ライフサイエンスコーパス: oligosaccharide

1 adP) recognizes the galabiose Galalpha1-4Gal-oligosaccharide.

2 tent (656.38 mg/g) with high amounts of DP 5 oligosaccharide.

3 thesized, using a chemically modified cyclic oligosaccharide.

4 ed together as functional groups on the same oligosaccharide.

5 fragmentation throughout the backbone of the oligosaccharide.

6 ition and modification of polysaccharide and oligosaccharide.

7 ule affecting conformational changes on a HS oligosaccharide.

8 mass spectral reference database of 219 milk oligosaccharides.

9 ing a potential role of IgG2 and specific AM oligosaccharides.

10 rapid syntheses of heptose (Hep)-containing oligosaccharides.

11 glycosyl donors in the synthesis of complex oligosaccharides.

12 al aspects and winemaking techniques on wine oligosaccharides.

13 spectra of CID fragments from two human milk oligosaccharides.

14 expression with the analysis of hormones and oligosaccharides.

15 so display activity on hemicelluloses and/or oligosaccharides.

16 gio- and stereoselective access to bioactive oligosaccharides.

17 ure and pH affects acetyl migration on manno-oligosaccharides.

18 nors is critical for assembly of fluorinated oligosaccharides.

19 nnogen, which is composed of beta-1,2-mannan oligosaccharides.

20 main challenge in the chemical synthesis of oligosaccharides.

21 is able to remove both galactoses from XLLG oligosaccharides.

22 itations in synthetic access to well-defined oligosaccharides.

23 s to 6 selectively mono- and bis-fucosylated oligosaccharides.

24 imensions capable of resolving some isomeric oligosaccharides.

25 is the central challenge in the synthesis of oligosaccharides.

26 standards showed a preference for the larger oligosaccharides.

27 tivation methods for GAGs and other sulfated oligosaccharides.

28 eotide derivatives, and 3/10 were human milk oligosaccharides.

29 ion of beta-1,6- rather than beta-1,4-linked oligosaccharides.

30 f both lowly sulfated and highly sulfated HS oligosaccharides.

31 Zy families may work sequentially to degrade oligosaccharides.

32 ulfate E, but not with neutral or sialylated oligosaccharides.

33 ce higher level of acetate than medium chain oligosaccharides.

34 hanced interactions with the former class of oligosaccharides.

35 accharides, beta-glucans, alpha-glucans, and oligosaccharides.

36 in the interpretation of spectra of unknown oligosaccharides.

37 olymers: oligonucleotides, polypeptides, and oligosaccharides.

38 nd detected separately from the APTS-labeled oligosaccharides.

39 well as chitooligosaccharides, but not other oligosaccharides.

40 lytic transformations of the mono-, di-, and oligosaccharides.

41 cules including DNA, peptides, proteins, and oligosaccharides.

42 oconjugate vaccines based on short synthetic oligosaccharides.

43 to groups given the synbiotic agents (fructo-oligosaccharides, 4 g twice per day, plus Bifidobacteriu

44 prebiotic potential of arabinoxylan-derived oligosaccharides (A)XOS.

45 f putative GTs, nucleotide sugar donors, and oligosaccharide acceptors will dramatically accelerate p

46 rd carbohydrate separation matrix, resolving oligosaccharides according to their charge to hydrodynam

47 0-times higher affinity compared to the GD1b oligosaccharide affinity) when present with GM1.

48 inkages from non-reducing end of short chain oligosaccharides, alkyl and aryl beta-D-glucosides and d

49 heparan sulfate (HS) molecules into smaller oligosaccharides, allowing for release of angiogenic gro

50 ourse monitoring of these AA9 LPMOs on cello-oligosaccharides also provides a useful model system for

51 , activity measurements using synthetic PNAG oligosaccharide analogs, and in vitro biofilm dispersal

52 gmin, involving cis interactions between the oligosaccharide and ceramide moieties of GT1b and the ju

53 ction of the enzyme with an acceptor/product oligosaccharide and elucidate the molecular basis of the

54 Suitable processing then leads to protein, oligosaccharide and nucleic acid cross-peak enhancements

55 as allergic response is directed against an oligosaccharide and the reactions can be both immediate

56 Glycan arrays display oligosaccharides and are used to report glycan hapten bi

57 ntil now, limited by the high flexibility of oligosaccharides and ensemble-averaged analytical method

58 enges in the assembly of glycosidic bonds in oligosaccharides and glycoconjugates pose a bottleneck i

59 tematic studies using homogeneous samples of oligosaccharides and glycoconjugates, which could be acc

60 to the cleavage of pyranosyl 4,6-diols from oligosaccharides and glycoconjugates.

