ライフサイエンスコーパス: polysaccharide

1 omparable to those of the full-length native polysaccharide.

2 y responses to this extremely complex fungal polysaccharide.

3 isation of the repeat unit of the spore coat polysaccharide.

4 M48 is essential for the CE1 activity on the polysaccharide.

5 ves adhesins, and RbmB, which digests matrix polysaccharides.

6 saminoglycans (GAGs), highly sulfated linear polysaccharides.

7 armonized deposition of cellulose and matrix polysaccharides.

8 al potential, due to its metabolites, mainly polysaccharides.

9 on various carbon sources, including chitin polysaccharides.

10 the presence of arabinogalactans as the main polysaccharides.

11 ify lignins and facilitate interactions with polysaccharides.

12 zed degraders of fucoidans and other complex polysaccharides.

13 ation, and poor immunogenicity in infants of polysaccharides.

14 n its partner's ability to degrade different polysaccharides.

15 l method for producing oligosaccharides from polysaccharides.

16 s of deposition of both cellulose and matrix polysaccharides.

17 e ability to synthesize and modify cell wall polysaccharides.

18 ding dimethylsulfoniopropionate and sulfated polysaccharides.

19 low extracellular hydrolysis rates of a few polysaccharides.

20 Staphylococcus aureus types 5 and 8 capsular polysaccharides.

21 PLWH) have increased plasma levels of fungal polysaccharide (1->3)-beta-D-Glucan (betaDG).

22 teromannans (~60%), slightly branched pectic polysaccharides (~25%), and xyloglucans possessing monom

23 ts were composed of cellulose (~49%), pectic polysaccharides (~30%), and xyloglucans (~15%), whereas

24 mensal, Bacteroides fragilis, but not with a polysaccharide A (PSA) deficient isogenic strain.

25 g Bacteroides fragilis and its OM-associated polysaccharide A, we determined that IFN-beta expression

26 -MS, (13)C was detected in starch and matrix polysaccharides after the formation of NDP sugars.

27 oic acid (WTA) synthesis, a common cell wall polysaccharide among Gram-positive organisms.

28 Plant cell wall polysaccharide analysis encompasses the utilization of a

29 ded cell wall-anchored adhesins (ebh, sdrD), polysaccharide and capsule synthesis genes, cell wall re

30 treatment caused hydrolysis of the attached polysaccharide and consequently lowered the height of th

31 Despite the immense variation in capsular polysaccharide and exopolysaccharide structures, pattern

32 ethylene biosynthesis, and the activation of polysaccharide and glycoprotein lectin, which are import

33 l component of clinically used NmW CPS-based polysaccharide and polysaccharide-conjugate vaccines.

34 ed products could be adapted to modify other polysaccharides and biopolymers in general.

35 lds and indicate that primary degradation of polysaccharides and fermentation may play an important b

36 edicated to the utilization of diverse plant polysaccharides and host glycans.

37 revealing new potential functions for these polysaccharides and linking them to diseases such as Alz

38 dwide and contains virulence factor capsular polysaccharides and lipopolysaccharides linked to the ce

39 rcome a greater diversity of plant cell wall polysaccharides and maximize access to the nutritionally

40 Here, we generated a panel of polysaccharides and oligosaccharides to determine the pr

41 ants and animals, which include a variety of polysaccharides and polypeptides.

42 lipid-binding activity and interactions with polysaccharides and polysaccharide molecular recognition

43 primary cell walls of plants are composed of polysaccharides and proteins.

44 xternal hydrolysis rates of a broad range of polysaccharides and reduced selfish uptake of polysaccha

45 reatments or prevention options are aimed at polysaccharides and surface-related proteins that play i

46 Sulphating naturally occurring polysaccharides and their synthetic analogs is challengi

47 olor kombucha extract displayed more complex polysaccharides, and a higher content of total polysacch

48 ll as plant cell wall-derived hemicellulosic polysaccharides, and carry out C4 oxidative cleavage.

49 talyse the biosynthesis of oligosaccharides, polysaccharides, and glycoconjugates.

50 microbial models for the utilization of soil polysaccharides, and many of their components have been

51 rticles), consisting of flaxseed protein and polysaccharides, and of the addition of thymol to the oi

52 tion and loss of crystallinity of cellulosic polysaccharides, and silicification.

53 ids, lipids, and ions to peptides, proteins, polysaccharides, and xenobiotics.

54 and fibre polysaccharides (cellulose, pectic polysaccharides, and xyloglucans, ~45%).

