ライフサイエンスコーパス: esterase

1 ceptor-destroying sialate-O-acetylesterase ("esterase").

2 on the oligomeric assembly of hemagglutinin-esterase.

3 with no significant change in acetylcholine esterase.

4 ied cells that express a substrate-selective esterase.

5 r hydrolysis reactions catalyzed by a serine esterase.

6 minal domain of calmodulin into an efficient esterase.

7 2 is not a potent inhibitor of acetylcholine esterase.

8 tion affecting the catalytic activity of the esterase.

9 0 cellulase-xylanase and a GH11-CE4 xylanase-esterase.

10 ases, pseudocholine esterase and cholesterol esterase.

11 rough binding the ColQ tail of acetylcholine esterase.

12 of any previously reported de novo designed esterases.

13 as well as controlled deactivation by plasma esterases.

14 esidue peptides that act as Zn(2+)-dependent esterases.

15 of additional not yet characterized lipases/esterases.

16 ggests that o(LA)(8) is a good substrate for esterases.

17 kbiting reaction in vitro, without requiring esterases.

18 o-methacrylates (mono-MAs), are prepared via esterases.

19 for the differences in activities in the two esterases.

20 structure of AF-Est2 with the human carboxyl esterase 1, which has CoA thioesterase activity, reveals

21 main with the typical fold of a carbohydrate esterase 4 and an N-terminal domain unique for this fami

22 e a highly potent inhibitor of acetylcholine esterase (AChE) and unsuitable for development.

23 used to follow the activity of acetylcholine esterase, AChE, and to probe its inhibition.

24 SsE(M28) possesses much lower esterase activities against triglycerides and other este

25 he mutant strain lost most of its lipase and esterase activities and displayed reduced virulence in c

26 In S. invicta, male alates had the highest esterase activities followed by workers then female alat

27 Esterase activities in S. invicta were always significan

28 petitive inhibition of the dehydrogenase and esterase activities of the enzyme.

29 Specific esterase activities were determined each 2 days over a p

30 Esterase activities were measured for workers and male a

31 ered significantly in monooxygenase and beta-esterase activities, but not in Vgsc gene mutation frequ

32 erted into the active species 2c by secreted esterase activities.

33 ae1A and BiFae1B, were functionally assigned esterase activities.

34 eviously observed to have either high or low esterase activity against artificial substrates.

35 esidues are positively correlated with fecal esterase activity and acetate level of human diabetes.

36 a significant reduction (p < 0.05) in mantle esterase activity and MgNACR transcript abundance (p < 0

37 We have validated the esterase activity of 80 selected genes, which belong to

38 Notably, the classical esterase activity of AChE is dispensable for this activi

39 opied the DeltahfsH mutant and abolished the esterase activity of HfsH.

40 , although each showed a higher ferulic acid esterase activity on methyl-ferulate.

41 binding or provide the protease, lipase, or esterase activity required for entry of the virus into a

42 ly higher levels of variation about the mean esterase activity than S. invicta.

43 more invasive S. invicta would have a higher esterase activity than S. richteri.

44 In BCoV, an HE lectin domain promotes esterase activity toward clustered substrates.

45 ver, one strong band (EST = S1; Rm: 27.4) of esterase activity was detected when using homogenates of

46 However, survival measured by esterase activity was higher for C. auris than C. paraps

47 able microorganisms exhibiting intracellular esterase activity were detected on >90% of both NC types

48 s seem to exhibit no significant protease or esterase activity when tested against analogous substrat

49 Optimized conjugate 16 was designed so that esterase activity will liberate 5 and cathepsin K cleava

50 m stems of these species exhibit only a weak esterase activity with caffeoyl shikimate.

51 le, fluorogenic probe was developed to sense esterase activity with single-molecule resolution.

52 are bifunctional enzymes containing a trans-esterase activity, which is responsible for nicking the

53 se/esterases and we demonstrated that it has esterase activity, with preference for short-chain fatty

54 r-coordinating aspartate residue that limits esterase activity.

55 sed to reconstruct a super-resolved image of esterase activity.

56 ls high in esterases over fibroblasts low in esterase activity.

57 proposed biosensor was obtained using 0.5 U esterase activity.

58 ogenic probes have been developed to monitor esterase activity.

59 tein and demonstrated that LipE has a lipase/esterase activity.

60 xhibiting NAD(+)-binding, ALDH activity, and esterase activity.

61 (III) as the basis for a continuous assay of esterase activity.

62 ic microenvironment, which shows significant esterase activity.

