ライフサイエンスコーパス: cellulose

1 ecomposing labile soil organic carbon (e.g., cellulose).

2 may reduce the intrinsic permeability of the cellulose.

3 h positive charge density of the regenerated cellulose.

4 ulose, nylon, poly(vinylidene fluoride), and cellulose.

5 s, but the strains did not appear to degrade cellulose.

6 nosyl substitutions, with close proximity to cellulose.

7 cellulase Cel7A and its insoluble substrate, cellulose.

8 alcitrant polysaccharides such as chitin and cellulose.

9 nities that are involved in the digestion of cellulose.

10 se (EG) with a preference for more amorphous cellulose.

11 F. succinogenes S85 in response to growth on cellulose.

12 between three-fold screw xylan and amorphous cellulose.

13 n gum, xanthan gum, and sodium carboxymethyl cellulose.

14 the walls, indicating changes in lignin and cellulose.

15 he pEtN group from membrane phospholipids to cellulose.

16 exopolysaccharide phosphoethanolamine (pEtN) cellulose.

17 es of degrading enzymes acting on lignin and cellulose, (2) co-option of genes present in saprotrophi

18 arbohydrates study revealed a composition of cellulose (27.68%), hemicellulose (8.2%) and lignin (26.

19 Cellulose (28%) and lignin (45.1%) were the main biopoly

20 16 short-term glucose (6-day), 16 short-term cellulose (30-day) and 16 long-term cellulose (729-day)

21 oscopy and polymers identified as: synthetic cellulose (33.3%), polypropylene (25%), polyacrylamides

22 tural and roasted hazelnuts were composed of cellulose (~49%), pectic polysaccharides (~30%), and xyl

23 ort-term cellulose (30-day) and 16 long-term cellulose (729-day) incubation datasets with soils from

24 Progress in these fronts renders cellulose a prospect of being effectuated in an array of

25 lower structural organization and increased cellulose accessibility.

26 aphene oxide (GO) and an additional layer of cellulose acetate.

27 ective in the current study was to fabricate Cellulose Acetate/Gelatin (CA/Gel) electrospun mat loade

28 pH dependant polymer hydroxyl-propyl-methyl-cellulose-acetate-succinate (HPMCAS).

29 MOs, here we generated a mutant library of a cellulose-active family AA10 LPMO from Streptomyces coel

30 Cellobiohydrolases effectively degrade cellulose and are of biotechnological interest because t

31 revealed that all these LPMOs are active on cellulose and cello-oligosaccharides, as well as plant c

32 oxyfluorinated, as well as carboxymethylated cellulose and chitin analogues with full control over th

33 of bacteria as well as genes responsible for cellulose and chitin degradation.

34 even though natural polysaccharides, such as cellulose and chitin, are key structural components of b

35 nd that GIWAXS can decouple diffraction from cellulose and epicuticular wax crystals in cell walls.

36 that lignin dissociates from itself and from cellulose and expands to form a random coil.

37 ies is sufficient for the co-fermentation of cellulose and hemicellulose.

38 ll models assume no covalent bonding between cellulose and hemicelluloses such as xyloglucan or mixed

39 he impact of the spatio-temporal dynamics of cellulose and homogalacturonan pectin distribution durin

40 h) to remove impurities present in microbial cellulose and increase membrane permeability.

41 chosen because of their specific binding to cellulose and intrinsic fluorescence.

42 cid metabolism, nucleotide biosynthesis, and cellulose and lignin biosynthesis, in line with breeding

43 s and platform compounds obtained from (hemi)cellulose and lignin derivatives.

44 balance of cell wall components, i.e., high cellulose and low xylan and lignin content, which could

45 ide a platform to coordinate the delivery of cellulose and matrix polysaccharides, but the underlying

46 l assembly requires harmonized deposition of cellulose and matrix polysaccharides.

47 t stabilizes the sites of deposition of both cellulose and matrix polysaccharides.

