ライフサイエンスコーパス: beta-glucosidase

1 glyceraldehyde-3-phosphate dehydrogenase and beta-glucosidase.

2 obiose, which can be converted to glucose by beta-glucosidase.

3 i = 8.2 nM) of the Thermotoga maritima TmGH1 beta-glucosidase.

4 es was evaluated with beta-galactosidase and beta-glucosidase.

5 ecific and multivalent interaction with acid beta-glucosidase.

6 n was found to be dependent on the bacterial beta-glucosidase.

7 elated with their activation effects on acid beta-glucosidase.

8 ort the identification of the H antigen as a beta-glucosidase.

9 nt activity of the lysosomal hydrolase, acid beta-glucosidase.

10 a for native and denatured broad specificity beta-glucosidase.

11 of the aglycones produced by hydrolysis with beta-glucosidase.

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

13 transcription factors, ABC transporters, and beta-glucosidases.

14 glutamates that play catalytic roles in the beta-glucosidases.

15 ated sequence homology with genes for fungal beta-glucosidases.

16 ajor differences between these two cytosolic beta-glucosidases.

17 including endoglucanases, exoglucanases, and beta-glucosidases.

18 d to interpret the glucose dependence of GH1 beta-glucosidases.

19 n of the beetle myrosinase from other insect beta-glucosidases.

20 d has up to 76% sequence similarity to other beta-glucosidases.

21 ously for other glycoside hydrolase family 3 beta-glucosidases.

22 valently modify the nucleophile of retaining beta-glucosidases.

23 the salvage pathway involving, in part, acid beta-glucosidase 1 (GBA1), which cleaves glucosylceramid

24 the present study, we examined whether acid beta-glucosidase 1 (GBA1), which hydrolyzes glucosylcera

25 e resulting from a defect in the enzyme acid beta-glucosidase 1.

26 Furthermore, only one beta-glucosidase 12 homolog has been characterized so fa

27 d and purified as follows: broad specificity beta-glucosidase 1460-fold and pyridoxine-beta-D-glucosi

28 describe the role of the ER-resident enzyme beta-glucosidase 2 (GBA2) in mice.

29 beta-Glucosidase 2 (GBA2) is a resident enzyme of the en

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

31 beta-glucosidase 2 is an enzyme with similar glucosylcer

32 a in these families within the gene encoding beta-glucosidase 2, GBA2.

33 27) was found to be a selective inhibitor of beta-glucosidase 2, with potency similar to NB-DNJ.

34 ogues were weakly active against rat-derived beta-glucosidase 2.

35 ession of a sulfur deficiency-activated gene beta-glucosidase 28 (BGLU28).

36 sm to that determined at 37 degreesC for the beta-glucosidase (abg) from the mesophilic bacterium, Ag

37 ceramide; the same reaction catalyzed by the beta-glucosidase acid 1 (GBA1) defective in subjects wit

38 of 70.2-380.9 nM in various cancer cells by beta-glucosidase activation inside of the tumor cells, w

39 While BGLC1 (At5g20950; for beta-glucosidase active against xyloglucan 1) is respons

40 says revealed marked differences in secreted beta-glucosidase activities from three H. capsulatum res

41 of these monolignol glucosides would involve beta-glucosidase activities.

42 The response functions were investigated for beta-glucosidase activity and isoflavone contents.

43 mice resulted in cellular decreases of acid beta-glucosidase activity and protein.

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

45 The beta-Glucosidase activity has been constant over time, s

46 beta-Glucosidase activity in 'Hayward' and 'Hort16A' rem

47 rlying Gaucher disease and the regulation of beta-glucosidase activity in general.

48 8.3 and 17 muM, and also inhibited lysosomal beta-glucosidase activity in live cells at low-micromola

49 The beta-glucosidase activity is thus focused at the immedia

50 H. capsulatum culture supernatants revealed beta-glucosidase activity near the predicted mobility of

51 A cell wall-associated beta-glucosidase activity that releases SA from this glu

52 beta-Glucosidase activity was measured using the synthet

53 The beta-glucosidase activity was reduced through soybean sl

54 Fecal beta-glucosidase activity was significantly higher in th

55 Intracellular beta-glucosidase activity was visualized using the fluor

56 and one intracellular beta-glucosidase lacks beta-glucosidase activity, but efficiently induces cellu

57 beta-glucosidase enzymes (Delta3betaG) lacks beta-glucosidase activity, but efficiently induces cellu

58 data indicated that the null genotypes have beta-glucosidase activity, but the enzyme occurs as inso

59 f salicin and d-arabinose, and expression of beta-glucosidase activity, correctly assigned each strai

60 metabolism of isoflavones other than higher beta-glucosidase activity.