63 ters are apparently important markers of LAB esterase activity.

64 ere are many fully characterized acetylxylan esterases (AcXEs); however, the enzymes deacetylating ma

65 A new carboxyl esterase, AF-Est2, from the hyperthermophilic archaeon A

66 activity of GH5 and GH26 mannanases and CE2 esterases against intact plant cell walls.

67 The lipase/esterase also elicited a hypersensitive response in grap

68 The activity of pectin methyl esterase and beta-glucosidase was enhanced in ET-treated

69 , temperature and substrate conditions using esterase and caseinolytic activity assays and time cours

70 ep enzymolysis by 2 esterases, pseudocholine esterase and cholesterol esterase.

71 terplay of the virion-attached hemagglutinin-esterase and fusion glycoproteins.

72 TI, a negative dipstick result for leukocyte esterase and nitrites excludes infection.

73 characterized a novel periplasmic trilactone esterase and suggested a new model of FeEnt acquisition

74 er hydrolysis reaction catalyzed by a serine esterase and, therefore, one no longer can simply assume

75 ester groups are processed by intracellular esterases and accumulate in cells.

76 Nature for activating modern enzymes such as esterases and dehydratases and also for proteins like op

77 ain removal from the different plasticizers (esterases and enzymes involved in the beta-oxidation pat

78 binding pockets of coronavirus hemagglutinin esterases and influenza virus C/D hemagglutinin-esterase

79 tible to the sequential actions of bacterial esterases and sialidases.

80 res similarities with other bacterial lipase/esterases and we demonstrated that it has esterase activ

81 ding an absence of protein, blood, leukocyte esterase, and nitrites.

82 e ester group and thus its susceptibility to esterase, and structural features critical to the lacton

83 ion and activity of the enzyme pectin methyl-esterase, and the chelation of calcium by pectic acids.

84 xylanase, arabinofuranosidase, and feruloyl esterase, and their combinations.

85 EGG pathway profiling predicts that kinases, esterases, and hydrolases may contribute to venom activi

86 rolases, polysaccharide lyases, carbohydrate esterases, and lytic polysaccharide monooxygenases.

87 gests that MHETase evolved from ferulic acid esterases, and two homologous enzymes are shown to exhib

88 have a cognate CBM48 domain and are feruloyl esterases, and wtsFae1A binds arabinoxylan.

89 Esterase- and phosphatase-sensitive H2S2 prodrugs with t

90 O-acetylation, and an O-acetylpeptidoglycan esterase (ape1) for de-O-acetylation.

91 was significantly elevated expression of an esterase, arylacetamide deacetylase (AADAC), in vascular

92 ibition of pancreatic lipase and cholesterol esterase, as well as cholesterol micelle formation and b

93 ses, polysaccharide lyases, and carbohydrate esterases, as well as accessory, redox-active enzymes fo

94 paradigm pimeloyl-ACP methyl ester carboxyl-esterase, BioH.

95 n be restored by the action of porcine liver esterase both in vitro and on the surface of living cell

96 lysis but is a highly reactive substrate for esterases both in vitro and in cellulo, yielding a brigh

97 or their capacities to inhibit acetylcholine esterase but, in contrast to the predictions from dockin

98 The sulfocoumarins were hydrolyzed by the esterase CA activity to 2-hydroxyphenyl-vinylsulfonic ac

99 Unlike coumarins which are hydrolyzed by the esterase CA activity to the corresponding 2-hydroxy-cinn

100 knockdown approach, we identified a specific esterase, carboxylesterase 1, whose function had a clear

101 Esterases catalyze the hydrolysis of esters to form a ca

102 on until entry into a cell, where endogenous esterases catalyze the hydrolysis of the masking groups,

103 tified a mutant G4C/S10C/T172R/G173Q cocaine esterase (CCRQ CocE) with an in vitro duration of action

104 contains a C-terminal family 4 carbohydrate esterase (CE4) catalytic domain, but unlike other MurNAc

105 arrel common to the family four carbohydrate esterases (CE4s) with the canonical motifs circularly pe

106 analysis identified a unique Ent trilactone esterase Cee (Cj1376) in C. jejuni.

107 The esterase Chath_Est1 from the anaerobic risk 1 strain Clo

108 ssay for total cholesterol using cholesterol esterase/cholesterol oxidase coupled with the luminol-H2

109 thrombin inhibitor as a single, macrocyclic esterase-cleavable (acyloxy)alkoxy prodrug.

