ライフサイエンスコーパス: hydrolyse

1 rst double bond from the ester linkage being hydrolysed.

2 A), a BphD substrate, which was subsequently hydrolysed.

3 endonucleolytic and exonucleolytic (EXO) DNA hydrolyses.

4 for alternative mechanisms for the enzymatic hydrolyses.

5 Cys59Ser mutant enzyme was shown to rapidly hydrolyse 4-methylumbelliferyl acetate in paraoxon-treat

6 e/S-adenosylhomocysteine nucleosidase, which hydrolyses 5'-methylthioadenosine, the product of MccD-c

7 exonuclease activity of p53, particularly in hydrolysing 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG

8 ressed as a recombinant protein and shown to hydrolyse a generic phosphatase substrate, and phosphoty

9 Activated HaCA42 carboxypeptidase hydrolysed a synthetic substrate for glutamate carboxype

10 These data indicate that human CBG hydrolyses a broad range of dietary glucosides and may p

11 ng an IC50 value of 138 mug/ml, was obtained hydrolysing a mixture of lupin alpha+beta conglutin.

12 em for chromatin assembly, we found that ACF hydrolyses about 2#150;4 molecules of ATP per base pair

13 Full-length NAT hydrolyses Ac-CoA but only in the presence of an arylami

14 Butyrylcholinesterase hydrolyses acetylcholine, which exerts immunoregulatory

15 tif 3-containing proteins have peptidoglycan-hydrolysing activity and that while this activity is not

16 A incorporated into the LCP retained its ATP-hydrolysing activity for 7 days, while the solubilized p

17 The H2O2 hydrolysing activity of purified catalase is necessary i

18 ne faecal microbes possessing beta-glycoside-hydrolysing activity.

19 tor (MRCA) is not expected to possess lactam-hydrolysing activity.

20 Results show that PPL preferentially hydrolyses ALA and DPA over EPA, DHA and STA, and this s

21 used proteinase K concentrations designed to hydrolyse all fragments resulting from an incomplete dig

22 remains on membranes after Arf1-GTP has been hydrolysed and dissociated.

23 structure, in which two molecules of ATP are hydrolysed and the rotor of the enzyme turns through two

24 tween 0.75 and 2.5 mg/ml, (p < 0.05) for the hydrolysed and unhydrolysed samples.

25 ate threadfin bream (Nemipterus hexodon) was hydrolysed and used to cultivate Enterobacter sp. C2361

26 ly on DNA at approximately 2000 bp s(-1) and hydrolyses approximately 1 ATP molecule per base pair tr

27 that the active site of HiAXHd3 is tuned to hydrolyse arabinofuranosyl or xylosyl linkages, and it i

28 , k(H(2)O)/k(D(2)O)) for the amine-catalyzed hydrolyses are 1.4 and 1.9 for the hydrolysis of N-benzo

29 Mechanisms for the two hydrolyses are drawn on the basis of the results, which

30 ves, R = i-propyl, s-butyl, t-butyl, t-amyl, hydrolyses are general-acid catalyzed.

31 oeni produces esterases that are capable of hydrolysing artificial substrates.

32 mining combined effect of enzymatic and acid hydrolyses, associations and fine structure of AX.

33 methylarginine dimethylaminohydrolase (DDAH) hydrolyses asymmetrically methylated arginine residues t

34 Lactose in milk whey was hydrolysed at comparatively higher rate than that of mil

35 with an interplay of alkali penetration and hydrolyses at various time points.

36 ilis FtsE mutants that are unable to bind or hydrolyse ATP cannot activate CwlO.

37 All type II topos hydrolyse ATP during their reactions; however, only DNA

38 sis in limiting the capacity of the heart to hydrolyse ATP in vivo.

39 contact with a translocating polypeptide to hydrolyse ATP to drive substrate spooling into ClpP, and

40 Kinesins hydrolyse ATP to transport intracellular cargoes along m

41 is unable to stably bind RNA or effectively hydrolyse ATP under physiological conditions, but additi

42 The Arp2 subunit has been shown to hydrolyse ATP, but the functional importance of Arp2/3 A

43 were expressing extracellular hydrolases to hydrolyse ATP.

44 influence the ability of FtsA to bind and/or hydrolyse ATP.

