ライフサイエンスコーパス: mucilage

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

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

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

4 itantly with the outer layer but produces no mucilage.

5 hich are present exclusively in the adherent mucilage.

6 produce the polysaccharide components of the mucilage.

7 demonstrated the interaction between oil and mucilage.

8 e proteins are genuinely associated with the mucilage.

9 rides and is required for production of seed mucilage.

10 ed solubility of the pectic component of the mucilage.

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

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

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

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

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

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

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

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

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

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

21 3 affect the speed of mucilage extrusion and mucilage adherence.

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

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

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

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

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

27 interactions between components in the seed mucilage and cellulose.

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

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

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

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

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

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

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

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

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

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

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

39 The sensory analysis showed that most mucilages are tasteless.

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

41 5 transcription factor mainly regulates seed mucilage biosynthesis and trichome branching, with only

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

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

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

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

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

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

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

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

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

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

52 Adherent mucilage contains rays composed of cellulose and pectin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 Applying mucilage from normal roots or substances with a consiste

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

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

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

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

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

79 Arabidopsis mucilage has both nonadherent and adherent layers.

80 Seed mucilage hydrocolloid was primarily composed of arabinog

81 1% citric acid were used to extract the seed mucilage hydrocolloid while 72% ethanol and 20mM HEPES b

82 The seed mucilage hydrocolloids that were extracted, using either

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

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

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

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

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

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

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

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

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

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

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

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

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

96 Mucilage is synthesized during seed development within m

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 The seed mucilage of Hyptis suaveolens contains neutral and acidi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 naling through membrane lipid metabolism and mucilage production.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 -2 cells to differentiate synchronously into mucilage-secreting cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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