55 que structure due, in part, to two lipidated polysaccharides-arabinogalactan and lipoarabinomannan.

56 nal IgG against the M. tuberculosis capsular polysaccharide arabinomannan (AM).

57 Presence of pectic polysaccharides, arabinoxylans and xyloglucans was infer

58 hile carbon-storage polymers such as surface polysaccharide are increased.

59 Vaccines based on the Vi capsular polysaccharide are licensed or in development against ty

60 ant cytokinesis, newly synthesized cell wall polysaccharides are deposited in a restricted region of

61 Polysaccharides are dominant features of most bacterial

62 Pure, completely defined linear and branched polysaccharides are essential to understand carbohydrate

63 Although capsular polysaccharides are good antigens for vaccine production

64 Capsular polysaccharides are important virulence factors in patho

65 ithin the body via biological processes, and polysaccharides are regarded as generally safe.

66 Our findings suggest that PLPE (in which polysaccharides are the major component) has potential a

67 Polysaccharides are the most abundant biomolecules in na

68 Polysaccharides are the most abundant biopolymers on ear

69 Vesicles containing matrix polysaccharides are thought to be transported by the FRA

70 ate polysaccharides, distinct from cell wall polysaccharides, are adhesive factors secreted by root a

71 constituted a potential source of high value polysaccharides as beta-glucans (average 12.2 +/- 1.7g/1

72 plete chemical and/or enzymatic syntheses of polysaccharides as long 92-mers.

73 are produced by dedicated Wzx/Wzy-dependent polysaccharide-assembly pathways distinct from that resp

74 membrane system facilitates the transport of polysaccharides, associated enzymes, and glycoproteins t

75 his report the chemical structure of the K15 polysaccharide, based on chemical analysis and nuclear m

76 Here, we report the first GAG polysaccharide-based photoaffinity probes for the system

77 am; 95% CI: 0.003, 0.04) and total nonstarch polysaccharides (beta = 0.02 per gram; 95% CI: 0.003, 0.

78 tion from mushrooms (A. bisporus) is rich in polysaccharides (beta-glucans) and proteins.

79 Long-chain polysaccharides bind and may bridge adjacent sites on th

80 porters implicated in O antigen and capsular polysaccharide biosyntheses with those facilitating teic

81 lete model of the Exo pathway for spore coat polysaccharide biosynthesis and export.

82 thus, the secretion of a novel biosurfactant polysaccharide (BPS) is spatially modulated within commu

83 y binding to lipopolysaccharides or capsular polysaccharides, but in other cases they suggested the p

84 rdinate the delivery of cellulose and matrix polysaccharides, but the underlying molecular mechanisms

85 The technique is first used to identify polysaccharides by oligosaccharide fingerprinting.

86 ted OLE, suggesting a protective role of the polysaccharides by the formation of non-covalent polysac

87 Polysaccharides can be taken up in a 'selfish' mode, whe

88 tain N-acetylglucosamine (GlcNAc)-containing polysaccharides can stabilize poliovirus.

89 Polysaccharides cannot be simply sequenced because they

90 The extracellular polysaccharide capsule of Klebsiella pneumoniae resists

91 pathogen Cryptococcus neoformans possesses a polysaccharide capsule that is a major virulence factor,

92 >90 serotypes, each of which has a distinct polysaccharide capsule.

93 shrimp boiling water (SBW) using food grade polysaccharides (carrageenan, alginate and carboxymethyl

94 azelnut skin made up lignin (~55%) and fibre polysaccharides (cellulose, pectic polysaccharides, and

95 f ~ 8 to ~ 20 galectin molecules binding per polysaccharide chain.

96 changes in the crystalline structure of the polysaccharide chains and led to an increased enzymatic

97 weight, the radii of gyration of the starch polysaccharide chains, and the distribution of the amylo

98 isation-repolymerisation reactions of starch polysaccharide chains.

99 We previously reported that the polysaccharide chitin, a key component of arthropod exos

100 The effect of different polysaccharides combinations on the stability of maqui e

101 es and explores the impact of pH and protein-polysaccharide complexation on overrun and foam stabilit

102 ticularly, these can be interlinked in multi-polysaccharide complexes.

