ライフサイエンスコーパス: mucilage

1 ed solubility of the pectic component of the mucilage.

2 ed cellulose, RG I, and ray size in adherent mucilage.

3 icantly in atgatl5-1 compared with wild-type mucilage.

4 S5 also play a role in the synthesis of seed mucilage.

5 itantly with the outer layer but produces no mucilage.

6 ated numerous diazotrophs from field sorghum mucilage.

7 lls that form a two-layered hydrogel, termed mucilage.

8 a, impaired in their production of spore tip mucilage.

9 demonstrated the interaction between oil and mucilage.

10 ifying action to chemically characterize the mucilage.

11 rides and is required for production of seed mucilage.

12 hich are present exclusively in the adherent mucilage.

13 produce the polysaccharide components of the mucilage.

14 e proteins are genuinely associated with the mucilage.

15 Arabidopsis (Arabidopsis thaliana) seed coat mucilage, a specialized layer of the extracellular matri

16 s synthesize and secrete large quantities of mucilage, a specialized secondary cell wall composed of

17 lls that contain pectin, including seed coat mucilage, a specialized secondary cell wall of seed coat

18 SCE cells produce mucilage, a specialized secondary wall that is rich in p

19 cleotide sugar transporters for altered seed mucilage, a structure rich in the GalA-containing polysa

20 alactouronic acid and fucose, Abroma augusta mucilage (AAM) exhibited shear thinning behavior (follow

21 Additionally, microcapsules of mucilage achieved the retention of betalains at more tha

22 Mucilage activity was greater in weakly basic (pH 9) and

23 disrupt other wall components suggests that mucilage adherence is maintained by complex interactions

24 LT-OVERLY SENSITIVE5 (SOS5) are required for mucilage adherence through unknown mechanisms.

25 A5) synthesizes cellulose necessary for seed mucilage adherence to seed coat epidermal cells of Arabi

26 esa5-1 sos5-2 has a much more severe loss of mucilage adherence, suggesting that SOS5 and CESA5 funct

27 3 affect the speed of mucilage extrusion and mucilage adherence.

28 t, reduced mucilage extrusion, and increased mucilage adherence.

29 porthe oryzae(1), powerful glycoprotein-rich mucilage adhesives(2) cement melanized and pressurized d

30 ts and produce an abundant carbohydrate-rich mucilage after rain.

31 ion in the rays of cellulose present in seed mucilage, along with an increased solubility of the pect

32 f MtWD40-1 expression blocks accumulation of mucilage and a range of phenolic compounds, including PA

33 wed a woody coat covered by a thick layer of mucilage and an embryo with two large cotyledons rich in

34 stems, and roots, and the production of seed mucilage and anthocyanin pigments.

35 defects appear to result from a lower DM in mucilage and are enhanced by the addition of Ca(2+) or c

36 aps of some mutants secrete small amounts of mucilage and are graviresponsive.

37 tophyte algae secretion of microbe-harboring mucilage and bacterial taxa such as Rhizobium and genes

38 interactions between components in the seed mucilage and cellulose.

39 A combination of cactus mucilage and ferric (Fe(III)) salt was investigated as a

40 , Cactaceae species produce large amounts of mucilage and fiber, although they can be also considered

41 nt xylose-rich component in Arabidopsis seed mucilage and is required to maintain its architecture.

42 The mucilage and outer wall then dehydrate to leave the colu

43 , suggesting compatibility between fermented mucilage and starch.

44 in the synthesis and structure of seed coat mucilage and that the FEI2/SOS5 pathway plays a role in

45 d apoplastic pocket filled with pectinaceous mucilage and the columella, a thick secondary cell wall.

46 is just beginning towards understanding root mucilage and the proposed adhesive polymers involved in

47 Hydrocolloids were extracted from seed mucilage and the pulp fractions from red tamarillo (Sola

48 lease a high molecular weight polysaccharide mucilage and thousands of living cells into the incipien

49 Their root caps secrete little or no mucilage and touch the root only at the extreme apex.

50 Negatively charged NPs did not adsorb to the mucilage and were able to translocate into the apoplast.

51 Although both flax mucilage and zein have excellent film-forming properties

52 wledge need, including the microstructure of mucilages and their compositional and regulatory dynamic

53 d composite coatings consisting of chitosan, mucilage, and levan, were applied on sweet cherry fruits

54 from others such as fruits, roots, flowers, mucilage, and seeds.

