ライフサイエンスコーパス: glucosidase

1 potent inhibitors of alpha-amylase and alpha-glucosidase.

2 tural inhibitors for alpha-amylase and alpha-glucosidase.

3 chanism-based covalent inhibitor of an alpha-glucosidase.

4 raldehyde-3-phosphate dehydrogenase and beta-glucosidase.

5 .2 nM) of the Thermotoga maritima TmGH1 beta-glucosidase.

6 coincubated with the recombinant human alpha-glucosidase.

7 l) displayed strong inhibition towards alpha-glucosidase.

8 e aglycones produced by hydrolysis with beta-glucosidase.

9 interpret the glucose dependence of GH1 beta-glucosidases.

10 the beetle myrosinase from other insect beta-glucosidases.

11 up to 76% sequence similarity to other beta-glucosidases.

12 for other glycoside hydrolase family 3 beta-glucosidases.

13 tly modify the nucleophile of retaining beta-glucosidases.

14 4.55, as found for most of the fungi of beta-glucosidases.

15 the extensive digestion by the mucosal alpha-glucosidases.

16 s of individual and collective mucosal alpha-glucosidases.

17 ding endoglucanases, exoglucanases, and beta-glucosidases.

18 ulting from a defect in the enzyme acid beta-glucosidase 1.

19 n-degrading extracellular enzymes (beta-1, 4-glucosidase, 1, 4-beta-cellobiosidase, beta-D-xylosidase

20 Furthermore, only one beta-glucosidase 12 homolog has been characterized so far.

21 beta-Glucosidase 2 (GBA2) is an enzyme that cleaves the membr

22 beta-glucosidase 2 is an enzyme with similar glucosylceramida

23 these families within the gene encoding beta-glucosidase 2, GBA2.

24 as found to be a selective inhibitor of beta-glucosidase 2, with potency similar to NB-DNJ.

25 were weakly active against rat-derived beta-glucosidase 2.

26 n of a sulfur deficiency-activated gene beta-glucosidase 28 (BGLU28).

27 Anthocyanin-rich extracts inhibited alpha-glucosidase (37.8%), alpha-amylase (35.6%), dipeptidyl p

28 enzymes with biological significance (alpha-glucosidase, acetylcholinesterase and butyrylcholinester

29 udy was to investigate how the mucosal alpha-glucosidases act with alpha-amylase to digest granular s

30 While BGLC1 (At5g20950; for beta-glucosidase active against xyloglucan 1) is responsible

31 lactate dehydrogenase and lysosomal alpha-d-glucosidase activities was also tested.

32 mbination of alpha-amylase and mucosal alpha-glucosidase activities, were applied to three granular m

33 aluating the lipase, alpha-amylase and alpha-glucosidase activities.

34 erived OC supported elevated phosphatase and glucosidase activities.

35 fluctuations in lysosomal and neutral alpha-glucosidase activities.

36 ese monolignol glucosides would involve beta-glucosidase activities.

37 nhibitory effects on alpha-amylase and alpha-glucosidase activities.

38 -) mice, pharmacological inhibition of alpha-glucosidase activity almost completely abolished residua

39 esponse functions were investigated for beta-glucosidase activity and isoflavone contents.

40 noterpenes inhibited alpha-amylase and alpha-glucosidase activity and stimulated glucose uptake and l

41 al DeltaSPD0247 strain had reduced 6-phospho-glucosidase activity and was attenuated in growth on cel

42 ated changes in glycogen, glucose, and alpha-glucosidase activity are also found in spinal cord tissu

43 A. oryzae IOC 3999/1998 expressed beta-glucosidase activity at 10.7 times higher than M. purpur

44 The beta-Glucosidase activity has been constant over time, showin

45 beta-Glucosidase activity in 'Hayward' and 'Hort16A' remained

46 g Gaucher disease and the regulation of beta-glucosidase activity in general.

47 nd 17 muM, and also inhibited lysosomal beta-glucosidase activity in live cells at low-micromolar con

48 Extracts with IC50 for alpha-glucosidase activity in the 0.010-0.079mgmL(-1) range sh

49 xtracts from certain berries inhibited alpha-glucosidase activity in vitro.

