ライフサイエンスコーパス: hemicellulose

1 ) to degrade lignin along with cellulose and hemicellulose.

2 apacity to hydrolyze amorphous cellulose and hemicellulose.

3 incomplete thermal degradation of lignin and hemicellulose.

4 zymes to efficiently hydrolyze cellulose and hemicellulose.

5 mplex carbohydrates, including cellulose and hemicellulose.

6 k the layers of polysaccharide chains within hemicellulose.

7 f interpenetrating networks of cellulose and hemicellulose.

8 annot metabolize pentose sugars derived from hemicellulose.

9 stion of glycan extracted from cellulose and hemicellulose.

10 nsumption pathway required for its growth on hemicellulose.

11 ent for the co-fermentation of cellulose and hemicellulose.

12 tural polysaccharides, such as cellulose and hemicellulose.

13 eractions between cellulose microfibrils and hemicelluloses.

14 ased upon coating the cellulose with various hemicelluloses.

15 n synthesis of xyloglucan and possibly other hemicelluloses.

16 whole cell walls was observed for acetylated hemicelluloses.

17 mnogalacturonan I, rhamnogalacturonan II and hemicelluloses.

18 ng capacity compared to low-molecular-weight hemicelluloses.

19 s suggested by the sugar composition of both hemicelluloses.

20 The hemicellulose 4-O-methyl glucuronoxylan is one of the pr

21 ose and fructooligosaccharides (0.8-169 mg), hemicellulose (77-763 mg), lignin (0-90 mg), and unknown

22 evealed a composition of cellulose (27.68%), hemicellulose (8.2%) and lignin (26.46%) in the solid fr

23 ards producing these compounds directly from hemicellulose, a major component of plant-derived biomas

24 Hemicelluloses, a family of heterogeneous polysaccharide

25 vent the breakdown of structurally important hemicelluloses, a major contributor to softening.

26 Further, hemicelluloses accumulated in Golgi at levels that contr

27 ve for the hydrolysis of pentose polymers in hemicellulose and also increase the access of enzymes to

28 to disrupt noncovalent interactions between hemicellulose and cellulose microfibrils.

29 hree main cell wall polysaccharides: pectin, hemicellulose and cellulose.

30 ogen bonds between cell wall polysaccharides hemicellulose and cellulose.

31 ading ruminal bacterium capable of utilizing hemicellulose and cellulose.

32 here they show versatility in degrading both hemicellulose and cellulose.

33 is required for the secretion of pectin and hemicellulose and distinguishes the role of the TGN in s

34 After partially removing amorphous hemicellulose and eliminating most lignin, the treated w

35 higher contents of dietary fiber, especially hemicellulose and insoluble fractions, and were characte

36 lignocellulosic hydrolysates, deriving from hemicellulose and lignin breakdown.

37 nal enzymes often associated with cellulose, hemicellulose and lignin degradation, an array of enzyme

38 olvent mixture liberates the majority of the hemicellulose and lignin from biomass, allowing unfetter

39 thick secondary wall comprised of cellulose, hemicellulose and lignin is deposited.

40 as lignocellulosic biomass is embedded in a hemicellulose and lignin matrix from which it needs to b

41 The results showed that hemicellulose and lignin were degummed at different rate

42 nents of lignocellulosic biomass (cellulose, hemicellulose and lignin), lignin has been treated as a

43 d its three constituent polymers, cellulose, hemicellulose and lignin, represent the largest renewabl

44 irectly activates the biosynthetic genes for hemicellulose and lignin, which are the other two major

45 f three major biopolymers, namely cellulose, hemicellulose and lignin.

46 posed of three major biopolymers: cellulose, hemicellulose and lignin.

47 believed to aid in a release of lignin from hemicellulose and may be involved in lignin solubilizati

48 s appears to be related to increased loss of hemicellulose and NDF soluble concentrations and not to

49 nt cell walls are comprised of cellulose and hemicellulose and other polymers that are intertwined, a

50 a role, in both monocot and dicot plants, of hemicellulose and pectin acetylation in plant defense ag

51 ted with matrix polysaccharide content (i.e. hemicellulose and pectin) in the stem tissue.

52 ose microfibrils embedded within a matrix of hemicellulose and pectin.

53 omposed of the polysaccharides cellulose and hemicellulose and the polyphenol lignin.

54 allows simultaneous conversion of cellulose, hemicellulose and, more significantly, lignin fractions

55 d that the mutations affect both pectins and hemicelluloses and alter overall wall structure, as indi

56 itrogen, lignin and ash, and negatively with hemicelluloses and carbohydrate content of substrates.

