戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 nsiderably greater in wines made by carbonic maceration.
2 ay winegrapes during twelve days of carbonic maceration.
3  greatest decrease of these compounds during maceration.
4 tivity were found following 6 and 10 days of maceration.
5 already consolidated in winemaking, carbonic maceration.
6  extracted by steam distillation and aqueous maceration.
7 d on seed surface have been quantified after maceration.
8 the wines as a function of time and stage of maceration.
9 erial densities and causing prominent tissue maceration.
10 t activity (up to 82 % DPPH scavenging) than maceration.
11  results compared to the benchmark of reflux maceration.
12 iques were the most effective techniques for maceration.
13 e lowest in the must pre-treatment by thermo-maceration.
14  altered, according to the time and stage of maceration.
15 olatile composition after a pre-fermentation maceration.
16 tarius deliciosus compared with conventional maceration.
17 aled a more efficient cell wall rupture with maceration.
18 ere assessed during a 72-hour skin simulated maceration.
19 nt and their extractability during simulated maceration.
20 teolin-7-O-glucoside extraction than dynamic maceration.
21 s from withered grape skins during simulated maceration.
22 itamin E concentrations were not affected by maceration.
23 lycopene-rich oleoresin using hexane solvent maceration.
24  alcoholic fermentation to post-fermentative maceration.
25 g enzymes and results in an extensive tissue maceration.
26 abilisation in comparison to the traditional maceration.
27 om the seeds were determined after simulated maceration.
28 anicum extract was prepared using continuous macerations.
29 erent copigment concentrations in grape skin macerations.
30 thout; tannin addition: 0-9 g/L; and time of maceration: 0-11 days) on tannin, pigment, and protein e
31    In the extract obtained by hydroalcoholic maceration, 24 compounds were characterized using liquid
32 e lowest in the must pre-treatment by thermo-maceration (2979.8 mg/100 mL).
33 volution of the determined parameters during maceration (90 and 180 days) allowed a number of interes
34                                       During maceration, a reduction in the crushed berry skin break
35            However, some mutants gave higher maceration activity in plant tissue and elicited greater
36 (DW) was more effective than the simple post-maceration addition to improve the phenolic structure of
37  hydroalcoholic (HHM), and aqueous enzymatic maceration (AEM) were applied to crude (CG) and waste gu
38 fied sweet wine (FSW) was also obtained: the maceration-alcoholic fermentation of Garnacha Tintorera
39 FSW presented the lowest content because the maceration-alcoholic fermentation was stopped through th
40                                              Maceration also helped reduce total processing time.
41                                    Cryogenic maceration also increased the levels of several varietal
42 e 2017 vintage, 40 had been made by carbonic maceration and 44 by destemming and crushing.
43            The influence of pre-fermentative maceration and ageing factors on the ester profiles of P
44 volatile markers related to pre-fermentative maceration and ageing time, reported for the first time
45                  The effects of the carbonic maceration and conventional winemaking on the volatile c
46 activity per se are involved in plant tissue maceration and elicitor activity.
47 ial, chemical, and microbial) after carbonic maceration and fermentation.
48                     3-DXAs were sensitive to maceration and germination (retentions of 69.6% and 69.9
49                                The impact of maceration and germination on the concentration of bioac
50                                              Maceration and germination reduced thiamine and pyridoxi
51 was evaluated in sorghum grains subjected to maceration and germination, using High Performance Liqui
52 was evaluated in sorghum grains subjected to maceration and germination, using High Performance Liqui
53  blot, glomerulus number determined via acid maceration and hormone changes by radioimmunoassay (RIA)
54 tic - are able to infect Mp and cause tissue maceration and host cell killing.
55 n further knowledge on the influence of chip maceration and micro-oxygenation related factors (oxygen
56 GA were maintained in the pulping, enzymatic maceration and microfiltration, leading to a concentrati
57  movement along the vascular parenchyma, and maceration and rotting of the petiole and central bud.
58                    The extraction by dynamic maceration and separation by ultra-high-performance liqu
59 ioactive components compared to conventional maceration and single-method methods.
60 tervention (blister) and two in the control (maceration and skin tear) groups.
61     Methanol and water extracts, obtained by maceration and Soxhlet extraction, were examined.
62                                              Maceration and Soxhlet methods were used to obtain metha
63 atty acids from the fourth to seventh day of maceration and the presence of oak chips during the ferm
64 ion between two winemaking methods: carbonic maceration and the standard method of destemming and cru
65 techniques (grape freezing, dry-ice and cold maceration) and a control treatment were measured.
66 cted using a conventional technique (dynamic maceration) and an emerging technology, such as pressuri
67 ent maceration techniques (microwave, thermo-maceration, and enzymatic treatment) on the content of p
68 d the effect of high pressure extraction and maceration, and four extraction solvents (three hydroalc
69 e extracts, produced with and without enzyme maceration, and the saliva protein-tannin precipitation
70                                 In wine-like maceration, anthocyanins quickly peaked and then decreas
71                         This study evaluated maceration as a pre-treatment combined with various proc
72  (ultrasound extraction) as modern, and MAC (maceration) as conventional extraction technique.