55 ss GalA, rhamnose, and xylose in the soluble mucilage, and the distal cell walls had decreased arabin

56 We propose that GGM scaffolds control mucilage architecture along with cellulosic rays and sho

57 sociated proteins that are required for seed mucilage architecture.

58 Mucilages are generally polysaccharide-rich and often oc

59 These mucilages are natural and compatible blends of different

60 The sensory analysis showed that most mucilages are tasteless.

61 Arabidopsis (Arabidopsis thaliana) seed coat mucilage as a model system to investigate interactions b

62 We are developing seed mucilage as a model to study the biochemical and biologi

63 is work the capacity of Opuntia ficus indica mucilage as a wall agent in the microencapsulation of Es

64 ons confirmed the flocculation action of the mucilage as visible flocs formed and settled to the bott

65 Some Colombian NCS producers employ natural mucilages as clarifiers; but the uncontrolled applicatio

66 racterization and production of 100% natural mucilage-based probiotic edible coatings with enhanced b

67 The shear-thinning behavior of the mucilage-betalain solutions was suitable for spray dryin

68 5 transcription factor mainly regulates seed mucilage biosynthesis and trichome branching, with only

69 ontrol of epidermal cell differentiation and mucilage biosynthesis by the mucilage transcription fact

70 sights into the complex regulation of PA and mucilage biosynthesis in M. truncatula.

71 plants, with myb5 also showing deficiency in mucilage biosynthesis.

72 , as does CESA5, but CESA5 also functions in mucilage biosynthesis.

73 r interface respectively indicating that the mucilage bonded and transported the arsenic to the air-w

74 (RG-I) present in mucilage-modified2 (mum2) mucilage, but not in wild-type mucilage; the retention o

75 Release of an Al-binding mucilage by border cells could play a role in protecting

76 ells detaching from the root) and associated mucilage can accumulate and trap NPs irrespective of par

77 Our results indicate that plant-sourced mucilage can potentially serve as a cost-effective and e

78 at breads and chocolate cakes made with chia mucilage can replace up to 50% of fat without affecting

79 in IQD9 as well as in KLCR1 lead to compact mucilage capsules with aberrant cellulose distribution,

80 g CESA3 show defects consistent with altered mucilage cellulose biosynthesis.

81 n extracting the Colocasia esculenta rhizome mucilage (CEM) using different green extraction methods

82 ores of hornworts (typically referred to as 'mucilage clefts').

83 offers innovative ingredients such as cactus mucilage (CM) and cladode flour (CF) for producing glute

84 Cactus mucilage (CMU) have been widely studied in various appli

85 To specifically engineer mucilage composition and avoid altering other cell types

86 es and the biosynthesis and secretion of the mucilage compounds of the Arabidopsis seed coat.

87 ral pH, removal was dependent on Fe(III) and mucilage concentration and the age of the Fe(III) soluti

88 The composition and structure of mucilage confers its unique properties of expansion, ext

89 The flax mucilage conjugate exhibited thermoplastic and elastic p

90 The flax mucilage conjugate had a water-holding capacity of 87-62

91 The mucilage contains a single heterogeneous polysaccharide

92 ysis of the muci10 mutants demonstrates that mucilage contains highly branched galactoglucomannan (GG

93 Adherent mucilage contains rays composed of cellulose and pectin

94 oil was nanoencapsulated utilizing chia seed mucilage (CSM) as wall material.

95 s and the aggregation behavior of cress seed mucilage (CSM)-beta-lactoglobulin (Blg) complexes were s

96 When compared to NTSF, the addition of plant mucilage decreased the moisture content while increasing

97 and several mucilage proteins are reduced in mucilage-deficient mutant seeds, suggesting that these p

98 he GGM backbone, the structure of cellulose, mucilage density, as well as the adherence of pectin.

99 red by formulating talipot starch with plant mucilage derived from shoeblack leaves, okra, and seeds

100 were prepared with different levels of chia mucilage dried at 50 degrees C or lyophilized as fat, re

101 ntent for both products when added with chia mucilage dried at 50 degrees C.