57 ligomeric hemicelluloses, isolated polymeric hemicelluloses and cell walls.

58 t substrates demonstrated high reductions in hemicelluloses and cellulose in contrast to lignin; fibr

59 mes for synthesis and degradation of lignin, hemicelluloses and cellulose were also differentially ex

60 hains, which may affect interactions between hemicelluloses and cellulose.

61 suggesting the partial enzyme hydrolysis of hemicelluloses and cellulose.

62 e found in xylem, are composed of cellulose, hemicelluloses and lignin and account for the bulk of pl

63 rstood how the polymer components cellulose, hemicelluloses and lignin co-operate to resist tensile s

64 action is divided into components cellulose, hemicelluloses and pectin, are all modified during fruit

65 ymerize a broad range of linear and branched hemicelluloses and pectin, despite the inability of F. s

66 etylation is a crucial substitution found in hemicelluloses and pectin, which are necessary for maint

67 Binding assays of commercially available hemicelluloses and pectins, and microfibrillar cellulose

68 ind to cell wall polymers such as cellulose, hemicelluloses and pectins.

69 lms changed after the addition of the chosen hemicelluloses and the films became less elastic but mor

70 which could be applied to effectively remove hemicelluloses and transform cellulose structure from ce

71 e, but some members also display activity on hemicelluloses and/or oligosaccharides.

72 ion, and catalytic transformation of lignin, hemicellulose, and cellulose.

73 of the cellulolytic one with some overlap to hemicellulose, and in its extent surprisingly high, sugg

74 scale materials and assemblies of cellulose, hemicellulose, and lignin as well as other biomaterials

75 in the coordinated regulation of cellulose, hemicellulose, and lignin biosynthetic pathways.

76 omponents of the plant cell wall (cellulose, hemicellulose, and lignin), paving the way for more effi

77 The wood polymers cellulose, hemicellulose, and lignin, common to all wood tissues, s

78 contains 56.26, 17.56, and 16.74% cellulose, hemicellulose, and lignin, respectively, while the densi

79 s a hierarchical matrix of mainly cellulose, hemicellulose, and lignin.

80 cal structures of its components: cellulose, hemicellulose, and lignin.

81 composite material, comprised of cellulose, hemicellulose, and lignin.

82 composed of a complex mixture of cellulose, hemicellulose, and pectin polysaccharides as well as pro

83 ed largely of the polysaccharides cellulose, hemicellulose, and pectin, along with approximately 10%

84 nts of the plant cell wall, i.e., cellulose, hemicellulose, and pectin.

85 d secondary cell wall composed of cellulose, hemicellulose, and pectin.

86 ormation about water proximity to cellulose, hemicellulose, and pectins as well as water mobility.

87 the noncovalent network formed by cellulose, hemicellulose, and pectins, but the CW target of expansi

88 major classes of polysaccharides: cellulose, hemicellulose, and pectins.

89 plants have lower contents of cellulose and hemicellulose, and thinner sclerenchyma and vascular bun

90 rast, the xylan backbone, galactomannan-type hemicelluloses, and cellulose were more resistant to deg

91 e interactions among cellulose microfibrils, hemicelluloses, and lignin are still not well understood

92 By depolymerizing cellulose, hemicelluloses, and lignin separately, monomer yields we

93 rent cell wall components, namely cellulose, hemicelluloses, and lignin, are coordinately expressed a

94 made up of cellulose microfibrils, pectins, hemicelluloses, and lignin.

95 e grouping of cell wall maturation (pectins, hemicelluloses, and oxalate) and membrane biogenesis mar

96 roduced by terrestrial plants are cellulose, hemicelluloses, and pectins.

97 Cell walls are made of cellulose, hemicelluloses, and pectins.

98 types of polysaccharides: cellulose, various hemicelluloses, and pectins.

99 nd dynamic network made mostly of cellulose, hemicelluloses, and pectins.

100 (Brachypodium distachyon) plants expressing hemicellulose- and pectin-specific fungal acetylesterase

101 ers derived from thermally altered cellulose/hemicellulose (anhydrosugars) and lignin (methoxyphenols

102 s involved in the digestion of cellulose and hemicellulose are highly expressed during the interactio

103 manganese peroxidases, whereas cellulose and hemicellulose are hydrolysed.