61 hich 3-HKG can be used as a general probe of beta-glucosidase activity.

62 of the active site completely abolishes the beta-glucosidase activity.

63 of detergent-independent membrane-associated beta-glucosidase activity; 3) was more variable among mo

64 We have shown that a beta-glucosidase aggregating factor (BGAF) is responsibl

65 ally interacts with a chimeric lectin called beta-glucosidase aggregating factor (BGAF), resulting in

66 omain and is similar to the maize (Zea mays) beta-glucosidase aggregating factor.

67 The specific beta-glucosidase-aggregating activity of BGAF is unequiv

68 We have shown that a beta-glucosidase-aggregating factor (BGAF) is responsibl

69 ble large quaternary complexes mediated by a beta-glucosidase-aggregating factor (BGAF).

70 protein, and BGAF is solely responsible for beta-glucosidase aggregation and insolubility and, thus,

71 neurodegenerative course had two novel acid beta-glucosidase alleles: a complex, maternally derived

72 GE by the endoplasmic reticulum and vacuolar beta-glucosidases allows the rapid formation of free ABA

73 ces cerevisiae) with an IC(50) of 600 nM and beta-glucosidase (almond) with an IC(50) of 20 muM.

74 ted against several glycosidases (alpha- and beta-glucosidase, alpha- and beta-galactosidase, alpha-

75 To promote their release, beta-glucosidase, alpha-arabinosidase, and alpha-rhamnos

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

77 to compare the levels of phenolic compounds, beta-Glucosidase and antioxidant activity during the age

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

79 imental design to optimise the production of beta-glucosidase and convert glycosidic isoflavones in a

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

81 The free beta-glucosidase and immobilised cells containing the en

82 is a 35-kD protein and binds specifically to beta-glucosidase and renders it insoluble during extract

83 based on sequence differences between maize beta-glucosidase and sorghum beta-glucosidase (dhurrinas

84 howed 54 and 48% identities to raucaffricine beta-glucosidase and strictosidine beta-glucosidase, res

85 pe, and it specifically interacts with maize beta-glucosidases and forms large insoluble aggregates.

86 olved in forming a site for binding to maize beta-glucosidases and thus provides a plausible explanat

87 this study was to monitor olive hydrolytic (beta-glucosidase) and oxidative (peroxydase, POX, and po

88 al hydrolysis by a novel mammalian cytosolic beta-glucosidase, and (d) exert a weak antagonistic effe

89 Conduritol B epoxide is an inhibitor of acid beta-glucosidase, and lowers glucosylceramide degradatio

90 ars exhibited specificity for almond-derived beta-glucosidase, and the 1-nonylazetidine 25 inhibited

91 ineered strains express cellulase, xylanase, beta-glucosidase, and xylobiosidase enzymes under contro

92 beta-Glucosidases are enzymes that hydrolyze beta-glycos

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

94 beta-Glucosidases are known to play a role in abiotic st

95 to interact directly with the substrates in beta-glucosidases are not conserved in hydroxyisourate h

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

97 describes novel preparations of immobilized beta-glucosidase as highly stable and active catalysts f

98 The x-ray structure of N370S mutant acid beta-glucosidase at acidic and neutral pH values indicat

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

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

101 gions to BGAF binding, we constructed mutant beta-glucosidases based on sequence differences between

102 orage disorder caused by deficient lysosomal beta-glucosidase (beta-Glu) activity.

103 -glucur) are both produced by E. coli, while beta-glucosidase (beta-gluco) is produced by Enterococcu

104 ase for irreversible inhibition of retaining beta-glucosidases, beta-aziridine ABPs do not.

105 endosperm beta -mannosidase and barley seed beta -glucosidase/ beta -mannosidase BGQ60.

106 The enzyme is a beta-glucosidase/beta-xylosidase that also shows beta-ga

107 mnosperms) against the potential activity of beta-glucosidase (BG), N-acetyl-glucosaminidase (NAG), a

108 To understand the mechanism of the beta-glucosidase-BGAF interaction, we constructed chimer

109 obacco (Nicotiana tabacum) plants expressing beta-glucosidase (Bgl-1) show modified development.

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

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

112 in binding protein, a protease (PepO), and a beta-glucosidase (BglX).

