ライフサイエンスコーパス: galactoside

1 of the cytoplasmic cavity in the presence of galactoside.

2 the chromogenic substrate o-nitrophenyl-beta-galactoside.

3 ined on induction with isopropyl thio-beta-D-galactoside.

4 , thiodigalactoside, and m-nitrophenyl-alpha-galactoside.

5 side was rapidly metabolized to peonidin-3-O-galactoside.

6 affinity for melibiose or nitrophenyl-alpha-galactoside.

7 te -1 to enable the binding of various alpha-galactosides.

8 FV was also affected in the presence of beta-galactosides.

9 modification blocks galectin binding to beta-galactosides.

10 ndary carbon sources such as alpha- and beta-galactosides.

11 recognition domain that interacts with beta-galactosides.

12 naling requires binding to cell surface beta-galactosides.

13 ratios despite intense selection on the pure galactosides.

14 ns that are selectively favored on different galactosides.

15 the utilization of raffinose and other alpha-galactosides.

16 hich is induced on exposure to galactose and galactosides.

17 transports sucrose but not lactose or other galactosides.

18 strates dissimilar to either glucuronides or galactosides.

19 ls to catalyze the formation of flavonol 3-O-galactosides.

20 ility of PllA as a probe for detecting alpha-galactosides.

21 anomerization to obtain good yields of alpha-galactosides.

22 yptophan, Wessely-Moser isomers apigenin-6-C-galactoside-8-C-arabinoside & apigenin-6-C-arabinoside-8

23 its three major lipids, acylated cholesteryl galactoside (ACGal), monogalactosyl diacyglycerol (MGalD

24 Furthermore when galactoside affinity is measured as a function of pH, an

25 gands to the B chain to block its binding to galactoside affinity matrixes.

26 Accumulation of galactoside against a concentration gradient does not in

27 ns between a tryptophan residue and the beta-galactoside alpha face are observed.

28 beta-1,3-glucosyltransferase (B3GLCT), beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GAL5), and

29 study we identified high expression of beta-galactoside alpha-2,3-sialyltransferase, ST3GAL6, in MM

30 Our results suggest that the beta-galactoside alpha-2,6-sialyltransferase 1 (ST6Gal-I) sia

31 ether inactivation of the UDP-galactose:beta-galactoside-alpha1-3-galactosyltransferase (alpha1,3GT)

32 Knockdown of beta-galactoside alpha2,6-sialyltransferase (ST6Gal-1) by RNA

33 s to inhibit galectin signaling, namely beta-galactoside alpha2,6-sialyltransferase (ST6Gal-I).

34 ation of the Fc fragment is mediated by beta-galactoside alpha2,6-sialyltransferase 1 (ST6Gal-1), act

35 from overexpression of the Golgi enzyme beta-galactoside:alpha2-6-sialyltransferase (ST6Gal-I).

36 prisingly, however, binding of high-affinity galactoside analogues is severely compromised in the mut

37 Here we show that DDAOG, a conjugate of beta-galactoside and 7-hydroxy-9H-(1,3-dichloro-9,9-dimethyla

38 ns, catalyzes the coupled translocation of a galactoside and a H(+) across the cytoplasmic membrane o

39 The effects of the di-galactoside and alternative glucose extension were also

40 ns, catalyzes the coupled translocation of a galactoside and an H(+) across the Escherichia coli memb

41 lix protein LacY that catalyzes symport of a galactoside and an H(+), was studied.

42 atalyzes coupled stoichiometric symport of a galactoside and an H(+).

43 DH-negative bacteria were impaired for alpha-galactoside and galactose metabolism.

44 n, respectively) together with quercetin-3-O-galactoside and quercetin-3-O-glucoside (15 and 140mugg(

45 and caffeic acids and between quercetin-3-O-galactoside and quercetin-3-O-glucoside.

46 in family defined by their affinity for beta-galactosides and by their conserved carbohydrate recogni

47 chia coli catalyzes coupled translocation of galactosides and H(+) across the cell membrane.