104 Associations with hemicelluloses are important for microfibril spacing and

105 Hemicelluloses are key chemical constituents of plant ce

106 hitecture, and xyloglucans (XyGs), the major hemicellulose, are often considered as spacers of cellul

107 mechanical sampling and molecular picture of hemicellulose arrangement around cellulose.

108 and composition of branches attached to the hemicellulose backbone can significantly alter the cell

109 ume and molecular packing in hydrolysate and hemicellulose-based barriers films, derived from process

110 fer of molecular wood cell interactions into hemicellulose-based materials may offer new design princ

111 ccurs synergistically and sequentially, with hemicellulose being degraded preferentially to cellulose

112 g on property and wood type, with lignin and hemicellulose being the most accurately determined and g

113 ns of these topologies on various aspects of hemicellulose biosynthesis are discussed.

114 ms to be involved in cellulose biosynthesis, hemicellulose biosynthesis, secondary cell wall developm

115 reduced expression of putative cellulose and hemicellulose biosynthetic genes.

116 We show that hemicellulose branches of arabinose, glucuronic acid, an

117 relative to N. corniger microbiota included hemicellulose breakdown and fixed-nitrogen utilization.

118 We show that such hemicellulose bridges exist and that the stripping of th

119 fibrils is reduced again and contact through hemicelluloses bridges is restored.

120 mented a cellulosome active on cellulose and hemicellulose by addition of an enzyme active on lignin.

121 s of pulp firmness, CSP, ISP, cellulose, and hemicellulose by enhancing the activities of PE, PG, Cx,

122 edict the contents of pectins, cellulose and hemicelluloses by partial least squares regression (PLS)

123 Deconstruction of cellulose and hemicellulose carbohydrate polymers into their constitue

124 a primary emphasis on engineering cellulose/hemicellulose catabolism, small molecule production, and

125 module directed against the mannan group of hemicellulose cell wall polysaccharides, we show that mo

126 ndividual layers, as well as to the protein, hemicellulose, cellulose, and lignin content.

127 ated the presence, in addition to lipids, of hemicellulose, cellulose, lignin, and proteins, dependin

128 resence of non-covalent interactions between hemicellulose chains attached to adjacent cellulose micr

129 re, we present an alternative model in which hemicellulose chains bridging continuously from one micr

130 y novel methods, the ordered, disordered and hemicellulose-coated cellulose components comprising eac

131 ydrogels and the aggregative effects amongst hemicellulose-coated fibrils.

132 rate in autoclaved corn fiber, including its hemicellulose component glucuronoarabinoxylan (GAX).

133 omplementing endoxylanase degradation of the hemicellulose component of lignocellulosic substrates.

134 sents the number of xylose residues]) in the hemicellulose component of lignocellulosics to biobased

135 r strains grow using either the cellulose or hemicellulose components of ionic liquid-pretreated biom

136 onoxylan and acetylated glucomannan as major hemicellulose components, respectively) were subjected t

137 We address the effect of hemicellulose composition on primary cell wall assembly

138 ecalcitrant network of lignin, cellulose and hemicelluloses comprising the plant secondary cell wall.

139 Hemicellulose concentrated from the different feedstocks

140 al including enzymes acting on cellulose and hemicellulose, confirmed by experimental assays.

141 Lignin, cellulose, hemicellulose content and saccharification rate showed a

142 wed by oxygen removal from its cellulose and hemicellulose content by catalytic processes results in

143 n wild-type plants, whilst the cellulose and hemicellulose content remained unchanged.

144 rring to chemical composition such as lignin/hemicellulose content, and biomass structure-relevant fa

145 wall thickness, a decrease in cellulose and hemicellulose contents, and an increase in lignin conden

146 al detergent fibre, acid detergent fibre and hemicelluloses contents were higher in CCWPs than in VOR

147 etabolize the pentose sugars abundant within hemicellulose creates specific challenges for microbial

148 We present a mathematical model of hemicellulose crosslink dynamics in an expanding cell wa

149 In contrast, elastic modulus of hemicellulose decreases constantly with MC.

150 sis (e.g., Elusimicrobium, nrfA), pectin and hemicellulose degradation (e.g., Sphaerochaeta), and pho

151 f the cellulosome paradigm for cellulose and hemicellulose degradation by R. champanellensis in the h

152 role of SLH domain GHs and demonstrate that hemicellulose degradation can be enhanced through non-na

153 alpha-L-arabinosidases that are involved in hemicellulose degradation, we screened the C. cellulovor

154 In addition, genes encoding hemicellulose-degrading enzymes, peptidases, and metabol

155 h are valuable substrates for characterizing hemicellulose-degrading enzymes.