61 Chemical syntheses of oligosaccharides and glycosides call utilization of many

62 antibodies did not differentiate the ganglio-oligosaccharides and mimics, the patient serum samples b

63 The measurement of both oligosaccharides and monosaccharides usually requires tw

64 time, that the migration of acetyl groups in oligosaccharides and polysaccharides may not be limited

65 gagement of two types of glycans, sialylated oligosaccharides and sulfated glycosaminoglycans (GAGs).

66 substantially broadens the coverage of milk oligosaccharides and thereby increases utility use of a

67 charides, xylo-oligosaccharides, arabinoxylo-oligosaccharides and uronic acids using CarboPac PA 200

68 ing process, and (iv) the connection between oligosaccharides and wine sensorial attributes.

69 standards was performed using disaccharide, oligosaccharide, and polysaccharide standards.

70 ial for the degradation of proteins, lipids, oligosaccharides, and nucleic acids.

71 ynthetic brush polymers of oligonucleotides, oligosaccharides, and oligopeptides, prepared via graft-

72 cosidic linkages derived from disaccharides, oligosaccharides, and polysaccharides present in complic

73 ion of 16 standards of monosaccharides, xylo-oligosaccharides, arabinoxylo-oligosaccharides and uroni

74 Free milk oligosaccharides are bioactive molecules that function a

75 Oligosaccharides are carbohydrates with a low polymeriza

76 The released oligosaccharides are characterized by advanced liquid ch

77 Acetylated oligosaccharides are common in nature.

78 Functional oligosaccharides are non-digestible food ingredients tha

79 Oligosaccharides are related to plant defense responses

80 with other HM immune markers, microbiome and oligosaccharides are required.

81 Oligosaccharides are the third most abundant component i

82 tigating cranberry should be keen to include oligosaccharides as part of the 'active' cocktail of che

83 hese LPMOs are active on cellulose and cello-oligosaccharides, as well as plant cell wall-derived hem

84 d based on the instructions carried in their oligosaccharide backbones or by a Ca2+-mediated process

85 efficiency and the difficulty in separating oligosaccharides because of their high structural simila

86 osynthesis of a dolichylpyrophosphate-linked oligosaccharide before its transfer onto acceptor protei

87 ge toward the synthesis of -amino human milk oligosaccharides (betaA-HMOs).

88 jor capsid protein VP1, a broad range of GAG oligosaccharides bind to recessed regions between VP1 ca

89 Griffithsin (GRFT) is high-mannose oligosaccharide binding lectin that has shown in vivo br

90 Furthermore, an additional oligosaccharide-binding site 20 angstrom away from the c

91 More strikingly, we found an oligosaccharide-binding site at the surface of domain A,

92 g28366) can hydrolyze fucose from xyloglucan oligosaccharides but were unable to complement a fucosid

93 d catalytic activity on de-N-acetylated PNAG oligosaccharides, but the molecular basis for this incre

94 ides which were converted to the desired NAc-oligosaccharides by an efficient one-step chemical trans

95 ort the efficient synthesis of type I LacNAc oligosaccharides by chemoselective glycosylation.

96 s of CUPRA substrates containing ganglioside oligosaccharides by the glycosyl hydrolase human neurami

97 Here, we showed that certain short-chain oligosaccharides can bind to poliovirus but do not incre

98 hilic molecules, they comprise a hydrophilic oligosaccharide chain attached to a hydrophobic membrane

99 Structural variations of the oligosaccharide chains of mAb-Ds are hypothesised to be

100 itosan (deacetylated chitin) microparticles, oligosaccharide chitin, or glucosamine.

101 ulose nanofibers (CNF) and kappa-carrageenan oligosaccharides (CO) nanoparticles for the treatment of

102 ly heterogeneous lipid A and a peculiar core oligosaccharide composed of an unusually high number of

103 oach that provided an unprecedented panel of oligosaccharides composed of the inner-core of the LOS o

104 0% and 30% of the wet matrix; however, their oligosaccharide composition has not been studied.