48 However, the minerals, total alpha-galactosides and inositol phosphates contents were reduc

49 ession of Mrt is exclusively up-regulated by galactosides and sucrose.

50 C-arabinoside & apigenin-6-C-arabinoside-8-C-galactoside, and 9,12,13-trihydroxy-trans-10-octadecenoi

51 luteolin 7-O-malonylglucoside, myricetin 3-O-galactoside, and naringenin tri glycoside.

52 noninducing species, orthonitrophenyl-beta-D-galactoside; and (3) transform an inducible switch to on

53 sion strain as a biosensor to determine that galactosides are released from the seeds of several diff

54 way, and could be involved in the sorting of galactoside-bearing glycoconjugates, since it was found

55 ha-L-arabinosides, beta-D-glucosides, beta-D-galactosides, beta-L-xylosides, beta-D-arabinosides), si

56 pK for binding is approximately 10.5); (iii) galactoside binding and dissociation, not microH+, are t

57 imately, these structural changes facilitate galactoside binding and may be involved in the storage o

58 However, galactoside binding by mutants defective in lactose-indu

59 driving forces for alternating access; (iv) galactoside binding involves induced fit, causing transi

60 Because the pK(a) value for galactoside binding is approximately 10.5, protonation o

61 Galectin-9 is a beta-galactoside binding lectin capable of modulating immune

62 Galectin-3 is a beta-galactoside binding lectin that is highly expressed in f

63 en-Friedenreich antigen (T antigen) and beta-galactoside binding lectins (galectins) have been implic

64 s performed with a model ligand on both beta-galactoside binding lectins showed additional interactio

65 G) analogues as recognition elements of beta-galactoside binding lectins.

66 ase (PI3K) and Ras is suppressed by the beta-galactoside binding protein (betaGBP) molecule, a cytoki

67 We report here that beta-galactoside binding protein (betaGBP), an antiproliferat

68 Galectin-3 (Gal-3), a member of the beta-galactoside binding protein family containing the NWGR a

69 ced cellular expression of the secreted beta-galactoside binding protein Galectin 1-like 2 (Drgal1-L2

70 Alterations in the production of the beta-galactoside binding protein galectin-3 and of MUC2 intes

71 The beta-galactoside binding protein galectin-3 modulates the exp

72 Galectin-3 is a beta-galactoside binding protein that has also been associate

73 Galectin-3, a beta-galactoside binding protein, contains a C-terminal carbo

74 Recently, the overexpression of a beta-galactoside binding protein, galectin-3 (LGALS3), has be

75 Galectin-3, a beta-galactoside binding protein, plays a significant role in

76 plasmic loop IV/V and in the vicinity of the galactoside binding site at the interface of helices IV,

77 Galactoside binding strongly modifies kinetic, energetic

78 conformational changes in LacY initiated by galactoside binding were monitored in real time by Trp q

79 teoliposomes and were compared with rates of galactoside binding.

80 e residues have been shown to participate in galactoside binding: Cys148 hydrophobically interacts wi

81 ing 6 of 8 conserved amino acids involved in galactoside-binding activity.

82 Galectin-3 is a member of the beta-galactoside-binding animal lectin family expressed in va

83 Galectin-3 is a member of a beta-galactoside-binding animal lectin family.

84 The beta-galactoside-binding animal lectin galectin-3 is predomin

85 Galectin-7 is a beta-galactoside-binding animal lectin specifically expressed

86 Galectin-3 is a member of a family of beta-galactoside-binding animal lectins expressed abundantly

87 Galectin-3 belongs to a family of beta-galactoside-binding animal lectins expressed in several

88 Galectins are a family of beta-galactoside-binding animal lectins with conserved carboh

89 3 is a member of the galectin family of beta-galactoside-binding animal lectins.

90 in-3 is a member of a growing family of beta-galactoside-binding animal lectins.