103 to evaluate the relationship between shared polysaccharide components and the frequency of serotype

104 be vital for NMR structure analysis of minor polysaccharide components of plant cell walls that are p

105 ate the presence of complex, highly branched polysaccharide components with a wide range of galactosy

106 hus, we identified, in addition to the major polysaccharide components, two minor polysaccharides, na

107 These patterns were correlated with shared polysaccharide components.

108 Polysaccharide composition of seed mucilage was successf

109 This work investigated the A. mearnsii gum polysaccharide composition, its cytotoxicity and the tec

110 cile relative quantitative analysis of their polysaccharide composition, utilizing only a few milligr

111 riptional responses, biofilm production, and polysaccharide composition.

112 Next, the polysaccharide compositions of food and feces are determ

113 were initially included in the pneumococcal polysaccharide conjugate vaccine (PCV) in 2000 before it

114 tested their role in the clinically relevant polysaccharide conjugate vaccine against Streptococcus p

115 Each component of current protein-polysaccharide conjugate vaccines (PCVs) generally induc

116 ically used NmW CPS-based polysaccharide and polysaccharide-conjugate vaccines.

117 A 20-valent PCV (PCV20) containing capsular polysaccharide conjugates of serotypes present in the 13

118 The repeating structure of the K15 polysaccharide consists of 4)-alpha-GlcpNAc-(1 -> 5)-alp

119 ch has the potential to be extended to other polysaccharides containing 2-amino uronic acids, as alre

120 ocytes to beta-glucan, a naturally occurring polysaccharide, contributes to the induction of innate i

121 to cleave the glycosidic linkage between the polysaccharide (core and O-antigen) and lipid A moieties

122 eria meningitidis serogroup W (NmW) capsular polysaccharide (CPS) and is a required structural compon

123 utations in the putative E. faecium capsular polysaccharide (cps) biosynthetic locus, with different

124 ulin G (IgG) antibodies against the capsular polysaccharide (CPS) offer S. pneumoniae serotype-specif

125 Bacteria express multiple diverse capsular polysaccharides (CPSs) for protection against environmen

126 ally produce several phase-variable capsular polysaccharides (CPSs), but their contributions to bacte

127 Processing of both the protein and the polysaccharide creates glycopeptides in the endosome of

128 structural analysis of cell wall-associated polysaccharides (CWPS) through MALDI-TOF MS and methylat

129 oK, MXAN_3262/ExoO and MXAN_3263/ExoP) and a polysaccharide deacetylase (MXAN_3259/ExoL) are importan

130 high content of genes involved in cell wall polysaccharides decomposition but low expression levels,

131 observed phenotypes (growth characteristics, polysaccharide degradation) do not necessarily correlate

132 ficans, that uniquely combines two different polysaccharide-degrading activities.

133 tification of an unknown product coming from polysaccharide depolymerization.

134 It is worth noting that polysaccharide dextran-modified NPs also exhibited evide

135 has been no equivalent enzyme for universal polysaccharide digestion.

136 rvations indicate that specific root exudate polysaccharides, distinct from cell wall polysaccharides

137 nic bacteria containing Pse on their surface polysaccharides (e.g., Helicobacter pylori and Enterobac

138 Previously, we found that bacterial polysaccharides enhance poliovirus stability against hea

139 ace-exposed carbohydrates like lipo- and exo-polysaccharides (EPS) is important for non-self recognit

140 olysaccharides and reduced selfish uptake of polysaccharides, except for laminarin.

141 The hypoglycemic effect of Phellinus linteus polysaccharide extract (PLPE) has been documented in sev

142 FTIR analysis of polysaccharide extracts showed dominant presence of poly

143 ile the immunological properties of kombucha polysaccharide extracts were determined in peripheral bl

144 iable synthesis of surface molecules such as polysaccharides, fimbriae, and outer surface proteins.

145 ) is a highly abundant, nontoxic, degradable polysaccharide found in marine organisms and hence is a

146 The polysaccharide fraction is divided into components cellu

147 te dissolution of both soluble and insoluble polysaccharide fractions of plant cell walls in organic

148 at bran into enriched protein and non-starch polysaccharide fractions, which show potential to be use

149 tive monoclonal antibody and a MenA capsular polysaccharide fragment were further elucidated at the a

150 udy, we successfully synthesized K2 capsular polysaccharides from tetra- to octasaccharides in highly

151 ived organic matter, much of it occurring as polysaccharides, fuels biogeochemical cycles driven by i

152 Here we show that the polysaccharide galactosaminogalactan (GAG) of A. fumigat

153 the limits of our understanding of how (lipo)polysaccharides, (glyco)lipids, and other bacterial secr

154 s loaded into the 75/25 blend films based on polysaccharides (gum Arabic (GAR), octenyl succinic anhy

155 Capsular polysaccharides have been confirmed to be an important v

156 Although polysaccharides have been well-studied nutrients for the

157 Drug delivery-related research involving polysaccharides have continuously cited minimal to zero

158 the deposition of an associated hormogonium polysaccharide (HPS).

