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1 longed due to the mucoadhesive nature of the polysaccharide.
2 h relative to bacteria experiencing a single polysaccharide.
3 the protective response against type III GBS polysaccharide.
4 ) synthesized in situ in alginate, a natural polysaccharide.
5 a naturally occurring catalytic antibody for polysaccharides.
6 way and immunised with a complex mixture of polysaccharides.
7 e with cell wall pectic rhamnogalacturonan-I polysaccharides.
8 er-dependent enzymes that oxidatively cleave polysaccharides.
9 and disfavor taxa that prefer complex plant polysaccharides.
10 des alginates and fucose-containing sulfated polysaccharides.
11 zymatic mechanism through which TTPA acts on polysaccharides.
12 tilizes a myriad of host dietary and mucosal polysaccharides.
13 n26A primarily formed mannobiose from mannan polysaccharides.
14 ents, including water insoluble proteins and polysaccharides.
15 in the absence of flagella, pili, or certain polysaccharides.
16 host glycans and the importance of microbial polysaccharides.
17 ntous fungus Aspergillus fumigatus comprises polysaccharides.
18 imal for fueling LPMO-catalyzed oxidation of polysaccharides.
21 and as reference substrates, glucose and the polysaccharide alginate, derived from brown algal cell w
22 re composed predominantly of the polyanionic polysaccharides alginates and fucose-containing sulfated
25 fumigatus cell wall is a complex network of polysaccharides among them galactofuran, which is absent
26 xin B and A subunits, V. cholerae O-specific polysaccharide and lipopolysaccharide, toxin coregulated
29 imulations to model the hydrodynamics of the polysaccharide and the interaction with guest species re
30 ions displayed greater levels of non-starchy polysaccharides and bioactive components as compared to
31 rotective antigens that include cell surface polysaccharides and cell-associated and cell-secreted pr
32 sible for remodeling the de novo synthesized polysaccharides and establishing the three-dimensional s
33 cA) is the precursor of many plant cell wall polysaccharides and is required for production of seed m
35 in the presence of total, acidic or neutral polysaccharides and oligosaccharides was tested using tu
36 s substrates, the mutant enzymes synthesized polysaccharides and oligosaccharides with changed linkag
38 alls are composed of an intricate network of polysaccharides and proteins that varies during the deve
39 lls form elastic films of bacteria, excreted polysaccharides and proteins, whereas PA14 cells move ac
43 c acid based polymers, sulfonamides, anionic polysaccharides, and anionic polypeptides) and polybases
45 e alternative ligands include proteoglycans, polysaccharides, and fibers like collagen, all of which
46 o to bacterial lipopolysaccharides, capsular polysaccharides, and lipoarabinomannans that contain the
47 transport and breakdown of a wide variety of polysaccharides, and to the regulation of these processe
51 ding domains for the highly diverse sulfated polysaccharides are important growth factors involved in
53 or the uptake and breakdown of many of these polysaccharides are transcriptionally regulated by hybri
54 simple sugars, and starch, leaving nonstarch polysaccharides as major nutrients reaching the microbio
61 nderpinnings of the complex process of plant polysaccharide biosynthesis are poorly understood, large
62 rkably, integrates several key activities in polysaccharide biosynthesis into a single polypeptide.
64 One spot comprising a mixture of capsular polysaccharide biosynthesis protein and other proteins w
67 s not orchestrate the degradation of a plant polysaccharide but targets a fungal cell wall glycan, 1,
68 pends of the degree of polymerization of the polysaccharide, but when applied to pasta products, both
69 characterizing the structure and dynamics of polysaccharides, but only relatively few such studies ex
72 jor component of the Cryptococcus neoformans polysaccharide capsule, hydrolyzed a peptide antigen mim
75 longevity through increased secretion of the polysaccharide colanic acid (CA), which regulates mitoch
76 ys containing chemically extracted cell wall polysaccharides collected from 331 genetically diverse B
79 pare the effect of ferrous sulfate with iron polysaccharide complex on hemoglobin concentration in in
80 t commonly prescribed oral iron despite iron polysaccharide complex possibly being better tolerated.
81 y anemia, ferrous sulfate compared with iron polysaccharide complex resulted in a greater increase in
83 bic fluorescent probes established that this polysaccharide complexes hydrophobic species, and NMR ex
84 ls of natural antibodies to the pneumococcal polysaccharide component phosphocholine were significant
88 with molecular-level characterization of the polysaccharide composition, mobility, hydration, and int
89 vision of energy from otherwise indigestible polysaccharides comprising part of the host diet, lining
91 tibodies against the capsule are protective, polysaccharide conjugate vaccines, which are constructed
94 tose, glucose and mannose whereas the acidic polysaccharides contain fucose, xylose and 4-O-methylglu
97 network of covalently linked plant cell wall polysaccharides containing galacturonic acid (GalA).