48 size the beta-1,4-linked glycan backbones of cellulose and most hemicellulosic polysaccharides that c

49 The molecular and macromolecular features of cellulose and the physicochemical properties of extracte

50 to elucidate supramolecular substructures of cellulose and their impact on enzyme accessibility.

51 associated proteins involved in adhesion to cellulose and transport and metabolism of cellulolytic p

52 ne (HDPE), and semisynthetic cellulose (S.S. Cellulose), and in Lake Erie samples were S.S. Cellulose

53 berin-based material harboring lignin, (hemi)cellulose, and extractable small molecules (primarily tr

54 Lignocellulosic biomass-the lignin, cellulose, and hemicellulose that comprise major compone

55 oad-bearing component of plant cell walls is cellulose, and how plants regulate its biosynthesis duri

56 lorescence stems revealed changes in lignin, cellulose, and matrix sugar composition indicating an ov

57 Diverse biological materials, such as bone, cellulose, and muscle, have as many as 10 hierarchical l

58 The reductive potential of the cellulose- and antioxidant-rich OP was validated using t

59 , recently developed VPA-loaded NPs based on cellulose- and dextran VPA esters were modified with sul

60 regenerated fibers, produced from dissolved cellulose are widely used today for clothes, upholstery,

61 acid as reducing agent and microfibrillated cellulose as a capping agent and demonstrate this materi

62 ent a high ratio of amorphous to crystalline cellulose as compared to dicots.

63 due to overproduction of c-di-GMP-regulated cellulose, as deletion of the cellulose synthase machine

64 ofilms, these membranes consist of microbial cellulose, bacteria, and extracellular polymers.

65 esigning and embedding wax channels onto the cellulose-based filter paper through printing and subjec

66 Here, various transparent and white cellulose-based materials produced so far are highlighte

67 pose serious negative environmental impacts, cellulose-based materials, owing to their biocompatibili

68 t cell walls, has yielded unique families of cellulose-based nanomaterials, which have leveraged the

69 f polygonally bent helical microfilaments of cellulose-based nanostructures coated by different layer

70 In this work, we describe a cellulose-based photoacoustic sensor for heparin.

71 The nanostructures were formed on cellulose-based rayon microfibers through selective etch

72 ecent advances in realizing highly efficient cellulose-based solar evaporators for alleviating the gl

73 ecent progress in designing highly efficient cellulose-based solar evaporators, including utilizing e

74 erformance, fully green TENG (FG-TENG) using cellulose-based tribolayers is reported.

75 Herein, we have fabricated a cellulose-based wearable patch, which further paired wit

76 in rate on the tensile response of bacterial cellulose (BC) nanopaper.

77 ronan (LM20) and by labelling with the CMB3a cellulose-binding module.

78 This novel silver nanoparticle-cellulose biocomposite synthesized by a green methodolog

79 gulation of morphogenesis, direct studies of cellulose biosynthesis and its impact on morphogenesis o

80 species into self-assembled networks during cellulose biosynthesis in a bacterial model, without alt

81 anchored endo-beta-1,4-glucanase involved in cellulose biosynthesis, provides a link between N-glycos

82 n photoperiodic flowering time regulator, in cellulose biosynthesis.

83 stablished the role of FKF1 in regulation of cellulose biosynthesis.

84 the morphology and the crystallinity of the cellulose bundles.

85 the nature of their direct interactions with cellulose, but can be related to the distinct molecular

86 Fungal AA9 LPMOs are active on cellulose, but some members also display activity on hem

87 rtical microtubules orient the deposition of cellulose by guiding the trajectory of cellulose synthas

88 As a model for cellulose, cellohexaose chains are observed in two confo

89 echanical properties of the cell wall and of cellulose-cellulose and cellulose-matrix interactions.