110 ICS1-AM, designed to permeate cells, undergo esterase cleavage, and allow intracellular calcium level

111 oxil bisphosphonate esters enter cells where esterases convert them to their active acids.

112 ave previously identified caffeoyl shikimate esterase (CSE) as an enzyme in the monolignol biosynthes

113 Caffeoyl shikimate esterase (CSE) was recently shown to play an essential r

114 -5-hydroxylase (F5H), and caffeoyl shikimate esterase (CSE), were targeted by MYB31 or MYB42, but in

115 yl transferase (HCT), and caffeoyl shikimate esterase (CSE).

116 Although CE2 esterases display similar specificities against acetylat

117 The majority of the 4 esterase-DMA combinations undergo the sequential enzyme-

118 three amino acids within a highly conserved esterase domain in putative PMR5 orthologs are necessary

119 inds to a conserved epitope in the vestigial esterase domain of hemagglutinin (HA) and blocks HA-medi

120 Sequence alignments of the esterase domains in BiFae1B with the feruloyl esterase f

121 in the Sia-binding sites of both lectin and esterase domains.

122 y modest architectural changes in lectin and esterase domains; and (iii) a single, inconspicuous Ala-

123 articles are fully degradable in response to esterases due to an embedded ester cross-linker in the p

124 due to the activity of beta-glucosidase and esterase during the first months of storage and then a s

125 apid hydrolysis, catalyzed by intrabacterial esterases (e.g., BioH and YjfP), to generate chloramphen

126 Feruloyl esterases (EC 3.1.1.73), belonging to carbohydrate ester

127 Moreover, esterase efficacy and selectivity on DMA enzymolysis are

128 ame enzyme acting in concert with a putative esterase encoded upstream.

129 Two purified esterases (EstA2 and EstB28) synthesised ethyl butanoate

130 Here, we describe a generalizable esterase-ester pair capable of targeted delivery of smal

131 of glutathione-S-transferase (GST), general esterases (ESTs) and phenol oxidase (PO) decreased in th

132 All of the new VoltageFluors targeted by esterase expression (VF-EXs) report single spikes in cul

133 ses (EC 3.1.1.73), belonging to carbohydrate esterase family 1 (CE1), hydrolyze ester bonds between f

134 GEs belong to the carbohydrate esterase family 15 (CE15), which is in turn part of the

135 , and is the founding member of carbohydrate esterase family CE18.

136 The carbohydrate esterases family 1 (CE1s) is a diverse group of enzymes

137 eliminating enzyme, reveals a deviant acetyl esterase fold.

138 rictions leave unexplored the specificity of esterases for aliphatic esters.

139 sterase domains in BiFae1B with the feruloyl esterase from Clostridium thermocellum suggest that both

140 inetic parameters for catalysis by pig liver esterase from either initial rates or the integration of

141 Here, we show that exposure to an esterase from Mycobacterium smegmatis (Msmeg_1529), hydr

142 O-Acetylpeptidoglycan esterase from Neisseria gonorrhoeae functions to release

143 ion catalyzed by the versatile lipase/sterol esterase from the ascomycete fungus O. piceae.

144 A chlorogenic acid esterase from this basidiomycete was expressed in good y

145 of eight aliphatic polyesters by two fungal esterases (FsC and Rhizopus oryzae lipase) at different

146 Secreted esterases further hydrolyze the adhesive polymer, exposi

147 ed amino acid substitutions in hemagglutinin-esterase fusion (HEF) glycoproteins suggests that antige

148 erases and influenza virus C/D hemagglutinin-esterase fusion glycoproteins.

149 Molecular modeling of the hemagglutinin esterase fusion protein of D/3-13 identified a mutation

150 sites of 43 active SHs encompassing lipases/esterases, GDSL lipases, proteases, Ser carboxypeptidase

151 -HKU14) were identified at the hemagglutinin esterase gene position.

152 hat the recently characterized acetylcholine esterase gene, choE (PA4921), is also regulated by GbdR.

153 n(2+) bimetallo core is an effective mono/di-esterase generalist and that the bimetallo cores were no

154 actors in only 1 h, yielding a collection of esterase genes.

155 even PYP/XES (Pale Yellow Petal/ Xanthophyll esterase) genes were identified in Citrus genomes, but o

156 Glucuronoyl esterases (GEs) catalyze the cleavage of ester linkages

157 Glucuronoyl esterases (GEs) catalyze the cleavage of ester linkages

158 tudy provides evidence that purified O. oeni esterases have the ability to both synthesise and hydrol

159 ycans via spike protein S with hemagglutinin-esterase (HE) acting as a receptor-destroying enzyme.