50 od-based assay to measure the level of alpha-glucosidase activity is the optimal initial test for con

51 The beta-glucosidase activity is thus focused at the immediate si

52 beta-Glucosidase activity was measured using the synthetic su

53 The beta-glucosidase activity was reduced through soybean slurry

54 and the potential ability to modulate alpha-glucosidase activity were tested.

55 l four subunits have alpha-1,4-exohydrolytic glucosidase activity, and the SI N-terminal subunit has

56 glucosidase enzymes (Delta3betaG) lacks beta-glucosidase activity, but efficiently induces cellulase

57 ne intracellular beta-glucosidase lacks beta-glucosidase activity, but efficiently induces cellulase

58 We show that alpha-glucosidase activity, i.e. glycogen debranching and/or l

59 um and rye extracts inhibited (p<0.05) alpha-glucosidase activity, whereas barley and sorghum extract

60 30 min to inactivate the undesirable beta-d-glucosidase activity.

61 he active site completely abolishes the beta-glucosidase activity.

62 tergent-independent membrane-associated beta-glucosidase activity; 3) was more variable among mouse t

63 lycosidase activity (GA) by 13.0%, alpha-1,4-glucosidase (AG) by 19.6%, beta-1,4-glucosidase (BG) by

64 vities of the three lysosomal enzymes (alpha-glucosidase (AG), beta-galactosidase (B-GAL) and beta-N-

65 the endoplasmic reticulum and vacuolar beta-glucosidases allows the rapid formation of free ABA in r

66 erevisiae) with an IC(50) of 600 nM and beta-glucosidase (almond) with an IC(50) of 20 muM.

67 toprostanes (PhytoPs) on four enzymes: alpha-glucosidase, alpha-amylase, acetylcholinesterase, and bu

68 To promote their release, beta-glucosidase, alpha-arabinosidase, and alpha-rhamnosidase

69 ted with metabolic syndrome, including alpha-glucosidase, amylase and lipase and exhibited antioxidan

70 ogical relevance of acid maltase (acid alpha-glucosidase, an enzyme that degrades lysosomal glycogen)

71 Here, we purified an A. niger beta-glucosidase (AnBgl1) and conducted its biochemical and b

72 d the inhibitory effect of extracts on alpha-glucosidase and alpha-amylase activities were investigat

73 nols from guarana were able to inhibit alpha-glucosidase and alpha-amylase activities.

74 For this purpose, alpha-glucosidase and alpha-amylase assays were assessed; amon

75 rdolino extracts exhibited the highest alpha-glucosidase and alpha-amylase inhibitory activity with I

76 antioxidant activities, inhibition of alpha-glucosidase and alpha-amylase, inhibition of angiotensin

77 mpare the levels of phenolic compounds, beta-Glucosidase and antioxidant activity during the ageing o

78 as selective competitive inhibitors of beta-glucosidase and are promising candidates as pharmacologi

79 al design to optimise the production of beta-glucosidase and convert glycosidic isoflavones in aglyco

80 green olives is due to the activity of beta-glucosidase and esterase during the first months of stor

81 e and comparable and lower activity on alpha-glucosidase and hyaluronidase, respectively.

82 The free beta-glucosidase and immobilised cells containing the enzyme

83 e highest inhibition of alpha-amylase, alpha-glucosidase and lipase (IC50: 0.38mg/mL, 0.87mug/mL and

84 L-cholesterol peroxidation, as well as alpha-glucosidase and lipase activities were demonstrated, the

85 as well as evaluation of inhibition of alpha-glucosidase and lipase activities.

86 ome-associated enzymes (alpha-amylase, alpha-glucosidase and lipase) was evaluated.

87 s inhibited the enzymes alpha-amylase, alpha-glucosidase and xanthine oxidase.

88 s unexpectedly associated with mucosal alpha-glucosidases and not just alpha-amylase.

89 study was to monitor olive hydrolytic (beta-glucosidase) and oxidative (peroxydase, POX, and polyphe

90 nzyme, enzyme type (cellulase, pectinase, ss-glucosidase), and hydrolysis time (1, 4, 8, 24 h) on the

91 ritol B epoxide is an inhibitor of acid beta-glucosidase, and lowers glucosylceramide degradation.