99 d apple - we have dissected cell wall matrix polysaccharide contents using sequential solubilisation
100 he present study, the 6-deoxyheptan capsular polysaccharide (CPS) from B. pseudomallei was purified,
102 cans resembling portions of the ST2 capsular polysaccharide (CPS) repeating unit were used to screen
103 onjugate vaccines based on isolated capsular polysaccharide (CPS) save millions of lives annually by
107 Streptococcus pneumoniae expresses capsular polysaccharides (CPSs) to protect itself from opsonophag
109 ion activity which occurs in active sites of polysaccharide deacetylases (PDAs) from bacterial pathog
110 ve framework to further identify enzymes for polysaccharide deconstruction in fungal genomes and will
114 cell wall degradation, either by catalysing polysaccharide degradation itself, or by targeting the v
115 teroidetes and should facilitate analyses of polysaccharide degradation systems and many other proces
120 dy processes such as cell wall biosynthesis, polysaccharide deposition, protein-carbohydrate interact
121 the production and characterization of plant polysaccharide-derived oligosaccharides and their attach
123 host-gut microbiota symbiosis beyond dietary polysaccharide digestion, including microbial interactio
127 ptidoglycan, lipopolysaccharide and capsular polysaccharide-either simultaneously or individually in
128 90% of the enzymes for deconstructing algal polysaccharides emanate from members of a single bacteri
129 ural basis of immune recognition of capsular polysaccharide epitopes can aid in the design of novel g
130 screened, a mutant lacking an extracellular polysaccharide (EPS) locus consistently failed to transm
131 entrations to investigate free extracellular polysaccharide (EPS) production during anaerobic digesti
134 nal properties, and biological activities of polysaccharides extracted from watermelon rinds (WMRP) w
135 s is featured with pre-loading proteins into polysaccharide fine particles via a self-standing aqueou
139 sidic bonds in the two foremost recalcitrant polysaccharides found in nature, namely cellulose and ch
140 s ranged from 39.8 to 43.3g/100g with pectic polysaccharide fraction constituted of rhamnogalacturona
142 tion and gelling ability, confirmed the main polysaccharide fractions were pectin with different acyl
144 The extent of growth increased with neutral polysaccharides from H. suaveolens corresponding to the
145 ncreasing concentrations of a highly charged polysaccharide, fucoidan, the microscale ordering of Fmo
146 ne-associated BoMan26B initially acts on the polysaccharide galactomannan, producing comparably large
147 (ACME), and a specific mutation in capsular polysaccharide gene cap5E Although the PVL-encoding phag
151 significantly more than the natural sulfated polysaccharide heparin, and promoted regeneration of bon
153 results reveal the important role of capsule polysaccharide in shielding OmpA and thereby inhibiting
154 of carboxymethyl cellulose, a commonly used polysaccharide in the food and pharmaceutics industry, c
156 t starch and wheat gluten was mixed with the polysaccharides in five concentrations: 3%, 6%, 9%, 12%
158 mportant implications for potential roles of polysaccharides in the pathogenesis and transmission of
159 hylesterification of pectin, one of the main polysaccharides in the plant cell wall, and are of criti
164 panied by gradual depolymerization of pectic polysaccharides, including homogalacturonans, rhamnogala
168 lysis by destabilising the tight networks of polysaccharides intertwining cellulose in the plant cell
171 lant cell wall xyloglucan, we show that this polysaccharide is secreted by a wide range of angiosperm
173 charide on the surfaces they inhabit; hence, polysaccharide is their immediate environment on many su
177 lution and storage was also inhibited by two polysaccharide layers coupled with copigmentation, which
178 is influenced by the cell wall composition (polysaccharides, lignins, pectins) and by the degree of
183 l, and functional screening, we identified a polysaccharide lyase family 7 enzyme that is unique to V
186 nts a significant enzymatic challenge to the polysaccharide lyases and sulfatases that mediate degrad
188 oxidase, were immobilized on a biocompatible polysaccharide matrix to develop a functional hydrogel c
189 ow little is known about the assembly of the polysaccharide matrix, and considers changes in the wall
190 B. thetaiotaomicron when faced with multiple polysaccharides may aid its competitiveness in the mamma
191 ve digestion of recalcitrant plant cell wall polysaccharides may offer solutions for sustainable indu
192 B307.30) was shown, suggesting that capsular polysaccharide mediated the inhibition of MAb binding to
193 bably was an important influencing factor in polysaccharide metabolism and adaptations of plants to s
194 properties influenced by four dietary fibre polysaccharides (microcrystalline cellulose, inulin, app
196 hese include adaptation to oxidative stress, polysaccharide modification and genes associated with re
199 sequences for glycoside hydrolases and lytic polysaccharide mono-oxygenases targeting cellulose, xyla
200 ional traits and the high frequency of lytic polysaccharide mono-oxygenases, as well as other physiol
201 n crystalline chitin was enhanced by a lytic polysaccharide monooxygenase that increases substrate ac
207 of oxygen activation by substrate free lytic polysaccharide monooxygenases and provide insights that
213 mly assigned to low-fiber [</=10 g nonstarch polysaccharide (NSP)/d], habitual-fiber (control), or hi
214 KIMO1 (ESK1), which encodes a plant-specific polysaccharide O-acetyltransferase involved in xylan ace
216 tic cell (DC) response to alpha-(1,3)-glucan polysaccharide of Aspergillus fumigatus and ensuing CD4+
217 pentasaccharide, related to the O-antigenic polysaccharide of Escherichia coli 120, as its p-methoxy
218 enic carrier protein coupled to the capsular polysaccharide of the bacterial pathogen, are the most e
219 allowing us to finish assembling the defined polysaccharides of 5-20 units within days rather than ye
220 ic pathway for carrageenans, major cell wall polysaccharides of red macroalgae, in the marine heterot
221 glucans are high-molecular-weight non-starch polysaccharides of that are great interest to the brewin
222 nthetic oligosaccharides instead of isolated polysaccharides offer an attractive alternative to the t
223 system by a combination of a thick layer of polysaccharide on the surface (the glycan shield) and mo
224 orming bacteria typically deposit a layer of polysaccharide on the surfaces they inhabit; hence, poly
226 YKL-40 is interacting with these alternative polysaccharides or proteins within the body, extending i
227 ich in anti-inflammatory components, such as polysaccharides, phenolic and indolic compounds, mycoste
229 oorganisms proficient at degrading insoluble polysaccharides possess large numbers of carbohydrate ac
231 production were all reduced, which suggested polysaccharide production was decreased in DeltaciaR.