105 A novel oligosaccharide compound AVR-25 selectively binds to the

106 This technique permits the exploration of oligosaccharide conformations, until now, limited by the

107 antigens for vaccine production and capsular oligosaccharides conjugate vaccines are proven effective

108 We show that highly glycosylated short oligosaccharide conjugates elicit functional immune resp

109 Complex oligosaccharides consist principally of neutral oligosac

110 d the identification of low molecular weight oligosaccharides contained in an EtOH/water extract of g

111 Then, the oligosaccharides contained in the different fractions as

112 to affect the composition and bioactivity of oligosaccharides contained in the grape seeds.

113 r synthesizing N-acetyl analogues of NmW CPS oligosaccharides containing 7-O-acetyl-N-acetylneuramini

114 nus dendrimers and either linear or branched oligosaccharides containing up to six monosaccharide uni

115 disialyllacto-N-hexose (FDSLNH) was the only oligosaccharide correlated to factor 3.

116 improved hydrolysis of fully acetylated PNAG oligosaccharides correlates with improved in vitro dispe

117 In this study, a group of cranberry pectic oligosaccharides (cPOS) were found to both inhibit quies

118 The product profiles from cello-oligosaccharide degradation suggest that the subtle diff

119 fically in genes coding for debranching- and oligosaccharide-degrading enzymes.

120 Our results demonstrate that desialylated N-oligosaccharides (DeNO) and N-acetylneuraminic acids (Ne

121 eneration of free N-glycans, or unconjugated oligosaccharides derived from N-linked glycoproteins, is

122 iency resulting from the competition between oligosaccharide diffusion and cellular uptake, with low

123 ne-pot, iterative glycosylations to generate oligosaccharides directly from monosaccharide building b

124 o choose to follow a diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and po

125 ited evidence that a diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and po

126 patients with IBS, a diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and po

127 A diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and po

128 re of the side chain, triterpenoid core, and oligosaccharide domain together orchestrate saponin adju

129 was limited to a ~20% reduction of released oligosaccharides during the intestinal phase.

130 ase of size- and charge-heterogeneous pectic oligosaccharide elicitors of PR gene expression.

131 The metabolic oligosaccharide engineering (MOE) strategy using unnatur

132 ged as a complementary approach to metabolic oligosaccharide engineering.

133 Based on its oligosaccharide fine specificity, SadP can be divided in

134 is first used to identify polysaccharides by oligosaccharide fingerprinting.

135 ints to the therapeutic potential of the GM1 oligosaccharide for treatment of sporadic Parkinson's di

136 is required to generate structurally defined oligosaccharides for a biological study.

137 gly, S. pneumoniae can utilize several plant oligosaccharides for growth in vitro, including raffinos

138 ation of comprehensive libraries of sulfated oligosaccharides for unlocking the "sulfation code" and

139 Membrane-bound oligosaccharides form the interfacial boundary between t

140 te antigens not well studied, such as chitin oligosaccharides, Forssman-related antigens, globo-type

141 rides origins, (ii) techniques for isolating oligosaccharide fraction and determining their content,

142 ere we present a separation method for Hp/HS oligosaccharide fractionation with cross-compatible solv

143 -induced protection, we generated a panel of oligosaccharide fragments of different lengths and teste

144 of an asymmetrical biantennary N-glycan from oligosaccharide fragments prepared by AGA and linear as

145 Convergent block coupling of 30- and 31-mer oligosaccharide fragments, prepared by AGA, yielded a mu

146 s, we prepared partially acetylated chitosan oligosaccharides from a chitosan polymer (DA = 35%, DP(w

147 emonstrate evidence that polysaccharides and oligosaccharides from marine algae can be used as prebio

148 plication of a chemical method for producing oligosaccharides from polysaccharides.

149 y, N-glycans, enzymatically released as free oligosaccharides from the GP, are screened against the G

150 evolved with the inability to synthesize the oligosaccharide galactose-alpha-1,3-galactose (alpha-Gal

151 -N-acetyllactosamine derivatives, human milk oligosaccharides, gangliosides and N-glycans.

152 lites was evaluated in comparison to galacto-oligosaccharide (GOS) and lactose and control without ad

153 Mice gavaged with lactose or fed fructo-oligosaccharides had increased abdominal sensitivity com

154 ars, breakthroughs in automated synthesis of oligosaccharides have also been achieved.

155 es is still under investigation, medium size oligosaccharides have been reported as the most active.

156 ride (LPS) molecules with negatively charged oligosaccharide headgroups.

