ライフサイエンスコーパス: hydrolysis

1 e remaining in a closed state for the second hydrolysis.

2 leading to a monomer-dimer cycle during GTP hydrolysis.

3 quential hydrolysis yielded higher degree of hydrolysis.

4 spectrometry following controlled enzymatic hydrolysis.

5 s by stimulating ParF adenosine triphosphate hydrolysis.

6 elical domain during different stages of GTP hydrolysis.

7 acid residue functions as a proton donor in hydrolysis.

8 midine hydrolysis and disfavour acetyllysine hydrolysis.

9 onformations, in agreement with the observed hydrolysis.

10 tereocenter, which is resistant to enzymatic hydrolysis.

11 in copper binding and those involved in ATP hydrolysis.

12 s that is tightly coupled to ATP binding and hydrolysis.

13 n targeting to the INM depends on nucleotide hydrolysis.

14 as seen for mammalian microtubules upon GTP hydrolysis.

15 agement, of the catalytic site following ATP hydrolysis.

16 cts were prepared and submitted to an acidic hydrolysis.

17 general base (in contrast to specific base) hydrolysis.

18 ring are perfectly designed for inducing ATP hydrolysis.

19 acids that showed the highest resistance to hydrolysis.

20 by Sec17 and Sec18:ATP without requiring ATP hydrolysis.

21 on is species-specific and requires RecN ATP hydrolysis.

22 he consensus site nucleotide is committed to hydrolysis.

23 local redox reactions between molecules, and hydrolysis.

24 NT), rather than AP, was responsible for ATP hydrolysis.

25 Intriguingly, GSH catalyzes their hydrolysis.

26 rage distances between turns reduce with GTP hydrolysis.

27 Thus, substrate is released prior to ATP hydrolysis.

28 cell membranes with energy derived from ATP hydrolysis.

29 ome of these organelles are degraded through hydrolysis.

30 nc-bound metalloamyloid that catalyzes ester hydrolysis.

31 c attack on PL at the C2-C3 olefin led to PL hydrolysis.

32 ubunit, greatly accelerating the rate of GTP hydrolysis.

33 some of which play important roles in starch hydrolysis.

34 nder gastric conditions caused no further GR hydrolysis.

35 trate binding primes the transporter for ATP hydrolysis.

36 d into macrophages, and catalyzes host lipid hydrolysis.

37 ophilic surface properties are restored upon hydrolysis.

38 n RNA synthesis and as a general base in RNA hydrolysis.

39 g them unavailable for actin binding and ATP hydrolysis.

40 d to be the highest throughout the course of hydrolysis.

41 thermally activated persulfate and alkaline hydrolysis (17 +/- 2 and 13.0 +/- 0.8, respectively) vs

42 Using the energy of ATP hydrolysis, ABC transporters catalyze the trans-membrane

43 their GTP-binding, GDP/GTP-exchange, and GTP-hydrolysis activities, but the extent to which these dif

44 possible single nonsynonymous mutations for hydrolysis activity of an amidase expressed in E. coli w

45 acting protein that selectively inhibits the hydrolysis activity of ATP synthase, which may render th

46 We further demonstrated that the hydrolysis activity of GIMAP6 was not essential for its

47 reover, inhibition of fusion or of lysosomal hydrolysis activity significantly reduced viral replicat

48 were pretreated with 1 g L(-1) urea (14-35% hydrolysis after 2 days).

49 es them unavailable for actin binding or ATP hydrolysis, although a small fraction of the myosin head

50 00 random pools initially seeking amide bond hydrolysis, although they both cleave simple single-stra

51 e iminophosphorane product was stable toward hydrolysis and aza-phosphonium ylide reactions.

52 s of compounds, their catalysis of Si-O bond hydrolysis and condensation was investigated with a rang

53 igations have described the mechanism of ATP hydrolysis and defined the architecture of ABC exporters

54 confer specificity for N(8)-acetylspermidine hydrolysis and disfavour acetyllysine hydrolysis.