45 s activities are dependent on its ability to hydrolyse ATP.

46 tion in which specialized activator proteins hydrolyse ATP.

47 RecA2201 binds, but does not hydrolyse ATP.

48 e subunits when the cassette dimer closes to hydrolyse ATP.

49 nt stalling if one subunit failed to bind or hydrolyse ATP.

50 way, and two nucleotide-binding domains that hydrolyse ATP.

51 system (sigma54-RNAP, Esigma54) and a slowly hydrolysed ATP analogue (ATPgammaS), we provide evidence

52 found that purified wild-type FtsA bound and hydrolysed ATP, whereas FtsA27 was defective in both act

53 Enzymatically active mouse Lon that hydrolyses ATP and degrades protein and peptide substrat

54 We found that T7 helicase binds and hydrolyses ATP and dTTP by competitive kinetics such tha

55 In carrying out these functions Hsp90 hydrolyses ATP as it cycles between ADP- and ATP-bound f

56 p33 alone hydrolyses ATP but exhibits no helicase activity.

57 The complex hydrolyses ATP in the absence of DNA; unwinds duplex reg

58 Apaf-1 binds to and hydrolyses ATP/dATP and their analogues.

59 Mutants of SecA capable of binding but not hydrolysing ATP do not elicit this conformationally acti

60 Recombinant SpyA was able to hydrolyse beta-NAD(+), and this activity was dependent o

61 ability of the Lab4 probiotic consortium to hydrolyse bile salts, assimilate cholesterol and regulat

62 asein hydrolysis kinetics and were active in hydrolysing BODIPY-FL casein to varying extents at postm

63 No specific peptidic hydrolysed bond was detected.

64 bacterial-derived protease (HT) extensively hydrolysed both meat protein extracts, producing peptide

65 Antimicrobial saponins are first hydrolysed by a fungal saponin-detoxifying enzyme.

66 family that requires ATP, which is bound and hydrolysed by a helicase-like domain.

67 defatted skipjack (Katsuwonous pelamis) roe, hydrolysed by Alcalase 2.4 L (RPH) with different degree

68 (Saccharomyces cerevisiae) was enzymatically hydrolysed by Alcalase, Protex or Viscozyme.

69 acellular space via SWEET9, where sucrose is hydrolysed by an apoplasmic invertase to produce a mixtu

70 L-cIDPR is surprisingly still hydrolysed by CD38, whereas 8-Br-L-cIDPR is not cleaved,

71 tic implications, because d peptides are not hydrolysed by endogenous proteases and may be administer

72 released when a starch-triiodide complex is hydrolysed by honey diastase.

73 Cell-wall components are hydrolysed by numerous plant glycosidase and glycanase a

74 Food proteins can also be isolated and hydrolysed by peptidases to produce hydrolysates.

75 High-molecular-weight kininogen can be hydrolysed by plasma kallikrein to bradykinin and cleave

76 Hemp protein isolates (HPIs) were hydrolysed by proteases (AFP, HT, ProG, actinidin and zi

77 About 15% of 2-AG in the brain is hydrolysed by serine hydrolase alpha-beta-hydrolase doma

78 w on sucrose, the disaccharide must first be hydrolysed by the enzyme invertase.

79 e related to the multiple natural substrates hydrolysed by the multiple sites of maltase activity.

80 ing the milk fermentation process it was not hydrolysed by the produced acids.

81 1-L140 and L149-I162 were found when BLG was hydrolysed by this strain.

82 Corn protein was hydrolysed by three microbial proteases and further sepa

83 entified product of this reaction is further hydrolysed by TM0413 (IolN) to form 5-keto-l-gluconate.

84 Bovine beta-casein (beta-CN) was hydrolysed by trypsin and fractionated by ultrafiltratio

85 FAD into the periplasmic space, where it is hydrolysed by UshA to FMN and adenosine monophosphate (A

86 Antioxidant peptides of mungbean meal hydrolysed by Virgibacillus sp. SK37 proteinases (VH), A

87 Fish skin gelatin was hydrolysed by visceral alkaline-proteases from Giant cat

88 ults suggest that peptide and phosphodiester hydrolyses by SgAP may share a common reaction mechanism

89 that EcpC has phosphodiesterase activity to hydrolyse c-di-GMP into linear pGpG.