92 xhibited specificity for almond-derived beta-glucosidase, and the 1-nonylazetidine 25 inhibited alpha

93 beta-Glucosidases are enzymes that hydrolyze beta-glycosidic

94 However, most beta-glucosidases are feedback inhibited by the glucose produ

95 beta-Glucosidases are known to play a role in abiotic stresse

96 tivity profiles on disaccharides, these beta-glucosidases are not functionally equivalent.

97 ribes novel preparations of immobilized beta-glucosidase as highly stable and active catalysts for in

98 , i.e., HPLC-SPE-ttNMR/high-resolution alpha-glucosidase assay.

99 y-2-fluoro-beta-glucosides react with a beta-glucosidase at rates differing by 10(6)-fold, despite th

100 Additionally, the beta-glucosidase BABG that is present in Brassica rapa but ab

101 owed promising results as inhibitor of alpha-glucosidase, being almost 9 times more effective than ac

102 ur) are both produced by E. coli, while beta-glucosidase (beta-gluco) is produced by Enterococcus spp

103 aucher disease is caused by mutations in the glucosidase, beta, acid gene that encodes glucocerebrosi

104 Glucosidase, beta, acid mutations often cause protein mi

105 Case) due to biallelic mutations in the GBA (glucosidase, beta, acid) gene causes the classic manifes

106 or irreversible inhibition of retaining beta-glucosidases, beta-aziridine ABPs do not.

107 The enzyme is a beta-glucosidase/beta-xylosidase that also shows beta-galacto

108 lpha-1,4-glucosidase (AG) by 19.6%, beta-1,4-glucosidase (BG) by 11.1%, beta-1,4-xylosidase (BX) by 2

109 erms) against the potential activity of beta-glucosidase (BG), N-acetyl-glucosaminidase (NAG), and pe

110 d, we designed a chimeric cohesin-fused beta-glucosidase (BglA-CohII) that binds directly to the cell

111 his study, we characterized a 6-phospho-beta-glucosidase (BglA3) encoded by SPD_0247.

112 High-resolution alpha-glucosidase biochromatograms of these extracts allowed f

113 primarily of stereochemistry-retaining beta-glucosidases but also contains a subfamily of beta-N-ace

114 opsis thaliana contain large amounts of beta-glucosidases, but the physiological functions of ER bodi

115 toggling of activities of the mucosal alpha-glucosidases by selective enzyme inhibition.

116 fy both catalytic residues of retaining beta-glucosidases by the combined use of cyclophellitol beta-

117 copyranoside hydrolysis by sweet almond beta-glucosidase can be generated based on 24 time-courses ta

118 Thus, mucosal alpha-glucosidases can have a synergistic effect with alpha-am

119 zymes of intact heterotrophic biofilms, beta-glucosidase (carbon-cycling) and l-leucin aminopeptidase

120 to non-homologous (putative) retaining beta-glucosidases categorized in GH1 and GH116: GBA2, GBA3, a

121 on of both enzymes, as a membrane-bound beta-glucosidase could specifically digest soluble xyloglucan

122 D) is a metabolic myopathy due to acid alpha-glucosidase deficiency and characterized by extensive gl

123 iated uptake of recombinant human acid-alpha-glucosidase during ERT in mice with Pompe disease follow

124 lises the diglycosidase alpha-rhamnosyl-beta-glucosidase (EC 3.2.1.168) to quantitatively hydrolyse h

125 ntrations were associated with enhanced beta-glucosidase enzyme activities (V max ) but short-term dr

126 showed more than 80% inhibition of the alpha-glucosidase enzyme at a concentration of 40mg/mL (dry sa

127 tors of glucocerebrosidase (GCase), the beta-glucosidase enzyme deficient in Gaucher disease (GD).

128 matic activities, results show that the beta-glucosidase enzyme is the key enzyme responsible for the

129 se compounds, which are bioactivated by beta-glucosidase enzymes (BGDs).