55 us to propose rate constant values for some hydrolysis and disproportionation reactions of dichloram

56 omplexation, making Fe species available for hydrolysis and effective coagulation.

57 inhibition of enzymes compared with separate hydrolysis and fermentation (SHF).

58 like process, namely successive dissolution, hydrolysis and fermentation in the same reaction pot.

59 und bacterial Z-rings that is powered by GTP hydrolysis and guides correct septal cell wall synthesis

60 ng peptides suffer from low stability due to hydrolysis and intramolecular side reactions.

61 of retinoschisin on Na/K-ATPase-mediated ATP hydrolysis and ion transport.

62 as mechanistic indicators of release such as hydrolysis and mass loss, was measured by direct analysi

63 reactive oxygen species (ROS) through water hydrolysis and may subsequently damage cellular lipids.

64 The G-domain, which catalyzes GTP hydrolysis and mediates downstream signaling, is 95% con

65 f a transposase dimer is responsible for two hydrolysis and one transesterification reaction at the s

66 dials and oleuropeindials), and to determine hydrolysis and oxidation levels.

67 es and differences were observed in terms of hydrolysis and oxidation.

68 wild-type-like enzyme turnover rate for ATP hydrolysis and rate of cellular K(+) uptake.

69 of the helix and engage the substrate, while hydrolysis and release promotes helix disassembly and su

70 combination with direct manipulation of ATP hydrolysis and release.

71 Pepsin-hydrolysis and sequential hydrolysis by pepsin and tryps

72 ation experiments by taking into account the hydrolysis and synthesis reactions occurring during thes

73 nts and obtaining the rate constants for the hydrolysis and synthesis reactions occurring during thes

74 lB mutant variant, which is deficient in ATP hydrolysis and T4P assembly, supports EPS production wit

75 pt glycosidic bonds via oxidation instead of hydrolysis and to enhance enzymatic digestion of recalci

76 , substrate-assisted activation of water for hydrolysis, and formation of a gem-diol intermediate.

77 g by the neighboring ester group, subsequent hydrolysis, and loss of methanol resulting in the format

78 temperatures, peak viscosity, extent of acid hydrolysis, and resistant starch content were higher in

79 pendent on the p97 adaptor NPLOC4-UFD1L, ATP hydrolysis, and substrate ubiquitination, with branched

80 e of the biocatalysts was tested for lactose hydrolysis, and the enzyme immobilized in SiQT10 and SiQ

81 Phosphoryl transfer and proofreading hydrolysis are controlled in part by a dynamic RNAP comp

82 twork and, furthermore, highlight GPI-anchor hydrolysis as a cell-intrinsic mechanism to alter cell b

83 udy of diphenylmethane deprotection via acid hydrolysis as well as a key lactone to tetrahydropyran c

84 DNA at sites of protein adducts requires ATP hydrolysis at both sites, as does the stimulation of ATM

85 demonstrates that the ultimate fate of DMMP hydrolysis at the Cs8[Nb6O19] catalyst is strong binding

86 Inhibition of 2-AG hydrolysis augments the number of mature oligodendrocyte

87 y generated from dichloroacetonitrile (DCAN) hydrolysis because the concentrations of these two compo

88 drance; Nas6 clashes with the lid in the ATP-hydrolysis-blocked proteasome, but clashes instead with

89 0-tetraols released from human DNA upon acid hydrolysis, BPDE-N(2)-dG adducts have rarely if ever bee

90 sm of condensin depends on the energy of ATP hydrolysis but how this activity specifically promotes p

91 ission reaction is strictly dependent on GTP hydrolysis, but how fission is mediated is still debated

92 thiocyanate (SCN(-)), relies upon microbial hydrolysis, but this process is sensitive to high loadin

93 ity of F. succinogenes OMVs is used to prime hydrolysis by destabilising the tight networks of polysa

94 u-GDP-Pi-Lys-tRNA(Lys) complex following GTP hydrolysis by EF-Tu.