91 ative trait locus for the transcript soluble galactoside-binding lectin 9 (LGALS9) that is in linkage

92 Here, we show that a beta-galactoside-binding lectin [galectin-3 (gal3)] that reco

93 Galectin (Gal)-3 is a beta-galactoside-binding lectin and currently intensely studi

94 Galectin-3 (gal-3) is a beta-galactoside-binding lectin expressed in diverse fibrotic

95 Galectin-1 is a galactoside-binding lectin expressed in multiple tissues

96 Galectin-3 (Gal-3) is a member of the beta-galactoside-binding lectin family and plays an important

97 we show that galectin-12, a member of a beta-galactoside-binding lectin family preferentially express

98 Galectin-1 is a member of the conserved beta-galactoside-binding lectin family that binds galactoside

99 acetylglucosamine, a ligand for a ubiquitous galactoside-binding lectin galectin-1.

100 acetylglucosamine, a ligand for a ubiquitous galactoside-binding lectin galectin-1.

101 mune surveillance by overexpressing the beta-galactoside-binding lectin galectin-1.

102 The role played by the beta-galactoside-binding lectin galectin-3 (Gal-3) in airway

103 Several lines of evidence implicate the beta-galactoside-binding lectin galectin-3 in development and

104 e hypothesized that human galectin-3, a beta-galactoside-binding lectin involved in immune regulation

105 es exhibited increased affinity for the beta-galactoside-binding lectin RCA-I in the presence of AZT,

106 Galectin-3 is a soluble ss-galactoside-binding lectin released by activated cardiac

107 Galectin-3 is a beta-galactoside-binding lectin that plays an important role

108 Galectin-3 is a beta-galactoside-binding lectin widely expressed on epithelia

109 show that ablation of galectin-3 (Gal-3), a galactoside-binding lectin, accelerates high-fat diet-in

110 Galectin-3 (GAL3), a beta-galactoside-binding lectin, confers chemoresistance to a

111 Galectin-1, a beta-galactoside-binding lectin, is involved in many physiolo

112 e show that expression of galectin-3, a beta-galactoside-binding lectin, is up-regulated in a mouse m

113 Galectin-1 (Gal-1), a beta-galactoside-binding lectin, plays a profound role in mod

114 -1 (Gal-1), an evolutionarily conserved beta-galactoside-binding lectin, plays essential roles in the

115 rminal sugar, the expression profile of beta-galactoside-binding lectins (galectins) in MDA-MB-435 ce

116 Galectin-1 is a member of a family of beta-galactoside-binding lectins that are soluble adhesion mo

117 Galectins are beta-galactoside-binding lectins that regulate diverse cell b

118 he prototype galectin family, which are beta-galactoside-binding lectins, exhibit subunit-specific al

119 Galectin-3 is a member of the beta-galactoside-binding protein family shown to be involved

120 tin (Gal)-3, a M(r) 31000 member of the beta-galactoside-binding protein family, is a multifunctional

121 Galectin-3 (Gal-3), a member of a beta-galactoside-binding protein family, is involved in RNA p

122 Galectin-7, a member of the beta-galactoside-binding protein family, is primarily express

123 Mammalian beta-galactoside-binding protein Galectin-3 (Gal-3) modulates

124 The beta-galactoside-binding protein galectin-3 has pleiotropic b

125 The galactoside-binding protein galectin-3 is increasingly r

126 The beta-galactoside-binding protein galectin-3 is widely express

127 The beta-galactoside-binding protein galectin-9 is critical in re

128 Galectin-1, a beta-galactoside-binding protein highly expressed in the thym

129 Galectin-3 is a multifunctional beta-galactoside-binding protein implicated in apoptosis, mal

130 Galectin-3 is a beta-galactoside-binding protein implicated in diverse biolog

131 Galectin-3 is a beta-galactoside-binding protein implicated in tumor progress

132 LGALS4, encoding a galactoside-binding protein involved in cell-cell and ce

133 Galectin-3 (Gal-3), a beta-galactoside-binding protein is expressed in a specific c

134 Galectin-3 (Gal-3) is a beta-galactoside-binding protein that is involved in cancer p

135 Galectin-3 is a beta-galactoside-binding protein that is secreted from many c

136 Galectin-1 (Gal-1), a beta-galactoside-binding protein, can alter fate and effector

137 msen-Friedenreich glycoantigen with the beta-galactoside-binding protein, galectin-3.