90 PDE4B hydrolyses cAMP and DISC1 may regulate cAMP signalling t

91 Phosphodiesterase (PDE) 4 hydrolyses cAMP and terminates cAMP/PKA signaling.

92 PDE10A hydrolyses cAMP/cGMP signalling cascades, thus having a

93 These MbetaLs hydrolyse carbapenems via a similar mechanism, with accu

94 athway, as well as functioning as xenobiotic-hydrolysing carboxyesterases.

95 brane adherence in a Mfn-dependent manner by hydrolysing cardiolipin to generate phosphatidic acid.

96 stigation of both peptide and phosphodiester hydrolyses catalyzed by SgAP.

97 The use of protease FPII to hydrolyse cattle plasma resulted in a hydrolysate with h

98 om Trichoderma reesei (TrCel7A) processively hydrolyses cellulose into cellobiose.

99 roduction from lignocellulosic feedstocks by hydrolysing cellulose under conditions typically employe

100 BG) is a xenobiotic-metabolizing enzyme that hydrolyses certain flavonoid glucosides, with specificit

101 the GH18 Cphy1799 and Cphy1800, synergize to hydrolyse chitin, a main component of the fungal cell wa

102 nt substrates, but have a reduced ability to hydrolyse chitinous substrates and fungal hyphae.

103 sparagus were evaluated for their ability to hydrolyse commercially available substrates and proteins

104 er, carbonic anhydrase (CA), the enzyme that hydrolyses COS, is expected to be light independent, and

105 ve been able to investigate how GH11 enzymes hydrolyse decorated substrates by solving the crystal st

106 Thus, the mechanism by which these enzymes hydrolyse decorated xylans is unclear and the structural

107 in 1) is known for its antiviral activity of hydrolysing deoxynucleotides required for virus replicat

108 ate: the method was linear for BADGE and its hydrolysed derivatives up to 1000mugkg(-1), for the rema

109 Uch37-Adrm1 or Uch37-Adrm1-S1 complexes can hydrolyse di-ubiquitin efficiently; rather, incorporatio

110 The Fhit tumor suppressor binds and hydrolyses diadenosine polyphosphates and the Fhit-subst

111 ch as the NaOH concentration, time needed to hydrolyse different collagen contents, buffer strength o

112 They are also able to hydrolyse DNA and RNA substrates from the 5'-end, libera

113 with the recent hypothesis that the E9 DNase hydrolyses DNA by two distinct, cation-dependent catalyt

114 es between them in the mean amounts of WU-AX hydrolysed during breadmaking.

115 lso indicated that beta-CN was substantially hydrolysed during the early stages of hydrolysis.

116 but glycosidically bound phenols can also be hydrolysed during the winemaking process, releasing the

117 both safety and efficacy of a low allergenic hydrolysed egg (HydE) preparation used in a double-blind

118 Hydrolysed egg products may be beneficial as low-allerge

119 rwent a double-blind food challenge with the hydrolysed egg remained completely free of symptoms.

120 ure content on physicochemical properties of Hydrolysed Egg White powder (HEW) was more severe than t

121 that, depending on the pH and cofactors, can hydrolyse either pyrophosphate (PPi ) or polyphosphate (

122 ess chemical-consuming and more effective in hydrolysing ellagitannins.

123 howed high efficiency of the purified Cee to hydrolyse Ent.

124 The extracts were additionally hydrolysed enzymatically (beta-glucuronidase/arylsulphat

125 ounds, antioxidant capacity and carbohydrate-hydrolysing enzyme inhibitory activity of roselle bevera

126 Apyrase (500 units ml(-1)), an ATP hydrolysing enzyme, dilated retinal arterioles by 40.4 +

127 l work, to design a highly efficient cocaine hydrolysing enzyme.

128 ich was a function of the specificity of the hydrolysing enzyme.

129 extracts through inhibition of carbohydrate-hydrolysing enzymes.

130 However, saponification also hydrolyses esterified carotenoids and is known to induce

131 ases have the ability to both synthesise and hydrolyse esters.