159 Large bottlebrush complexes formed from the polysaccharide hyaluronan (HA) and the proteoglycan aggr

160 fore ovulation, HCs are transferred onto the polysaccharide hyaluronan (HA) to form covalent HC.HA co

161 Alternatively, polysaccharides hydrolyzed by cell-surface attached or f

162 synthesize rare intracellular polymethylated polysaccharides implicated in the modulation of fatty ac

163 Mannans are an abundant cell wall polysaccharide in bryophytes, seedless vascular plants a

164 seed starch (JSS), an underutilized natural polysaccharide in conjugation with soy protein isolate (

165 O antigens are important cell surface polysaccharides in gram-negative bacteria where they ext

166 Unlike the ones from other sources, pectic polysaccharides in IDFs had lower proportion of smooth r

167 on and distribution of lignin and structural polysaccharides in leatherwood xylem in comparison with

168 However, commercial use of microbial polysaccharides in other areas as well as the positive r

169 Unlike the polysaccharides in the assembled capsule, isolated exopo

170 ese data reveal the central role of secreted polysaccharides in the intricate behaviors coordinating

171 arides (XGOs) - and, we now show, xyloglucan polysaccharide - in vitro, thus exhibiting CXE (cellulos

172 charide extracts showed dominant presence of polysaccharides, in addition to phenols, lipids and prot

173 tems for the utilization of hemicellulolytic polysaccharides, including xylan, arabinan, and galactan

174 Vi polysaccharide is a homopolymer of alpha-1,4-N-acetylgal

175 spp., and the succinyl modification to this polysaccharide is critical.

176 solubility, while the chemical synthesis of polysaccharides is challenging with few reported example

177 mponents and biosynthetic pathways for these polysaccharides is key to our ability to design vaccines

178 and the ability of microorganisms to secrete polysaccharides is reduced, which makes the nutrients ne

179 The visual appearance of gums (water-soluble polysaccharides) is so similar to other plant exudates,

180 Polysaccharide isolation provides heterogeneous mixtures

181 l surface polysaccharides, such as K-antigen polysaccharide (KPS) and lipopolysaccharide (LPS), might

182 nation with glycoconjugates of MenA capsular polysaccharide led to an almost complete elimination of

183 To address the impact of polysaccharide length, typhoid conjugates made with shor

184 f these organisms also mediate hydrolysis of polysaccharides, likely from cyanobacterial blooms.

185 s can be stabilized by bacteria or bacterial polysaccharides, limiting inactivation and aiding transm

186 hesis of conjugate vaccines, consisting of a polysaccharide linked to a protein, can be technically c

187 vance to the structure analysis of insoluble polysaccharide materials that otherwise are not easily i

188 Concentration level and polysaccharide matrix of encapsulating agent significant

189 ynergism within a consortium by heterogenous polysaccharide metabolism.

190 ty and interactions with polysaccharides and polysaccharide molecular recognition systems coordinate

191 ng avenue is to exploit the vast quantity of polysaccharide molecules contained in green wastes.

192 Lytic polysaccharide monooxygenase (LPMO) and copper binding p

193 381 contains an N-terminal family AA10 lytic polysaccharide monooxygenase (LPMO), a family 5 chitin-b

194 Lytic polysaccharide monooxygenases (LPMOs) are a recently dis

195 Lytic polysaccharide monooxygenases (LPMOs) are microbial enzy

196 Lytic polysaccharide monooxygenases (LPMOs) have a unique abil

197 Lytic polysaccharide monooxygenases (LPMOs) have been proposed

198 ucture analysis of insoluble plant cell wall polysaccharides, more so of minor cell wall components t

199 e major polysaccharide components, two minor polysaccharides, namely, <5% 3-linked arabinoxylan (swit

200 Allergen-polysaccharide neoglycogonjugates increase immunization

201 In contrast, the long-chain O-antigen polysaccharide (O-PS) shows remarkable structural divers

202 saccharides by the formation of non-covalent polysaccharides-OE complexes.