113 in of BGAF is responsible for its lectin and beta-glucosidase binding and aggregating activities.

114 which of the two BGAF domains is involved in beta-glucosidase binding and aggregation.

115 ar-binding site of BGAF is distinct from the beta-glucosidase-binding site.

116 sists primarily of stereochemistry-retaining beta-glucosidases but also contains a subfamily of beta-

117 lucoside hydrolase but not broad specificity beta-glucosidase, but both were inhibited by the mechani

118 rabidopsis thaliana contain large amounts of beta-glucosidases, but the physiological functions of ER

119 sidases, consistent with known inhibition of beta-glucosidases by 6-phosphogluconolactone.

120 dentify both catalytic residues of retaining beta-glucosidases by the combined use of cyclophellitol

121 l glucopyranoside hydrolysis by sweet almond beta-glucosidase can be generated based on 24 time-cours

122 ar enzymes of intact heterotrophic biofilms, beta-glucosidase (carbon-cycling) and l-leucin aminopept

123 in C binding and further enhancement of acid beta-glucosidase catalytic activity.

124 ed it to non-homologous (putative) retaining beta-glucosidases categorized in GH1 and GH116: GBA2, GB

125 Cytosolic beta-glucosidase (CBG) from mammalian liver is known for

126 stine, spleen and kidney contain a cytosolic beta-glucosidase (CBG) that hydrolyses various beta-d-gl

127 which is encoded by an operon with a phospho-beta-glucosidase (CelA) and a cellobiose-specific sugar

128 i has been cloned, and the encoded 6-phospho-beta-glucosidase (cellobiose-6-phosphate [6P] hydrolase;

129 The double dockerin binds to the GH3 beta-glucosidase component of the fungal cellulosome, wh

130 n mutant had increased expression of several beta-glucosidases, consistent with known inhibition of b

131 ization of both enzymes, as a membrane-bound beta-glucosidase could specifically digest soluble xylog

132 AxlA together with beta-glucosidase depolymerized xyloglucan heptasaccharid

133 . Moench) has two isozymes of the cyanogenic beta-glucosidase dhurrinase: dhurrinase-1 (Dhr1) and dhu

134 s between maize beta-glucosidase and sorghum beta-glucosidase (dhurrinase 2, Dhr2), which does not bi

135 nd Gu2, to which BGAF binds, and the sorghum beta-glucosidase (dhurrinase) isozyme Dhr1, to which BGA

136 Plant beta-glucosidases display varying substrate specificitie

137 In certain maize genotypes, called "null," beta-glucosidase does not enter gels and therefore canno

138 In certain maize genotypes (nulls), beta-glucosidase does not enter the gel and therefore ca

139 d utilises the diglycosidase alpha-rhamnosyl-beta-glucosidase (EC 3.2.1.168) to quantitatively hydrol

140 a TP antigen revealed that it functions as a beta-glucosidase (EC 3.2.1.21).

141 ein from the native expression system showed beta-glucosidase enzymatic activity in substrate gels an

142 A loss in lysosomal acid-beta-glucosidase enzyme (GCase) activity due to bialleli

143 concentrations were associated with enhanced beta-glucosidase enzyme activities (V max ) but short-te

144 lasmid pMAD401 displayed increased levels of beta-glucosidase enzyme activity and H protein expressio

145 determine whether H. capsulatum contained a beta-glucosidase enzyme activity and whether this activi

146 nhibitors of glucocerebrosidase (GCase), the beta-glucosidase enzyme deficient in Gaucher disease (GD

147 enzymatic activities, results show that the beta-glucosidase enzyme is the key enzyme responsible fo

148 defense compounds, which are bioactivated by beta-glucosidase enzymes (BGDs).

149 N. crassa mutant carrying deletions of three beta-glucosidase enzymes (Delta3betaG) lacks beta-glucos

150 re, a mutant lacking genes encoding both the beta-glucosidase enzymes and cellodextrin transporters (

151 eletions of two genes encoding extracellular beta-glucosidase enzymes and one intracellular beta-gluc

152 ed considerable homology with members of the beta-glucosidase family of enzymes.

153 cells through the action of an intracellular beta-glucosidase following import by a high-affinity cel

154 The highest production of beta-glucosidase for both strains occurred when adding 1

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

156 hydrolysis of the sugar moiety by intestinal beta-glucosidases for uptake to the peripheral circulati

157 enzyme and the immobilised cells containing beta-glucosidase, for 2h at 40 degrees C, promoted effic

158 es were assayed to catalyze the process, and beta-glucosidase from Aspergillus niger was selected.