73       For this purpose, the applied methods: maceration, ASE and SFE coupled with ASE were incorporat
74 s on more than 600 plant species with tissue maceration being the most prominent symptom.
75  different techniques (cold pre-fermentative maceration, beta-galactosidase enzyme addition and enzym
76 gns of fungal infection, cracks/fissures, or maceration between toes (36.3%); 30.9% had some tenderne
77 rs affecting the v-dPCR performance were the maceration buffer composition, the target DNA amplicon l
78 ate strengths at different times during cold maceration (CM) (0, 2 and 4days) was more efficient for
79                                     Carbonic maceration (CM) consists in placing intact grape bunches
80 e monomeric phenolic composition of carbonic maceration (CM) wines.
81    As an alternative to traditional carbonic maceration (CM), this study explores the use of nitrogen
82 rganic-walled microfossils extracted by acid maceration, complemented by studies using thin sections
83                         The pre-fermentative maceration consisted of the skin-maceration of musts at
84 accharide and monosaccharide content to long maceration control wines.
85  subjected to either 10 or 240 days extended maceration (Control and EM).
86 ion of Teran red wine were studied: standard maceration (control C), cold pre-fermentation maceration
87 nfandel wines were produced with traditional maceration (Control), and extended maceration for one (1
88 mpounds and flavonoids from I. laurina using maceration (conventional), ultrasonic bath and probes, c
89 aceration (control C), cold pre-fermentation maceration (CPM), saignee (S), pre-fermentation heating
90  In this work, impact of extraction methods (maceration, decoction, MAE, and UAE) on TPC, antioxidant
91        Sparkling wines with pre-fermentative maceration displayed higher contents of ethyl esters of
92 fect of different pre- and post-fermentation maceration durations on the chemical and sensory charact
93                              The double post-maceration (DW) was more effective than the simple post-
94                                              Maceration enhanced the oxidative stability of the teste
95 (TM), Prefermentative Cold Maceration (PCM), Maceration Enzyme (ENZ) and grape-Seed Tannins additions
96  phenolic extraction with a pectolytic-based maceration enzyme with that of favoring both phenolic ex
97 pared with the wine made using a traditional maceration enzyme.
98 nidin-cell wall interactions when commercial maceration enzymes are present in the solution.
99             Wines made with pre-fermentation maceration exhibited floral attributes, citrus and white
100 a response surface method comparing with the maceration extraction (MAE) method.
101          As compared to ultrasonic (UAE) and maceration extraction (ME), MAE showed significantly (p<
102 ined by supercritical fluid, antisolvent and maceration extraction in different solvents were compare
103          The effects of the variables of the maceration extraction of betacyanins have not been prope
104                                  Traditional maceration fermentation conditions gave the highest conc
105 of crushed skin mechanical properties during maceration-fermentation, as also affected by grape ripen
106                                          The maceration/fermentation of coffee berries generated inte
107 hnological applications to traditional grape maceration for avoiding the common loss of colour of win
108 ydrodynamic cavitation (HC) and conventional maceration for extracting bioactive compounds from A.nod
109 a more efficient, sustainable alternative to maceration for maximizing bioactive compound recovery an
110 aditional maceration (Control), and extended maceration for one (1 month-EM), and six months (6 month
111   Conventional extraction techniques such as maceration, grinding or pressing have reported low yield
112 from sonicated grapes at 28 kHz and with mid maceration had higher rhamnogalacturonans type II and PR
113 her anthocyanin content and retention during maceration, higher antioxidant capacity, presented simil
114                                          C2 (maceration + immersion) reduced tannin content by 3-fold
115  UAE significantly outperformed conventional maceration in carotenoid yield, depending on the solvent
116 y chronic, recurrent vesicles, erosions, and maceration in flexural areas.
117                                              Maceration in methanol allowed recovering the highest cu
118  autolysis, concomitant to post-fermentation maceration in red winemaking.
119 traction from berries in wines and from skin macerations in model solutions have been studied for two
120                                    Cryogenic maceration increased phenolics and antioxidant activity.
121 in pomace at higher temperatures or extended maceration indicated enhanced extraction and subsequent
122 aims to investigate which extraction method (maceration, infusion, or Soxhlet) and which green solven
123                            Pectolytic enzyme maceration is common for producing red wines, but the ef
124                                       Longer macerations led to less wine anthocyanins.
125     In contrast, Pr2 (pressure cooking after maceration) led to a ~ 40 % reduction in nutritional and
126 nd (UAE), microwave (MAE), and conventional (maceration (MAC)) was applied using two"green" solvents
127     Five eco-friendly extractive techniques [maceration (MAC), digestion (DIG), accelerated solvent e
128 se obtained using the conventional method of maceration (ME).