157 Human milk oligosaccharides (HMO) are a diverse range of sugars sec

158 Human milk oligosaccharides (HMO) are favorable macromolecules whic

159 Human milk oligosaccharides (HMOs) and bioactive breast milk protei

160 o explore the association between human milk oligosaccharides (HMOs) and late-onset sepsis in very-lo

161 Human milk oligosaccharides (HMOs) are free glycans naturally prese

162 wing interest towards synthesized human milk oligosaccharides (HMOs) as baby formula additives, and i

163 andem mass spectral library of 74 human milk oligosaccharides (HMOs) derived from results of combined

164 Human milk oligosaccharides (HMOs) function as prebiotics for benef

165 Human milk oligosaccharides (HMOs) promote the development of the n

166 Human milk oligosaccharides (HMOs) shape gut microbiota during infa

167 actions among the gut microbiota, human milk oligosaccharides (HMOs), and osteoclast and osteoblast b

168 in human milk components, such as human milk oligosaccharides (HMOs), is associated with programming

169 tion of human milk is composed of human milk oligosaccharides (HMOs), which are resistant to digestio

170 y of bifidobacteria to metabolize Human Milk Oligosaccharides (HMOs).

171 charyltransferase hydrolysis of lipid-linked oligosaccharides in the ER lumen, followed by ENGase and

172 a wide array of product ions throughout the oligosaccharide including cross-ring fragments that illu

173 We have prepared well-defined unnatural oligosaccharides including methylated, deoxygenated, deo

174 -O-acetylations on any mannose residue in an oligosaccharide, including double acetylated mannoses, w

175 hod led to the identification of another 145 oligosaccharides, including an additional 80 HMOs from r

176 Deep infiltration of the oligosaccharides into the active site cleft imposes a sh

177 Aggregation of synthetic oligosaccharides into well-defined architectures has not

178 a major component of fucosylated human milk oligosaccharides, is beneficial to human health in vario

179 ibiting hexasaccharides identified from a HS oligosaccharide library screen demonstrates that the app

180 ELISA-presented alpha2,3-linked sialic acid oligosaccharide ligand.

181 and GlcNAcbeta1-2Man reveal that a range of oligosaccharide ligands can be accommodated in an open b

182 rns and show that synthetic anticoagulant HS oligosaccharides limit liver ischemia reperfusion injury

183 y reconstituting the eukaryotic lipid-linked oligosaccharide (LLO) pathway.

184 glycans, requires transport of lipid-linked oligosaccharide (LLO) precursors across the membrane by

185 MD-based binding energies of KS oligosaccharide-loaded galectins support experimental da

186 tion that has induced antibodies to the lipo-oligosaccharide (LOS) that cross-react with gangliosides

187 he TGN/post-Golgi vesicles, but its N-linked oligosaccharide maturation as well as that of a co-trans

188 ants/children, and suggest that certain milk oligosaccharides may have therapeutic utility in this se

189 HS oligosaccharides may represent a potential new therapeut

190 The total synthesis of the oligosaccharide moiety of disialosyl globopentaosylceram

191 ficity and differs in both its reactivity to oligosaccharide motifs within AM and its functions in ba

192 as evaluated by analysis of monosaccharides, oligosaccharides, N-glycans released from glycoproteins,

193 n-reactive Abs were largely directed against oligosaccharide (O)-antigenic determinant of LPS that S

194 -focused glycan microarray platform based on oligosaccharides obtained by chemical synthesis.

195 BALB/c mice indicate that truncating the C28 oligosaccharide of the natural product to the tetrasacch

196 that BcelPL6 initially releases unsaturated oligosaccharides of a degree of polymerization of 2-7 fr

197 eydew honey was found to contain 37.8% total oligosaccharides of which 27.4% was melezitose, and 2.5%

198 -rich (TEL) patch and the N terminus of TPP1-oligosaccharide/oligonucleotide-binding (NOB) region.

199 s been mapped to 2 regions of the N-terminal oligosaccharide/oligonucleotide-binding (OB) domain, nam

200 a zinc finger (ZF) sub-ring followed by the oligosaccharide/oligonucleotide-binding (OB) fold ring.