159 7 cDNA encodes a protein similar to the BGL4 beta-glucosidase from Brassica napus.

160 e functional characterization of CsBGlu12, a beta-glucosidase from Crocus sativus.

161 An intracellular beta-glucosidase from Debaryomyceshansenii UFV-1 was pro

162 e alignment of the amino acid sequences of P-beta-glucosidase from Escherichia coli and F. mortiferum

163 gous expressed OeGLU, an oleuropein-specific beta-glucosidase from olive (Olea europaea), had enzymat

164 Here, the beta-glucosidase from the hyperthermophilic archaeon Pyr

165 egions were fused to the bglC ORF encoding a beta-glucosidase from the thermophilic bacterium Thermob

166 different Arabidopsis (Arabidopsis thaliana) beta-glucosidases from glycoside hydrolase family 3.

167 Database searches revealed homology with beta-glucosidases from several sources (plant, bacteria,

168 validated the method by using the retaining beta-glucosidase GBA (CAZy glycosylhydrolase family GH30

169 results from the deficient activity of acid beta-glucosidase (GBA).

170 The lysosomal acid beta-glucosidase GBA1 and the non-lysosomal beta-glucosi

171 beta-glucosidase GBA1 and the non-lysosomal beta-glucosidase GBA2 degrade glucosylceramide (GlcCer)

172 a-epoxide (CBE), as well as the nonlysosomal beta-glucosidase (GBA2) inhibitor N-butyldeoxygalactonoj

173 eramidase (GBA), and the cytosolic retaining beta-glucosidase, GBA3.

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

175 Human lysosomal enzymes acid-beta-glucosidase (GCase) and acid-alpha-galactosidase (a

176 , is caused by insufficient activity of acid beta-glucosidase (GCase) and the resultant glucosylceram

177 Inherited deficiency of acid beta-glucosidase (GCase) due to biallelic mutations in t

178 Gaucher disease is caused by defective acid beta-glucosidase (GCase) function.

179 Defective lysosomal acid beta-glucosidase (GCase) in Gaucher disease causes accum

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

181 Acid beta-glucosidase (GCase) is a 497-amino acid, membrane-a

182 ited disease caused by mutations at the acid beta-glucosidase (GCase) locus (GBA).

183 somal sphingolipid degradation pathway, acid beta-glucosidase (GCase) requires saposin C for optimal

184 se is caused by mutations in the enzyme acid beta-glucosidase (GCase), the most common of which is th

185 cosylceramide (GC) cleavage activity by acid beta-glucosidase (GCase).

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

187 tic patients with Gaucher disease (GD) (acid beta-glucosidase [Gcase] deficiency) are treated with in

188 ritance reported for the null alleles at the beta-glucosidase gene is actually for the BGAF protein,

189 es, all resulting from mutations in the acid beta-glucosidase gene.

190 order caused by deficiency in lysosomal acid beta-glucosidase (GlcCerase), the enzyme responsible for

191 The acid beta-glucosidase (glucocerbrosidase (GCase)) binding seq

192 Human cytosolic beta-glucosidase (hCBG) is a xenobiotic-metabolizing enz

193 addition of exogenous noncellulosomal enzyme beta-glucosidase; however, because the cellulosome is ad

194 Screening a library of over 100 beta-glucosidases identified a number of enzymes that ca

195 Here we show that PYK10, the most abundant beta-glucosidase in A. thaliana root ER bodies, hydrolyz

196 acute increases in serum levels of cytosolic beta-glucosidase in animal models of liver injury may re

197 estigated which cell types express cytosolic beta-glucosidase in guinea pig liver, and characterized

198 tes by CCl4 resulted in release of cytosolic beta-glucosidase in parallel with the hepatocyte marker

199 estigate the possible role of a brush border beta-glucosidase in the hydrolysis of PNG, lactase phlor

200 e, and support the hypothesis that cytosolic beta-glucosidase in the liver functions to hydrolyze sma

201 The most abundant beta-glucosidase in the mesophilic fungus Hypocrea jecor

202 Interestingly, expression of individual beta-glucosidases in Escherichia coli K-12 enabled this

203 amin B6 in plants, we detected two cytosolic beta-glucosidases in jejunal mucosa.