160 outbreaks have shown that the hemagglutinin-esterase (HE) genes of the viruses fall into two of the

161 It is also unclear whether hemagglutinin-esterase (HE) protein plays a role in viral entry.

162 hCoV-HKU1 encodes a hemagglutinin-esterase (HE) protein that is unique to the group a beta

163 complex of the ISAV F and ISAV hemagglutinin esterase (HE) proteins in an unknown stoichiometry prior

164 Hemagglutinin-esterases (HEs) are bimodular envelope proteins of ortho

165 Hog liver esterase (HLE) hydrolyzed chlorogenic acid lactones (CQA

166 Both purified esterases hydrolysed ethyl butanoate, ethyl hexanoate an

167 fferences were observed and strains with low esterase hydrolysis activity against artificial substrat

168 QALs, FQALs) selectively, while chlorogenate esterase hydrolyzed all chlorogenic acids (CQAs, FQAs) a

169 f alcohol acyl-transferase EEB1 and the acyl esterase IAH1.

170 Exposure to the esterase immediately releases free mycolic acids, while

171 rface and two effectors, glucose oxidase and esterase, immobilized on the Au face.

172 t drug 1 in vivo by alkaline phosphatase and esterase in a stepwise manner, providing higher exposure

173 ly suggested that Cee is the sole trilactone esterase in C. jejuni.

174 etic peptide-derived cGMP hydrolysis by this esterase in diseased heart myocardium.

175 We overexpressed this esterase in human primary VSMCs and VSMCs differentiated

176 sterase is more effective than pseudocholine esterase in maintaining sequential degradation until >90

177 Interestingly, expression of the esterase in normal fibroblasts or endothelial cells had

178 usceptible to enzymatic hydrolysis by plasma esterases in a controllable manner, while their metaboli

179 , and its utility is evident with unpurified esterases in bacterial and human cell lysates.

180 odel are employed to compare the efficacy of esterases in DMA enzymolysis.

181 Detailed characterization of this esterase including elucidation of the crystal structure

182 ts received intravenous recombinant human C1 esterase inhibitor (50 IU/kg; maximum 4200 IU) twice wee

183 cks of hereditary angioedema (HAE) due to C1 esterase inhibitor (C1-INH) deficiency (C1-INH-HAE) incl

184 C1 esterase inhibitor (C1-INH) is a soluble regulator of co

185 To explore whether C1 esterase inhibitor (C1INH), an endogenous inhibitor of t

186 we demonstrate that secreted protease of C1 esterase inhibitor (StcE), a bacterial protease from Esc

187 ngioedema (HAE) in the presence of normal C1 esterase inhibitor activity (FXII-HAE).

188 Hereditary angioedema with normal C1 esterase inhibitor and mutations in the F12 gene (HAE-FX

189 Infusions of plasma-derived C1 esterase inhibitor deter attacks of hereditary angio-oed

190 assess the efficacy of recombinant human C1 esterase inhibitor for prophylaxis of hereditary angio-o

191 urvival implications for individuals with C1-esterase inhibitor functional deficiency.

192 prophylactic effect of recombinant human C1 esterase inhibitor has not been rigorously studied.

193 In general, high-dose C1-esterase inhibitor infusion down-regulated the systemic

194 Simultaneously, C1-esterase inhibitor infusion in sepsis patients was assoc

195 4200 IU) twice weekly, recombinant human C1 esterase inhibitor once weekly and placebo once weekly,

196 ATION: Prophylaxis with recombinant human C1 esterase inhibitor provided clinically relevant reductio

197 n hIL1ra(Ast)(+/+) mice, the cholinergic ACh esterase inhibitor pyridostigmine increases ACh levels a

198 XII-driven coagulation and the ability of C1-esterase inhibitor to bind and inhibit activated FXII we

199 assays using the P450 inhibitor PBO, or the esterase inhibitor TPP resulted in markedly increased mo

200 nificantly reduced with recombinant human C1 esterase inhibitor twice weekly (2.7 attacks [SD 2.4]) a

201 ents given twice-weekly recombinant human C1 esterase inhibitor, 13 (45%) of 29 patients given the on

202 y plasmin, escape from inhibition through C1 esterase inhibitor, and elicit excessive bradykinin form

203 lated to treatment with recombinant human C1 esterase inhibitor, but both resolved without additional

204 rmacokinetic profile of recombinant human C1 esterase inhibitor, our results suggest that efficacy of

205 with methylprednisolone, furosemide, and C1 esterase inhibitor.