90 second flow layer was comprised of a grade 1 cellulose chromatography paper with wax-printed four cha

91 ions for monovalent ions, 0.2% carboxymethyl cellulose (CMC) 700 kg mol(-1) as the dispersing agent,

92 n effects between xanthan (X), carboxymethyl cellulose (CMC) and kappa-carrageenan (kappa-C) (0-0.3%)

93 (NaCAS) and a polysaccharide, carboxymethyl cellulose (CMC) or gum Arabic (GA), to retain polyphenol

94 des (carrageenan, alginate and carboxymethyl cellulose (CMC)) as flocculants was investigated at diff

95 h as (Chitosan, potato starch, carboxymethyl cellulose (CMC), corn starch and Arabic gum) can improve

96 ge of anionic polysaccharides [carboxymethyl cellulose (CMC), gum Arabic (GA), alginate (AL), and iot

97 ocrystals (CNC), and kaolin-microfibrillated cellulose composite.

98 as applied to overcome the low-solubility of cellulose compounds.

99 The effectiveness of the low-cost cellulose cone tips used as a solid fourth phase also co

100 In this work, cellulose cone tips were used as a hydrophilic sorbent s

101 level negatively correlated with lignin and cellulose content, and positively correlated with matrix

102 ented by WT CESA6 in regard to plant growth, cellulose content, cellulose microfibril organization, C

103 reduction in p-coumaric acid, Glc, Man, and cellulose contents.

104 epresents an opportunity for introduction of cellulose conversion technology.

105 ectins increases under conditions of reduced cellulose crystallinity.

106 talline, although the orientational order of cellulose crystallites normal to the plane of the cell w

107 A preferred orientational alignment of cellulose crystals could be an important determinant of

108 f GIWAXS and X-ray rocking scans reveal that cellulose crystals have a preferred crystallographic ori

109 This orientational ordering of cellulose crystals, termed texturing in materials scienc

110 A phenotype suppression screen using a cellulose deficient mutant cesa1(aegeus),cesa3(ixr1-2) (

111 enes involved in carbohydrate metabolism and cellulose degradation.

112 at 78 degrees C and is the most thermophilic cellulose degrader known.

113 Importantly, this work supports the use of cellulose delta(18) O to infer T(L-AW) , but does not su

114 T(L-AW) values calculated from cellulose delta(18) O vs crown fluxes were remarkably co

115 ared these data to T(L-AW) derived from wood cellulose delta(18) O.

116 ith the oxygen isotopic composition of alpha-cellulose (delta(18) O(cell) ) to shifts in relative hum

117 Herein, a diverse group of newly synthesized cellulose derivatives was evaluated for their ability to

118 ver a wide temperature range (>25 degrees C) cellulose disruption occurs only above 150 degrees C.

119 t the larger surface area of nanofibrillated cellulose enables stronger binding between the binder an

120 e which explains the origin of the different cellulose environments observed in the NMR experiments.

121 hanism underlying pEtN derivatization of the cellulose exopolysaccharide remains elusive.

122 n equivalent amount of nonfermentable fiber (cellulose) expelled worms normally.

123 Nanostructured cellulose fabric with an air-bubble-enhanced anti-oil fo

124 lied as fire retardant and pest repellent in cellulose fiber insulation (CFI) in Europe since the 198

125 i.e., crystalline cellulose) occurred at the cellulose fiber surface, which was interspersed by zones

126 isting shear forces and adhering bacteria to cellulose fibers in the human gut.

127 sms as well as the hierarchical structure of cellulose fibers, one of the main building blocks of pla

128 The hierarchical structure of cellulose fibers, one of the main constituents of plant

129 ms made from polylactic acid (PLA) and micro cellulose fibrils (MCF).

130 obiose to glucose in the saccharification of cellulose for second-generation ethanol production, and

131 The abundance of cellulose found in natural resources such as wood, and t

132 secretomes, and their ability to break down cellulose has been successfully exploited in textile and

133 d fibre, a thick secondary wall comprised of cellulose, hemicellulose and lignin is deposited.