95 n either phosphoryl transfer or proofreading hydrolysis by Escherichia coli RNAP.

96 Ester hydrolysis by extracellular carboxylesterases is conside

97 These allosteric effects thus reduce ATP hydrolysis by inactive proteasomes and nonspecific prote

98 m transport through KdpA is coupled with ATP hydrolysis by KdpB remains poorly understood.

99 and bound to ATP until ORC-Cdc6 triggers ATP hydrolysis by MCM, promoting both Cdt1 ejection and MCM

100 Rapid GTP hydrolysis by monomeric Cdc10 drives assembly of the cor

101 e gained insights into the mechanism of acyl hydrolysis by observing differing arrangements of PEG an

102 Pepsin-hydrolysis and sequential hydrolysis by pepsin and trypsin hydrolyzed all heavy mo

103 bound RecA protein increases the rate of ATP hydrolysis catalysed by RecN during the DNA pairing reac

104 , but clashes instead with the CP in the ATP-hydrolysis-competent proteasome.

105 speciation models attributed this to Pu(IV) hydrolysis competing with ligand complexation, increasin

106 rotein hydrolysates generated under the same hydrolysis conditions differ.

107 h GEF-mediated exchange and GAP-mediated GTP hydrolysis, consistent with NMR-detected structural pert

108 Our findings explain how GTP hydrolysis controls septin assembly, and uncover mechani

109 igh yield of CO2 (>98%), suggesting that CGA hydrolysis could be the rate limiting step for CO2 forma

110 Consequently, hydrolysis could occur during food processing and during

111 of Tpm1.12 extends the time required per ATP hydrolysis cycle 3.7-fold, whereas it is shortened by 27

112 reveals two mechanical substates of the ATP hydrolysis cycle of the superfamily 2 helicase Hel308 du

113 in nanodiscs were never far apart during the hydrolysis cycle, and we never observed the NBD-NBD dist

114 ction with sodium borohydride and subsequent hydrolysis decarboxylation generated the corresponding 3

115 The adducts could further undergo hydrolysis/decarboxylation to generate the products whic

116 Accordingly, the ATP hydrolysis-defective dna2-K1080E mutant is less able to

117 bottom DNA strands, respectively, in an NTP-hydrolysis dependent reaction.

118 vertebrate orthologue of Sey1p, forms a GTP-hydrolysis-dependent network on its own, serving as both

119 ular motor capable of adenosine triphosphate hydrolysis-dependent translocation along double-stranded

120 ics simulations provide insight into how ATP hydrolysis destabilizes strand exchange products.

121 The degree of hydrolysis (DH) observed suggests that proteolytic cleav

122 The degree of hydrolysis (DH) of casein was observed to be the highest

123 Degree of hydrolysis (DH), amino acid composition, solubility, emu

124 90, and 120min to yield different degrees of hydrolysis (DH).

125 iments through the calculation of degrees of hydrolysis (DH).

126 Upon GTP hydrolysis, dynamin breaks these necks, a reaction calle

127 At room temperature, blocking ATP hydrolysis effectively abolished slow endocytosis and ra

128 periments reveal that in the presence of ATP hydrolysis even 75 bp sequence-matched strand exchange p

129 tubulin dimers change shape, triggered by a hydrolysis event.

130 recruits BiP through the stimulation of ATP hydrolysis, forcibly disrupting IRE1 dimers.

131 rted by the observed increase in kcat of ATP hydrolysis, from 7.8 +/- 0.1 min-1 to 457.7 +/- 9.2 min-

132 tically competent manner, suggesting that IP hydrolysis has a role in plant pathogenesis.

133 olved in a functional cycle accompanying ATP hydrolysis has been investigated in unprecedented detail

134 elevated temperatures with eventual backbone hydrolysis have not been reported to date.

135 nd 8-NH2-L-cIDPR inhibit CD38-mediated cADPR hydrolysis (IC50 7 muM and 21 microM respectively) with

136 arginine finger, R158, indispensable for ATP hydrolysis; (iii) the location of this arginine is conse

137 novo synthesis inhibition, not sphingomyelin hydrolysis, improved glucose tolerance and dyslipidemia.