201 donors to selected synthetic plant cell wall oligosaccharides on the array and that the transferred m

202 However, the role of N-linked oligosaccharides on the structural and immunological pro

203 were confirmed as the main asparagine-linked oligosaccharides on the surface of TBEV derived from hum

204 Research has focused in wine oligosaccharides only in the last decade.

205 They include: (i) wine oligosaccharides origins, (ii) techniques for isolating

206 Partially acetylated chitosan oligosaccharides (paCOS), consisting of beta-1,4-linked

207 , and correlations between the abundances of oligosaccharide pairs were identified, potentially indic

208 has been ascribed to high concentrations of oligosaccharides, particularly melezitose.

209 (ASRDelta2) in complex with different gluco-oligosaccharides pinpointed key residues in binding site

210 of enzymes that catalyse the biosynthesis of oligosaccharides, polysaccharides, and glycoconjugates.

211 content and lack of interactions between the oligosaccharide portion of GM1 with specific membrane pr

212 It was observed that short chain oligosaccharides produce higher level of acetate than me

213 d dissociation (CID) of these phosphorylated oligosaccharides produces simple MS/MS spectra with most

214 e examined the factors affecting bovine milk oligosaccharide production among cattle in the dairy ind

215 Alginate lyases can be used for alginate oligosaccharide production and for structural characteri

216 Improving our understanding of oligosaccharide production will aid in developing strate

217 ] reaction while producing the same oxidized oligosaccharide products.

218 The oligosaccharide profiles further demonstrated that the e

219 Here, we report that six synthetic oligosaccharides, ranging from dimers to hexamers, self-

220 iable and universal approaches that assemble oligosaccharides rapidly and stereoselectively.

221 neumoniae recognizes sialylated and sulfated oligosaccharide receptors to colonize the respiratory tr

222 molecular basis of coronavirus attachment to oligosaccharide receptors, we determined cryo-EM structu

223 entified on CD11b/CD18 included high Mannose oligosaccharides recognized by the Galanthus Nivalis lec

224 ractions by expression of O-antigen and with oligosaccharides reduces infectivity.

225 p < 0.001), led to an eight-fold increase in oligosaccharides release (p < 0.001), and reduced the fl

226 The stereoselective synthesis of oligosaccharides remains one of the biggest challenges i

227 he optimal nutrition source for infants, and oligosaccharides represent the third most abundant compo

228 at room temperature, while hexoses and their oligosaccharides require mild heating (i.e., 50 degrees

229 ved reduced laminaripentaose and transferred oligosaccharides, resulting in polymers of 6 and 7 gluca

230 growth in vitro, including raffinose-family oligosaccharides (RFOs, which are alpha-(1->6)-galactosy

231 gosaccharides consist principally of neutral oligosaccharides rich in arabinose and glucose.

232 Adding purified bovine sialylated milk oligosaccharides (S-BMO) with structures similar to thos

233 ategies combining chemical depolymerization, oligosaccharide sequencing, and monosaccharide and glyco

234 6B generated a mixture of (galactosyl) manno-oligosaccharides shorter than mannohexaose.

235 ay and SPR assays of structurally defined HS oligosaccharides show that a rare 3-O-sulfation (3-O-S)

236 that target the polyLacNAc structures within oligosaccharide side chains of both animal and human muc

237 tself constructed using the hybrid search of oligosaccharide spectra in the NIST 17 Tandem MS Library

238 Enzyme action on oligosaccharide standards showed a preference for the la

239 of differentially fucosylated and sialylated oligosaccharides starting from a single chemically synth

240 was illustrated by synthesizing partial core oligosaccharide structure present in the lipopolysacchar

241 ach, we found a wealth of hybrid and complex oligosaccharide structures reminiscent of those in highe

242 , enveloped viruses also utilize these large oligosaccharide structures to prevent access to surface

243 Fucosylated oligosaccharide structures were widely identified among

244 rovides the opportunity to determine unknown oligosaccharide structures, which is particularly advant

245 ally reduced brain levels of ganglioside and oligosaccharide substrates and reversed well-established

246 ally reduced brain levels of ganglioside and oligosaccharide substrates and reversed well-established

247 We found that relatively short GlcNAc oligosaccharides, such as a six-unit GlcNAc oligomer, ca

248 ecific activity on red algal neo-carrageenan oligosaccharides, such as those found in both family 127

249 ective acylation of S-glycosides streamlines oligosaccharide synthesis and will have wide application

250 Automated chemical oligosaccharide synthesis is an attractive concept that

251 fully automated process for enzyme-mediated oligosaccharide synthesis that can give easy access to d

252 protecting groups that are commonly used in oligosaccharide synthesis, these protecting groups are n

253 To help navigate within many methods of oligosaccharide synthesis, this Perspective offers a cri

254 fit into selective activation strategies for oligosaccharide synthesis.