132 Both purified esterases hydrolysed ethyl butanoate, ethyl hexanoate and ethyl oc

133 indicate that subgroup 6 has the ability to hydrolyse extracellular plant-derived carbohydrates, and

134 Pepsin-hydrolysed FBS, at a 5% degree of hydrolysis (DH), showe

135 A piperacillin-BSA adduct with cyclized and hydrolysed forms of the hapten bound to eight lysine res

136 fumonisins that were then converted to their hydrolysed forms.

137 s at high risk of allergic disease recommend hydrolysed formula if formula is introduced before 6 mon

138 thaliana (AtF2KP), which both generates and hydrolyses fru-2,6-P2, is also regulated by phosphorylat

139 response, corresponding to the catalytic ATP-hydrolysing function of NKA incorporated into the LCP, w

140 in epiphytic lichens (e.g. 11.3 mumol InsP6 hydrolysed g(-1) h(-1) in Bryoria fuscescens) but low in

141 y mild acid treatment, which renders an acid-hydrolysed gliadin/peptide mixture (AHG).

142 re by natural enemies, the myrosinase enzyme hydrolyses glucosinolates, releasing defense molecules.

143 iger propyl-endoprotease (AN-PEP), which can hydrolyse gluten, has been proposed to prevent the harmf

144 hospholipase A2 beta enzyme that selectively hydrolyses glycerophospholipids to release free fatty ac

145 olases, indicating the ability of MGIIa_P to hydrolyse glycosidic bonds in complex sugars in PRE.

146 d with a productivity of 22.2 g of substrate hydrolysed/gram of biocatalyst/hour.

147 sults showed the ability of oral bacteria to hydrolyse grape aroma precursors, releasing different ty

148 storage quality of a commercial spray-dried hydrolysed hen egg white powder (HEW).

149 glucosidase (EC 3.2.1.168) to quantitatively hydrolyse hesperidin to hesperetin, and the last is meas

150 lization on the content of fumonisins (FBs), hydrolysed (HFBs) and partially hydrolysed (PHFBs) fumon

151 The adsorbed proteins were hydrolysed in situ, which resulted in the separation of

152 respectively, into the enzyme biofluids, and hydrolysed in the solvent-free state.

153 Hydrolyses in D(2)O (pD 1.7-3.1) of dimethyl (7), methyl

154 wever, whether one ATP hydrolysis or two ATP hydrolyses in the homodimer of ABCG2 with the NBD.ATP.AT

155 their respective tRNAs, but also selectively hydrolyse incorrectly activated non-cognate amino acids

156 ccharides than infusions, which seemed to be hydrolysed, increasing the content of monosaccharides.

157 Capacity to hydrolyse InsP6 appears widespread amongst lichens poten

158 -32P]-GTP is used to polymerize FtsZ, GTP is hydrolysed instantaneously.

159 tored as triglycerides in lipid droplets are hydrolysed into fatty acids for energy.

160 d forms, for a safe and efficient process to hydrolyse isoflavone glycosides in soy molasses.

161 cteria use metallo-beta-lactamase enzymes to hydrolyse lactam rings found in many antibiotics, render

162 The enzyme could also hydrolyse lactose, with an optimum pH of 4.0 at 40 degre

163 Strain 83-1 furthermore hydrolysed laminarin, pullulan and xylan, and correspond

164 Caa had twice the phospholipid-hydrolysing (lecithinase) activity, 1.5 times the haemol

165 g beta-fructosidase SacC, which specifically hydrolyses levan, contains the founding member of CBM fa

166 oxic form of PEI called dPEI (a nearly fully hydrolysed linear PEI with 11% additional free protonata

167 arations were evaluated for their ability to hydrolyse meat myofibrillar and connective tissue protei

168 indicated that at least three SUR1 must bind/hydrolyse MgATP to open the mutant K(ATP) channel.

169 hobic resin (Toyopearl(R) Butyl) and used to hydrolyse milk lipids in a batch reactor.

170 The rate of available lysine loss in lactose-hydrolysed milk was mostly affected by the presence of g

171 c acid (DHA) and stearidonic acid (STA) were hydrolysed more slowly.