204 poxide, a potent inhibitor of lysosomal acid beta-glucosidase, inhibited pyridoxine-beta-D-glucoside

205 propyl" analogue would be a potent retaining beta-glucosidase inhibitor for those enzymes reacting th

206 ophellitol aziridine-both covalent retaining beta-glucosidase inhibitors-we postulated that the corre

207 pectral changes indicated saposin C and acid beta-glucosidase interaction only in the presence of NCP

208 with the recently identified ipecac alkaloid beta-glucosidase Ipeglu1.

209 These data indicate that cytosolic beta-glucosidase is a hepatocyte-specific enzyme, and su

210 Acid beta-glucosidase is a lysosomal membrane protein that cl

211 beta-Glucosidase is an ubiquitous enzyme which has enorm

212 The nasturtium beta-glucosidase is ascribed a role in xyloglucan mobili

213 Southern-blot data suggested that beta-glucosidase is encoded by a small multigene family

214 rufin beta-glucoside revealed that cytosolic beta-glucosidase is expressed in all hepatocytes, with n

215 In the present work Aspergillus niger beta-glucosidase is immobilized within nanoscale polymer

216 A conformational change of acid beta-glucosidase is shown to accompany activity reconsti

217 lpha-galactosidase, and cellobiose-inducible beta-glucosidase is unaffected in the ccpA strain, sugge

218 onicus found that only one of four predicted beta-glucosidases is required in a physiological context

219 The Sorghum bicolor beta-glucosidase isoenzyme Dhr1 has a strict specificity

220 oside), whereas its close homolog, the maize beta-glucosidase isoenzyme Glu1, which shares 72% sequen

221 ave any effect on the binding of BGAF to the beta-glucosidase isozyme 1 (Glu1), and the BGAF-Glu1 com

222 y-1,4-benzoxaxin-3-one), whereas the sorghum beta-glucosidase isozyme Dhr1 (SbDhr1) hydrolyzes exclus

223 -1,4-benzoxazin-3-on e), whereas the sorghum beta-glucosidase isozyme Dhr1 hydrolyzes exclusively its

224 The maize beta-glucosidase isozyme Glu1 (ZmGlu1) hydrolyzes a broa

225 1-T29, E50-N127, and F466-A512) on the maize beta-glucosidase isozyme Glu1 are involved in interactio

226 The maize beta-glucosidase isozyme Glu1 hydrolyzes a broad spectru

227 enzymes by domain swapping between the maize beta-glucosidase isozymes Glu1 and Gu2, to which BGAF bi

228 howed 70% identity with two maize (Zea mays) beta-glucosidase isozymes.

229 r hydrological legacy alters the response of beta-glucosidase kinetics (i.e. type of inhibition) to s

230 ta-glucosidase enzymes and one intracellular beta-glucosidase lacks beta-glucosidase activity, but ef

231 mber of this family ( At3g06510; sfr2 ) is a beta -glucosidase-like gene that belongs to a distinct l

232 an M20b peptidase-like protein, and SLW3, a beta-glucosidase-like protein, in defense and the leaf-s

233 abolite repressor gene, cre-1, in the triple beta-glucosidase mutant resulted in a strain that produc

234 distinct subtypes result from different acid beta-glucosidase mutations encoding enzymes with absent

235 The cytosolic beta-glucosidase of mammalian liver has been implicated

236 dicted protein sequence displays homology to beta-glucosidases of other organisms, but a recombinant

237 Remarkably, some beta-glucosidases of the glycoside hydrolase (GH) 1 fami

238 studies have also suggested that the 120-kDa beta-glucosidase participates in wall modification durin

239 st the insect but can be cleaved by a spruce beta-glucosidase, PgbetaGLU-1, which releases the active

240 tive surfaces with OM inputs had the highest beta-glucosidase, phosphatase, NAGase and cellobiohydrol

241 Plant beta-glucosidases play a crucial role in defense against

242 data support our hypothesis that the 120-kDa beta-glucosidase plays a morphogenetic role in the paras

243 The ability of olive endogenous enzymes beta-glucosidase, polyphenol oxidase (PPO) and peroxidas

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

245 astomic plants as a vehicle for heterologous beta-glucosidase production for the cellulosic ethanol i

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

247 nternal sequences obtained from the purified beta-glucosidase protein, and a motif resembling plant s

248 ucose, and benzaldehyde by the action of the beta-glucosidase prunasin hydrolase (PH) and mandeloniti

249 These studies show that acid beta-glucosidase requires interfaces composed of NCPs, c

250 affricine beta-glucosidase and strictosidine beta-glucosidase, respectively.

