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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 ng an IC50 value of 138 mug/ml, was obtained hydrolysing a mixture of lupin alpha+beta conglutin.
9                        Butyrylcholinesterase hydrolyses acetylcholine, which exerts immunoregulatory
10 tif 3-containing proteins have peptidoglycan-hydrolysing activity and that while this activity is not
11 A incorporated into the LCP retained its ATP-hydrolysing activity for 7 days, while the solubilized p
12                                     The H2O2 hydrolysing activity of purified catalase is necessary i
13 ne faecal microbes possessing beta-glycoside-hydrolysing activity.
14 tor (MRCA) is not expected to possess lactam-hydrolysing activity.
15         Results show that PPL preferentially hydrolyses ALA and DPA over EPA, DHA and STA, and this s
16 used proteinase K concentrations designed to hydrolyse all fragments resulting from an incomplete dig
17 P and NAD(P)H, which subsequently need to be hydrolysed and oxidized, respectively, in order to resto
18 structure, in which two molecules of ATP are hydrolysed and the rotor of the enzyme turns through two
19 tween 0.75 and 2.5 mg/ml, (p < 0.05) for the hydrolysed and unhydrolysed samples.
20 ate threadfin bream (Nemipterus hexodon) was hydrolysed and used to cultivate Enterobacter sp. C2361
21 ly on DNA at approximately 2000 bp s(-1) and hydrolyses approximately 1 ATP molecule per base pair tr
22  that the active site of HiAXHd3 is tuned to hydrolyse arabinofuranosyl or xylosyl linkages, and it i
23 ht lower than 38 kDa were noticed, while non-hydrolysed arabinoxylan had only peaks corresponding to
24 plexes during baking from samples containing hydrolysed arabinoxylan were associated with limited swe
25 , 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
26                       Mechanisms for the two hydrolyses are drawn on the basis of the results, which
27  oeni produces esterases that are capable of hydrolysing artificial substrates.
28 mining combined effect of enzymatic and acid hydrolyses, associations and fine structure of AX.
29                     Lactose in milk whey was hydrolysed at comparatively higher rate than that of mil
30  with an interplay of alkali penetration and hydrolyses at various time points.
31 ilis FtsE mutants that are unable to bind or hydrolyse ATP cannot activate CwlO.
32                            All type II topos hydrolyse ATP during their reactions; however, only DNA
33 sis in limiting the capacity of the heart to hydrolyse ATP in vivo.
34                                     Kinesins hydrolyse ATP to transport intracellular cargoes along m
35  is unable to stably bind RNA or effectively hydrolyse ATP under physiological conditions, but additi
36           The Arp2 subunit has been shown to hydrolyse ATP, but the functional importance of Arp2/3 A
37 way, and two nucleotide-binding domains that hydrolyse ATP.
38 influence the ability of FtsA to bind and/or hydrolyse ATP.
39 s activities are dependent on its ability to hydrolyse ATP.
40 tion in which specialized activator proteins hydrolyse ATP.
41                 RecA2201 binds, but does not hydrolyse ATP.
42 e subunits when the cassette dimer closes to hydrolyse ATP.
43  were expressing extracellular hydrolases to hydrolyse ATP.
44 system (sigma54-RNAP, Esigma54) and a slowly hydrolysed ATP analogue (ATPgammaS), we provide evidence
45 found that purified wild-type FtsA bound and hydrolysed ATP, whereas FtsA27 was defective in both act
46          We found that T7 helicase binds and hydrolyses ATP and dTTP by competitive kinetics such tha
47                                    p33 alone hydrolyses ATP but exhibits no helicase activity.
48                                  The complex hydrolyses ATP in the absence of DNA; unwinds duplex reg
49                                           It hydrolyses ATP to remodel chromatin structure by sliding
50                          Apaf-1 binds to and hydrolyses ATP/dATP and their analogues.
51   Mutants of SecA capable of binding but not hydrolysing ATP do not elicit this conformationally acti
52 e authors suggested that cardosins could not hydrolyse beta-lactoblogulin.