102 ological sections revealed the prevalence of mucilage ducts within stipes and fronds (absent in Lesso

103 The plant mucilages enhanced the crosslinking of the filmogenic so

104 The mucilage exhibited swelling as well as pseudo plastic be

105 mum5-1 mucilage exhibited very weak adsorption to cellulose.

106 The mucilages exhibited high yields (8.9 to 21.54%), high co

107 Only mucilage extracted at low temperature and precipitated w

108 Protein was detected in the mucilage extracted by each method and is ideal for the e

109 Specifically, we study the aqueous mucilage extracted from flax seeds (Linum usitatissimum)

110 The mucilage extracted from the convection-dried cladodes of

111 , structural and technological properties of mucilages extracted from seven cladodes of cacti native

112 emical, functional and sensory properties of mucilages, extracted from seven Italian flax cultivars,

113 e of this study was to analyze existing taro mucilage extraction techniques for extraction of a pure

114 Five taro mucilage extraction techniques were analyzed which used

115 e to the mucilage that is important for both mucilage extrusion and adherence.

116 tions in CESA5 and CESA3 affect the speed of mucilage extrusion and mucilage adherence.

117 iled around the columella and unwinds during mucilage extrusion to form a linear ray.

118 cuticular wax deposition, aberrant seed coat mucilage extrusion, and delayed secondary cell wall colu

119 ch displays primary wall detachment, reduced mucilage extrusion, and increased mucilage adherence.

120 utant displays altered embryo morphology and mucilage extrusion, both of which are a consequence of d

121 set of rays that radiate from the seed upon mucilage extrusion, serving to anchor the pectic compone

122 ed a coating based on Opuntia cochenillifera mucilage fermented with Lactobacillus gasseri and starch

123 All three seed mucilage films exhibited high moisture retention regardl

124 ic moduli and elongation at break than basil mucilage films.

125 e produced by using guar gum (GG), flax seed mucilage (FM) and polyvinyl alcohol (PVA), supplemented

126 copious amounts of dispensable, pectinaceous mucilage followed by a thick cellulosic secondary cell w

127 explored zein protein conjugation with flax mucilage for packaging material development.

128 e outcomes could support the use of flaxseed mucilages for industrial applications.

129 ial of using cacti as a source of functional mucilages for use in food applications.

130 several genotypes between seed longevity and mucilage formation at the seed surface, suggesting that

131 nection between dormancy, ABA, and a cripple mucilage formation due to a naturally occurring mutation

132 aride matrix may be ancestral to the complex mucilage formed by multicellular members of the Chlamydo

133 hydrocolloids from the anthocyanin-rich seed mucilage fraction of the tamarillo and its carotenoid-ri

134 with reduced overall methylesterification of mucilage fractions and demucilaged seeds.

135 st, soluble sugars were barely detectable in mucilage freshly secreted from glands.

136 Applying mucilage from normal roots or substances with a consiste

137 n associated with a redistribution of pectic mucilage from the inner to the outer layer, in agreement

138 these connections are rapidly broken as the mucilage fully hydrates.

139 ting the importance of this pectin for outer mucilage function.

140 From the results, mucilages functional properties showed good water and oi

141 replacement of 75% of fat, for both types of mucilage, had a significant reduction in fat content of

142 inant constituents of polysaccharides in the mucilage, had little or no inhibitory effect on hormogon

143 In addition, we found that attachment of the mucilage halo to the parent seed following extrusion is

144 A maize aerial root mucilage has been found that harbors nitrogen fixing bac

145 Arabidopsis mucilage has both nonadherent and adherent layers.

146 ouette apparatus, show that the as-extracted mucilage has comparable drag reduction performance under

147 Seed mucilage hydrocolloid was primarily composed of arabinog

148 1% citric acid were used to extract the seed mucilage hydrocolloid while 72% ethanol and 20mM HEPES b

149 The seed mucilage hydrocolloids that were extracted, using either

150 The outer cell layer secretes mucilage in a ring between the plasma membrane and the o

151 ting anthocyanins, root hairs, and seed coat mucilage in addition to trichomes.

152 l the important function of border cells and mucilage in interactions of plants with charged NPs.

153 ner layer, which alters the structure of the mucilage in response to hydration.

154 f anthocyanins, proanthocyanidins (PAs), and mucilage in the seed and the development of trichomes an

155 cellulose as an important component of seed mucilage in various species.