203 One obstacle is that the capsular polysaccharide of a dominated Klebsiella pneumoniae sero

204 erial cell wall polymers, including capsular polysaccharide of streptococcal species and arabinogalac

205 ce-determining glycan motifs in the capsular polysaccharides of bacterial pathogens.

206 glycosides such as are found in the capsular polysaccharides of numerous pathogenic bacteria.

207 lycosyltransferases that build the lipidated polysaccharides of the mycobacterial cell envelope, and

208 eties into a shell structure (e.g., protein, polysaccharide or lipid-based material).

209 PGs hydrolyze the cell wall polysaccharide pectin and are among the first enzymes to

210 hain exposed at the bacterial surface, named polysaccharide pellicle (PSP), and a more conserved rham

211 addition on the CWPS components rhamnan and polysaccharide pellicle (PSP), respectively, whereas csd

212 lysaccharides, and a higher content of total polysaccharides, phenols and flavonoids compared to L. e

213 lular and extracellular biopolymers, such as polysaccharides, polyamides, polyesters, polyphosphates,

214 mblies comprising millions of functionalized polysaccharide-polynucleotide coacervate droplets.

215 mbrane fragments on the surface of preformed polysaccharide-polynucleotide coacervate micro-droplets

216 nor constituents (i.e., minerals, non-starch polysaccharides, polyphenols (flavonolignans), macaenes,

217 The alpha-2,8-linked form of the polysaccharide polysialic acid (PSA) has widespread impl

218 Polysaccharides possessing charged functional groups, su

219 of potato protein (PPT) with selected pectic polysaccharides (PPS) and modulation of the conjugation

220 10% encapsulating polysaccharide produced best results, with maltodextrin

221 The main classes of cell wall polysaccharides produced by terrestrial plants are cellu

222 ifficile biofilm formation and extracellular polysaccharide production.

223 era supports the case for licensure of a GBS polysaccharide-protein conjugate vaccine based on immuno

224 Licensure of a Group B streptococcus (GBS) polysaccharide-protein conjugate vaccine for protecting

225 The ability of GBS polysaccharide-protein conjugate vaccines currently unde

226 Polysaccharide-protein conjugates have been developed to

227 rix that is composed of a complex mixture of polysaccharides, proteins, and DNA.

228 They are made of polysaccharides, proteins, and other biomolecules and ha

229 Quick access to polysaccharides provides the basis for future material s

230 to the immunologically relevant zwitterionic polysaccharide PS A1 via an oxime link.

231 Oral streptococci often harbor capsular polysaccharide (PS) synthesis loci (cps).

232 describe the development of a method for Vi polysaccharide quantification based on acid hydrolysis w

233 onal antibodies have enabled the tracking of polysaccharide release along root axes of young seedling

234 se-causing serotype, the associated capsular polysaccharide remains poorly characterized.

235 t the fate of fucoidan-their major cell wall polysaccharide-remains poorly understood.

236 Agarose is a prominent marine polysaccharide representing reversible thermogelling beh

237 both complex hemicellulosic and pectinaceous polysaccharides requires the production of alpha-l-arabi

238 l changes that result from permethylation of polysaccharide residues.

239 Mucilages are generally polysaccharide-rich and often occur in the form of visco

240 pied by a dense mixture of proteins, lipids, polysaccharides, RNA, and DNA.

241 interaction, this activity was restored when polysaccharide size was reduced by enzymatic treatment,

242 , NMR structure analysis of 10 permethylated polysaccharide standards was undertaken to generate chem

243 ent structural proposals of the many complex polysaccharide structures that exist in the complex matr

244 o not directly reflect cereal root cell wall polysaccharide structures.

245 Analysis of the reactivity in the absence of polysaccharide substrate by stopped-flow absorption and

246 powerful in the degradation of recalcitrant polysaccharides such as chitin and cellulose.

247 ciations with legumes, and rhizobial surface polysaccharides, such as K-antigen polysaccharide (KPS)

248 on of fucoidans is slower than that of other polysaccharides, suggesting that fucoidans are more reca

249 However, while these CSLD polysaccharide synthases are essential, the nature of th

250 GS)-based method to characterize the capsule polysaccharide synthesis (cps) locus, classify N. mening

251 comprising most components of a Wzx/Wzy-type polysaccharide synthesis and export system.

252 roteins with homology to enzymes involved in polysaccharide synthesis and export, as well as sugar mo

253 are part of a Wzx/Wzy-dependent pathway for polysaccharide synthesis and export; however, key compon

254 , similarly to C. acnes supernatant, reduced polysaccharide synthesis by S. epidermidis.