53  ability of the Lab4 probiotic consortium to hydrolyse bile salts, assimilate cholesterol and regulat
54 asein hydrolysis kinetics and were active in hydrolysing BODIPY-FL casein to varying extents at postm
55                         No specific peptidic hydrolysed bond was detected.
56 this esterase proved a remarkable ability to hydrolyse both natural and synthetic polyesters.
57  bacterial-derived protease (HT) extensively hydrolysed both meat protein extracts, producing peptide
58  falciparum phosphodiesterase beta (PDEbeta) hydrolyses both cAMP and cGMP and is essential for blood
59 defatted skipjack (Katsuwonous pelamis) roe, hydrolysed by Alcalase 2.4 L (RPH) with different degree
60 (Saccharomyces cerevisiae) was enzymatically hydrolysed by Alcalase, Protex or Viscozyme.
61 acellular space via SWEET9, where sucrose is hydrolysed by an apoplasmic invertase to produce a mixtu
62                L-cIDPR is surprisingly still hydrolysed by CD38, whereas 8-Br-L-cIDPR is not cleaved,
63 ivo assays show that the cow's milk proteins hydrolysed by CgLP and CapLP exhibited no immune reactio
64  released when a starch-triiodide complex is hydrolysed by honey diastase.
65                     Cell-wall components are hydrolysed by numerous plant glycosidase and glycanase a
66       Food proteins can also be isolated and hydrolysed by peptidases to produce hydrolysates.
67       High-molecular-weight kininogen can be hydrolysed by plasma kallikrein to bradykinin and cleave
68 ol 4,5-bisphosphate (PIP(2) ), the substrate hydrolysed by PLC, and intracellular Ca(2+) .
69            Hemp protein isolates (HPIs) were hydrolysed by proteases (AFP, HT, ProG, actinidin and zi
70            About 15% of 2-AG in the brain is hydrolysed by serine hydrolase alpha-beta-hydrolase doma
71 w on sucrose, the disaccharide must first be hydrolysed by the enzyme invertase.
72 ing the milk fermentation process it was not hydrolysed by the produced acids.
73 1-L140 and L149-I162 were found when BLG was hydrolysed by this strain.
74                             Corn protein was hydrolysed by three microbial proteases and further sepa
75 entified product of this reaction is further hydrolysed by TM0413 (IolN) to form 5-keto-l-gluconate.
76             Bovine beta-casein (beta-CN) was hydrolysed by trypsin and fractionated by ultrafiltratio
77  FAD into the periplasmic space, where it is hydrolysed by UshA to FMN and adenosine monophosphate (A
78        Antioxidant peptides of mungbean meal hydrolysed by Virgibacillus sp. SK37 proteinases (VH), A
79                        Fish skin gelatin was hydrolysed by visceral alkaline-proteases from Giant cat
80 ults suggest that peptide and phosphodiester hydrolyses by SgAP may share a common reaction mechanism
81  that EcpC has phosphodiesterase activity to hydrolyse c-di-GMP into linear pGpG.
82                                        PDE4B hydrolyses cAMP and DISC1 may regulate cAMP signalling t
83                    Phosphodiesterase (PDE) 4 hydrolyses cAMP and terminates cAMP/PKA signaling.
84                                       PDE10A hydrolyses cAMP/cGMP signalling cascades, thus having a
85                                These MbetaLs hydrolyse carbapenems via a similar mechanism, with accu
86 athway, as well as functioning as xenobiotic-hydrolysing carboxyesterases.
87 brane adherence in a Mfn-dependent manner by hydrolysing cardiolipin to generate phosphatidic acid.
88 stigation of both peptide and phosphodiester hydrolyses catalyzed by SgAP.
89                  The use of protease FPII to hydrolyse cattle plasma resulted in a hydrolysate with h
90 om Trichoderma reesei (TrCel7A) processively hydrolyses cellulose into cellobiose.
91 roduction from lignocellulosic feedstocks by hydrolysing cellulose under conditions typically employe
92 BG) is a xenobiotic-metabolizing enzyme that hydrolyses certain flavonoid glucosides, with specificit
93 the GH18 Cphy1799 and Cphy1800, synergize to hydrolyse chitin, a main component of the fungal cell wa
94 nt substrates, but have a reduced ability to hydrolyse chitinous substrates and fungal hyphae.
