ライフサイエンスコーパス: beta-glucosidase

1 er inhibiting also butyrylcholinesterase and beta-glucosidase.

2 e, soluble beta-glucosidase and GPI-anchored beta-glucosidase.

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

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

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

6 ecific and multivalent interaction with acid beta-glucosidase.

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

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

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

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

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

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

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

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

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

16 valently modify the nucleophile of retaining beta-glucosidases.

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

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

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

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

21 including endoglucanases, exoglucanases, and beta-glucosidases.

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

23 s to understand the glucose tolerance in GH3 beta-glucosidases.

24 ctosidase (3.42), beta-xylosidase (0.07) and beta-glucosidase (0.28) on low-cost copra meal (CM) in S

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

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

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

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

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

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

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

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

33 beta-glucosidase 2 is an enzyme with similar glucosylcer

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

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

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

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

38 Here, the extremophilic beta-glucosidase A from Halothermothix orenii, (BglA) ha

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

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

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

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

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

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

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

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

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

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

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

50 8.3 and 17 muM, and also inhibited lysosomal beta-glucosidase activity in live cells at low-micromola

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

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

53 We then used HPLC-MS/MS to assess the beta-glucosidase activity of purified enzymes on p-nitro

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

55 The beta-Glucosidase activity was 6 and 14% higher with manu

56 beta-Glucosidase activity was measured using the synthet

57 The beta-glucosidase activity was reduced through soybean sl

58 Fecal beta-glucosidase activity was significantly higher in th

59 Ectomycorrhizal fungal richness and beta-glucosidase activity were strongly reduced by burni

60 CWEC, CWEN, and enzyme activities especially beta-Glucosidase activity were the key determinants of M

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

86 eta-galactosidase, alpha-fucosidase, soluble beta-glucosidase and GPI-anchored beta-glucosidase.

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

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

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

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

91 GH161 genes co-localize with genes encoding beta-glucosidases and ATP-binding cassette transporters,

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

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

94 ta-galactosidase, soluble and membrane-bound beta-glucosidases and two alpha-fucosidases.

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

96 ency in glucocerebrosidase (GBA, a retaining beta-glucosidase), and deficiency in GBA constitutes the

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

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

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

100 beta-Glucosidases are enzymes that hydrolyze beta-glycos

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

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

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

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

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

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

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

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

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

110 In addition, soluble beta-glucosidase BdBGLC1 (Bd1g08550) complemented a gluc

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

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

113 in cell wall metabolism (beta-galactosidase, beta-glucosidase, beta-amylase, chitinase, pectate lyase

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

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

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

117 Four glycosidases, alpha-glucosidase (AG), beta-glucosidase (BG), beta-xylosidase (BX), cellobiohyd

118 nced potential activities of cellulase (CL), beta-glucosidase (BG), lignin peroxidase (LiP), and mang

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

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

121 acterize a family 3 glycosyl hydrolase (GH3) beta-glucosidase (Bgl) produced by Malbranchea pulchella

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

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

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

125 n to be in an operon with a putative phospho-beta-glucosidase (bglB) downstream and a predicted antit

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

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

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

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

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

131 structural basis of glucose tolerance in GH1 beta-glucosidases but also demonstrate a strategy to imp

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

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

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

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

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

137 beta-glucosidases catalyze the hydrolysis beta-1,4, beta

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

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

140 haracterized the corresponding GH1 6-phospho-beta-glucosidase, Cel1A.

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

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

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

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

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

146 AxlA together with beta-glucosidase depolymerized xyloglucan heptasaccharid

147 jCel3A is, thus, preferable as an industrial beta-glucosidase despite its lower activity caused by tr

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

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

150 Plant beta-glucosidases display varying substrate specificitie

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

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

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

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

155 beta-Glucosidases enhance enzymatic biomass conversion b

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

157 ts of the beta-glucoside permease (bglP) and beta-glucosidase enzyme (bglB) in 5448, we showed that b

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

180 tivity of the industrially relevant family 3 beta-glucosidases from Hypocrea jecorina, HjCel3A and Hj

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

198 is caused by mutations in GBA1 encoding acid beta-glucosidase (GCase).

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

200 ons leading to functional deficiency of acid-beta-glucosidase (GCase).

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

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

203 n Enterococcus faecalis, encodes a 6-phospho-beta-glucosidase (GenA) and a phosphotransferase system

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

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

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

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

208 improved the functional properties of a GH1 beta-glucosidase highly expressed by Trichoderma harzian

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

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

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

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

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

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

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

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

217 Addition of 8U of beta-glucosidase into soymilk significantly increased th

218 A range of enzymes, namely beta-glucosidase, invertase, beta-galactosidase, and cat

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

220 beta-Glucosidase is an ubiquitous enzyme which has enorm

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

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

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

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

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

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

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

228 -1,4-benzoxazin-3-on e), whereas the sorghum beta-glucosidase isozyme Dhr1 hydrolyzes exclusively its

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

230 1-T29, E50-N127, and F466-A512) on the maize beta-glucosidase isozyme Glu1 are involved in interactio

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

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

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

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

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

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

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

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

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

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

241 the screen, and the Exg1 gene (coding for a beta-glucosidase) of D. bruxellensis was cloned and puri

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

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

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

245 beta-glucosidases play a critical role among the enzymes

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

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

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

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

250 breakdown of beta-1, 4-glycosidic linkages, beta-glucosidases produce free fermentable glucose and a

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

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

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

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

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

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

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

258 pite this benefit, most characterised fungal beta-glucosidases show weak activity at high glucose con

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

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

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

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

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

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

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

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

267 ,6-beta-glucanase, BT3312, and a periplasmic beta-glucosidase that targets primarily 1,6-beta-glucans

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

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

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

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

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

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

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

275 beta-Glucosidase was covalently immobilised onto spent c

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

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

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

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

299 ts of HjCel3A and other structurally similar beta-glucosidases would have a significant economic effe

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