138 ver, pilocarpine blocked CCh-stimulated PIP2 hydrolysis in M3R-overexpressing cells, thus, it acted a

139 ery urination event was able to inhibit urea hydrolysis in synthetic urine and real urine as indicate

140 gate this type of force originating from ATP hydrolysis in the chaperonin GroEL, by applying forces o

141 At its heart are two main ideas: i) ATP hydrolysis in the CI domain provides the thermodynamic d

142 of the CII domain provides the timer for the hydrolysis in the CI domain.

143 The presence of proteins provoked a higher hydrolysis in triglycerides, a lower decrease of polyuns

144 Our data suggest hydrolysis-independent closure of the NBD dimer, which i

145 reased linearly (p<0.05), whereas the starch hydrolysis index decreased linearly (p<0.05) by raising

146 wherein PL is a prodrug whose intracellular hydrolysis initiates the formation of the hPL-GSH conjug

147 n how superfamily 1 and 2 helicases turn ATP hydrolysis into motion along DNA.

148 The effects of PGE2-G required its hydrolysis into PGE2, were not observed with the non-hyd

149 l be a useful tool for understanding how ATP hydrolysis is coupled to LPS transport.

150 ucleolytic processing of DNA ends, while ATP hydrolysis is essential for Mre11 endonuclease activity

151 y the TS for guanosine 5'-triphosphate (GTP) hydrolysis is higher in energy when RhoA is complexed wi

152 ation of the NPR2 guanylyl cyclase, and cGMP hydrolysis is increased by activation of the PDE5 phosph

153 Additionally, we reveal that actin ATP hydrolysis is not required for VASP-mediated filament as

154 d zwitterionic carboxy groups by spontaneous hydrolysis is possible in the pCB brushes.

155 Experiments also indicate that when ATP hydrolysis is present, flanking heterologous dsDNA regio

156 ATP hydrolysis is related to detachment of EHD2 from the mem

157 mulation of the metabolite Mg(2+) from MgATP hydrolysis is required to make dantrolene administration

158 0.02% Tween 80 pH7.4, including rate of PLGA hydrolysis, mass loss and water uptake.

159 mal processing, pressurization and enzymatic hydrolysis may reduce the allergenic properties of food

160 retreated with 10 g L(-1) urea, whereas slow hydrolysis occurred when they were pretreated with 1 g L

161 We show that in fibroblasts, dynamin GTP hydrolysis occurs as stochastic bursts, which are random

162 nalysis of one such enzyme showed that ether hydrolysis occurs via the analogous mechanisms found for

163 h-throughput colorimetric assay based on the hydrolysis of 4-nitrophenyl silyl ethers.

164 ls of bond breaking and formation during the hydrolysis of a chemical warfare nerve agent simulant ov

165 lowed for the first quantitative analysis of hydrolysis of a nonphospholipid as a novel substrate of

166 ing the acetylcholinesterase (AChE) mediated hydrolysis of acetylthiocholine to thiocholine where the

167 Mild acid hydrolysis of adducts affords barbituric acid derivative

168 CD39 is a key purinergic enzyme in the hydrolysis of adenosine triphosphate (ATP) and increased

169 ssion in E. coli confirmed its functions for hydrolysis of AHLs, and the gene was designated as aidP

170 docosapentaenoic acid (DPA-n6) after partial hydrolysis of algal oil.

171 Whereas most CCPs catalyze hydrolysis of alpha-carboxyl-linked glutamates, CCP5 uni

172 lyst and show maximum NiPd catalysis for the hydrolysis of ammonia borane (H3 NBH3 , AB) with a turno

173 bilized enzyme, reaching a similar degree of hydrolysis of approximately 6-8% after 20h.

