ライフサイエンスコーパス: hydrolysis

1 of UPF1 to release RNA upon ATP binding and hydrolysis.

2 longed protein stability against proteolytic hydrolysis.

3 orm organic sulfur that is resistant to acid hydrolysis.

4 the target C-N coupling product upon in situ hydrolysis.

5 kinetic steps are accelerated by faster ATP hydrolysis.

6 erone "helper" proteins, and ATP binding and hydrolysis.

7 mation on ATPase domain architecture and ATP hydrolysis.

8 e before conversion to the derived ketone by hydrolysis.

9 and this cycle is linked to GTP binding and hydrolysis.

10 d convert into benzoic acids due to C-F bond hydrolysis.

11 iotics is via their beta-lactamase-catalyzed hydrolysis.

12 ng catalysis and how they are coupled to ATP hydrolysis.

13 y of protein synthesis at the expense of GTP hydrolysis.

14 d 70S ribosomes in vitro, independent of GTP hydrolysis.

15 es and the cytosolic headpiece mediating ATP hydrolysis.

16 steadily increased with increasing degree of hydrolysis.

17 the allosteric transition that triggers ATP hydrolysis.

18 y of prepared compounds toward acid-promoted hydrolysis.

19 by HPLC coupled to tandem MS after enzymatic hydrolysis.

20 s the levels of cellular dNTPs through their hydrolysis.

21 l cores, whose formation requires MukBEF ATP hydrolysis.

22 , and eight presented 72.74-84.54% of starch hydrolysis.

23 nhibited heparanase and was resistant toward hydrolysis.

24 s host-pathogen lipid imaging following acid hydrolysis.

25 aining mycobacterial GyrB are limited by ATP hydrolysis.

26 -anticodon interactions before and after GTP hydrolysis.

27 f receptor subtypes, and the dynamics of ACh hydrolysis.

28 ine, which results in unproductive glutamine hydrolysis.

29 hey showed faster (higher k) in vitro starch hydrolysis (0.0140 vs 0.0050) with lower estimated glyce

30 study of lactose digestion showed levels of hydrolysis (82.8%) at 0.2 mg*mL(-1) and the highest hydr

31 the product of the PLC-catalyzed PI(4,5)P(2) hydrolysis, activates protein kinase C (PKC).

32 oteins exhibit conserved GTP-binding and GTP-hydrolysis activities, and function in maintaining overa

33 atient, both have gain-of-function Rad50 ATP hydrolysis activity that results not from faster associa

34 enome replication, RNA-binding affinity, ATP hydrolysis activity, and helicase-mediated unwinding act

35 d at the 9(th) carbon due to decreased FAHFA hydrolysis activity.

36 prised of a cytoplasmic V(1) complex for ATP hydrolysis and a membrane-embedded V(o) complex for prot

37 Strictly sequential models of ATP hydrolysis and a power stroke that moves two residues of

38 motifs that were linked to enzyme-catalyzed hydrolysis and are therefore candidates for incorporatio

39 omplexes reveals preferred conformations for hydrolysis and beta-lactone formation.

40 ylation abolishes the K(+)-dependence of ATP hydrolysis and blocks the catalytic cycle after formatio

41 requires fuel consumption in the form of ATP hydrolysis and coordination of the catalytic cycles betw

42 e results challenge sequential models of ATP hydrolysis and coupled mechanical work by ClpAP and prov

43 ed proteins retained drug stimulation of ATP hydrolysis and drug binding affinities.

44 A simultaneous hydrolysis and extraction method was developed using met

45 expression of specific genes involved in TAG hydrolysis and fatty acid oxidation, and that PA relieve

46 The FeOx were prepared by Fe(III) hydrolysis and Fe(II) oxidation, in the absence and pres

47 rolysis rate constant for the first stage of hydrolysis and final hydrolysis extent.

48 ecies relevant to Br(-) oxidation, and Cl(2) hydrolysis and formation reactions (Cl2 + H2O + A- k-4k4

49 ntein fusion approach suffers from premature hydrolysis and low compatibility with denatured conditio

50 After this power stroke, ATP hydrolysis and phosphate release launch the return to th

51 ni, perhaps due to inefficient polyubiquitin hydrolysis and proteasome-mediated degradation.