156 The proteins identified in mucilage include those previously identified by genetic

157 cept that the molecular weight of the mutant mucilage increased 63% compared with that of the wild ty

158 e rays of cellulose observed across the seed mucilage inner layer, which alters the structure of the

159 This mucilage is almost exclusively made up of rhamnogalactur

160 ment, cytological evidence suggests that the mucilage is coiled around the columella and unwinds duri

161 ot occurs via an apoplastic pathway, and (c) mucilage is necessary for normal communication between t

162 ed that the emulsifying power of the studied mucilage is primarily caused by the protein content alon

163 This mucilage is primarily formed by arabinogalactans connect

164 h demonstrated that the Cassia uniflora seed mucilage is rich in the polysaccharides residues (B-d-gl

165 This aerial root mucilage is similar to that observed in landraces of mai

166 This mucilage is structured into two domains: an outer diffus

167 Mucilage is synthesized during seed development within m

168 Compositional analyses of the mucilage isolated from the atgatl5-1 mutant demonstrated

169 s in structure were observed between soluble mucilage isolated from wild-type and mutant seeds, excep

170 Al induced a thicker mucilage layer around detached border cells of both cult

171 ultivar Dade border cells produced a thicker mucilage layer in response to 25 microM Al compared with

172 On hydration, seeds release an adherent mucilage layer strongly attached to the seed in addition

173 mpounds produced during removal of the fruit mucilage layer, including esters, higher alcohols, aldeh

174 rs involved in the formation of the adherent mucilage layer.

175 on in the amount of RGI present in the outer mucilage layer; cuaoalpha1 mutants validated its role in

176 Mucilage (M) and soluble protein (SP) extracted from chi

177 s an adhesion role between the extracellular mucilage matrix and the parent cell in seed coat epiderm

178 d encapsulated with maltodextrin and cladode mucilage MD-CM and only with MD.

179 crateriforme as the dominant species in the mucilage microbial communities, thriving in multiple sun

180 o be modulated by GLABRA2 and LEUNIG HOMOLOG/MUCILAGE MODIFIED1, as expression of PMEI6 is reduced in

181 Double-mutant analyses with mutations in MUCILAGE MODIFIED2 and FLYING SAUCER1 that reduce mucila

182 ying beta-galactosidase (BGAL)-encoding gene MUCILAGE-MODIFIED2 (MUM2) and complement the mum2 mutant

183 ns of rhamnogalacturonan-I (RG-I) present in mucilage-modified2 (mum2) mucilage, but not in wild-type

184 due to a naturally occurring mutation in the MUCILAGE-MODIFIED2 gene is proposed, and this is an inte

185 -ABUNDANT2 (TBA2), PEROXIDASE36 (PER36), and MUCILAGE-MODIFIED4 (MUM4), to express the cell wall modi

186 acid, and rhamnose was evidenced, except for mucilage modified5-1 (mum5-1; a mutant showing a redistr

187 ervation techniques with Opuntia (Cactaceae) mucilage (Mu) and with a combination of Mu with chitosan

188 The viscous seed mucilage of flax (Linum usitatissimum) is a mixture of r

189 The seed mucilage of Hyptis suaveolens contains neutral and acidi

190 The seed mucilage of Hyptis suaveolens L. includes acid - and neu

191 ducted a microbiome study of the aerial root mucilage of maize and sorghum and isolated numerous diaz

192 within the middle lamella, and possibly the mucilage of wild-type seed coat epidermal cells, through

193 Nitrogen fixation in sorghum aerial root mucilage offers a promising avenue to reduce reliance on

194 These results suggested that the mucilage or higher sugar content of CP increased the hyg

195 Known as mucilages or exudates, they are secreted by seeds, roots

196 nd that Takakia root-analogs produce lateral mucilage organs that are more complex than generally und

197 ion do not develop rhizoids, slime papillae, mucilage papillae, or gemmae.

198 We explore the application of cactus mucilage, pectic polysaccharide extracts from Opuntia fi

199 mum5-1; a mutant showing a redistribution of mucilage pectin from the inner adherent layer to the out

200 Mucilage, phenethylamines, flavonol glycosides, betalain

201 ell wall synthesis, result in a similar seed mucilage phenotype.