174 highly selective in promoting the reductive hydrolysis of aromatic ethers in aqueous phase at relati

175 Rate constants for spontaneous hydrolysis of aryl glycosides and their analogous valien

176 ges in F-actin structure associated with the hydrolysis of ATP and release of inorganic phosphate (Pi

177 e the stable docked SBP from the transporter hydrolysis of ATP is required.

178 hosphate (ATP)-bound DnaA and stimulates the hydrolysis of ATP to inactivate DnaA.

179 AA+ proteases and remodeling machines couple hydrolysis of ATP to mechanical unfolding and translocat

180 CD157, CD38) for the accelerated release and hydrolysis of ATP, cAMP, AMP, and NAD to adenosine.

181 ngement of local motifs, and the binding and hydrolysis of ATP.

182 correlations show that the rho value for the hydrolysis of benzylidene acetals is about -4.06, which

183 produced from acetylthiocholine (ATC) by the hydrolysis of butyrylcholinesterase (BChE), could cause

184 CRPH was obtained by enzymatic hydrolysis of discarded roe by using Alcalase 2.4L for 3

185 nd high-throughput analysis of the enzymatic hydrolysis of eight aliphatic polyesters by two fungal e

186 upregulation of the enzymatic machinery for hydrolysis of extracellular adenosine triphosphate and n

187 ctivity revealed that CsBGlu12 catalyzes the hydrolysis of flavonol beta-glucosides and cello-oligosa

188 In vitro hydrolysis of food proteins using commercial proteolytic

189 the design, synthesis, serum stability, and hydrolysis of four kinetin riboside ProTides.

190 rChiA is active in the hydrolysis of glycol chitin and tetra-N-acetylchitotetra

191 After hydrolysis of GR by the endogenous enzyme myrosinase, su

192 subunit inhibits the binding and induces the hydrolysis of GTP by the other.

193 f the encapsulated ligand can be achieved by hydrolysis of hydrazones to disrupt the sandwich complex

194 Pyrophosphatases catalyze the hydrolysis of inorganic phosphate (PPi) to inorganic pho

195 lysophosphatidic acid (LPA) in blood through hydrolysis of lysophosphatidyl choline (LPC).

196 The hydrolysis of MOF-1201 in water makes it the first examp

197 The process was optimized for hydrolysis of MP into p-nitrophenol (PNP).

198 The enzyme catalyzes hydrolysis of N-acetyl-beta-d-glucosamine-(1-->4)-1,6-an

199 s of N-nitrosoamide from N-alkyl amides, (2) hydrolysis of N-methoxyamides to carboxylic acids, (3) m

200 Hydrolysis of oleuropein, the main phenol in olive (Olea

201 he development of such a library for abiotic hydrolysis of organic chemicals under environmentally re

202 ested that iPLA2gamma is responsible for the hydrolysis of oxidized CL and subsequent signaling media

203 Due to hydrolysis of pharmaceutical metabolites back to the par

204 critical importance to better understand the hydrolysis of PLA driven by water molecules either in li

205 as powerful tools for the study of enzymatic hydrolysis of polymeric amphiphiles due to the monodispe

206 similar peptide profiles were obtained after hydrolysis of pressure-treated proteins using trypsin.

207 The hydrolysis of protein concentrate under in vitro gastroi

208 However, despite the hydrolysis of protein peptide bonds by peptidases being

209 RhoA-GTP with the RhoGAP domain, reduces the hydrolysis of RhoA-GTP, the binding of other DLC1 ligand

210 Rhizomucor miehei lipase mediated-hydrolysis of sardine oil was conducted at several water

211 The tubules rapidly fragment when GTP hydrolysis of Sey1p is inhibited, indicating that networ

212 The bound phenolics extracted after acid hydrolysis of sonicated protein co-precipitates showed i

213 ons show that the mechanism for the alkaline hydrolysis of squaramic acids is quite similar to that o

214 At the same temperature and [OH(-)], the hydrolysis of squaramides usually displays biphasic spec

215 and squaramic acids, the product of partial hydrolysis of squaramides, has been evaluated by UV spec

216 Enzymatic hydrolysis of starch was restricted by the presence of a

217 of different sized soil particles, including hydrolysis of sugars, revealing a pattern of size depend

218 We found that hydrolysis of the acid-labile linker is incomplete becau

219 s been the apparent lack of cooperativity in hydrolysis of the ATP in each protomer.