130 assa mutant carrying deletions of three beta-glucosidase enzymes (Delta3betaG) lacks beta-glucosidase

131 mutant lacking genes encoding both the beta-glucosidase enzymes and cellodextrin transporters (Delta

132 ons of two genes encoding extracellular beta-glucosidase enzymes and one intracellular beta-glucosida

133 -4B is an iminosugar that inhibits the alpha-glucosidase family of enzymes and subsequently the foldi

134 The highest production of beta-glucosidase for both strains occurred when adding 10 mL

135 Finally, Bgl3D is the crucial beta-glucosidase for XyG utilization.

136 que and shared roles of the individual alpha-glucosidases for alpha-glucans persisting after starch i

137 me and the immobilised cells containing beta-glucosidase, for 2h at 40 degrees C, promoted efficient

138 most potent (IC50: 0.25mug/mL) against alpha-glucosidase; Fraction IV from black turtle bean was the

139 re assayed to catalyze the process, and beta-glucosidase from Aspergillus niger was selected.

140 to be low micromolar inhibitors of the alpha-glucosidase from baker's yeast with Ki's near to 2 muM.

141 ctional characterization of CsBGlu12, a beta-glucosidase from Crocus sativus.

142 An intracellular beta-glucosidase from Debaryomyceshansenii UFV-1 was produced

143 expressed OeGLU, an oleuropein-specific beta-glucosidase from olive (Olea europaea), had enzymatic ki

144 i-casuarine is a strong inhibitor of alpha-d-glucosidase from rice and of rat intestinal sucrase.

145 n in the active site of the homologous alpha-glucosidase from Sulfolobus solfataricus resulted in a s

146 rent Arabidopsis (Arabidopsis thaliana) beta-glucosidases from glycoside hydrolase family 3.

147 somal glycogen-hydrolyzing enzyme acid alpha-glucosidase (GAA) activity, which results in lysosomal g

148 or gene replacement therapy with acid alpha-glucosidase (GAA) has achieved only partial efficacy in

149 d to and degraded in lysosomes by acid alpha-glucosidase (GAA) in mammals, but it is unclear why and

150 disorder characterized by lack of acid-alpha glucosidase (GAA) resulting in ubiquitous lysosomal glyc

151 to improve lysosomal delivery of acid alpha-glucosidase (GAA), the enzyme deficient in patients with

152 d enzyme replacement therapy with acid alpha-glucosidase (GAA), which has been attributed to ineffici

153 uscles of young-, mid-, and late-stage alpha-glucosidase (GAA)-deficient mice.

154 eficiency of the lysosomal enzyme acid alpha-glucosidase (GAA).

155 dated the method by using the retaining beta-glucosidase GBA (CAZy glycosylhydrolase family GH30) and

156 The lysosomal acid beta-glucosidase GBA1 and the non-lysosomal beta-glucosidase

157 -glucosidase GBA1 and the non-lysosomal beta-glucosidase GBA2 degrade glucosylceramide (GlcCer) to gl

158 xide (CBE), as well as the nonlysosomal beta-glucosidase (GBA2) inhibitor N-butyldeoxygalactonojirimy

159 dase (GBA), and the cytosolic retaining beta-glucosidase, GBA3.

160 Isofagomine (IFG) is an acid beta-glucosidase (GCase) active site inhibitor that acts as a

161 caused by insufficient activity of acid beta-glucosidase (GCase) and the resultant glucosylceramide (

162 Inherited deficiency of acid beta-glucosidase (GCase) due to biallelic mutations in the GB

163 Defective lysosomal acid beta-glucosidase (GCase) in Gaucher disease causes accumulati

164 CBE-N2a) was created by inhibiting acid beta-glucosidase (GCase) in N2a cells with conduritol B epoxi

165 that encodes the lysosomal enzyme acid beta-glucosidase (GCase).

166 The acid beta-glucosidase (glucocerbrosidase (GCase)) binding sequence

167 ion of exogenous noncellulosomal enzyme beta-glucosidase; however, because the cellulosome is adsorbe

168 his pathway in maize smut (Ustilago maydis), glucosidase I (Gls1) and glucosidase II beta-subunit (Ga

169 lacking Erv41-Erv46 function, the ER enzyme glucosidase I (Gls1) was mislocalized and degraded in th

170 Processing alpha-glucosidase I (GluI) is a key member of the eukaryotic N

171 e glucosidase (OsMOGS), an ortholog of alpha-glucosidase I in Arabidopsis, which trims the terminal g

172 nce capacity and effectively inhibited alpha-glucosidase (IC(50): 0.83 mg/ml) and pancreatic lipase (

173 pea showed inhibitory activity against alpha-glucosidase (IC50 6967 +/- 343 and 2885 +/- 85.4 mug/ml,

174 (bran) and 148.23 mug/ml (hulls)] and alpha-glucosidase [IC50, 62.1 mug/ml (bran) and 68.14 mug/ml (

175 Screening a library of over 100 beta-glucosidases identified a number of enzymes that catalyz

176 structures of the main ERQC enzyme, ER alpha-glucosidase II (alpha-GluII; from mouse), alone and in c

177 and genetic approaches, we demonstrate that glucosidase II (GII) mediates glycan trimming of TRPP2.