52 d had the highest degree of in-vitro protein hydrolysis and protein digestibility.

53 terminal subunit, which likely promotes ATP hydrolysis and rapid phosphate release.

54 an energy-consuming futile cycle between TG hydrolysis and resynthesis, leading to inhibition of mTO

55 ione transport activity, suggesting that ATP hydrolysis and substrate transport by Atm1 may involve a

56 Purified Smc5/6 exhibits DNA-dependent ATP hydrolysis and SUMO E3 ligase activity.

57 WS) and Lotus stem (LS) by using mild alkali hydrolysis and ultra-sonication process has been present

58 P-loop NTPase fold enzymes that catalyze ATP-hydrolysis and utilize its free energy for a staggering

59 Nucleotide hydrolysis and/or product release leads to an increase o

60 molecular machines by coupling ATP binding, hydrolysis, and phosphate release to translocation of di

61 opose a model of how substrate cleavage, ATP hydrolysis, and substrate translocation are coordinated

62 otor rotation, negative cooperativity in ATP hydrolysis, and the energetic requirement for at least 1

63 a subunits in G-proteins, accelerate the GTP hydrolysis, and thereby rapidly dampen GPCR signaling.

64 ues play in regulating ribosome binding, GTP hydrolysis, and translation initiation both in vitro and

65 olar mass of milk saccharides throughout the hydrolysis are discussed.

66 Features of the cyanobacterial RNAP hydrolysis are reminiscent of the Gre-assisted reaction-

67 the S-nitrosylation assay, 5.8 in the NAD(+) hydrolysis assay, and 6.8 in the enzymatic ADP-ribosyltr

68 Here, using MS-based FAHFA hydrolysis assays, LC-MS-based lipidomics analyses, and

69 nge tested had a minor effect on bound-forms hydrolysis, being both free and bound forms equally affe

70 beta-glucosidases catalyze the hydrolysis beta-1,4, beta-1,3 and beta-1,6 glucosidic li

71 on and dissociation steps do not require ATP hydrolysis, but subsequent forward and reverse kinetic s

72 r results show that substrate stimulates ATP hydrolysis by accelerating the IF-to-OF transition.

73 quence of the ability of ClpS to repress ATP hydrolysis by ClpA, but several lines of evidence show t

74 GTP hydrolysis by dynamin triggers disassembly of fully asse

75 s identified 2-AG as the main product of LPI hydrolysis by GDE3.

76 red for HSP70's role: we have found that ATP hydrolysis by HSP70, the nucleotide exchange activity of

77 -5 tails decrease microtubule-stimulated ATP-hydrolysis by specifically engaging motor domains in the

78 ATP binding and hydrolysis by StXPB could lead to a spiral translocation

79 to restart elongation via stimulation of RNA hydrolysis by the active centre of RNA polymerase (RNAP)

80 settes strongly influence RNA-stimulated ATP hydrolysis by the N-terminal cassette.

81 Here, we compare ESOC hydrolysis by the parent enzyme KPC-2 and its clinically

82 coated pits is spatially segregated from its hydrolysis by the PI(3,4)P(2)-specific inositol polyphos

83 rkably, 5' end recognition and pyrophosphate hydrolysis by the PPsome complex also contribute to mRNA

84 lied for real-time monitoring of beta-casein hydrolysis by trypsin at various conditions for the firs

85 in a closed conformation and stimulates ATP hydrolysis by XPB while AfBax1 maintains AfXPB in the op

86 Back hydrolysis can be prevented by hydrogenating C=N bonds u

87 Hydrolysis conditions with neutralization post-treatment

88 Under such hydrolysis conditions, the peptides produced have the hi

89 s used for the identification of the optimal hydrolysis conditions.

90 ction of ribosomes from Fe(2+)-mediated rRNA hydrolysis correlates with the restoration of cell viabi

91 Thus, KIF1A spends the majority of its hydrolysis cycle in a one-head-bound state.

92 suggesting a coordinated and directional GTP-hydrolysis cycle.