220 Hydrolysis of the extracted proteins with either trypsin

221 ell, where endogenous esterases catalyze the hydrolysis of the masking groups, generating fluorescenc

222 is pathway, LigY is proposed to catalyze the hydrolysis of the meta-cleavage product (MCP) 4,11-dicar

223 ylate bonds at the interface, as a result of hydrolysis of the methoxy group, is observed by ATR-FTIR

224 Under mild conditions, 1 catalyzes both hydrolysis of the nerve agent simulant, diethyl cyanopho

225 lysis of FDL to fluorescein during enzymatic hydrolysis of the polyester.

226 Lipase AS catalyzes the selective hydrolysis of the rear foot of macrocyclized walkers (an

227 lkyl protecting group, followed by enzymatic hydrolysis of the resulting phosphoramidate monoester.

228 Contrary, the hydrolysis of the second one was highly affected by the

229 sive study of the nonenzymatic (spontaneous) hydrolysis of these same substrates, wherein an approxim

230 rehalases (Nth), enzymes responsible for the hydrolysis of trehalose to glucose, compared with trehal

231 nversion model could adequately describe the hydrolysis of triacylglycerides, formation of FFAs and M

232 low recovery from N deprivation, compromised hydrolysis of triacylglycerols7 (cht7), was included to

233 idence that chloroform is formed through the hydrolysis of trichloroacetyl compounds in natural, orga

234 ion equation is proposed to characterize the hydrolysis of urea that accounts for both the ionization

235 ge in the local pH produced by the catalyzed hydrolysis of urea.

236 The process involves hydrolysis of vegetable oil blend using Candida cylindra

237 lti-functional bioactive peptides due to the hydrolysis of whey proteins.

238 LC-MS/MS study (without isotopic labeling or hydrolysis) of primary oxidation sites of p53 exon 7.

239 been adapted for transamidation, rather than hydrolysis, of acyl-enzyme intermediates to yield cyclic

240 Lack of compaction might reflect slower GTP hydrolysis or a different degree of allosteric coupling

241 around the IT, but mutations that affect GTP hydrolysis or GTP/GDP exchange modified this localizatio

242 nd amplifying wave regulate ATP levels using hydrolysis or secretion, respectively, whereas release a

243 To achieve high hydrolysis performance with the multi-activity enzyme Vi

244 The impact of the hydrolysis process on the r-betaLg structure and the rhe

245 branches controlled by base strength in the hydrolysis process.

246 the cell wall structure was carried out by a hydrolysis process.

247 peratures by amines reacting with nitrite (a hydrolysis product of NOx), but they can also thermally

248 sure/release, ptDNA binding/release, and ATP hydrolysis/product release.

249 nd tri-substituted sugar complexes and their hydrolysis products of mono-ribosylated N(6) and N(9) ad

250 ortant, but yet underestimated glucosinolate hydrolysis products that are released instead of the can

251 sponses to the consumption of starch and its hydrolysis products would benefit from convenient source

252 DeltaCTL also displays a reduced GTP hydrolysis rate compared with WT, but this altered activ

253 The restriction starch hydrolysis rate markedly reduced the GI of biscuits.

254 gh-duty ratio, monomeric motor, this altered hydrolysis rate would reduce activity to extremely low l

255 While hydrolysis rates for both enzymes increased with decreas

256 ane-targeting sequence stimulated higher ATP hydrolysis rates than the full-length protein, indicatin

257 tant (k) and activation energy (Ea) for this hydrolysis reaction are detailed; the results demonstrat

258 Iterative macrocyclization and hydrolysis reactions lead to 68% of walkers taking two s

259 low Fe/NOM ratio, however, NOM inhibited Fe hydrolysis, reduced zeta potential, and suppressed the f

260 protein and includes electron transfer, ATP hydrolysis, release of Pi, and dissociation of the oxidi

261 cise roles of the TL/TH in RNA synthesis and hydrolysis remain unclear.