178 resent in a protein with enzymatic activity, glucosidase II (GII).

179 The non-catalytic beta subunit of glucosidase II (GIIbeta) is encoded by PRKCSH, one of th

180 sylation of N-glycans, and oppositely acting glucosidase II (GlucII), and that vIL-6 can promote prot

181 (Ustilago maydis), glucosidase I (Gls1) and glucosidase II beta-subunit (Gas2), are essential for it

182 with a missense mutation in GANAB, encoding glucosidase II subunit alpha (GIIalpha).

183 unctions as the noncatalytic beta subunit of Glucosidase II, an endoplasmic reticulum (ER)-resident e

184 e we show that PYK10, the most abundant beta-glucosidase in A. thaliana root ER bodies, hydrolyzes in

185 edly enhanced expression of human acid-alpha-glucosidase in nonhuman primates.

186 The most abundant beta-glucosidase in the mesophilic fungus Hypocrea jecorina i

187 Interestingly, expression of individual beta-glucosidases in Escherichia coli K-12 enabled this non-c

188 lpha-Amylase combined with the mucosal alpha-glucosidases in the intestinal extract showed higher glu

189 reatic alpha-amylases and four mucosal alpha-glucosidases, including N- and C-terminal subunits of bo

190 range of dietary NSP intake, although alpha-glucosidase increased on a resistant starch-enriched die

191 However, no alpha-glucosidase inhibition activity was observed under the c

192 alpha-Glucosidase inhibition activity, cell viability and ther

193 his study was to evaluate the in vitro alpha-glucosidase inhibition and antioxidant activity of hexan

194 his study was to evaluate the in vitro alpha-glucosidase inhibition and antioxidant activity of hexan

195 In in vitro alpha-glucosidase inhibition and antioxidant activity, the met

196 al platform based on a high-resolution alpha-glucosidase inhibition assay in combination with hyphena

197 variate data analysis, high-resolution alpha-glucosidase inhibition assays and HPLC-HRMS-SPE-NMR with

198 xtract of H. biflora (HBMe) showed 50% alpha-glucosidase inhibition at the concentration of 480.20 +/

199 ore investigated using high-resolution alpha-glucosidase inhibition profiling combined with high-perf

200 30-50% alpha-glucosidase inhibition was observed in ultrasound, Flavo

201 Therefore, the combination of alpha-glucosidase inhibition with its antiradical capacity ope

202 anticancer activity, alpha-amylase and alpha-glucosidase inhibition, angiotensin-converting-enzyme (A

203 nificant potential to use as a natural alpha-glucosidase inhibition, antioxidant agent.

204 for pinpointing HPLC peaks displaying alpha-glucosidase inhibition.

205 ter fraction (WF) of ME was a stronger alpha-glucosidase inhibitor (EC50 2.9 mug/mL) than quercetin,

206 SMD, 0.33 [95% CI, 0.13 to 0.52]), and alpha-glucosidase inhibitor (SMD, 0.35 [95% CI, 0.12 to 0.58])

207 The effect of the alpha-glucosidase inhibitor acarbose on cardiovascular outcome

208 l" analogue would be a potent retaining beta-glucosidase inhibitor for those enzymes reacting through

209 tive synthesis of nectrisine, a potent alpha-glucosidase inhibitor, was carried out starting from but

210 WF was a competitive alpha-glucosidase inhibitor.

211 increased amount of quercetin, a known alpha-glucosidase inhibitor.

212 Alpha-glucosidase inhibitors play a potential role in the trea

213 phenolic sub-classes were more potent alpha-glucosidase inhibitors than the clinical drug, acarbose

214 Iminosugars, which are glucosidase inhibitors, can interfere with the initial s

215 litol aziridine-both covalent retaining beta-glucosidase inhibitors-we postulated that the correspond

216 es revealed to be potent and selective alpha-glucosidase inhibitors.