134 cell wall is a hierarchical matrix of mainly cellulose, hemicellulose, and lignin.

135 ccharide fraction is divided into components cellulose, hemicelluloses and pectin, are all modified d

136 ccharides produced by terrestrial plants are cellulose, hemicelluloses, and pectins.

137 the multiscale architecture of the bacterial cellulose hydrogels.

138 egradation tests showed that the presence of cellulose in PLA improved the compostability of the foam

139 Here, the crystalline structures of cellulose in primary cell walls of onion (Allium cepa),

140 cture of lignin and on its interactions with cellulose in the cell wall drives multiple synergistic m

141 xpression increases deposition of lignin and cellulose in the xylem vessels and their surrounding cel

142 eport, multiscale mechanics understanding of cellulose, including the key role of hydrogen bonding, t

143 Comparing multiple subsets of cellulose incubations (i.e., 6, 30, 90, 180, 360, 480 an

144 The comparison with microcrystalline cellulose indicates that the larger surface area of nano

145 mbly of a bio-derived polymer, hydroxypropyl cellulose, into a cholesteric liquid crystalline phase s

146 fferent hydroclimate signals: earlier season cellulose is a better recorder of RH while late-season c

147 is a better recorder of RH while late-season cellulose is a better recorder of the source water.

148 Microbial cellulose is an effective membrane filtration medium, an

149 Cellulose is an essential plant cell wall component and

150 It is well established that cellulose is crystalline, although the orientational ord

151 In plants, cellulose is synthesized at the cell surface by plasma m

152 Cellulose is synthesized by cellulose synthase complexes

153 Plant cellulose is synthesized by rosette-structured cellulose

154 Primary cell wall cellulose is synthesized by the cellulose synthase compl

155 hitin, the second most ample polymer next to cellulose, is insoluble and resistant to degradation.

156 ane surface is smoothed by deposition of the cellulose layer and modified with azidophenyl groups, al

157 ale prevents lignin aggregation and disrupts cellulose, leading to improvements in deconstruction at

158 s, down to the molecular architecture of the cellulose, lignin, and hemicelluloses that comprise its

159 the structure, properties, and reactions of cellulose, lignin, and wood cell walls, studied using de

160 and cellulose nanofibrils (CNF)) and natural cellulose materials (wood and bacterial nanocellulose (B

161 articles via bottom-up assembly CNF, natural cellulose materials with intrinsic hierarchical structur

162 Silver nanoparticles were obtained in the cellulose matrix with an average size of 140 nm and with

163 the cell wall and of cellulose-cellulose and cellulose-matrix interactions.

164 re based on polyethylene glycol (PEG)/methyl cellulose (MC) core with anthocyanidin and sodium acetat

165 PCL NPs were incorporated into a supporting cellulose membrane which promoted LPS adsorption further

166 onductive layer between touching hydrophilic cellulose membranes instead of polyacrylamide gel is use

167 motrimer that suggests a molecular basis for cellulose microfibril formation.

168 crotubule network, which leads to disordered cellulose microfibril organization in the cell wall.

169 n regard to plant growth, cellulose content, cellulose microfibril organization, CSC dynamics and sub

170 (CMTs), which in turn mediate deposition of cellulose microfibrils (CMFs).

171 ibrils within the cell wall layers, and that cellulose microfibrils are highly anisotropic and have h

172 Cellulose microfibrils are the major load-bearing compon

173 the recent success of in vitro synthesis of cellulose microfibrils by a single recombinant cellulose

174 tion by intimately binding to the surface of cellulose microfibrils in a semi-crystalline fashion.

175 orm a gel-like matrix between stress-bearing cellulose microfibrils in growing plant cell walls.

176 The organization of cellulose microfibrils is critical for the strength and

177 This is due to the distinct orientation of cellulose microfibrils within the cell wall layers, and

178 , indicates they most likely reflect nascent cellulose microfibrils.