156 nd 6 dockerins are predominantly appended to hemicellulose-degrading enzymes.

157 hydrodeoxygenation of lignin, cellulose, and hemicellulose-derived oligomers into liquid alkanes with

158 e resulting liquid phases, containing mainly hemicellulose-derived saccharides, were refined by physi

159 In general, hemicelluloses did not form specific clusters in the cel

160 r very efficient hydrolysis of cellulose and hemicellulose due to the spatial proximity of synergisti

161 evelopment requires massive up-regulation of hemicellulose (e.g. glucuronoxylan) biosynthesis in the

162 lulose structural changes and differences in hemicellulose epitopes between switchgrass pretreatments

163 the accumulation of specific root pectin and hemicellulose epitopes.

164 mnogalacturonan I, rhamnogalacturonan II and hemicellulose epitopes.

165 of a set of enzymes required to depolymerize hemicellulose, especially xylan that is composed of a ma

166 ement suggests an ability to utilize certain hemicelluloses, especially beta-glucans and xyloglucan,

167 The incorporated hemicelluloses exhibit both a rigid phase having close i

168 The wood hemicelluloses exhibit distinct biomechanical contributi

169 Notably, high-molecular-weight hemicelluloses exhibited superior emulsifying capacity c

170 Hydrothermal treatment is commonly used for hemicelluloses extraction from lignocellulosic materials

171 of plant cell walls, including cellulose and hemicellulose, facilitated by a diverse set of glycoside

172 mosaccharolyticum or several other described hemicellulose-fermenting thermophilic bacteria can only

173 ied by the partial removal of its lignin and hemicellulose, followed by hot-pressing.

174 Efforts toward the utilization of hemicellulose for bioconversion into cellulosic biofuels

175 Xyloglucan (XyG) is the principal hemicellulose found in the primary cell walls of most pl

176 action (DASS), a 1M sodium hydroxide-soluble hemicellulose fraction (1MASS), a 4M sodium hydroxide-so

177 ction (1MASS), a 4M sodium hydroxide-soluble hemicellulose fraction (4MASS) and a cellulose-rich resi

178 Furthermore, the DAc of the hemicellulose fraction (LiCl-DMSO) was shown to be negat

179 ction constituted of rhamnogalacturonans and hemicellulose fraction consisted of arabinogalactans, xy

180 Direct bacterial conversion of the hemicellulose fraction of hardwoods and crop residues to

181 that the degree of acetylation (DAc) of the hemicelluloses fraction (LiCl-DMSO) increased during app

182 abolic potential for bacterial conversion of hemicellulose fractions of hardwood and crop residues to

183 a coli, to grow using both the cellulose and hemicellulose fractions of several types of plant biomas

184 se were the main sugar constituents of these hemicellulose fractions.

185 Hemicellulose fragmentation and altered cellulose nanost

186 The constant increase of hemicellulose free volume, however, causes the aggregati

187 rasslands and metabolizes both cellulose and hemicellulose from plant cell walls.

188 the wild and metabolizes both cellulose and hemicellulose from plant cell walls.

189 Brown rot decay removes cellulose and hemicellulose from wood--residual lignin contributing up

190 trast, the tandem MS images of cellulose and hemicellulose generated by plotting characteristic fragm

191 ze a moving stream of wood chips for lignin, hemicellulose, glucan, and extractives content.

192 Hemicellulose glues lignin and cellulose fiber together

193 sferases (UGTs), crucial enzymes involved in hemicellulose glycosylation.

194 roscopy, we observed that about one-third of hemicellulose had decomposed after three centuries, acco

195 idly growing cells, and that the presence of hemicelluloses has an effect on cellulose utilization by

196 . the branched structure and the size of the hemicelluloses have an influence over the extent of the

197 Hemicelluloses have emerged as a promising alternative t

198 element approach to study the hypothesis of hemicellulose (HC) tethering with the cellulose microfib

199 evidence does not confirm the importance of hemicellulose-hemicellulose association in the cohesion

200 e complex polysaccharides like cellulose and hemicellulose, highlighting the adaptation of the WBR mi

201 re resistant to the mixture of inhibitors in hemicellulose hydrolysates, confirming the importance of

202 oside hydrolases that catalyze cellulose and hemicellulose hydrolysis, few are more enigmatic than fa

203 wn to exhibit various activities involved in hemicellulose hydrolysis.