255 We found that the GM1 oligosaccharide, systemically administered, reaches the

256 Secretors had higher amounts of total oligosaccharides than nonsecretors (11.45 g/L; IQR: 0.77

257 alactose-alpha-1,3-galactose (alpha-Gal), an oligosaccharide that is present in cells and tissues of

258 targeted HS library, we demonstrate that an oligosaccharide that possesses both anticoagulant activi

259 Therefore, we sought to generate an oligosaccharide that would bind Tau and block its cellul

260 initial attack on galactomannan, generating oligosaccharides that after transport to the periplasm a

261 Cyclodextrins are cyclic glucan oligosaccharides that form inclusion complexes with a nu

262 hat can provide libraries of heparan sulfate oligosaccharides that have glucosamine residues modified

263 matory target, decreases injury greater than oligosaccharides that only bind to HMGB1 or only have an

264 We have identified 13 oligosaccharides that vary significantly by breed, with

265 we generated a panel of polysaccharides and oligosaccharides to determine the properties required fo

266 GA) aims at accelerating access to synthetic oligosaccharides to meet the demand for defined glycans

267 hat oral administration of lactose or fructo-oligosaccharides to mice increases abdominal sensitivity

268 es mainly cleaved unsaturated guluronic acid oligosaccharides to monomers.

269 First, we used short heparan sulfate oligosaccharides to remove lipoproteins already deposite

270 a-EPD combines UVPD of negatively charged oligosaccharides to yield abundant charge-reduced radica

271 stral state in angiosperms, with fucosylated oligosaccharides transported across the plasma membrane.

272 tally straightforward preparation of complex oligosaccharide units from simple building blocks.

273 resent a new synthetic approach to HS and DS oligosaccharides using chemoselective glycosylation whic

274 , we report online LC-MS/MS sequencing of HS oligosaccharides using hydrophilic interaction liquid ch

275 hesis of type I LacNAc (Galbeta1 -> 3GlcNAc) oligosaccharides usually suffers from low yields.

276 A series of synthetic HS oligosaccharides varying in chain length (tetramers and

277 associated with mice given lactose or fructo-oligosaccharides vs controls.

278 at 160 degrees C, whereas the maximum fucose oligosaccharides was obtained at 180 degrees C.

279 The coverage of oligosaccharides was significantly extended using milks

280 Lacto-N-tetraose, another common human milk oligosaccharide, was also obtained en route to the targe

281 The most abundant oligosaccharides were 2'-fucosyllactose, lacto-N-fucopen

282 Hep-containing oligosaccharides were assembled directly from building b

283 After global deprotection, these oligosaccharides were coupled with carrier protein keyho

284 The obtained oligosaccharides were identified as arabino-xylooligosac

285 mass spectrometry, complex-type biantennary oligosaccharides were identified as major N-glycan struc

286 The abundances of several oligosaccharides were increased in second-parity cows, a

287 The compounds and corresponding ganglio-oligosaccharides were printed as a microarray to examine

288 ther with a number of previously prepared HS oligosaccharides, were printed as a glycan microarray to

289 acetylated analogues of O-acetylated NmW CPS oligosaccharides which can serve as structurally stable

290 monosaccharides or derivatives to form N(3)-oligosaccharides which were converted to the desired NAc

291 assembling densely substituted arabinoxylan oligosaccharides, which are valuable substrates for char

292 Pectin oligosaccharides, which can be obtained from fruit waste

293 approach of studying well-defined synthetic oligosaccharides will form the foundation of our underst

294 Here, we synthesized HS oligosaccharides with defined sulfation patterns and sho

295 In this study, a variety of HS oligosaccharides with different chain lengths and N- and

296 Membrane-bound oligosaccharides with specific chemistries are known to

297 Furthermore, transacetylation of oligosaccharides with the 2-O-specific RiCE17 provided i

298 up of mice were fed a diet containing fructo-oligosaccharides, with or without pyridoxamine in drinki

299 anase (HTG) grafts cellulose onto xyloglucan oligosaccharides (XGOs) - and, we now show, xyloglucan p

300 Xylo- and arabinoxylo-oligosaccharides (XOS and AXOS) are of interest for thei