172 se extract was found to be more effective at hydrolysing myofibrillar and collagen proteins than the

173 AT exhibited chymotrypsin-like activity and hydrolysed N-Suc-Ala-Ala-Pro-Phe-pNa and N-Suc-Ala-Ala-P

174 is a zinc containing metallohydrolase which hydrolyses N-succinyl L,L diaminopimelic acid (L,L-NSDAP

175 This preparation hydrolysed NADH, ATP and FAD to generate AMP and was inh

176 d the cognate nucleoside monophosphate, YtkD hydrolyses nucleoside triphosphates in a stepwise fashio

177 regulators, including ENTPD7, an enzyme that hydrolyses nucleotides.

178 The optimum pH of the enzyme was 2.8 and it hydrolysed o-nitrophenyl beta-d galactopyranoside (ONPG)

179 3 (HiAXHd3), a GH43 arabinofuranosidase that hydrolyses O3-linked arabinose of doubly substituted xyl

180 ic extrusion or enzymatic, alkaline and acid hydrolyses occasionally assisted with microwave or ultra

181 The hydronium ion-catalyzed hydrolyses of 5-methoxyindene 1,2-oxide and of 6-methoxy

182 The hydrolyses of AMP-Im and of AMP-N-MeIm by H96G-Fhit are

183 Wild-type Fhit is also found to catalyze the hydrolyses of AMP-Im and of AMP-N-MeIm nearly as efficie

184 he temperature dependence of the spontaneous hydrolyses of aryl sulfate monoesters, which proceed by

185 -O bond breaking in the transition state for hydrolyses of benzaldehyde acetals with secondary and te

186 Hydrolyses of benzaldehyde acetals, PhCH(OR)(2), are spe

187 receptor (SR) form a unique complex in which hydrolyses of both guanosine triphosphates (GTP) are act

188 We report the pH-k(obs) profiles for the hydrolyses of phosphodichloridate and thiophosphodichlor

189 Examination of the base-catalyzed hydrolyses of two other saturated pyrimidine lesions, 5,

190 The hydrolysed okra extract contained 0.6% beta-1, 3-D-gluca

191 t must be prepared from glycyrrhizin (GL) by hydrolysing one terminal glucuronic acid.

192 , we show that these eight ATP molecules are hydrolysed over the next 50 s, after which hydrolysis sl

193 ment of an advanced rupture-prone plaque, to hydrolyse oxidized phospholipid and generate significant

194 rotein-associated phospholipase A2 (Lp-PLA2) hydrolyses oxidized low-density lipoproteins into proinf

195 istidine-glutamic acid triads on each helix, hydrolyses p-nitrophenyl acetate with catalytic efficien

196 ing pure or co-culture with a beta-glycoside-hydrolysing Parabacteroides distasonis.

197 Recombinant PfPARE hydrolyses pepstatin esters and de-esterifies MMV011438.

198 In this compartment, the effectors hydrolyse peptidoglycan, thereby providing a fitness adv

199 ucing two lysis enzymes, Lysin A (LysA) that hydrolyses peptidoglycan, and Lysin B (LysB), a novel my

200 It hydrolyses peptidyl substrates l-Ala-pNA with highest af

201 s for the apparent stoichiometry of two ATPs hydrolysed per molecule of drug transported.

202 there is tight coupling (that is, one ATP is hydrolysed per power stroke), but this has not been dire

203 Enzymes that hydrolyse PG are critical for these processes, but their

204 isins (FBs), hydrolysed (HFBs) and partially hydrolysed (PHFBs) fumonisins in maize was investigated

205 PLCs of P. aeruginosa (PlcH, PlcN and PlcB) hydrolyse phosphatidylcholine (PC), only PlcB is active

206 Phospholipase C gamma 1 (PLC-gamma 1) hydrolyses phosphatidylinositol-4,5-bisphosphate to the

207 ociated with the biofilm lifestyle, c-di-GMP hydrolysing phosphodiesterases (PDEs) have been identifi

208 R/PMH hydrolyses phosphonate monoesters and phosphate diesters

209 ain, bromelain, FP400 and FPII) were used to hydrolyse plasma which was separated from slaughterhouse

210 e (PC) and sphingomyelin (SM) and is able to hydrolyse plasmenylcholine phospholipids (plasmalogens).

211 t, elaborated an enzyme (EnvD) which rapidly hydrolysed poly-gamma-d-glutamic acid (PDGA), the consti

212 seasoning) was produced using enzymatically hydrolysed poultry proteins isolate (PPI).