93 enzymatic models were fitted with degree of hydrolysis (d(h)) profiles to provide kinetic and mechan

94 ntestinal digestion showed a 4.2-fold higher hydrolysis degree in the protein concentrate than the fl

95 testinal digestion by RSIE, resulting in low hydrolysis degrees (20.4%) after 5 h reaction.

96 priming (recovery stroke) while slowing ATP hydrolysis, demonstrating that it uncouples these two st

97 roscopy was applied to predict the degree of hydrolysis (DH%) and weight-average molecular weight (M(

98 s food formulation effects on the degrees of hydrolysis (DH) of both proteins and lipids throughout i

99 that can potentially influence the degree of hydrolysis (DH), equivalent umami concentration (EUC), a

100 ATP molecules to the SMC subunits and their hydrolysis drive dynamics of these complexes.

101 imulates the adenosine 5'-triphosphate (ATP) hydrolysis-driven motor activity of DNA2 involved in the

102 her bacterial diversity in cheese on protein hydrolysis during simulated human digestion, Raclette-ty

103 controlled precipitation and to inhibit urea hydrolysis during storage until further treatment in mor

104 ) between 1.15 and 0.59 mg/mL), although the hydrolysis enhanced the bioactivity of HQE (p = 0.014).

105 This study demonstrates that enzymatic hydrolysis enhances the functional and antioxidant prope

106 0 aa) steps, each coupled to hundreds of ATP hydrolysis events.

107 for the first stage of hydrolysis and final hydrolysis extent.

108 antification method based on strong alkaline hydrolysis followed by High Performance Anion Exchange C

109 We measured the rate of enzyme-free hydrolysis for 17 phosphoramidates of ribonucleotides wi

110 is the widely preferred method over chemical hydrolysis for MOS production.

111 brane-embedded enzymes use the energy of ATP hydrolysis for transmembrane transport of a wide range o

112 in SO, SI showed slightly higher or similar hydrolysis (free fatty acids and diacylglycerols), simil

113 ime during thermal treatment, and decoupling hydrolysis from fibril self-assembly helped to identify

114 ide mixture, either endogenous or by protein hydrolysis, from other food matrices.

115 Enzymatic hydrolysis has been demonstrated, but a spontaneous chem

116 Hydrolysis improved solubility of faba proteins at acidi

117 al a function for INPP4-mediated PI(3,4)P(2) hydrolysis in local regulation of growth factor and nutr

118 (Phi(u)), low susceptibility to spontaneous hydrolysis in the dark, and good aqueous solubility.

119 nizes transmembrane substrates and catalyzes hydrolysis in the lipid bilayer is unclear.

120 (OPA) intermediate can proceed via alkaline hydrolysis in the presence of D(2) O to provide alpha-de

121 mismatch recognition, ATP converts MutS to a hydrolysis-independent, diffusive mobile clamp that no l

122 Acid-mediated hydrolysis initiated skeletal rearrangement processes th

123 mulations of 1) adenosine triphosphate (ATP) hydrolysis into adenosine monophosphate (AMP) and 2) AMP

124 te alanine mutants indicates that carbapenem hydrolysis is a concerted effort involving multiple resi

125 Cl(2) formation are acid-catalyzed and Cl(2) hydrolysis is base-catalyzed, but the impact of carbonat

126 uble in these conditions, confirming the HHM hydrolysis is caused by a heterogeneous reaction of the

127 taken up in a 'selfish' mode, where initial hydrolysis is coupled to transport into the periplasm, s

128 When the speed of GTP hydrolysis is faster than dimer recruitment, the loss of

129 DQ-OVA, a substrate for proteases which upon hydrolysis is fluorescent) was compared in vitro and the

130 ortant DOP hydrolase, although extracellular hydrolysis is involved.

131 Notably, ATP hydrolysis is required to alter the conformation of MutS

132 ics (AIMD) simulations confirm that aluminum hydrolysis is strongly promoted at the interface.