206 We hypothesized that application of C1-esterase-inhibitor (C1-INH) in LTX-recipients showing ea

207 C1 esterase-inhibitor (C1INH) deficiency or gain-of-functio

208 unctional proteome analysis using lipase and esterase inhibitors revealed a subset of candidate genes

209 bled eight copies of a C3-symmetric trimeric esterase into a well-defined octahedral protein cage by

210 shown that high expression of a non-specific esterase is critical for the low overall ester content o

211 However, cholesterol esterase is more effective than pseudocholine esterase i

212 falciparum Prodrug Activation and Resistance Esterase) is required for activation of esterified pepst

213 io-3-oxobutyl groups have been introduced as esterase-labile phosphodiester protecting groups that ad

214 determination of infection enzyme leukocyte esterase (LE) in human synovial (joint) fluid and urine.

215 ized and tested as a substrate for leukocyte esterase (LE), an enzyme produced by leukocytes (white b

216 the Xf secretome revealed a putative lipase/esterase (LesA) that was abundantly secreted in bacteria

217 mal UA finding (greater-than-trace leukocyte esterase level, positive nitrite test result, or pyuria)

218 n-regulated genes including juvenile hormone esterase-like protein et al.

219 pv oryzae (a bacterial pathogen) or lipaseA/esterase (LipA; a cell wall-degrading enzyme of X. oryza

220 motif and is encoded by a member of the GDSL esterase/lipase gene family.

221 This study demonstrates that ABH is an esterase/lipase with catalytic Ser-His-Asp triad.

222 e slr2103, with sequence similarity to plant esterase/lipase/thioesterase (ELT) proteins, is essentia

223 ty of catalytic tandem reactions that employ esterases, lipases or alcohol dehydrogenases and gold(I)

224 Prodrugs that release hydrogen sulfide upon esterase-mediated cleavage of an ester group followed by

225 Importantly, we also demonstrate that the esterase-mediated rapid lysis of M. tuberculosis signifi

226 crystal structure of the metal-ion dependent esterase MGS0169 from the amidohydrolase superfamily rev

227 water-soluble p-nitrophenolate catalyzed by esterase-mimic SAE.

228 lity = 85%, chi(2) = 134.04, p < 0.0001) and esterases (mortality = 56%, chi(2) = 47.31, p < 0.0001).

229 circularly permuted family four carbohydrate esterase motifs.

230 Parasites with esterase mutations are resistant to pepstatin esters and

231 g protein 6, also known as neuropathy target esterase (NTE), which is the target of toxic organophosp

232 that LipC is a novel cell surface-associated esterase of M. tuberculosis that is highly immunogenic a

233 The esterases of pimelate moiety synthesis show remarkable g

234 e similarity to the family CE-3 carbohydrate esterases of the CAZy classification system.

235 ophytic fungus Eupenicillium shearii FREI-39 esterase on halloysite, using graphite powder, multi-wal

236 ding reactivity, inhibition of acetylcholine esterase or uncoupling of oxidative phosphorylation.

237 on level of specific enzymes like proteases, esterases or glycosidases is often higher in tumor cells

238 DA-ZP1-TPP is insensitive to intracellular esterases over a 2-h period and is impervious to proton-

239 gene expression in the cancer cells high in esterases over fibroblasts low in esterase activity.

240 t in TraB proteins, but also in erythromycin esterase (Pfam ID: PF05139), DUF399 (domain of unknown f

241 nt parasite mutants, we find that a parasite esterase, PfPARE (P. falciparum Prodrug Activation and R

242 with the surface glycoprotein hemagglutinin esterase phylogeny, were observed between the two lineag

243 Esterases play a crucial role in toxic tolerance of inse

244 (2-ethyl)norleucinate (4) with porcine liver esterase (PLE) immobilized on Sepabeads.