213 inoid (eCB) 2-arachidonoylglycerol (2-AG) is hydrolysed primarily by monoacylglycerol lipase (MAGL).

214 e studies investigated a mix of whole versus hydrolysed protein and found conflicting results related

215 idant and copper chelating activities of the hydrolysed protein isolate.

216 te in hydrolytic Pu colloid is influenced by hydrolysed Pu(IV) species to a greater extent than in so

217 The prodrug was hydrolysed rapidly to 2-mycophenoloyl glycerol (2-MPA-MG

218 ed at the vertebrate nerve-muscle synapse is hydrolysed rapidly to choline (Cho), so endplate recepto

219 ed at the vertebrate nerve-muscle synapse is hydrolysed rapidly to choline (Cho), so endplate recepto

220 by a specialised activator protein in an ATP-hydrolysing reaction.

221 ater, these malto-oligosaccharides are fully hydrolysed resulting in that way in a correct and lower

222 A treatment to hydrolyse rhamnogalacturonan II borate diester bonds nei

223 (SAHH), the only mammalian enzyme capable of hydrolysing S-adenosylhomocysteine (SAH).

224 The most hydrolysed sample showed high angiotensin I converting e

225 Extensively hydrolysed samples showed higher sourness outputs.

226 which has a highly specialized function and hydrolyses seed-storage xyloglucan rather than modifying

227 owever, the enzyme is capable of binding and hydrolysing sequences that differ from the dcm target si

228 osylases were evaluated for their ability to hydrolyse SG under milder conditions.

229 e suite of surface-bound lichen enzymes that hydrolyse simple organic forms of phosphorus (P) and nit

230 The kinetics of Maillard reaction in lactose-hydrolysed skim milk powder and related systems containi

231 ry process, including hydrosoluble fraction, hydrolysed soap, distillation residue and purified fatty

232 sed on the incorporation of the membrane ATP-hydrolysing sodium/potassium transporter Na(+)/K(+)-ATPa

233 Optimized conditions were: a hydrolysing solution volume 10 ml with 50% ethanol, a pH

234 The results showed that the interaction of hydrolysing solution volume with ethanol ratio, volumes

235 enzyme expressed in intestinal mucosa, which hydrolyses sphingomyelin (SM) to ceramide and inactivate

236 and by the extent of retrogradation between hydrolysed starch chains.

237 athway's role in the metabolism of partially hydrolysed starch derivatives and demonstrate its involv

238 The percentage of hydrolysed starch during in vitro digestion was signific

239 alpha-Amylase hydrolyses starch molecules to produce smaller oligosacc

240 ptidases (FAEE, C-terminal Glu), but did not hydrolyse substrates for carboxypeptidase A or B (FAPP o

241 pane derivative prepared via this method was hydrolysed successfully to form the corresponding linear

242 ct, and optical rotation measurements of the hydrolysed sugar moiety.

243 tide bond, suggesting that the peptidase can hydrolyse tachykinin-related peptides with different str

244 )O-H(2)O show that these reactions are ester hydrolyses that proceed by C(acyl)-O bond cleavage proce

245 Only BGD2 is able to hydrolyse the alpha-HNGs.

246 -labelled cell walls of M. luteus; and (iii) hydrolyse the artificial lysozyme substrate, 4-methylumb

247 Endo-beta1,4-xylanases (xylanases) hydrolyse the beta1,4 glycosidic bonds in the backbone o

248 hosphonate compounds to ATP and subsequently hydrolyse the C-P bond.

249 ns, but may also remodel ubiquitin chains to hydrolyse the isopeptide bond.

250 Chitinase enzymes hydrolyse the polysaccharide chitin, an abundant archite

251 using oxazolines as donors, but which do not hydrolyse the reaction products.

252 self-assembly was induced by an enzyme that hydrolysed the ester.

253 GE activity was highly specific and hydrolysed the peptide bond predominantly on the carboxy

254 h the addition of RNase H, which selectively hydrolyses the hybridized RNA.

255 id ceramidase (AC) - a cysteine amidase that hydrolyses the proapoptotic lipid ceramide - is abnormal

256 ed with pancreatic phospholipase A(2), which hydrolyses the release of membrane-bound AA.