95 sparagus were evaluated for their ability to hydrolyse commercially available substrates and proteins
96 er, carbonic anhydrase (CA), the enzyme that hydrolyses COS, is expected to be light independent, and
97                           Amidases typically hydrolyse crosslinked peptidoglycan between daughter cel
98 ve been able to investigate how GH11 enzymes hydrolyse decorated substrates by solving the crystal st
99   Thus, the mechanism by which these enzymes hydrolyse decorated xylans is unclear and the structural
100 in 1) is known for its antiviral activity of hydrolysing deoxynucleotides required for virus replicat
101 ate: the method was linear for BADGE and its hydrolysed derivatives up to 1000mugkg(-1), for the rema
102  Uch37-Adrm1 or Uch37-Adrm1-S1 complexes can hydrolyse di-ubiquitin efficiently; rather, incorporatio
103          The Fhit tumor suppressor binds and hydrolyses diadenosine polyphosphates and the Fhit-subst
104 ch as the NaOH concentration, time needed to hydrolyse different collagen contents, buffer strength o
105                        They are also able to hydrolyse DNA and RNA substrates from the 5'-end, libera
106 es between them in the mean amounts of WU-AX hydrolysed during breadmaking.
107 lso indicated that beta-CN was substantially hydrolysed during the early stages of hydrolysis.
108 but glycosidically bound phenols can also be hydrolysed during the winemaking process, releasing the
109 s and is converted by the microglial ATP/ADP hydrolysing ectoenzyme CD39 into AMP; AMP is then conver
110 both safety and efficacy of a low allergenic hydrolysed egg (HydE) preparation used in a double-blind
111                                              Hydrolysed egg products may be beneficial as low-allerge
112 rwent a double-blind food challenge with the hydrolysed egg remained completely free of symptoms.
113 ure content on physicochemical properties of Hydrolysed Egg White powder (HEW) was more severe than t
114 h hypoallergenic label [pHF-HA], extensively hydrolysed [eHF], soya) and solid food introduction were
115 that, depending on the pH and cofactors, can hydrolyse either pyrophosphate (PPi ) or polyphosphate (
116 ess chemical-consuming and more effective in hydrolysing ellagitannins.
117  rituximab as the crosslinkers are gradually hydrolysed, enhancing the CNS levels of the antibody by
118 howed high efficiency of the purified Cee to hydrolyse Ent.
119               The extracts were additionally hydrolysed enzymatically (beta-glucuronidase/arylsulphat
120 ounds, antioxidant capacity and carbohydrate-hydrolysing enzyme inhibitory activity of roselle bevera
121           Apyrase (500 units ml(-1)), an ATP hydrolysing enzyme, dilated retinal arterioles by 40.4 +
122 l work, to design a highly efficient cocaine hydrolysing enzyme.
123 ich was a function of the specificity of the hydrolysing enzyme.
124  extracts through inhibition of carbohydrate-hydrolysing enzymes.
125                 However, saponification also hydrolyses esterified carotenoids and is known to induce
126 ases have the ability to both synthesise and hydrolyse esters.
127                      Both purified esterases hydrolysed ethyl butanoate, ethyl hexanoate and ethyl oc
128  indicate that subgroup 6 has the ability to hydrolyse extracellular plant-derived carbohydrates, and
129                                       Pepsin-hydrolysed FBS, at a 5% degree of hydrolysis (DH), showe
130        Major muscle proteins are extensively hydrolysed firstly by endogenous endo-peptidases followe
131  A piperacillin-BSA adduct with cyclized and hydrolysed forms of the hapten bound to eight lysine res
132 fumonisins that were then converted to their hydrolysed forms.
133 s at high risk of allergic disease recommend hydrolysed formula if formula is introduced before 6 mon
134 ow's milk, similar to a commercial partially hydrolysed formula.
135 response, corresponding to the catalytic ATP-hydrolysing function of NKA incorporated into the LCP, w
136  in epiphytic lichens (e.g. 11.3 mumol InsP6 hydrolysed g(-1) h(-1) in Bryoria fuscescens) but low in
137 y mild acid treatment, which renders an acid-hydrolysed gliadin/peptide mixture (AHG).