204 Grass xylan, the major hemicellulose in both primary and secondary cell walls,

205 Xyloglucan constitutes most of the hemicellulose in eudicot primary cell walls and function

206 idetes and contributes to the degradation of hemicellulose in the rumen.

207 Xylan is the principal hemicellulose in the secondary cell walls of eudicots an

208 Since GGM is the most abundant hemicellulose in the secondary walls of gymnosperms, und

209 Arabinoxylan (AX) is an abundant hemicellulose in wheat bran and an important functional

210 noxylans (MeGXn) are the major components of hemicellulose in woody biofuel crops.

211 Glucuronoarabinoxylans (GAXs) are the major hemicelluloses in grass cell walls, but the proteins tha

212 Branching of xylan, one of the main hemicelluloses in softwood secondary cell walls, with gl

213 ra crassa, NcLPMO9C, indeed degrades various hemicelluloses, in particular xyloglucan.

214 An in-depth understanding of the hemicellulose inherent structural and property features

215 oside hydrolases to break down cellulose and hemicellulose into sugars, which this organism then ferm

216 ve processes for breaking down cellulose and hemicellulose into their constituent sugars.

217 owed even distribution of both cellulose and hemicellulose ions; in contrast, the tandem MS images of

218 and in dicot secondary cell walls, the major hemicellulose is a polymer of beta-(1,4)-linked xylose u

219 Hemicellulose is one of the major components of the cell

220 Hemicellulose is the next most abundant plant cell wall

221 nd further explored using defined oligomeric hemicelluloses, isolated polymeric hemicelluloses and ce

222 poorly understood innermost xyloglucan-rich hemicellulose layers of unfermented grape pomace.

223 FT-IR results for acetylated hemicelluloses (LiCl-DMSO) were grouped by term using PC

224 e, including sugars related to cellulose and hemicellulose, lignin-related phenolic acid, and amino a

225 linkage (1-->3,1-->4)-beta-d-glucan (MLG), a hemicellulose long thought to be confined to certain Poa

226 volved in xylose, arabinose, cellobiose, and hemicellulose metabolism.

227 Xyloglucan is the major hemicellulose of dicotyledon primary cell walls, affecti

228 Xyloglucan (XG), the principal load-bearing hemicellulose of dicotyledonous plants, has a terminal f

229 ansglycosylase (XET) which acts on the major hemicellulose of the plant cell wall.

230 ansins do not hydrolyze the major pectins or hemicelluloses of the cucumber wall.

231 the MCC particles and complete digestion of hemicellulose on the cellulosic substrate by acid.

232 , the effect of the degree of acetylation of hemicelluloses on fruit softening during storage.

233 a to use labile C (glucose), intermediate C (hemicellulose or cellulose), or recalcitrant C (lignin).

234 s of oligosaccharide fragments of cellulose, hemicellulose, pectin, and arabinogalactans, as well as

235 is composed of a complex array of cellulose, hemicellulose, pectins and proteins, the modification an

236 iofuel production, is composed of cellulose, hemicelluloses, pectins and lignin.

237 matrix and crosslinked through a network of hemicellulose polymers.

238 ls that depict separate protein, pectin, and hemicellulose polysaccharide networks.

239 Hemicellulose polysaccharides influence assembly and pro

240 Moreover, acetylated hemicelluloses predominated at the post-harvest storage,

241 Xyloglucan (XyG) is the dominant hemicellulose present in the primary cell walls of dicot

242 provide an excellent system for deciphering hemicellulose production.

243 The effect of particle size on hemicellulose recovery upon pretreatment was studied usi

244 that particle size significantly influences hemicellulose recovery, as particles below 120 um result

245 e direction, and water severely disturbs the hemicellulose-related hydrogen bonds.

246 srupted the plant fiber matrix, facilitating hemicelluloses release while preserving its amphiphilic

247 reas soluble sugars, proteins, and amorphous hemicelluloses showed a positive impact.

248 ALDI-LIT MS analyses of cellulose and xylan (hemicellulose) standards were performed to determine mas

249 The family of hemicelluloses stands out as a very promising natural re

250 The lack of PMEI expression does not affect hemicellulose strengthening, callose deposition, and the

251 o undetected LPMO activities on recalcitrant hemicellulose structures.