245 an be removed by the action of porcine liver esterase (PLE) to reveal the bright unmodified VoltageFl

246 esterification via decreasing pectin methyl esterase (PME) activity in roots and leaves under unstre

247 The inactivation kinetics of pectin methyl esterase (PME) during the shelf life (4 degrees C-180 da

248 ntially demethyl esterified by pectin methyl esterase (PME) to strengthen or loosen plant cell walls

249 ppressed by a null allele of a pectin methyl esterase (PME3) whose activity normally leads to cross-l

250 gues seem the sole pimeloyl-ACP methyl ester esterase present in the Helicobacter species and their o

251 We recently reported that the secreted esterase produced by serotype M1 GAS (SsE(M1)) reduces n

252 The heterologous overexpression of this esterase proved a remarkable ability to hydrolyse both n

253 r kinetic studies of 2-step enzymolysis by 2 esterases, pseudocholine esterase and cholesterol estera

254 Importantly, ISAV hemagglutinin-esterase receptor engagement does not initiate conformat

255 An esterase-responsive charge-reversal polymer mediates sel

256 hydrophilic polyethylene glycol (PEG) and an esterase-responsive hydrophobic dendron, to prepare and

257 protein resistance to inhibitors of choline esterase (RIC-3).

258 Here we present two carbohydrate esterases, RiCE2 and RiCE17, from the Firmicute Roseburi

259 click chemistry", to develop new fluorogenic esterase sensors.

260 the CovRS-controlled secreted streptococcal esterase (SsE).

261 counts were examined by using chloroacetate esterase staining.

262 eal a conserved epitope in the HA1 vestigial esterase subdomain that is some distance from the recept

263 How the switch in esterase substrate specificity was realized remained unr

264 core of the transition in lectin ligand and esterase substrate specificity; (ii) in consequence, the

265 were seen or if either nitrates or leukocyte esterase testing was positive.

266 ed by a combination of nitrite and leukocyte esterase tests can be used.

267 Nitrite, leukocyte esterase tests, and urine microscopy alone were of poor

268 es were evaluated with nitrite and leukocyte esterase tests, using urine culture and/or dipslide with

269 ble antimalarial; (2) PfPARE is a functional esterase that is capable of activating prodrugs; (3) Mut

270 work has shown that Oenococcus oeni produces esterases that are capable of hydrolysing artificial sub

271 ation loci, including novel, mannan-specific esterases that are critical to its deconstruction.

272 ely, most microorganisms encode carbohydrate esterases that strip readily accessible methyl and acety

273 ilarity to a class of proteins that includes esterases, the heme-binding protein ChaN, and an unchara

274 ast to previously described chlorogenic acid esterases, the reUmChlE was also active towards feruloyl

275 When treated with hog liver esterase, these groups were removed by enzymatic deacyla

276 ed by using flow cytometry and chloroacetate esterase tissue staining.

277 he persulfide prodrug can be activated by an esterase to generate a "hydroxymethyl persulfide" interm

278 ctin (NP) was de-esterified by pectin methyl esterase to produce modified pectins [MP (42, 37, and 33

279 f taurine and D-peptide allows intracellular esterase to trigger intracellular self-assembly of the D

280 a xylan binding CBM reduced the capacity of esterases to deacetylate xylan in tobacco walls.

281 Sacubitril is converted by esterases to LBQ657, which inhibits neprilysin, the enzy

282 rability and efficacy of a novel cholesterol esterase transfer protein (CETP) inhibitor TA-8995 in pa

283 After esterase treatment, micelle-delivered beta-lap-dC3 and -

284 recognition, excellent cellular uptake, and esterase-triggered release.

285 ible hollow cage comprising 20 copies of the esterase trimer, 60 protein subunits in total, with over

286 the crystal structures of ISAV hemagglutinin-esterase unbound and complexed with receptor.

287 of carbofuran pesticide by inhibition of the esterase using square-wave voltammetry (SWV).

288 rgistic combination of xylanase and feruloyl esterase was found to be the most efficient enzymatic tr

289 tyl Neu5Ac by lentiviral transduction of the esterase was lethal to ALL cells in vitro even in the pr

290 HbA1c but no association with acetylcholine esterase was noticed.

291 Cholesterol oxidase and cholesterol esterase were assembled on the surface of graphene by in

292 ALE: Phosphodiesterase 2 is a dual substrate esterase, which has the unique property to be stimulated

293 Phosphodiesterase 2 is a dual substrate esterase, which has the unique property to be stimulated

294 side hydrolases, sulfatases and carbohydrate esterases, which are primarily located on a 0.89-megabas

295 nascent esters are substrates for endogenous esterases, which regenerate native protein.

296 or CB receptors and is deactivated by plasma esterases while the respective acid metabolite is inacti

297 , and (iii) the discovery of a new versatile esterase with a high biotechnological potential.

298 itive hits, Est WY was identified as a novel esterase with high catalytic efficiency and distinct evo

299 It has been demonstrated to be a serine esterase with sequence similarity to the family CE-3 car

300 egrating cholesterol oxidase and cholesterol esterase with the hybrid material.