179 matically loosen noncovalent bonding between cellulose microfibrils.

180 ing a CBM1 carbohydrate-binding module, bind cellulose more strongly and were less susceptible to ina

181 posed of oleic acid (OA, 1, 2, and 3%, w/w), cellulose nanocrystal (CNC, 0.1, 0.3, and 0.5%, w/w), an

182 In this study, bacterial cellulose nanocrystals (BCNCs) were obtained from bacter

183 combinations of cellulose nanofibrils (CNF), cellulose nanocrystals (CNC), and kaolin-microfibrillate

184 ulsions using interactions between rice bran cellulose nanocrystals (CNCs) and lauric arginate (LAE),

185 Aqueous suspensions of cellulose nanocrystals (CNCs) are known to self-assemble

186 s introduced, namely, aqueous dispersions of cellulose nanocrystals (CNCs) that form superstructured,

187 order for sustainable nanomaterials such as cellulose nanocrystals (CNCs) to be utilized in industri

188 ed, water-dispersible 'nanocage' composed of cellulose nanocrystals (CNCs), which are magnetically po

189 sions stabilised by hydrophobically modified cellulose nanocrystals (MCNCs).

190 erties of extracted cellulose nanoparticles (cellulose nanocrystals and cellulose nanofibrils (CNF))

191 Cellulose nanocrystals and nanofibrils may readily bind

192 ures with the natural chiral organization of cellulose nanocrystals are fabricated.

193 plementary amphiphilic character of CQDs and cellulose nanocrystals in the organized nematic phase.

194 quantum dot (CQD) microcrystals on organized cellulose nanocrystals templates at the liquid-air inter

195 h as thermosets, thermoplastics, composites, cellulose nanocrystals, and nanofibers.

196 using a casting method, which consisted of a cellulose nanofiber/whey protein matrix containing titan

197 rystals (BCNCs) were obtained from bacterial cellulose nanofibers (BCNFs) by controlled hydrolysis of

198 antimicrobials loaded hydrogels composed of cellulose nanofibers (CNF) and kappa-carrageenan oligosa

199 s the sensitivity of LFs based on the use of cellulose nanofibers (CNF).

200 The cellulose nanofibers in our engineered material backscat

201 also be easily disposed of due to the use of cellulose nanofibril paper as the circuit substrate.

202 with passive impedance matching networks on cellulose nanofibril paper.

203 The novel use of aqueous suspensions of cellulose nanofibrils (CNF) as an adhesive/binder in lig

204 mposites based on wood, fungal mycelium, and cellulose nanofibrils (CNF) were developed and investiga

205 se nanoparticles (cellulose nanocrystals and cellulose nanofibrils (CNF)) and natural cellulose mater

206 m formulations prepared from combinations of cellulose nanofibrils (CNF), cellulose nanocrystals (CNC

207 lecular structure and mechanical behavior of cellulose nanofibrils whereby molecular defects may be i

208 Long, aligned cellulose nanofibrils with dramatically increased hydrog

209 orts are presented for preparing and forming cellulose nanomaterial nanocomposites.

210 Cellulose nanomaterials (CNMs) are a class of materials

211 omprised largely of egg-derived polymers and cellulose nanomaterials as a conformal coating onto fres

212 the wide spectrum of structural diversity of cellulose nanomaterials in the form of micro-nano-sized

213 Nanocellulose network in the form of cellulose nanopaper is an important material structure a

214 ly, which allows for pre-designed control of cellulose nanoparticle orientations at the mesoscale.

215 the physicochemical properties of extracted cellulose nanoparticles (cellulose nanocrystals and cell

216 r evaporators, including utilizing extracted cellulose nanoparticles via bottom-up assembly CNF, natu

217 ssfully measured together with nanofibrillar cellulose (NFC) and ranked according to their binding co

218 rapped by negatively charged nanofibrillated cellulose (NFC) fibers to form multiple 2D confined spac

219 at a high degree of order (i.e., crystalline cellulose) occurred at the cellulose fiber surface, whic

220 Cellulose of natural origin, especially those derived fr

221 for the content of ethanolic extractives and cellulose of the commercial and wild cultivars.