257 dritic cells, restricts HIV-1 replication by hydrolysing the majority of cellular dNTPs, thus inhibit

258 cides to their bioactive herbicidal acids by hydrolysing the respective ester precursors have been id

259 For pepsin and combined pepsin-trypsin hydrolyses, the highest degree of hydrolysis (DH) was ob

260 oplasm of susceptible cells and kill them by hydrolysing their DNA, the colicin must interact with th

261 o-beta-lactamases (MbetaLs), enzymes able to hydrolyse these life-saving drugs.

262 The generated peptides may be further hydrolysed through the gastrointestinal digestion result

263 more rapidly than long chain FAs which were hydrolysed to a greater degree from PC.

264 FBS was hydrolysed to a greater extent than RD regardless of pro

265 molecular mechanisms through which XyGs are hydrolysed to component monosaccharides for further meta

266 The 24h urine samples were hydrolysed to determine the flavanones concentration by

267 to folate synthesis precursors: pABAGlu was hydrolysed to p-aminobenzoate and glutamate, and dihydro

268 questions remain as to why multiple ATPs are hydrolysed to prepare for DNA sliding.

269 The triphosphate moiety of RPnTP is hydrolysed to pyrophosphate and alpha-D-ribose-1-methylp

270 olar extract of tomato fruits, enzymatically hydrolysed to remove the glycosyl residues from the phen

271 s (deoxy)nucleoside triphosphates, which are hydrolysed to their monophosphate counterparts in order

272 ORAC test showed that AAA and semi hydrolysed total phenol (s-TP) fractions were significan

273 Lipoprotein lipase hydrolyses triglycerides in chylomicrons at the luminal

274 Deubiquitinases hydrolyse ubiquitin modifications from proteins and are

275 is DUBs react with activity-based probes and hydrolyse ubiquitinated and neddylated substrates.

276 general rate differences with which they are hydrolysed under various basic conditions.

277 When mince and W-MR-Al were hydrolysed using Alcalase for up to 120 min, a higher de

278 Chicken thigh and breast skin proteins were hydrolysed using alcalase or a combination of pepsin and

279 horse mackerel (Trachurus mediterraneus) was hydrolysed using Alcalase or trypsin.

280 grain protein-enriched isolate (BSG-PI) was hydrolysed using Alcalase, Corolase PP, Flavourzyme and

281 pre-treated whey protein isolate (WPI) were hydrolysed using alpha-chymotrypsin (chymotrypsin), peps

282 a fisheri) protein after agar extraction was hydrolysed using bromelain (enzyme activity=119,325 U/g)

283 Bean protein isolate and phaseolin were hydrolysed using pepsin and pancreatin, and the resultin

284 c acid and Fuscus vesiculosus extract), were hydrolysed using Protease P "Amano" 6 at pH 8 and 36 deg

285 and pig blood, obtained from abattoirs, was hydrolysed using protease preparations from plant (papai

286 tain a cytosolic beta-glucosidase (CBG) that hydrolyses various beta-d-glycosides, but whose physiolo

287 The impact of this work is targeted to add hydrolysed vegetable proteins to reformulated functional

288 Both hydrolyses were found to proceed via different mechanism

289 ycoside hydrolase family 5 (GH5) was used to hydrolyse wheat and rye arabinoxylan, and the product pr

290 39mg/l, which is comparable to enzymatically hydrolysed whey protein.

291 3-month period, while receiving extensively hydrolysed whey-formula (dairy-free diet).

292 lubilisation precipitation process (ISP) was hydrolysed with Alcalase and glycated with glucosamine (

293 an aqueous Palmaria palmata protein extract hydrolysed with Corolase PP.

294 SPI was hydrolysed with Flavourzyme for 2 h to obtain the hydrol

295 ce capacity (ORAC) value was obtained for WP hydrolysed with papain at constant pH of 7.0 compared to

296 WP hydrolysed with papain-like activity under pH regulation

297 tein concentrate from germinated soybean was hydrolysed with pepsin/pancreatin and fractionated by ul

298 In this study, serum albumin was hydrolysed with trypsin after several heat treatments an

299 n concentrate rich in beta-lactoglobulin was hydrolysed with trypsin and fractionated using a chromat

300 VVPF) were identified in camel milk proteins hydrolysed with trypsin.