252 The abundance of hemicellulose such as xylan suggests that their hydrolys

253 nctional differences between plant cell wall hemicelluloses such as glucomannan, xylan, and xylogluca

254 me no covalent bonding between cellulose and hemicelluloses such as xyloglucan or mixed-linkage beta-

255 clerenchyma cells and enhances cellulose and hemicellulose synthesis, making the cell walls stiffer a

256 product yields (ethanol and succinate) from hemicellulose syrups were equal to control fermentations

257 ellulosic biomass-the lignin, cellulose, and hemicellulose that comprise major components of the plan

258 es occurred in the contents of cellulose and hemicellulose that increased 37% and 28%, respectively,

259 r architecture of the cellulose, lignin, and hemicelluloses that comprise its chemical makeup.

260 oxidatively cleaving chitin, cellulose, and hemicelluloses that contain beta(1-->4) linkages between

261 y act on other substrates, in particular the hemicelluloses that tether to cellulose microfibrils.

262 In this regard, cellulose and hemicellulose, the carbohydrate fraction of lignocellulo

263 m aromatic aldehydes derived from lignin and hemicellulose, the major by-products of lignocellulosic

264 ddition to the insolubility of cellulose and hemicellulose, the tight association of lignin with thes

265 ating the post-Golgi secretion of pectin and hemicellulose, the two major cell wall polysaccharides,

266 Hemicelluloses, the polysaccharide component of plant ce

267 transmitted between microfibrils by bridging hemicelluloses these might have been expected to show di

268 binoxylans, which are the main components of hemicellulose, they are part of microbial xylanolytic sy

269 rolysis of the polysaccharides cellulose and hemicellulose to fermentable sugars is a research priori

270 role in TGN-mediated secretion of pectin and hemicellulose to the cell wall in dark-grown hypocotyls

271 Compositional (lignin, cellulose, hemicelluloses, total uronic acids, proteins, and solubl

272 However, the contribution of each hemicellulose type to the mechanical properties of secon

273 with pectin utilization and one with pectin/hemicellulose utilization (ARA-1).

274 the phylum Bacteroidetes that contributes to hemicellulose utilization within the bovine rumen.

275 nalysis reveals a decrease in cellulose- and hemicellulose-utilizing bacteria and enzymes, along with

276 late cellulose assembly and interaction with hemicelluloses via binding to emerging cellulose microfi

277 Enzymatic hydrolysis of hemicellulose was optimised using response surface metho

278 hich promotes the digestion of cellulose and hemicellulose, was significantly increased.

279 Ferulates decorating hemicelluloses were not altered.

280 and extensive depolymerization of structural hemicelluloses, whereas polyuronide depolymerization was

281 the reactions are similar for cellulose and hemicellulose, which contain C(6) and C(5) sugars, respe

282 biofuel production through the metabolism of hemicellulose, which is composed of d-xylose and l-arabi

283 lans (BCX) is involved in the degradation of hemicellulose, which is one of the most abundant renewab

284 d component is caused by depolymerization of hemicelluloses, which occurs independently of or require

285 nd mainly composed of lignin, cellulose, and hemicellulose while the soluble fiber was amorphous and

286 lia were possibly pectic polysaccharides and hemicellulose, while C. tora WSP was mainly composed of

287 As the most abundant hemicellulose, XyG is considered important in eudicot PC

288 g the various pectic polysaccharides and the hemicelluloses xylan, mannan, and xyloglucan.

289 erent combinations of extracted and purified hemicelluloses (xylans and glucomannans) from softwood a

290 ing mutants with altered structures of their hemicellulose xyloglucan (axy mutants) using oligosaccha

291 The predominant structure of the hemicellulose xyloglucan (XyG) found in the cell walls o

292 iana mutant with an altered structure of its hemicellulose xyloglucan (XyG; axy-8) identified by a fo

293 ABP1 also functions in the modulation of hemicellulose xyloglucan structure.

294 synthesis and xxt1 xxt2 mutants lacking the hemicellulose xyloglucan, stomatal apertures, changes in

295 walls of syncytia contain cellulose and the hemicelluloses xyloglucan and heteromannan.

296 e is the dominant binding component, whereas hemicelluloses (xyloglucan and arabinoxylan) apparently

297 om xyloglucan oligosaccharides to long-chain hemicelluloses (xyloglucan, water-soluble cellulose acet

298 ellulosic polysaccharides examined, only the hemicelluloses (xyloglucan, xylan, glucomannan, B-d-gluc

299 Among land-plant hemicelluloses, xyloglucan is ubiquitous, whereas mixed-

300 Within hemicellulose, xylose value was high in IL 6-3, IL 7-2 a