217 ural source of potent antioxidants and alpha-glucosidase inhibitors.

218 cient method for the identification of alpha-glucosidase inhibitors.

219 The alpha-glucosidase inhibitory activities of the VJ and FVJ were

220 lues following fermentation, while the alpha-glucosidase inhibitory activities ranged from 95.2 to 19

221 ima were evaluated for antiradical and alpha-glucosidase inhibitory activities.

222 tes were evaluated for antioxidant and alpha-glucosidase inhibitory activities.

223 X2C gave a subfraction, with enhanced alpha-glucosidase inhibitory activity (IC50=6.15mug/mL), with

224 -bioassay/HPLC-HRMS-SPE-NMR showed the alpha-glucosidase inhibitory activity of A. nodosum, F. vesocu

225 The antioxidant capacity and the alpha-glucosidase inhibitory activity of the duodenal extract

226 oside-A showed concentration-dependent alpha-glucosidase inhibitory activity with IC50=35.01 mug/ml.

227 identification of three analytes with alpha-glucosidase inhibitory activity, and subsequent HPLC-HRM

228 Samples showing more than 60% alpha-glucosidase inhibitory activity, at a concentration of 1

229 H), polyphenol content (GAE) and yeast alpha-glucosidase inhibitory activity.

230 ere screened for their antioxidant and alpha-glucosidase inhibitory activity.

231 acts of seaweeds for alpha-amylase and alpha-glucosidase inhibitory effects.

232 d stronger antioxidant activity and an alpha-glucosidase inhibitory property than positive controls.

233 lemon myrtle fractions had pronounced alpha-glucosidase-inhibitory activities (IC(50): 0.30 and 0.13

234 beta-Glucosidase is an ubiquitous enzyme which has enormous b

235 In the present work Aspergillus niger beta-glucosidase is immobilized within nanoscale polymeric ma

236 Inhibition of alpha-amylase and/or alpha-glucosidases is a strategy for treatment of type 2 diabe

237 s found that only one of four predicted beta-glucosidases is required in a physiological context.

238 rological legacy alters the response of beta-glucosidase kinetics (i.e. type of inhibition) to short-

239 ucosidase enzymes and one intracellular beta-glucosidase lacks beta-glucosidase activity, but efficie

240 nces glucose generation at the mucosal alpha-glucosidase level.

241 l-NBDNJ is able to enhance lysosomal alpha-glucosidase levels in Pompe disease fibroblasts, either

242 lic syndrome, including alpha-amylase, alpha-glucosidase, lipase and hydroxyl methyl glutaryl CoA red

243 compounds did not affect inhibition of alpha-glucosidase (maltase) activity, which remained relativel

244 n hydrolyzed to glucose by the mucosal alpha-glucosidases, maltase-glucoamylase (MGAM) and sucrase-is

245 and biallelic MOGS (mannosyl-oligosaccharide glucosidase) mutations (GenBank: NM_006302.2; c.[65C>A;

246 l synthase 2, 12-oxophytodienoate reductase, glucosidase, MYB transcription factor, and alcohol dehyd

247 Remarkably, some beta-glucosidases of the glycoside hydrolase (GH) 1 family ar

248 at coded a putative mannosyl-oligosaccharide glucosidase (OsMOGS), an ortholog of alpha-glucosidase I

249 ties and inhibitory activities against alpha-glucosidase, pancreatic lipase and angiotensin I-convert

250 ct and its inhibiting activity against alpha-glucosidase, pancreatic lipase and hyaluronidase were de

251 e insect but can be cleaved by a spruce beta-glucosidase, PgbetaGLU-1, which releases the active agly

252 surfaces with OM inputs had the highest beta-glucosidase, phosphatase, NAGase and cellobiohydrolase a

253 The ability of olive endogenous enzymes beta-glucosidase, polyphenol oxidase (PPO) and peroxidase (PO

254 These differences could be due to beta-glucosidase, POX and PPO activities changes during olive

255 Inhibition of acid beta-glucosidase promoted faster axonal elongation in an in v

256 Only the mucosal alpha-glucosidases provide the final hydrolytic activities to

257 , and benzaldehyde by the action of the beta-glucosidase prunasin hydrolase (PH) and mandelonitirile