255 ogen or starch (both alpha-glucans) or other polysaccharides tested.

256 Pel is a GalNAc-rich bacterial polysaccharide that contributes to the structure and fun

257 the overproduction of colanic acid capsular polysaccharide that defends against a wide array of phag

258 ronmental resistance depends on a spore coat polysaccharide that is synthesised by the ExoA-I protein

259 ckbones of cellulose and most hemicellulosic polysaccharides that comprise plant cell walls.

260 n sulfates are structurally diverse sulfated polysaccharides that reside at the surface of all animal

261 LPMOs modify biomass by oxidatively cleaving polysaccharides, thereby enhancing the efficiency of gly

262 e synthases are essential, the nature of the polysaccharides they synthesize has remained elusive.

263 A from plant tissue rich in starch and other polysaccharides, they invariably yield less and poor qua

264 ults indicate the importance of the capsular polysaccharide to G. parasuis virulence as well as nasal

265 the C. neoformans capsule and its associated polysaccharides to unravel their roles in fungal virulen

266 in filaments, thus diminishing noncellulosic polysaccharide transport to the cell wall and increasing

267 n agrC, P3.1 regained production of capsular polysaccharide type 5 (CP5) and staphyloxanthin.

268 ating unit of Staphylococcus aureus capsular polysaccharide type 5, which is also a potential antigen

269 by the HGM; and 3D crystal structures of the polysaccharide utilisation loci encoded sulfatases.

270 We tracked changes in the mode of polysaccharide utilization by heterotrophic bacteria dur

271 presence of genes encoding GH110 enzymes in polysaccharide utilization loci from marine bacteria sug

272 of the human intestinal microbiota, encodes polysaccharide utilization loci PULs, the apparatus requ

273 ations differentially express AcGGM-specific polysaccharide utilization loci, including novel, mannan

274 This effect of Bacteroidetes requires the polysaccharide utilization locus of their conserved comm

275 e (PCV13) followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 2 months later is recomm

276 >=19 years old in series with the 23-valent polysaccharide vaccine (PPSV23) in 2012.

277 urrently, followed by 23-valent pneumococcal polysaccharide vaccine (PPV23) 2 months later.

278 Vaccination with the 23-valent pneumococcal polysaccharide vaccine (PPV23) is available in the Unite

279 d by either a dose of 23-valent pneumococcal polysaccharide vaccine (PSV23) or a fourth PCV dose in t

280 t) and the percentage of cases caused by the polysaccharide vaccine PPV23 serotypes lowest (numerical

281 of PCV13 followed 1 month later by 23-valent polysaccharide vaccine.

282 sms, such as the production of extracellular polysaccharides, vesiculation and protein secretion.

283 n assembly (AGA) enables access to a 100-mer polysaccharide via a 201-step synthesis within 188 h.

284 e against the type III group B Streptococcus polysaccharide was comprised within 2 of the repeating u

285 the recovery of extract rich in antioxidant polysaccharide was reported.

286 The modified polysaccharides were comprehensively characterized and a

287 ns (e.g. preservation of esters or cuticular polysaccharides), which in combination with the solution

288 acterized into 15 serovars by their capsular polysaccharide, which has shown a correlation with isola

289 acteria produce abundant long-chain capsular polysaccharides, which can maintain a strong association

290 mediated by the extracellular hydrolysis of polysaccharides, which can trigger social behaviors in b

291 process occurring through rubbery amorphous polysaccharides, which contradicts previous assertions t

292 e with short- and long-chain fractions of Vi polysaccharide with average sizes of 9.5, 22.8, 42.7, 82

293 eparan sulfate and heparin are highly acidic polysaccharides with a linear sequence, consisting of al

294 Hemicelluloses, a family of heterogeneous polysaccharides with complex molecular structures, const

295 used to obtain extracts rich in antioxidant polysaccharides with pharmacological and food potential.

296 ached hydrophobic moieties also provided new polysaccharides with self-assembling ability.

297 oth showed peaks and bands characteristic of polysaccharides with semi-crystalline structure (14.50-3

298 assay was achieved by capturing pneumococcal polysaccharides with serotype-specific monoclonal antibo

299 ide modified starch (OSA), water soluble soy polysaccharides (WSSP)) and gelatin (GEL).

300 nd selectively secrete less of the cell wall polysaccharide xyloglucan.