138 interacting with endothelium-expressed beta-galactoside-binding protein, galectin-3.

139 e Lgals3 gene encodes a multifunctional beta-galactoside-binding protein, galectin-3.

140 Galectin-3, a beta-galactoside-binding protein, has been implicated in a va

141 Galectin-3 (Gal-3), a beta-galactoside-binding protein, has been implicated in a va

142 Galectin-3, a beta-galactoside-binding protein, has been implicated in Wnt

143 an galectin-1 (dGal-1), a small dimeric beta-galactoside-binding protein, induces phosphatidylserine

144 Galectin-3, a beta-galactoside-binding protein, is implicated in cell growt

145 Galectin-1 (Gal-1) is a beta-galactoside-binding protein, the expression of which is

146 Galectin-3 (Gal-3), a pleiotropic beta-galactoside-binding protein, was shown to be involved in

147 ), which directly killed NK cells using beta-galactoside-binding protein.

148 ted C4S, which binds less galectin-3, a beta-galactoside-binding protein.

149 Galectin-3 (gal-3), a member of the beta-galactoside-binding proteins family, was identified as a

150 a member of a growing family of animal beta-galactoside-binding proteins shown to be involved in cel

151 Galectins are a family of beta-galactoside-binding proteins that are widely found among

152 Galectins are a family of mammalian beta-galactoside-binding proteins that positively and negativ

153 er of the galectin family consisting of beta-galactoside-binding proteins with conserved carbohydrate

154 Consistent with their role as galactoside-binding proteins, the interaction with their

155 roteoliposomes reveals dramatic increases in galactoside-binding rates induced by interaction with th

156 A linear dependence of galactoside-binding rates on sugar concentration is obse

157 Tumor-derived galectin-1 (Gal-1), a beta-galactoside-binding S-type lectin, has been shown to enc

158 d were very poor inhibitors of the canonical galactoside-binding site for the tested galectins, with

159 own inhibitors of galectin-3 target its beta-galactoside-binding site in the carbohydrate recognition

160 r inhibition of the evolutionarily conserved galactoside-binding site of galectins has not been demon

161 HUK-921 bind galectin-3 outside of its beta-galactoside-binding site.

162 Two separate galactoside-binding sites have been clearly established

163 The galactoside-binding sites of ricin B chain can be blocke

164 we transferred the Gal-1-KO mutation (lectin galactoside-binding soluble 1(-/-) ) from the B6 strain

165 Lectin galactoside-binding soluble 3 binding protein (LGALS3BP,

166 cking Gal-1-mediated angiogenesis or lectin, galactoside-binding, soluble, 1 deficiency results in a

167 The data further show that beta-galactosides block the interaction between FV and Gal8.

168 del was built for the three considered alpha-galactosides both in the seed and in the soaking water,

169 greatly reduced or no growth on sucrose and galactosides but did not affect growth on monosaccharide

170 ntially incapable of oxidizing galactose and galactosides, but instead efficiently catalyse the oxida

171 in compound, followed by cyanidin-3-xyloside-galactoside (C3XG, 49.56-70.12mg/L).

172 Final alpha-galactoside concentrations were low in all sourdoughs.

173 ntaneous hydrolysis of the 2,4-dinitrophenyl galactosides, confirming earlier studies on the role pla

174 The substrate, a caged D-luciferin-galactoside conjugate, must first be cleaved by beta-gal

175 ns are soluble-type lectins recognizing beta-galactoside containing glycans.

176 alectin family that has an affinity for beta-galactoside containing glycoconjugates.

177 n proteins that show binding to various beta-galactoside-containing glycans.