222 tum hetero-trans-beta-glucanase (HTG) grafts cellulose onto xyloglucan oligosaccharides (XGOs) - and,

223 epresents a previously unreported measure of cellulose organization and contradicts the predominant h

224 planar cellulose substrates (air-laid paper, cellulose paper, and cotton fabric) is reviewed.

225 ses, the addition of phosphoric acid-swollen cellulose (PASC) had a major effect on activity: NcLPMO9

226 up lignin (~55%) and fibre polysaccharides (cellulose, pectic polysaccharides, and xyloglucans, ~45%

227 hin one cage, and carried bedding materials (cellulose pellets) from their nesting cages to their lat

228 With PEDOT:PSS coated onto cellulose/polyester cloth, the SC shows specific capacit

229 Several materials (cellulose/polyethylene terephthalate/glass fiber, nontre

230 ts, forms three channels occupied by nascent cellulose polymers.

231 llulose), and in Lake Erie samples were S.S. Cellulose, polypropylene (PP), and poly(vinyl chloride)

232 Plant polysaccharides such as starch and cellulose present in ENB substrate (wheat grains plus ri

233 ranes produced sustainably through microbial cellulose production can have filtration properties alte

234 essed as a fractional percentage of the pure cellulose reference.

235 he main building blocks for synthesis of the cellulose-rich cyst wall, leading to subversion of amoeb

236 nsity polyethylene (HDPE), and semisynthetic cellulose (S.S. Cellulose), and in Lake Erie samples wer

237 ave sparked a tremendous interest to utilize cellulose's intriguing mechanical properties in designin

238 high-performance functional materials, where cellulose's structure-mechanics relationships are pivota

239 nanotube patches composed of nanofibrillated cellulose/single-walled carbon nanotube ink 3-dimensiona

240 nd structural properties of a well-described cellulose-specific LPMO from Thermoascus aurantiacus (Ta

241 We used a gold nanoparticle-bacterial cellulose substrate and "hot spot"-normalized surface-en

242 cessive cycle of CBHs, dissociation from the cellulose substrate is rate limiting, but the molecular

243 ucture (wood and BNC), and commercial planar cellulose substrates (air-laid paper, cellulose paper, a

244 icroorganisms that have structural cell wall cellulose, suggesting expansins evolved in ancient marin

245 rapid fiber fragmentation and an increase in cellulose surface crystallinity.

246 nanoclusters (R(g) ~ 0.5 nm) on the nonpolar cellulose surfaces and on hydrophobic lignin, and equiva

247 equivalent water-rich nanoclusters on polar cellulose surfaces.

248 Members of the cellulose synthase (CESA) and cellulose synthase-like (C

249 ll surface by plasma membrane (PM)-localized cellulose synthase (CESA) complexes (CSCs).

250 llulose is synthesized by rosette-structured cellulose synthase (CESA) complexes (CSCs).

251 , which carries nonlethal point mutations in CELLULOSE SYNTHASE A 1 (CESA1) and CESA3, resulted in id

252 We determined the structure of a poplar cellulose synthase CesA homotrimer that suggests a molec

253 ry cell wall cellulose is synthesized by the cellulose synthase complex (CSC) containing CELLULOSE SY

254 trolling microfibril organization by guiding cellulose synthase complexes [1-4].

255 Our data suggest how cellulose synthase complexes assemble and provide the mo

256 , we reveal such a mechanism by showing that cellulose synthase complexes can interact with the trail

257 Cellulose is synthesized by cellulose synthase complexes in the plasma membrane and

258 Supramolecular plant cellulose synthase complexes organize multiple linear gl

259 nt for the microtubule-dependent guidance of cellulose synthase complexes.