138                        Actinidin efficacy in hydrolysing gliadin was compared with that of other glut
139 re by natural enemies, the myrosinase enzyme hydrolyses glucosinolates, releasing defense molecules.
140                         Actinidin is able to hydrolyse gluten proteins under simulated gastric condit
141 iger propyl-endoprotease (AN-PEP), which can hydrolyse gluten, has been proposed to prevent the harmf
142 hospholipase A2 beta enzyme that selectively hydrolyses glycerophospholipids to release free fatty ac
143 olases, indicating the ability of MGIIa_P to hydrolyse glycosidic bonds in complex sugars in PRE.
144 d with a productivity of 22.2 g of substrate hydrolysed/gram of biocatalyst/hour.
145 sults showed the ability of oral bacteria to hydrolyse grape aroma precursors, releasing different ty
146  storage quality of a commercial spray-dried hydrolysed hen egg white powder (HEW).
147 glucosidase (EC 3.2.1.168) to quantitatively hydrolyse hesperidin to hesperetin, and the last is meas
148 lization on the content of fumonisins (FBs), hydrolysed (HFBs) and partially hydrolysed (PHFBs) fumon
149                   The adsorbed proteins were hydrolysed in situ, which resulted in the separation of
150                            Lactose is mostly hydrolysed in the small intestine, whereas lactulose, re
151 respectively, into the enzyme biofluids, and hydrolysed in the solvent-free state.
152 wever, whether one ATP hydrolysis or two ATP hydrolyses in the homodimer of ABCG2 with the NBD.ATP.AT
153 their respective tRNAs, but also selectively hydrolyse incorrectly activated non-cognate amino acids
154 ccharides than infusions, which seemed to be hydrolysed, increasing the content of monosaccharides.
155                                  Capacity to hydrolyse InsP6 appears widespread amongst lichens poten
156 tored as triglycerides in lipid droplets are hydrolysed into fatty acids for energy.
157                                    The shell hydrolyses into 'flocs' and destabilizes and enmeshes co
158 d forms, for a safe and efficient process to hydrolyse isoflavone glycosides in soy molasses.
159 cteria use metallo-beta-lactamase enzymes to hydrolyse lactam rings found in many antibiotics, render
160                        The enzyme could also hydrolyse lactose, with an optimum pH of 4.0 at 40 degre
161                      Strain 83-1 furthermore hydrolysed laminarin, pullulan and xylan, and correspond
162 g beta-fructosidase SacC, which specifically hydrolyses levan, contains the founding member of CBM fa
163 oxic form of PEI called dPEI (a nearly fully hydrolysed linear PEI with 11% additional free protonata
164 arations were evaluated for their ability to hydrolyse meat myofibrillar and connective tissue protei
165 indicated that at least three SUR1 must bind/hydrolyse MgATP to open the mutant K(ATP) channel.
166 hobic resin (Toyopearl(R) Butyl) and used to hydrolyse milk lipids in a batch reactor.
167 The rate of available lysine loss in lactose-hydrolysed milk was mostly affected by the presence of g
168 ds decreased during digestion and that their hydrolysed molecules increased.
169 c acid (DHA) and stearidonic acid (STA) were hydrolysed more slowly.
170 se extract was found to be more effective at hydrolysing myofibrillar and collagen proteins than the
171  AT exhibited chymotrypsin-like activity and hydrolysed N-Suc-Ala-Ala-Pro-Phe-pNa and N-Suc-Ala-Ala-P
172  is a zinc containing metallohydrolase which hydrolyses N-succinyl L,L diaminopimelic acid (L,L-NSDAP
173 regulators, including ENTPD7, an enzyme that hydrolyses nucleotides.