178 drate-binding protein with affinity for beta-galactoside-containing glycoconjugates, is upregulated u

179 Galectin-8 (Gal8) interacts with beta-galactoside-containing glycoproteins and has recently be

180 basis for PllA's high specificity for alpha-galactoside-containing ligands, and we show that PllA ca

181 Peonidin-3-O-galactoside, cyanidin-3-O-arabinoside, and cyanidin-3-O-

182 ide, delphinidin-3-O-glucoside, cyanidin-3-O-galactoside, cyanidin-3-O-glucoside, cyanidin-3-O-arabin

183 that delphinidin-3-glucoside, delphinidin-3-galactoside, delphinidin-3-arabinoside and petunidin-3-a

184 Delphinidin-3-O-galactoside, delphinidin-3-O-glucoside, cyanidin-3-O-gal

185 of cultured malignant T cells induced a beta-galactoside-dependent inhibition of normal T-cell prolif

186 diate that undergoes alternating access; (v) galactoside dissociates, releasing the energy of binding

187 produced coupled reaction-diffusion of alpha-galactosides during the soaking-cooking process with a g

188 The mutant no longer requires galactoside for IIA(Glc) binding as demonstrated by both

189 nize a wide variety of glycans with terminal galactosides for conferring epithelial cell adhesion.

190 Produced, diffused and degraded alpha-galactoside fractions were identified by performing a ma

191 mutant hardly catalyzes transport, but binds galactosides from either side of the membrane with the s

192 The major anthocyanins mono-galactoside, -glucoside and -arabinoside isomers of delp

193 black carrot pomace with cyanidin-3-xyloside-galactoside-glucoside-ferrulic acid (C3XGGF, 60.85-74.22

194 Galactoside/H(+) symport across the cytoplasmic membrane

195 c membrane protein, catalyzes stoichiometric galactoside/H(+) symport by an alternating access mechan

196 mutants exhibit poor affinity for sugar, and galactoside/H(+) symport is abolished as well.

197 The lactose permease (LacY) catalyzes galactoside/H(+) symport via an alternating access mecha

198 n H(+) across the Escherichia coli membrane (galactoside/H(+) symport).

199 he cytoplasmic membrane of Escherichia coli (galactoside/H(+) symport).

200 perties of the N-terminal domain to initiate galactoside/H(+) symport.

201 Few side chains in the galactoside/H(+) symporter LacY (lactose permease of Esc

202 Delphinidin-3-galactoside has the highest capacity (13.062 +/- 2.729 m

203 -3-O-rhamnogalactoside, rutin, quercetin-3-O-galactoside (hyperoside), quercetin-3-O-glucoside (querc

204 Herein we report that isobutyl-beta-C-galactoside (IBCG) is also a promising inducer of gene e

205 ivers with 5-bromo-4-chloro-3-indolyl beta-d-galactoside in any of the 18 recipient mice analyzed wer

206 y undescribed demonstration of a cholesteryl galactoside in bacteria.

207 concluded that indole-3-acetyl-myo-inositol galactoside in the endosperm supplies about 2 picomoles

208 Gal3 bound to N-linked beta-galactosides in Dsg2 extracellular domain and co-sedimen

209 eriments examining microbial growth on alpha-galactosides in seed wash suggested that alpha-galactosi

210 sulfated carbohydrate ligands as 6-sulfated galactosides in the Ca(2+)-dependent binding site.

211 2) is responsible for the breakdown of alpha-galactosides in the lysosome.

212 evidence that it has high affinity for beta-galactosides in vitro.

