R343V) showed enhanced binding to mannan relative to wild type and R343A.

257 Allergoids conjugated to nonoxidized mannan represent suitable vaccines for AIT.

258 the conserved fungal components zymosan and mannan require ASC and Cryopyrin for caspase-1 activatio

259 The hydrolysis of polysaccharides containing mannan requires endo-1,4-beta-mannanase and 1,4-beta-man

260 crobial mannanases can be used to break down mannan rich agro-residues to yield MOS.

261 In murine experiments, beta-mannan selectively promotes beneficial gut bacteria, exe

262 Direct fluorescence imaging using a mannan-specific carbohydrate-binding module and sequenti

263 accharide utilization loci, including novel, mannan-specific esterases that are critical to its decon

264 anced its catalytic efficiency on glucan and mannan substrates by 175 and 1,600%, respectively.

265 ns and those microbes devoid of cell-surface mannan such as the gram-negative bacterium E. coli.

266 l gold particles was used to label the alpha-mannan sugar in the cell wall of the yeast Saccharomyces

267 This binding was blocked by the addition of mannan, suggesting mannose receptor involvement in the D

268 Ca(2+) and by preincubation of DC-SIGN with mannan, suggesting that C1q binds to DC-SIGN at its prin

269 Blocking experiments with laminarin and mannan supported the conclusion that differences in cell

270 ose synthase (CESA4, CESA7, and CESA8) and a mannan synthase (CSLA9) genes.

271 In addition, in vitro mannan synthase activity from the stems of msr1 single a

272 pecific MSR cofactors were indispensable for mannan synthase activity of a coffee CSLA or modulated a

273 B46 (At5g12870) is a direct regulator of the mannan synthase CLSA9.

274 Previous studies led to the conclusion that mannan synthase enzymes in several plant species are enc

275 members of the CslA gene family encode beta-mannan synthases.

276 tive GTs have also been implicated in (gluco)mannan synthesis, but their roles have been difficult to

277 nvolved in mannan biosynthesis, we named it 'mannan synthesis-related' (MSR).

278 MANNAN-SYNTHESIS RELATED (MSR) putative GTs have also be

279 n-1, was incorporated into the original beta-mannan tetanus toxoid conjugate providing a tricomponent

280 ive vaccine against Candida albicans, a beta-mannan tetanus toxoid conjugate showed poor immunogenici

281 y the tricomponent vaccine, but not the beta-mannan tetanus toxoid vaccine, showed activation of BMDC

282 e showed that the reducing end region of the mannan that is attached to inositol has 5-7 unbranched a

283 Its cell surface is enriched with mannan that is resistant to complement activation.

284 APS is a phosphorylated branched mannan that shares a common epitope with posttranslation

285 e to exogenous microbial components, such as mannan, that can induce and exacerbate Ps and PsA.

286 tinct molecular structure of wood xylans and mannans, the multiphase architecture of the hydrogels an

287 s of enzymatic synthesis of MOS from various mannans, their structural characteristics and their pote

288 nd YCW-b-MP1' contained mannoproteins with a mannan to protein ratio of 3.5 and 6.9, respectively.

289 weight (MW) distribution and variability of mannan to protein ratio of purified mannoproteins (MP),

290 and conjugated to the fungal cell wall beta-mannan trisaccharide [beta-(Man)(3)] by novel saccharide

291 oncanavalin A (Con A) and glycogen and Con A-mannan using quartz crystal microbalance (QCM), cost and

292 ein and provides a framework for engineering mannan utilization capabilities for microbial fermentati

293 the beta-mannan PUL and involved in the beta-mannan utilization pathway in B. ovatus.

294 Mannan was absent from the highly lignified compound mid

295 phenomenon in parenchyma systems, and masked mannan was found to be a feature of cell wall regions at

296 Xylan and mannan were detected in all lignified xylem cell types (

297 ogy as well as the storage carbohydrate beta-mannan, which is an essential virulence factor for survi

298 s, R. intestinalis shares the available beta-mannan with Bacteroides ovatus, demonstrating that the a

299 o the inner Araf-alpha(1-->5)-Araf unit) and mannan (with fewer 6-Manp residues and more substitution

300 Low-MW YCW-b-MP2' was mainly comprised of mannan, with a ratio of 181, whereas low-MW Agrimos(R)-M