174  The optimum pH of the enzyme was 2.8 and it hydrolysed o-nitrophenyl beta-d galactopyranoside (ONPG)
175 3 (HiAXHd3), a GH43 arabinofuranosidase that hydrolyses O3-linked arabinose of doubly substituted xyl
176 ic extrusion or enzymatic, alkaline and acid hydrolyses occasionally assisted with microwave or ultra
177 he temperature dependence of the spontaneous hydrolyses of aryl sulfate monoesters, which proceed by
178 receptor (SR) form a unique complex in which hydrolyses of both guanosine triphosphates (GTP) are act
179          Glycoside hydrolases (GHs) catalyze hydrolyses of glycoconjugates in which the enzyme choreo
180     We report the pH-k(obs) profiles for the hydrolyses of phosphodichloridate and thiophosphodichlor
181            Examination of the base-catalyzed hydrolyses of two other saturated pyrimidine lesions, 5,
182                                          The hydrolysed okra extract contained 0.6% beta-1, 3-D-gluca
183 t must be prepared from glycyrrhizin (GL) by hydrolysing one terminal glucuronic acid.
184 , we show that these eight ATP molecules are hydrolysed over the next 50 s, after which hydrolysis sl
185 he starch in bread and 30% of that in pasta, hydrolysing over half of it into oligosaccharides.
186 rotein-associated phospholipase A2 (Lp-PLA2) hydrolyses oxidized low-density lipoproteins into proinf
187 istidine-glutamic acid triads on each helix, hydrolyses p-nitrophenyl acetate with catalytic efficien
188 ing pure or co-culture with a beta-glycoside-hydrolysing Parabacteroides distasonis.
189 any choline-utilizing gut microorganisms can hydrolyse PC using a phospholipase D (PLD) enzyme and fu
190                           Recombinant PfPARE hydrolyses pepstatin esters and de-esterifies MMV011438.
191           In this compartment, the effectors hydrolyse peptidoglycan, thereby providing a fitness adv
192 ucing two lysis enzymes, Lysin A (LysA) that hydrolyses peptidoglycan, and Lysin B (LysB), a novel my
193                                           It hydrolyses peptidyl substrates l-Ala-pNA with highest af
194 there is tight coupling (that is, one ATP is hydrolysed per power stroke), but this has not been dire
195                                 Enzymes that hydrolyse PG are critical for these processes, but their
196 isins (FBs), hydrolysed (HFBs) and partially hydrolysed (PHFBs) fumonisins in maize was investigated
197 cilitates G(i/o) activation of TRPC4 through hydrolysing phosphatidylinositol 4,5-bisphosphate (PIP(2
198 ociated with the biofilm lifestyle, c-di-GMP hydrolysing phosphodiesterases (PDEs) have been identifi
199                                        R/PMH hydrolyses phosphonate monoesters and phosphate diesters
200 ain, bromelain, FP400 and FPII) were used to hydrolyse plasma which was separated from slaughterhouse
201 t, elaborated an enzyme (EnvD) which rapidly hydrolysed poly-gamma-d-glutamic acid (PDGA), the consti
202 Results indicated that applied enzymes could hydrolyse polymeric arabinoxylan while their synergistic
203  seasoning) was produced using enzymatically hydrolysed poultry proteins isolate (PPI).
204 inoid (eCB) 2-arachidonoylglycerol (2-AG) is hydrolysed primarily by monoacylglycerol lipase (MAGL).
205 tonucleotidases such as CD39 and CD73, which hydrolyse pro-inflammatory ATP to generate immunosuppres
206 e studies investigated a mix of whole versus hydrolysed protein and found conflicting results related
207 idant and copper chelating activities of the hydrolysed protein isolate.
208 te in hydrolytic Pu colloid is influenced by hydrolysed Pu(IV) species to a greater extent than in so
209                              The prodrug was hydrolysed rapidly to 2-mycophenoloyl glycerol (2-MPA-MG
210 ed at the vertebrate nerve-muscle synapse is hydrolysed rapidly to choline (Cho), so endplate recepto
211 ed at the vertebrate nerve-muscle synapse is hydrolysed rapidly to choline (Cho), so endplate recepto
212 by a specialised activator protein in an ATP-hydrolysing reaction.