213 alectin-3, an animal lectin recognizing beta-galactosides, in regulating dendritic cell motility both

214 ceable residue was mutated individually, and galactoside-induced opening or closing of periplasmic or

215 The addition of isopropyl-beta-D-thio-galactoside (IPTG) destabilizes but does not eliminate t

216 competitive inhibitor isopropyl thio-beta-D-galactoside (IPTG) requires the mutant enzyme to adopt i

217 olecules suggest that the O6 hydroxyl on the galactoside is essential for establishing a water-mediat

218 er exclusion"), and with lactose permease, a galactoside is required for unphosphorylated IIA(Glc) bi

219 rate-binding proteins with affinity for beta-galactosides, is a key modulator of diverse cell functio

220 a special lectin with high affinity to beta-galactosides, is implicated in protection against ischem

221 lthough the P. squamosus lectin binds beta-D-galactosides, it has an extended carbohydrate-combining

222 e to form an alpha 1-3 link with beta-linked galactosides; it is part of a family of homologous retai

223 ricin glycome is enriched with terminal beta-galactosides, known binding partners for a family of mul

224 Indole-3-acetyl-myo-inositol galactoside labeled with 3H in the indole and 14C in the

225 mber of the galectin family of secreted beta-galactoside lectins containing a conserved carbohydrate

226 Thus, beta-galactoside-mediated intravascular heterotypic and homot

227 ack of DLDH results in a deficiency in alpha-galactoside metabolism and galactose transport.

228 resents five copies of m-nitrophenyl-alpha-D-galactoside (MNPG) rather than five copies of beta-D-gal

229 ntal conditions, benzochlorin without a beta-galactoside moiety or the related glucose conjugate did

230 l-04 binds alpha-(1,6)-linked glucosides and galactosides of varying size, linkage, and monosaccharid

231 ed us to visualize the localized presence of galactosides on and around roots in unsterilized soil, a

232 the anomeric group, namely, either an alpha-galactoside or an alpha-glucoside.

233 rene-based glycoclusters functionalized with galactosides or fucosides have been synthesized.

234 g concentrations of either lactulose, methyl-galactoside, or a 72:28 mixture of the two.

235 A member of the LacS subfamily of galactoside-pentose hexuronide translocators was identif

236 de, pelargonidin-3-O-glucoside, peonidin-3-O-galactoside, peonidin-3-O-glucoside, cyanidin-3-O-xylosi

237 olymorphism was preserved had switched their galactoside preference.

238 Galactoside presence in seed wash and sterile root washe

239 tor of a known ECA via affinity for the beta-galactosides present on this receptor.

240 otes efflux and prevents accumulation of the galactoside, probably by converting the proton symporter

241 ilization during competition for mixtures of galactosides produces frequency-dependent selection at l

242 ned in the extracts from quince, quercetin-3-galactoside (Q-Ga), quercetin-3-rutinoside (Q-Ru), querc

243 de, quercetin 3-O-rutinoside, quercetin 3'-O-galactoside, quercetin 3'-O-glucoside, quercetin 3'-O-rh

244 constituents gallic acid, rutin, quercetin-3-galactoside, quercetin-3-glucoside, myricetin, quercetin

245 econdary carbon sources, including the alpha-galactosides raffinose and stachyose.

246 phism is protected only in a narrow range of galactoside ratios despite intense selection on the pure

247 24B11 blocked ricin attachment to galactoside receptors on primary mouse splenocytes and o

248 lectin-binding data indicate a possible beta-galactoside-recognized protein specificity of the galact

249 ncubated with lactose (known to bind to beta-galactoside-recognized proteins) prior to the addition o

250 chloro-9,9-dimethylacridin-2-on-7-yl) beta-D-galactoside, reducing the inhibitor concentration to K(i

251 a 200-800-fold lower catalytic rate on aryl galactosides relative to the WT enzyme.

252 galactoside-binding lectin family that binds galactoside residues on cell surface glycoconjugates.

253 ptations specific to lactulose and to methyl-galactoside, respectively.

254 eferentially recognizes alpha-2,6 sialylated galactosides showed strong binding reactivity with undif

255 ns needed for utilization of alpha- and beta-galactosides, slowed growth on diverse carbon sources, a

256 atterns by 5-bromo-4-chloro-3-indolyl beta-D-galactoside staining and lacZ immunostaining.

257 ch control attachment of a galalpha1-4gal di-galactoside structure (lic2A and lgtC phase-on) or an al

258 n vitro to catalyze the hydrolysis of a beta-galactoside substrate 500 times more efficiently (k(cat)

259 lactose transfer from UDP-Gal to beta-linked galactosides, such as lactose, and in the absence of an

260 67) because neither VGVAPG-like peptides nor galactoside sugars altered adhesion.