262 The hydrolysis-resistant aryl silicon fragment is promising

263 Hydrolysis resulted in higher yield (15.1-15.4%) compare

264 Mutants lacking TAG or impaired of TAG hydrolysis show spore wall assembly defects, supporting

265 t folds, and the post-adenosine triphosphate hydrolysis state of KaiC create a hub around which night

266 localization is driven by MinD-catalyzed ATP hydrolysis, stimulated by interactions with MinE's anti-

267 ts using a mutant form of ARF1 affecting GTP hydrolysis suggest that ARF1[GTP] is functionally requir

268 is achieved through expending energy via ATP hydrolysis, suggesting that it is coupled to TFIIH's est

269 sover conformational shift, catalyzed by GTP hydrolysis, that converts the dimer from a "prefusion" t

270 Remarkably, after the first hydrolysis, the dimer undergoes a flip in the asymmetry

271 of verapamil, a substrate that activates ATP hydrolysis, the NBDs of Pgp reconstituted in nanodiscs w

272 ion was carried out with or without alkaline hydrolysis to determine if these molecules accumulate in

273 tidrug transporter that uses energy from ATP hydrolysis to export many structurally dissimilar hydrop

274 set of proteins that use the energy from ATP hydrolysis to form dynamic, linear polymers.

275 ATLs harness the energy of GTP hydrolysis to initiate a series of conformational change

276 diate p31(comet)-Mad2 binding and couple ATP hydrolysis to local unfolding of Mad2.

277 ols to imidates, directed C-H amination, and hydrolysis to NH2).

278 15)N5]dG-gx-dA as internal standards, enzyme hydrolysis to release the cross-links as nucleosides, en

279 , RarA couples the energy of ATP binding and hydrolysis to separating the strands of duplex DNA, crea

280 The Alcalase-containing enzymatic hydrolysis treatments generated a greater proportion of

281 ps retain the filament helical structure and hydrolysis triggers filament stiffening upon disassembly

282 Our results show that ATP hydrolysis triggers sequential conformational waves." Th

283 number of myosin motors leaving the off, ATP hydrolysis-unavailable state characteristic of the diast

284 atalyzed cyclopropanation, followed by ester hydrolysis under epimerizing conditions.

285 Autoclaving and enzymatic hydrolysis under sonication separately induced a measura

286 duced by urea, since complete and very rapid hydrolysis, up to 4 g L(-1) h(-1) of urea, was observed

287 ing as an accelerator that enables rapid ATP hydrolysis upon contact with ptDNA and RFC-D Arg-101 ser

288 end of digestion, whereas an almost complete hydrolysis was observed for the other two emulsions.

289 and peptide profiles, obtained after protein hydrolysis, was investigated.

290 H solutions and subsequent in-situ enzymatic hydrolysis were thoroughly characterized.

291 und that they are also able to perform ester hydrolysis when attached to a protein.

292 is protected, up to a certain limit, against hydrolysis when it is aggregated with a strongly polar p

293 d E1CB elimination mechanism during alkaline hydrolysis) where a secondary AKIECl (1.00045 +/- 0.0000

294 On the contrary, hydrolysis with an alpha-l-arabinofuranosidase, removing

295 ion of free aglycones was observed following hydrolysis with Pektopol PT.

296 HT generated more antioxidant activity than hydrolysis with pepsin.

297 MPa, 5min or 20min at 20 degrees C) prior to hydrolysis with trypsin only and trypsin-pronase.

298 n endonucleases catalyze phosphodiester bond hydrolysis within or close to their DNA target sites, th

299 so supported these evidences indicating that hydrolysis yielded an intermediate (non-native) beta-Lg

300 lar weight chains of collagen but sequential hydrolysis yielded higher degree of hydrolysis.