258 -bound drug for recombinant human alpha acid glucosidase (rhGAA) in plasma from patients suffering fr

259 y leaves was resistant to conversion by beta-glucosidase-rich ingredients, but was converted to apige

260 and the 1-nonylazetidine 25 inhibited alpha-glucosidase (Saccharomyces cerevisiae) with an IC(50) of

261 All four alpha-glucosidases share digestion of linear regions of alpha-

262 A glucosidase side-activity, present in the crude sulphata

263 The IC(50) values show that the four alpha-glucosidase subunits could be differentially inhibited.

264 Glucosidase targets for therapy include viral envelope g

265 perior inhibition of alpha-amylase and alpha-glucosidase than foxtail millet cultivars.

266 o-component defense system comprising a beta-glucosidase that activates oleuropein into a toxic gluta

267 ered was JMB19063, a novel three-domain beta-glucosidase that belongs to the GH3 (glycoside hydrolase

268 ) is an intestinal membrane-associated alpha-glucosidase that breaks down di- and oligosaccharides to

269 ropose to redefine GBA2 activity as the beta-glucosidase that is sensitive to inhibition by N-butylde

270 ta-glucanase, BT3312, and a periplasmic beta-glucosidase that targets primarily 1,6-beta-glucans.

271 on by mechanism-based inhibitors of GH1 beta-glucosidases that utilize a double displacement retainin

272 , the gene encoding mannosyl-oligosaccharide glucosidase (the first enzyme in the processing pathway

273 rients involves the action of 6-phospho-beta-glucosidase to convert them into usable monosaccharaides

274 ing with alpha-amylase and followed by alpha-glucosidase to produce glucose.

275 ion of ICHO and ICOOH derivative pools after glucosidase treatment revealed that, in response to AgNO

276 beta-Glucosidase was covalently immobilised onto spent coffee

277 resence of active polyphenoloxidase and beta-glucosidase was determined by HPLC and UV-Visible spectr

278 activity of pectin methyl esterase and beta-glucosidase was enhanced in ET-treated berry skins, sugg

279 of the samples, only the inhibition of alpha-glucosidase was preserved.

280 e flavour combined with P. purpurogenum beta-glucosidase was studied.

281 tarch by mammalian recombinant mucosal alpha-glucosidases was observed which shows that these enzymes

282 e dehydrogenase activity, but not of alpha-d-glucosidase, was observed.

283 east cells containing the intracellular beta-glucosidase were immobilised in calcium alginate.

284 y properties against alpha-amylase and alpha-glucosidase were investigated.

285 mutation(s) in GBA, which encodes acid beta-glucosidase, were recruited at the SZMC Gaucher Clinic.

286 osomal acid maltase, two major hepatic alpha-glucosidases, were unaltered in L-G6pc(-/-) mice, pharma

287 GBA1 and GBA2 are both beta-glucosidases, which cleave glucosylceramide (GlcCer) to

288 er is known to secrete large amounts of beta-glucosidases, which have a variety of biotechnological a

289 se tolerance and stimulation of the GH1 beta-glucosidases will be crucial to improve their applicatio

290 highly specific inhibition of mammalian beta-glucosidase with a marked dependence of the potency upon

291 lted in the thermo-stabilization of the beta-glucosidase with an increase in optimum temperature and

292 lack currant and rowanberry, inhibited alpha-glucosidase with IC(50) values respectively of 20 and 30

293 were found to be potent inhibitors of alpha-glucosidase with IC50 values of 0.32 and 0.49 mug/ml.

294 found to be potent inhibitors of rice alpha-glucosidase with K(i) and IC(50) values in the nanomolar

295 Beta-glucosidase with putative algicidal capability was ident

296 mary and tertiary structures of two GH1 beta-glucosidases with distinct glucose dependence, some puta

297 ommercial samples were able to inhibit alpha-glucosidase, with EC(50) values lower than that found fo

298 ractions X1C and X2C notably inhibited alpha-glucosidase, with IC50=9.89 and 8.05mug/mL, respectively

299 insoluble substrate only a fraction of beta-glucosidase would be available to the cellulosome.

300 s of volatiles released enzymatically with a glucosidase, (Z)-3-hexenyl beta-D-glucopyranoside and li