133 Enzymatic hydrolysis is the widely preferred method over chemical

134 hydrolysis rate, r(0), and rate constant of hydrolysis, k(h), and enzyme inactivation, k(d).

135 Measurements of the hydrolysis kinetics of CUPRA substrates containing gangl

136 KIF3C retain their intrinsic ATP-binding and hydrolysis kinetics.

137 tch again instead of bypassing it; thus, ATP hydrolysis licenses the MutS mobile clamp to rebind the

138 MR kinetic experiments constrain the 1,2-IHN hydrolysis lifetime to less than 10 s in deuterium oxide

139 mutant enzyme exhibits decreased ceftazidime hydrolysis, lower thermostability, and decreased protein

140 -shaped pH/rate profile but are at odds with hydrolysis mechanisms in the classic literature.

141 d water volume, we show that condensed-phase hydrolysis of 1,2-IHN can account for this loss process.

142 rogression and simultaneously inhibiting the hydrolysis of 8oxodGTP.

143 ATPase (enzymatic hydrolysis of adenosine triphosphate to inorganic phosph

144 An in silico theoretical hydrolysis of amandin subunits corroborated with the res

145 ographic product quantification, compared to hydrolysis of amylose and amylopectin estimated using 3,

146 velopment of a model in which the sequential hydrolysis of ATP is coupled to motions of ClpX loops th

147 During the hydrolysis of ATP, the alpha(3)beta(3) domain undergoes

148 mplexes catalyzing the bicarbonate-dependent hydrolysis of ATP, which is the first half-reaction cata

149 olerae is blocked by gut microbiome-mediated hydrolysis of bile acids.

150 tained higher levels of terpenes (indicating hydrolysis of bound forms) and fermentation-derived vola

151 Hydrolysis of c-di-AMP is critical for normal growth and

152 iesterase type 4 (PDE4), which catalyzes the hydrolysis of cAMP.

153 he CTX-M enzyme, result in 10-fold increased hydrolysis of ceftazidime.

154 termediates have elucidated how hExo1 exerts hydrolysis of DNA phosphodiester bonds.

155 Here, we investigated whether CD73-mediated hydrolysis of extracellular ATP (eATP) could affect inte

156 nzoic acid) allosterically activates ERAP1's hydrolysis of fluorogenic and chromogenic amino acid sub

157 identified that a DspB mutant with improved hydrolysis of fully acetylated PNAG oligosaccharides cor

158 The rate of gastric degree of hydrolysis of gliadin was greater (P < 0.05) by actinidi

159 The gastric degree of hydrolysis of gluten proteins was influenced by an inter

160 pression) in the tubulin dimer following the hydrolysis of GTP have been suggested to generate stress

161 ese changes were attributed to increased net hydrolysis of IHTG and partitioning of the resulting fat

162 interaction with substrate polypeptides upon hydrolysis of its bound ATP.

163 lks, including breast milk, during enzymatic hydrolysis of lactose by supplemental beta-galactosidase

164 The hydrolysis of lactose over beta-galactosidase converted

165 in and punicalagin were weaker inhibitors of hydrolysis of maltoheptaoside (<50% inhibition) than amy

166 Here, the solvation and hydrolysis of MG at the air/liquid water interface is st

167 onstrate that the MHETase lid is crucial for hydrolysis of MHET and, furthermore, that MHETase does n

168 ere show that MTH1 efficiently catalyzes the hydrolysis of N6-methyl-dATP to N6-methyl-dAMP and furth

169 hesized and characterized the photolysis and hydrolysis of NB moieties containing different labile bo

170 similar in nature to those for the alkaline hydrolysis of neutral arylsulfonate monoesters or charge

171 One infers from our results that the hydrolysis of NO(2) in clouds must be catalyzed by organ

172 h the average intracellular pH minimizes the hydrolysis of nucleotides by slowing their reaction with

173 The acid hydrolysis of oleuropein was faster with lactic and citr

174 Fungal functional genes involved in hydrolysis of organic matter increased with ambient N de

175 demonstrated that 60% sorbitol could retard hydrolysis of OVT completely for a period of time during

176 Soil extracellular phosphatases catalyze the hydrolysis of P from soil organic matter, an important a

177 hosphocholine phosphatase that catalyzes the hydrolysis of phosphocholine (PC) to choline.