260 r investigate the structure and functions of cellulose synthase complexes.

261 on of cellulose by guiding the trajectory of cellulose synthase complexes.

262 Expression levels of secondary cell wall cellulose synthase genes (CesA) in the bk4 single mutant

263 nt, which could be caused by upregulation of cellulose synthase genes upon the expression of Pt x tER

264 llulose microfibrils by a single recombinant cellulose synthase isoform reconstituted into proteolipo

265 etics to investigate the role of Arabidopsis cellulose synthase like-C (CSLC) proteins in XyG biosynt

266 -GMP-regulated cellulose, as deletion of the cellulose synthase machinery restored virulence to a str

267 The bacterial cellulose synthase subunit G (BcsG) is a predicted inner

268 However, cellulose synthase trajectories can be maintained when m

269 hases and microfibrils, can maintain aligned cellulose synthase trajectories, while a microtubule gui

270 d to a change in the dominant orientation of cellulose synthase trajectories.

271 ted ones that comprised two cellulases and a cellulose synthase was conserved among the Frankia and o

272 Members of the cellulose synthase (CESA) and cellulose synthase-like (CSL) families encode glycosyltr

273 Cas9 to generate mutations in members of the Cellulose synthase-like (Csl) gene superfamily that enco

274 gated by glycosyltransferases (GTs) from the cellulose synthase-like A (CSLA) family.

275 iana) FRA1 kinesin physically interacts with cellulose synthase-microtubule uncoupling (CMU) proteins

276 cellulose synthase complex (CSC) containing CELLULOSE SYNTHASE1 (CESA1), CESA3 and one of four CESA6

277 IN-FORMED1) and cell wall development (i.e., CELLULOSE SYNTHASE1) and expansin homologous genes were

278 nomous system, involving interaction between cellulose synthases and microfibrils, can maintain align

279 pectin) and increased expression of putative cellulose synthases indicated that auxins may preserve c

280 the proportion of exchangeable oxygen during cellulose synthesis (P(ex) ) was kept constant.

281 cular mechanism through which CESA catalyzes cellulose synthesis and whether its catalytic activity i

282 that represents a powerful tool for studying cellulose synthesis in plants.

283 n conserved catalytic domains for catalyzing cellulose synthesis, other domains such as plant-conserv

284 n important role in determining the level of cellulose synthesized.

285 erutilized C6-platform chemical derived from cellulose that is ideal to prepare next-generation value

286 Among the natural materials, cellulose, the most abundant biopolymer in the world wit

287 Cellulose, the most abundant biopolymer on earth, is a v

288 thought to be composed of only underivatized cellulose, the pEtN modification present in these matric

289 However, fully exploiting defects in cellulose to benefit biobased materials and conversion a

290 ll walls and tested whether expansin exposes cellulose to HTG by disrupting hydrogen bonds.

291 s the glucose redirected to the synthesis of cellulose to maintain a slow-replicating, metabolically

292 a rigid phase having close interactions with cellulose, together with a flexible phase contributing t

293 signing a quantitative method to analyze the cellulose ultrastructure and accessibility, this study g

294 m vacancy-rich ReSe(2) @carbonized bacterial cellulose (V(r) -ReSe(2) @CBC) nanofibers between two CB

295 roduction from the fermentation of starch or cellulose were decreased by oil supplementation.

296 ns between taste compounds and nanofibrillar cellulose were studied.

297 s, highly elongated, and contain nearly pure cellulose when mature.

298 ase (CBH), with high activity on crystalline cellulose, whereas TrCel7B is an endoglucanase (EG) with

299 We demonstrated covalent cellulose-xyloglucan bonding in plant cell walls and sho

300 ysaccharide - in vitro, thus exhibiting CXE (cellulose:xyloglucan endotransglucosylase) activity.