261 mino acids that are crucial for binding beta-galactoside sugars.

262 y member, the Drosophila galectin bound beta-galactoside sugars.

263 d respond to the information encoded by beta-galactoside sugars.

264 metastasis via its interactions with various galactoside-terminated glycans.

265 ealed a strict specificity of PllA for alpha-galactoside-terminating glycoconjugates.

266 mbrane; (ii) LacY must be protonated to bind galactoside (the pK for binding is approximately 10.5);

267 We found that di-galactoside, the alternative glucose extension, ChoP, an

268 ng sialic acid to the nonreducing end of the galactosides through a sialyltransferase-catalyzed enzym

269 ctins are a family of lectins that bind beta-galactosides through their conserved carbohydrate recogn

270 bolizable galactose analogue thiomethyl-beta-galactoside (TMG) by a permease-catalyzed sugar:H(+) sym

271 pant with respect to the data for thiomethyl galactoside (TMG).

272 droxyls of sialic acids and C-3 hydroxyls of galactosides to reactive primary alcohols.

273 lacF lacR double mutant (lacF encodes a beta-galactoside transport protein) grown in medium containin

274 assays, revealed that MRT was a sucrose and galactoside transporter.

275 ould be transported by the overproduced beta-galactoside transporters and cause the induction of alph

276 model in which lacR mutants overproduce beta-galactoside transporters, thereby overwhelming the induc

277 ference is also reflected in the alpha-(1,6)-galactoside uptake profile of the bacterium.

278 an efficient route for the synthesis of beta-galactosides using a bacterial beta-4-galactosyltransfer

279 lactosides in seed wash suggested that alpha-galactoside utilization could play an important role in

280 t cause the constitutive expression of alpha-galactoside utilization genes but caused the aberrant ex

281 buted to the constitutive expression of beta-galactoside utilization genes in lacR mutants.

282 ransporters and cause the induction of alpha-galactoside utilization genes in the presence of both su

283 alpha-Mannoside or beta-galactoside was immobilized on a gold disk electrode usi

284 Indole-3-acetyl-myo-inositol galactoside was not transported into either the shoot or

285 a narrow periplasmic opening and an occluded galactoside was obtained, confirming many observations a

286 Among the anthocyanins, cyanidin-3-O-galactoside was rapidly metabolized to peonidin-3-O-gala

287 Specialists on each galactoside were isolated from chemostats that maintaine

288 , cyanidin-3-O-arabinoside, and cyanidin-3-O-galactoside were the predominant anthocyanins characteri

289 Galactosides were present in patches around zones of lat

290 yzes the coupled stoichiometric symport of a galactoside with a cation (either Na(+), Li(+), or H(+))

291 a coli catalyzes stoichiometric symport of a galactoside with an H(+), using a mechanism in which sug

292 found in this study was m-nitrophenyl alpha-galactoside with an IC50 of 0.6 (2) mM in the LT ELISA a

293 cificity, with preferences for glucosides or galactosides with alkyl or aryl substituents.

294 galactose from UDP-galactose to beta-linked galactosides with retention of its alpha configuration.

295 containing 5-bromo-4-chlor-3-indolyl beta-D galactoside (X-gal).

296 r depectinisation, two more ACNs (cyanidin-3-galactoside-xyloside and cyanidin-3-galactoside-xyloside

297 cid as the major ACN, followed by cyanidin-3-galactoside-xyloside-glucoside-coumaric acid, and cyanid

298 Unclarified BCJ contained cyanidin-3-galactoside-xyloside-glucoside-ferulic acid as the major

299 anidin-3-galactoside-xyloside and cyanidin-3-galactoside-xyloside-glucoside-sinapic acid) were also i

300 side-glucoside-coumaric acid, and cyanidin-3-galactoside-xyloside-glucoside.