202 anner in which cellulose is deposited in the mucilage pocket are unknown.

203 TBA proteins are secreted to the mucilage pocket during differentiation.

204 alize to the plasma membrane adjacent to the mucilage pocket.

205 n seed coat epidermal cells at the time when mucilage polysaccharides are accumulated.

206 pose that FLY1 regulates the DM of pectin in mucilage, potentially by recycling pectin methylesterase

207 ment biosynthesis and the differentiation of mucilage-producing cells of the seed coat.

208 ion: positively charged NPs induced a higher mucilage production and adsorbed to it, which prevented

209 er research on the regulatory role of ABA in mucilage production and its multiple effects on germinat

210 d and sole role for spermine in facilitating mucilage production by mitigating endoplasmic reticulum

211 ed abortion in the indehiscent programme and mucilage production by the mucilaginous seed coat.

212 s during outer seed coat differentiation and mucilage production in Aethionema arabicum, the Brassica

213 s hair development, tannin accumulation, and mucilage production in Arabidopsis.

214 of the inner testa (or seed coat) layer and mucilage production in specialized cells of the outer te

215 defective anthocyanin production, seed coat mucilage production, and position-dependent root hair sp

216 factors that are known to regulate seed coat mucilage production.

217 naling through membrane lipid metabolism and mucilage production.

218 es identified MUCI10 as a key determinant of mucilage properties.

219 identified by genetic analysis, and several mucilage proteins are reduced in mucilage-deficient muta

220 The most abundant mucilage proteins include a family of proteins named TES

221 Altogether, these results highlight the mucilage proteome as a model for cell walls in general,

222 Therefore, chia mucilage proved to be a new alternative for replacing fa

223 r by using kappa-carrageenan and quince seed mucilage (QSM) hydrogels and red cabbage anthocyanin.

224 A coexpression search for MUCILAGE-RELATED (MUCI) genes identified MUCI10 as a key

225 equence-based strategy, we predicted several MUCILAGE-RELATED (MUCI) genes that encode glycosyltransf

226 coding a putative glycosyltransferase called MUCILAGE-RELATED70 (MUCI70).

227 x in the stk mutant contribute to defects in mucilage release and seed germination under water-stress

228 is thaliana accession Djarly are affected in mucilage release from seed coat epidermal cells.

229 AGE MODIFIED2 and FLYING SAUCER1 that reduce mucilage release through pectin modification suggest tha

230 In pmei6, mucilage release was delayed and outer cell walls of epi

231 We propose that mucilage remains attached to the seed coat through inter

232 r cascade and their downstream cell wall and mucilage remodelling genes.

233 om Opuntia ficus indica (OFI) cladodes after mucilage removal was attempted using the response surfac

234 The results suggest that chia seed mucilage represents a promising alternative to substitut

235 dietary fiber ratio (4.3 and 1.79 seeds and mucilage respectively), fat and ash content.

236 rce of protein (19.52% and 15.81%, seeds and mucilage respectively), insoluble/soluble dietary fiber

237 from 734.5mug/g to 923.9mug/g for seeds and mucilage respectively.

238 n in the regulation of the final size of the mucilage rhamnogalacturonan I.

239 A simplified recipe involved, dried mucilage-rich jute leaves, tomato paste and olive oil, f

240 we have discovered a gene, RUBY PARTICLES IN MUCILAGE (RUBY), encoding a protein that is annotated as

241 r cv. Rosa by-products (epicarp and endocarp mucilage's), in order to evaluate their interest as sour

242 Mucilage sealing around the appressorial pore facilitate

243 -2 cells to differentiate synchronously into mucilage-secreting cells.

244 ria enter Gunnera through transiently active mucilage-secreting glands on stems.

245 ld-up(2), but the molecular underpinnings of mucilage secretion and appressorial adhesion are unknown

246 L ESTERIFIED SEEDS (HMS), is abundant during mucilage secretion, peaking at 7 d postanthesis in both

247 rotein response, thereby critically reducing mucilage secretion.

248 elopment within maternally derived seed coat mucilage secretory cells (MSCs), and is released to surr

249 nally derived seed coat epidermal cells into mucilage secretory cells is a common adaptation in angio

250 er genes involved in cellulose deposition in mucilage secretory cells.