213 ater, these malto-oligosaccharides are fully hydrolysed resulting in that way in a correct and lower
214                               A treatment to hydrolyse rhamnogalacturonan II borate diester bonds nei
215 es when they form part of the DNA strand, or hydrolyse RNA when it base-pairs with DNA in structures
216 (SAHH), the only mammalian enzyme capable of hydrolysing S-adenosylhomocysteine (SAH).
217                                     The most hydrolysed sample showed high angiotensin I converting e
218                                  Extensively hydrolysed samples showed higher sourness outputs.
219 (ABTS) radicals in comparison with those non-hydrolysed samples.
220  which has a highly specialized function and hydrolyses seed-storage xyloglucan rather than modifying
221 significantly greater in PHM over 28% of the hydrolysed sequence.
222 osylases were evaluated for their ability to hydrolyse SG under milder conditions.
223 e suite of surface-bound lichen enzymes that hydrolyse simple organic forms of phosphorus (P) and nit
224 The kinetics of Maillard reaction in lactose-hydrolysed skim milk powder and related systems containi
225 ry process, including hydrosoluble fraction, hydrolysed soap, distillation residue and purified fatty
226 sed on the incorporation of the membrane ATP-hydrolysing sodium/potassium transporter Na(+)/K(+)-ATPa
227                 Optimized conditions were: a hydrolysing solution volume 10 ml with 50% ethanol, a pH
228   The results showed that the interaction of hydrolysing solution volume with ethanol ratio, volumes
229 enzyme expressed in intestinal mucosa, which hydrolyses sphingomyelin (SM) to ceramide and inactivate
230  and by the extent of retrogradation between hydrolysed starch chains.
231 athway's role in the metabolism of partially hydrolysed starch derivatives and demonstrate its involv
232                            The percentage of hydrolysed starch during in vitro digestion was signific
233                                alpha-Amylase hydrolyses starch molecules to produce smaller oligosacc
234 pane derivative prepared via this method was hydrolysed successfully to form the corresponding linear
235 ct, and optical rotation measurements of the hydrolysed sugar moiety.
236 in from S. plantesis (ProS) was more rapidly hydrolysed than proteins from D. salina (ProD) because o
237 )O-H(2)O show that these reactions are ester hydrolyses that proceed by C(acyl)-O bond cleavage proce
238                         Only BGD2 is able to hydrolyse the alpha-HNGs.
239           Endo-beta1,4-xylanases (xylanases) hydrolyse the beta1,4 glycosidic bonds in the backbone o
240 hosphonate compounds to ATP and subsequently hydrolyse the C-P bond.
241 ns, but may also remodel ubiquitin chains to hydrolyse the isopeptide bond.
242 n), while all exogenous enzymes were able to hydrolyse the pentapeptide epitopes effectively.
243                            Chitinase enzymes hydrolyse the polysaccharide chitin, an abundant archite
244 using oxazolines as donors, but which do not hydrolyse the reaction products.
245  self-assembly was induced by an enzyme that hydrolysed the ester.
246          GE activity was highly specific and hydrolysed the peptide bond predominantly on the carboxy
247  tyrosyl-DNA phosphodiesterase (TDP1), which hydrolyses the bond that links a tyrosine in the active
248 h the addition of RNase H, which selectively hydrolyses the hybridized RNA.
249 id ceramidase (AC) - a cysteine amidase that hydrolyses the proapoptotic lipid ceramide - is abnormal
250 ed with pancreatic phospholipase A(2), which hydrolyses the release of membrane-bound AA.
251 dritic cells, restricts HIV-1 replication by hydrolysing the majority of cellular dNTPs, thus inhibit
252       For pepsin and combined pepsin-trypsin hydrolyses, the highest degree of hydrolysis (DH) was ob
253 o-beta-lactamases (MbetaLs), enzymes able to hydrolyse these life-saving drugs.
254 anabolic processes and by nucleotidases that hydrolyse these metabolites into nucleosides.
255 eceptor to prevent alkaline phosphatase from hydrolysing these substrates.
256        The generated peptides may be further hydrolysed through the gastrointestinal digestion result
257  more rapidly than long chain FAs which were hydrolysed to a greater degree from PC.