178 Fatiguing exercise causes hydrolysis of phosphocreatine, increasing the intracellu

179 atases (HP2P) able to carry out the stepwise hydrolysis of phytate.

180 Enzymatic hydrolysis of plant-derived proteins can improve their q

181 Many of these organisms also mediate hydrolysis of polysaccharides, likely from cyanobacteria

182 the major structural levers to modulate the hydrolysis of proteins (final DH between 51.7 and 58.3%)

183 Numerous bacteria are responsible for hydrolysis of proteins during cheese ripening.

184 Enzymatic hydrolysis of proteins produces bioactive peptides that

185 , we demonstrate that DXO also catalyzes the hydrolysis of RNAs bearing a 5'-hydroxyl group (5'-OH RN

186 Overall, using seawater in hydrolysis of seaweed increased sugar hydrolysis yield a

187 d; their increase could be mainly due to the hydrolysis of sucrose, which decreased in the same perio

188 l cellulose nanofibers (BCNFs) by controlled hydrolysis of sulfuric and hydrochloric acids.

189 olyzed by most beta-lactamases owing to slow hydrolysis of the acyl-enzyme intermediate.

190 idenced that prolonged heat treatment caused hydrolysis of the attached polysaccharide and consequent

191 nd nucleotide and thereby down-regulates ATP hydrolysis of the complex.

192 After hydrolysis of the conjugated form (mainly glucuronide) o

193 Furthermore, prior hydrolysis of the crosslinked peptide stem from the sacc

194 The generation of nascent-HBr from the slow hydrolysis of the dispersed catalyst, benzyl bromide, wi

195 he final enzyme-inhibitor complex due to the hydrolysis of the ester linkage.

196 Thus, the hydrolysis of the fish bycatch allows the release of bio

197 The alkali hydrolysis of the FITC@SiO(2)-NH(2)-anti-IgG released FI

198 Complete hydrolysis of the main whey proteins, beta-Lactoglobulin

199 Enzymatic hydrolysis of the oil hemp seed (FINOLA variety) cake an

200 eaction of NaPH(2) with carbon dioxide or by hydrolysis of the phosphaethynolate ion (PCO(-) ).

201 Hydrolysis of the phosphoramidate liberates the nucleoti

202 Hydrolysis of the precipitate then liberates the (S)-lig

203 Hydrolysis of the resulting benzophenone azine affords h

204 lso related to a higher resistance to enzyme hydrolysis of the retrograded starches.

205 ic fraction, after saponification and acidic hydrolysis of the samples, are extracted by solvent and

206 Remarkably, the stability to hydrolysis of the sulfimide varied more than 10-fold dep

207 COMPROMISED HYDROLYSIS OF TRIACYLGLYCEROLS7 (CHT7) in Chlamydomonas

208 The Chlamydomonas reinhardtii Compromised Hydrolysis of Triacylglycerols7 (CHT7) protein has been

209 e (LPL) to GPIHBP1 focuses the intravascular hydrolysis of triglyceride-rich lipoproteins on the surf

210 nnosidase II (GMII) catalyzes the sequential hydrolysis of two mannosyl residues from GlcNAcMan(5)Glc

211 In contrast to the quick hydrolysis of TzB, the N-acylated thiazolidines exhibit

212 Therefore, the enzymatic hydrolysis of whey protein concentrate (WPC 35) to produ

213 One hour hydrolysis of WPC-80 reduced the protein antigenicity, w

214 haracterized TF genes increased total glucan hydrolysis on average compared to control.

215 actamases, suggesting it promotes carbapenem hydrolysis only in the context of KPC-2.

216 /MS methods were developed and validated for hydrolysis optimization and for quantification of eight

217 also demonstrate that mutants perturbing ATP hydrolysis or DNA cleavage in vitro impair P2 OLD-mediat

218 eptide bonds with varied susceptibilities to hydrolysis or exchange by mTG.