251 ucomannan found in Arabidopsis thaliana seed mucilage significantly modulates cell wall architecture

252 nents has caused a risk of extinction in the mucilage source plants.

253 er cell wall proteomes while also containing mucilage-specific features.

254 ding the structure-function relationships of mucilages such as for the secretions that allow growing

255 ansporter plays a key role defining the seed mucilage sugar composition and that its absence produces

256 esults in a cell containing large amounts of mucilage surrounding and completely outside of a highly

257 As(V) solutions, ferric nitrate, and mucilage suspensions were mixed and left to stand for va

258 tes seed coat epidermal cell defects both in mucilage synthesis and cell adhesion.

259 y expressed in this cell type at the time of mucilage synthesis and localize to the plasma membrane a

260 ntributes to a further mechanism controlling mucilage synthesis.

261 Arabidopsis (Arabidopsis thaliana) seed coat mucilage system to examine cell wall polymer interaction

262 ther plants are surrounded by a pectinaceous mucilage that aids in seed hydration and germination.

263 ity arises from adaptations in extracellular mucilage that allow ice diatoms to adhere to ice, essent

264 the root cap and secrete massive amounts of mucilage that contains polysaccharides and proteoglycans

265 ivorous sundew plants (Drosera spp.) secrete mucilage that hosts microorganisms, but whether this mic

266 mella, providing a distinct structure to the mucilage that is important for both mucilage extrusion a

267 oat epidermal cells produce large amounts of mucilage that is released upon imbibition.

268 English ivy (Hedera helix) exude a yellowish mucilage that promotes the capacity of this plant to cli

269 Based on the absence of starch in extracted mucilage the CWE method was used to optimize spray-dryin

270 ified2 (mum2) mucilage, but not in wild-type mucilage; the retention of branched RG-I in the seed fol

271 res, which adhere to substrata via seed coat mucilage, thereby preventing dispersal (antitelechory).

272 with RGI production only impaired for outer mucilage, this indicates that CuAOalpha1 contributes to

273 o determine the chemical composition of taro mucilage (TM) and explain its emulsification properties

274 to RG-I chains and mediate the adsorption of mucilage to cellulose microfibrils.

275 e modified further in about one-third of the mucilage to form composites with enhanced viscosity.

276 rving to anchor the pectic component of seed mucilage to the seed surface.

277 anchoring the pectic component of seed coat mucilage to the seed surface.

278 tances with a consistency similar to that of mucilage to tips of mutant roots causes these roots to b

279 a publicly available data set of outer seed mucilage traits of over 300 accessions showed little nat

280 erentiation and mucilage biosynthesis by the mucilage transcription factor cascade and their downstre

281 Mucilage treatment improved As removal (over Fe(III)-onl

282 a ficus indica (OFI) cladodes after removing mucilage using the xylanase and cellulase.

283 by minimizing the temperature sensitivity of mucilage viscosity.

284 The mucilage was also explored for its gelling ability.

285 ), and the majority of HG found in wild-type mucilage was in fact derived from outer cell wall fragme

286 Polysaccharide composition of seed mucilage was successfully modified using three seed coat

287 The acidified mucilage was used as an extracting medium for betalains

288 ans to identify the active PMEs in seed coat mucilage, we identified seven PMEs expressed during seed

289 Films from flax and quince mucilage were found to be more thermally stable and mech

290 and -OH (hydroxyl) functional groups of the mucilage were involved in the interaction with the arsen

291 We observed that the prevailing phyla in the mucilage were Pseudomonadota, Bacteroidota, and Bacillot

292 The colloidal suspensions without mucilage were stable for up to 1 week.

293 niques, cold extraction was found to provide mucilage with good emulsion activity and stability, maki

294 the high potential to be used as a source of mucilages with different technological functions that ca

295 s (>=2 MDa) polysaccharides in the extracted mucilage, with an acidic fraction comprising negatively

296 (RG I) is the primary component of adherent mucilage, with homogalacturonan, cellulose, and xylogluc

297 d as a common structural feature for all the mucilages, with some variations depending on the cultiva

298 we summarise knowledge on plant exudates and mucilages within the concept of their functions in micro

299 to modify polysaccharide composition in seed mucilage without obvious negative consequences to the re

300 one-pot method for developing the novel flax mucilage/zein conjugate.