251 riodic infusions of macrophage-targeted acid beta-glucosidase reverse hepatosplenomegaly, hematologic

252 celery leaves was resistant to conversion by beta-glucosidase-rich ingredients, but was converted to

253 ther) derivatives are substrates for phospho-beta-glucosidase(s) belonging to Families 1 and 4 of the

254 munoblot analysis performed using maize-anti-beta-glucosidase sera detected two distinct dhurrinases

255 ich was confirmed by 3-fold inhibition using beta-glucosidase specific inhibitor [2,5-dihydroxymethy-

256 In certain maize genotypes (nulls), beta-glucosidase specifically interacts with a chimeric

257 ctivity was visualized using the fluorescent beta-glucosidase substrate, resorufin beta-D-glucoside,

258 a two-component defense system comprising a beta-glucosidase that activates oleuropein into a toxic

259 iscovered was JMB19063, a novel three-domain beta-glucosidase that belongs to the GH3 (glycoside hydr

260 azinoid-specific UDP-glucosyltransferase and beta-glucosidase that catalyze the enzymatic functions r

261 As expected, one was broad specificity beta-glucosidase that hydrolyzed aryl beta-D-glycosides

262 BGAF also precipitates beta-glucosidase that is added exogenously to supernatan

263 we propose to redefine GBA2 activity as the beta-glucosidase that is sensitive to inhibition by N-bu

264 In contrast to the strictosidine beta-glucosidase that stereospecifically hydrolyzes 3 al

265 ,6-beta-glucanase, BT3312, and a periplasmic beta-glucosidase that targets primarily 1,6-beta-glucans

266 ibition by mechanism-based inhibitors of GH1 beta-glucosidases that utilize a double displacement ret

267 Compared with the broad specificity maize beta-glucosidase, this different binding mode explains t

268 el system', the Thermotoga maritima family 1 beta-glucosidase, TmGH1.

269 e nutrients involves the action of 6-phospho-beta-glucosidase to convert them into usable monosacchar

270 The glucoside is hydrolyzed by beta-glucosidase to release the p-nitrophenolate chromop

271 e final enzymatic step uses laminarinase and beta-glucosidase to release the remaining beta-1,3-gluca

272 ide, and shown to be caused by the cytosolic beta-glucosidase using the inhibitors, conduritol beta-e

273 e (gluc78) encoding an antifungal glucan 1,3-beta-glucosidase was cloned from strain P1 of the biocon

274 beta-Glucosidase was covalently immobilised onto spent c

275 the presence of active polyphenoloxidase and beta-glucosidase was determined by HPLC and UV-Visible s

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

277 Cytosolic beta-glucosidase was expressed in hepatocytes and not in

278 Maize (Zea mays L.) beta-glucosidase was extracted from shoots of a wild-typ

279 The most highly induced beta-glucosidase was nuclear localized and preferred fla

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

281 Yeast cells containing the intracellular beta-glucosidase were immobilised in calcium alginate.

282 ubstrate specificity further, eight chimeric beta-glucosidases were constructed by replacing peptide

283 Four MJ-induced beta-glucosidases were expressed as recombinant enzymes

284 ism of substrate specificity further, mutant beta-glucosidases were generated by replacing Phe198, Ph

285 athepsin A (PPCA), neuraminidase (Neu1), and beta-glucosidase, were readily taken up and restored lys

286 rying mutation(s) in GBA, which encodes acid beta-glucosidase, were recruited at the SZMC Gaucher Cli

287 gh homology to several other reported fungal beta-glucosidases which are members of the family 3 glyc

288 this cluster shows high sequence homology to beta-glucosidases, which catalyze the hydrolysis of the

289 GBA1 and GBA2 are both beta-glucosidases, which cleave glucosylceramide (GlcCer

290 s niger is known to secrete large amounts of beta-glucosidases, which have a variety of biotechnologi

291 mino acid, membrane-associated lysosomal exo-beta-glucosidase whose defective activity leads to the G

292 glucose tolerance and stimulation of the GH1 beta-glucosidases will be crucial to improve their appli

293 owed highly specific inhibition of mammalian beta-glucosidase with a marked dependence of the potency

294 resulted in the thermo-stabilization of the beta-glucosidase with an increase in optimum temperature

295 Beta-glucosidase with putative algicidal capability was

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

297 or allergic reactions and antibodies to acid beta-glucosidase within the first 6 months of treatment.

298 g assays indicated that the JRL domain binds beta-glucosidase without causing it to aggregate.

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

300 A combination of AxlA, beta-glucosidase, xyloglucanase, and beta-galactosidase