219 control over system properties (e.g., rapid hydrolysis or slow photolysis).

220 ofiles are major determinants of beta-casein hydrolysis patterns.

221 e nucleotide-binding-domain dimer, while ATP hydrolysis per se does not reset MRP1 to the resting sta

222 motor (BFM), ATP (adenosine-5'-triphosphate) hydrolysis probably drives both motor rotation and filam

223 trix scoring multiplex qPCR assays utilize a hydrolysis probe, providing sensitive and specific F. tu

224 The hydrolysis probe-based multiplex dPCR assay quantifies S

225 Here, we developed a hydrolysis probe-based tetraplex real-time PCR assay tha

226 ur calculations suggest that sulfate diester hydrolysis proceeds through loose transition states, wit

227 s remained mostly in the sediments after the hydrolysis process in the Flavorpro treated samples, whi

228 reduces the BN heterocyclic ring, which upon hydrolysis produces a rare example of a macrocyclic para

229 gh the transition state until release of the hydrolysis product, despite changes in ring conformation

230 on the relative levels of beta-lactones and hydrolysis products formed.

231 ycation, oxidation and nitration and related hydrolysis products, glycation, oxidation and nitration

232 s shown that, in addition to the established hydrolysis products, the reaction of the class D nucleop

233 s adept control of Pu(IV) coordination under hydrolysis-prone conditions, provides an opportunity to

234 Powered by the energy of ATP binding and hydrolysis, protease-containing ABC transporters (PCATs)

235 The previously reported carbonate hydrolysis protocol reaches its limitation when confront

236 As a byproduct of PLC-mediated PIP(2) hydrolysis, protons have been shown to play an important

237 sis (82.8%) at 0.2 mg*mL(-1) and the highest hydrolysis rate constant (k(obt)).

238 ide chains and led to an increased enzymatic hydrolysis rate constant for the first stage of hydrolys

239 scription of proteolysis in terms of initial hydrolysis rate, r(0), and rate constant of hydrolysis,

240 oom phase was characterized by high external hydrolysis rates of a broad range of polysaccharides and

241 ctivity was accompanied by low extracellular hydrolysis rates of a few polysaccharides.

242 4a has significantly higher stepping and ATP hydrolysis rates than does GiKIN14a-Deltatail.

243 ower turnover number and transfructosylation/hydrolysis ratio.

244 e intermediate is a central milestone in the hydrolysis reaction catalyzed by these enzymes.

245 tons, the enzyme eliminates water, a reverse hydrolysis reaction, to yield the benzoxazole and avoids

246 t facilitates the acyl formation step of the hydrolysis reaction.

247 The kinetics of the hydrolysis reactions of 4-methoxybenzoyl chloride (OMe)

248 In this work, two hydrolysis reactions were used as a probe to investigate

249 lation, oxidative decarboxylation, and amide hydrolysis reactions.

250 Cellular DNA can be damaged by spontaneous hydrolysis, reactive oxygen species, aberrant cellular m

251 iration from ATP synthesis or increasing ATP hydrolysis restores NAD(+)/NADH homeostasis and prolifer

252 in either LPL or GPIHBP1 impair triglyceride hydrolysis, resulting in severe hypertriglyceridemia.

253 features in the enzyme, such as a nucleotide hydrolysis site or multiple intermediate conformations.

254 mic tail of SLC38A9 in the pre- and post-GTP hydrolysis state of RagC, which explain how SLC38A9 dest

255 ignificantly, kinking of TM6 in the post-ATP hydrolysis state stabilized by MgADPVO(4) eliminates thi

256 However, it remains unclear how binding and hydrolysis structurally alters the SL receptor to enable

257 e found that uptake by the 14A mutant is ATP hydrolysis-, substrate concentration-, and time-dependen

258 s for the kinetic analysis of peanut protein hydrolysis that lead to high reduction rate (K) of the I

259 Based on the results of the sinigrin hydrolysis, the AITC surface exchange rate and the AITC

260 After hydrolysis, the IgE-binding properties of the peanut sol

261 roinitiator to protect the NCA monomers from hydrolysis through spontaneous in situ self-assembly (IS

262 ASNU/Kg), water percentage (30 and 90%), and hydrolysis time (1 and 3 h).

263 f the immune system either directly or after hydrolysis to adenosine.