258                                      FBS was hydrolysed to a greater extent than RD regardless of pro
259  molecular mechanisms through which XyGs are hydrolysed to component monosaccharides for further meta
260                   The 24h urine samples were hydrolysed to determine the flavanones concentration by
261  to folate synthesis precursors: pABAGlu was hydrolysed to p-aminobenzoate and glutamate, and dihydro
262 questions remain as to why multiple ATPs are hydrolysed to prepare for DNA sliding.
263          The triphosphate moiety of RPnTP is hydrolysed to pyrophosphate and alpha-D-ribose-1-methylp
264 olar extract of tomato fruits, enzymatically hydrolysed to remove the glycosyl residues from the phen
265 s (deoxy)nucleoside triphosphates, which are hydrolysed to their monophosphate counterparts in order
266  these vesicles, 1-arseno-3-phosphoglycerate hydrolyses to release arsenate, which is then reduced by
267           ORAC test showed that AAA and semi hydrolysed total phenol (s-TP) fractions were significan
268                           Lipoprotein lipase hydrolyses triglycerides in chylomicrons at the luminal
269                              Deubiquitinases hydrolyse ubiquitin modifications from proteins and are
270 is DUBs react with activity-based probes and hydrolyse ubiquitinated and neddylated substrates.
271 general rate differences with which they are hydrolysed under various basic conditions.
272                  When mince and W-MR-Al were hydrolysed using Alcalase for up to 120 min, a higher de
273  Chicken thigh and breast skin proteins were hydrolysed using alcalase or a combination of pepsin and
274 horse mackerel (Trachurus mediterraneus) was hydrolysed using Alcalase or trypsin.
275  grain protein-enriched isolate (BSG-PI) was hydrolysed using Alcalase, Corolase PP, Flavourzyme and
276  pre-treated whey protein isolate (WPI) were hydrolysed using alpha-chymotrypsin (chymotrypsin), peps
277 a fisheri) protein after agar extraction was hydrolysed using bromelain (enzyme activity=119,325 U/g)
278                      Bovine whey protein was hydrolysed using cardosins A and B purified from dried f
279      Bean protein isolate and phaseolin were hydrolysed using pepsin and pancreatin, and the resultin
280 c acid and Fuscus vesiculosus extract), were hydrolysed using Protease P "Amano" 6 at pH 8 and 36 deg
281  and pig blood, obtained from abattoirs, was hydrolysed using protease preparations from plant (papai
282                                    Actinidin hydrolysed usually resistant peptide bonds adjacent to p
283   The impact of this work is targeted to add hydrolysed vegetable proteins to reformulated functional
284 at specific sites and that a subset of these hydrolyses was conserved across enzyme pools derived fro
285                                         Both hydrolyses were found to proceed via different mechanism
286 ycoside hydrolase family 5 (GH5) was used to hydrolyse wheat and rye arabinoxylan, and the product pr
287 39mg/l, which is comparable to enzymatically hydrolysed whey protein.
288  3-month period, while receiving extensively hydrolysed whey-formula (dairy-free diet).
289 lubilisation precipitation process (ISP) was hydrolysed with Alcalase and glycated with glucosamine (
290  an aqueous Palmaria palmata protein extract hydrolysed with Corolase PP.
291                                      SPI was hydrolysed with Flavourzyme for 2 h to obtain the hydrol
292 formula (regular, pre-/probiotics, partially hydrolysed with hypoallergenic label [pHF-HA], extensive
293   In the present work, the chia expeller was hydrolysed with Papain and the antioxidant properties of
294 ce capacity (ORAC) value was obtained for WP hydrolysed with papain at constant pH of 7.0 compared to
295                                           WP hydrolysed with papain-like activity under pH regulation
296 tein concentrate from germinated soybean was hydrolysed with pepsin/pancreatin and fractionated by ul
297             In this study, serum albumin was hydrolysed with trypsin after several heat treatments an
298 n concentrate rich in beta-lactoglobulin was hydrolysed with trypsin and fractionated using a chromat
299 (w/w) protein) was prepared and subsequently hydrolysed with trypsin at different temperatures, enzym
300 VVPF) were identified in camel milk proteins hydrolysed with trypsin.

 
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