232 ecially argB gene, the ciaR mutation reduced polysaccharide production, resulting in the formation of
233 ine polymeric material (WPM), which includes polysaccharides, proteins, and polyphenolic compounds, i
234 olutes including water-soluble organic dyes, polysaccharides, proteins, enzymes, and DNA, and can be
236 the solubilization of soluble proteins (PN), polysaccharides (PS), nucleic acids (NA) and humic-like
241 unlike bacteria, fungi's ability to degrade polysaccharides relies on apparent redundancy in functio
242 of the Staphylococcus aureus type 5 capsular polysaccharide repeating unit, a trisaccharide consistin
243 cellulose, the most abundant plant cell wall polysaccharide, requires the cooperative activity of a l
245 ally, a screening of more than 300 bacterial polysaccharides revealed highly diverging avidity and se
248 rally complex glycan known: the plant pectic polysaccharide rhamnogalacturonan-II, cleaving all but 1
251 introduced into adult gnotobiotic mice fed a polysaccharide-rich diet, and (ii) in situ hybridization
254 ioxidant activities of crude and sulphonated polysaccharides (S.PEPS and S.EPS) were investigated usi
255 tional pectinolytic metabolism targeting the polysaccharide's two most abundant classes: homogalactur
256 semble by binding to the secondary cell wall polysaccharide (SCWP) via S-layer homology (SLH) domains
257 serologically distinct pneumococcal capsular polysaccharides (serotypes) are recognized, but they are
258 Both the cartilage and skin sulfated GAG polysaccharides showed greater ferritin formation compar
259 CBM56, we propose that it binds a quaternary polysaccharide structure, most likely the triple helix a
260 water that accumulates on the surface of the polysaccharide substrate after compression or to compres
262 examined how the physical characteristics of polysaccharide substrates influence the behavior of the
263 cleavage of glycosidic bonds in recalcitrant polysaccharides, such as cellulose and chitin, and are o
264 mprehension of the degradation of macroalgal polysaccharides suffers from the lack of genetic tools f
266 l domain of the trans-cisternae accompanying polysaccharide synthesis with a mathematical model.
268 he C. diphtheriae GlfT2 gave rise to shorter polysaccharides than those obtained with the M. tubercul
269 nal macrophages and produces a large soluble polysaccharide that activates a specific MSK/CREB-depend
270 anne et al. (2017) report that Hh produces a polysaccharide that induces an anti-inflammatory respons
272 strongly influenced by the rhizobial surface polysaccharides that affect NCR-induced differentiation
273 , peptidoglycan is decorated by polyrhamnose polysaccharides that are critical for cell envelope inte
275 Heparan sulfates (HS) are linear sulfated polysaccharides that modulate a wide range of physiologi
276 nd fructo-oligosaccharides (FOS) are reserve polysaccharides that offer an interesting combination of
278 Despite the biological importance of these polysaccharides, their biosynthetic pathways have receiv
279 k the mucoadhesive nature of a commonly used polysaccharide to the organoleptic properties of a food.
280 vaccines achieve this by coupling bacterial polysaccharides to a carrier protein that recruits heter
282 e funnel to guide the positively charged Pel polysaccharide toward an exit channel formed by PelB.
287 ific glycans are organized into co-regulated polysaccharide utilization loci, with the archetypal loc
290 ypes contained in the 23-valent pneumococcal polysaccharide vaccine (PPV23) decreased at similar rate
291 splantation and the response to pneumococcal polysaccharide vaccine was significantly lower posttrans
292 ve a single dose of Vi-conjugate (Vi-TT), Vi-polysaccharide (Vi-PS), or control meningococcal vaccine
297 Food grade sulfated glycosaminoglycan (GAG) polysaccharides were successfully extracted from chicken
298 and the monosaccharide composition of these polysaccharides were then determined using chemical comp
300 aceans offered a substantial supply of plant polysaccharides, with added dividends of animal protein
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