264 ied on the flavonoid rutin to understand its hydrolysis to aglycones, antioxidant capacity and optica

265 elicases couple adenosine triphosphate (ATP) hydrolysis to conformational changes of their catalytic

266 -Cope reaction with formaldehyde followed by hydrolysis to eliminate unmask redox reporter N-alkylate

267 ers chemomechanically couple ATP binding and hydrolysis to large-scale conformational changes, ultima

268 balance between peptidoglycan synthesis and hydrolysis to maintain proper cell morphology.

269 nergy of nucleoside triphosphate binding and hydrolysis to mechanical movement along a polymer lattic

270 mechanoenzyme that uses the energy from ATP hydrolysis to physically reshape and remodel, and thus m

271 xes, cohesin, condensin, and Smc5/6, use ATP hydrolysis to power a plethora of functions requiring or

272 NA configurations and uses the energy of ATP hydrolysis to promote their compaction.

273 AAA+ protein, Skd3 (human ClpB), couples ATP hydrolysis to protein disaggregation and reactivation.

274 teases are degradation machines that use ATP hydrolysis to unfold protein substrates and translocate

275 in myrosinase activity, which stimulated GLs hydrolysis to yield health-promoting sulforaphane.

276 site of MoFe-protein and how energy from ATP hydrolysis transduces the ET processes.

277 In this hydrolysis transformation, a new mechanism is proposed f

278 n hull was performed by means of an alkaline hydrolysis treatment, which was optimized by the respons

279 ncreatic cells; importantly, Zn(II)-mediated hydrolysis triggers cargo activation.

280 s catalyst or degraded to small molecules by hydrolysis under acidic conditions.

281 mpounds (up to 178 mg/100 g) while the basic hydrolysis underestimates the phenolic concentration.

282 et of DspB in PNAG substrate recognition and hydrolysis using a combination of site-directed mutagene

283 cted arabinoxylan was subjected to enzymatic hydrolysis using individual xylanase, arabinofuranosidas

284 ing properties improved only until degree of hydrolysis values of 1.5% (neural endoprotease) and 1.9%

285 The highest studied degree of hydrolysis was 5.4% corresponding to 55.2% protein solub

286 Acidic hydrolysis was able to extract the highest amount of tot

287 The estimated rate of the sn-1/3 hydrolysis was around two- to thirty-fold faster compare

288 P < 0.05), whereas the pentapeptide epitopes hydrolysis was influenced only by the actinidin concentr

289 Using mutated human tubulin with blocked GTP hydrolysis, we demonstrate that EBs bind with high affin

290 ally reduce cephalosporin but not penicillin hydrolysis, we suggest that clavulanic acid paired with

291 w that N-trifluoromethyl amines are prone to hydrolysis, whereas N-trifluoromethyl azoles have excell

292 for uncoupling substrate reduction from ATP hydrolysis, which may provide new avenues for studying t

293 y adding a previous step including enzymatic hydrolysis with a xylanase, a functional evaluation of D

294 polysaccharide quantification based on acid hydrolysis with concomitant use of trifluoroacetic and h

295 gh SDS-PAGE analysis, an increased degree of hydrolysis with longer fermentation time was confirmed.

296 es demonstrate the recovery of free GMT upon hydrolysis, with biological activity as assessed by cyto

297 cellular homeostasis through macromolecular hydrolysis within their lumen and metabolic signaling by

298 ter in hydrolysis of seaweed increased sugar hydrolysis yield and subsequent bioethanol production.

299 eatment process was developed to improve the hydrolysis yield of brown (Laminaria digitata), green (U

300 ched or free extracellular enzymes (external hydrolysis) yield LMW products available to the wider ba