129          This work is about improvement of a maceration method in order to achieve a green process fo
130 ion of accelerated solvent extraction (ASE), maceration method of extraction, and using of volatile n
131                                  Traditional maceration method was used for the extraction of polyphe
132                     No thermal pre-treatment maceration methods gave lighter or redder must.
133 cts were obtained by hot extraction and cold maceration methods using aqueous and methanolic solvents
134 CM), this study explores the use of nitrogen maceration (NM) to create anoxic conditions during winem
135 ed on the comparison between CM and nitrogen maceration (NM).
136       The optimal extraction conditions were maceration of 0.75mm size berries by 50% ethanol, with s
137 s is vermouth, a fortified wine based on the maceration of a large number of herbs, fruits, barks, se
138 ared to AC5006, AC5061 causes more extensive maceration of celery petioles.
139 y aimed to evaluate the effect of ultrasound maceration of cold-pressed oils with freeze-dried mullei
140 cyanins in the pomace, and both cold and hot maceration of fresh unblanched berries with enzyme the l
141                                         Cold maceration of frozen berries without enzyme addition gav
142 s: ice wine production, berry freezing, cold maceration of grape must, and cryoconcentration of grape
143 cts of different grape lots were obtained by maceration of grapes in hydroalcoholic solution; afterwa
144 ermentative maceration consisted of the skin-maceration of musts at 10 degrees C for 6h.
145 ed wines Cannonau, liqueurs obtained by cold maceration of myrtle (Myrtus communis L.) berries and bi
146 s and lyases which are very effective in the maceration of plant cell walls.
147         As well as Deltaexl1 exhibiting less maceration of potato plants, fewer bacteria are observed
148 mber of traditional liqueurs are obtained by maceration of red fruits in aqueous ethanol liquor, name
149 nded to separate berry skin before enzymatic maceration of the berry flesh must.
150 nded to maintain berry skin during enzymatic maceration of the must.
151 e (HHP) processing in parallel with oak chip maceration on the physicochemical and sensory properties
152 ion of flavan-3-ol monomers into wine during maceration operations, heightening bitterness.
153 , 4.00; 95% CI: 1.75, 9.16), medial meniscal maceration (OR, 1.84; 95% CI: 1.13, 2.99), effusion (OR,
154 l repair, and 3 = displaced tear, resection, maceration, or destruction.
155 dget" concept, highlighting the interplay of maceration parameters shaping 'Nebbiolo' wine phenolics.
156 daily anthocyanin extraction during carbonic maceration, particularly from the sixth day.
157 tional Maceration (TM), Prefermentative Cold Maceration (PCM), Maceration Enzyme (ENZ) and grape-Seed
158 cts from three different extraction methods (maceration, percolation and Soxhlet).
159 uce massive pectinolytic activity during the maceration phase.
160  (S), pre-fermentation heating with extended maceration (PHT) or juice fermentation (PHP), and post-f
161                      The extract obtained by maceration presented a total phenolic content twice the
162                       Wines made by carbonic maceration presented higher aromatic quality due to thei
163 ne model solution was used for the simulated maceration procedure.
164                                          The maceration procedures applied to guarana contributed to
165                                The effect of maceration process on the profile of phenolic compounds,
166 g, the incorporation of these plants using a maceration process reduced the polar compounds by 69% an
167                                    After the maceration process, oils' were subjected to their oxidat
168  volatile profile was slightly influenced by maceration process, which occurred at room temperature (
169         Comparing the variation of metals at maceration process, with the variation of monomeric anth
170 ide value, but lower p-anisidine value after maceration process.
171 ls, while others showed an increase with the maceration process.
172 revious studies have indicated that carbonic maceration processing can be used to obtain a wine fract
173 and esters, and wines from post-fermentation maceration resulted in an increase in oxidation and agin
174             Wines made with pre-fermentation maceration showed a notable increase in the levels of te
175                     Meanwhile, those without maceration showed higher levels of ethyl esters of fatty
176             Wine made with post-fermentation maceration showed more complex attributes, such as notes
177                                    Method by maceration showed the highest phenolic yield when applie
178                         Mw2 (microwave after maceration) showed high protein content and a favorable
179 ults indicate that, after germination and/or maceration, sorghum had important nutritional and functi
180 t extraction techniques (steam distillation, maceration, Soxhlet extraction) were used to reveal the
181 ing (100 degrees C, 40 s), defatting method (maceration, Soxhlet) and solvent polarity (hexane, ethan
182  this context, different methods (enzymatic, maceration, Soxhlet, etc.) and solvents (variable polari
183   Five extraction techniques were evaluated: maceration, Soxhlet, sonication (UAE), microwave (MAE) a
184 tudy aimed at testing the use of alternative maceration technique (NM) in alternative to CM, to creat
185                            The pre-treatment maceration technique significantly (p < 0.05) affected t
186                            The pre-treatment maceration technique significantly (p < 0.05) affected t
187                For both rind and rachis, the maceration technique yielded extracts with the strongest
188 sma technique, respectively, compared to the maceration technique.
189 esent the effects of different pre-treatment maceration techniques (microwave, thermo-maceration, and
190                                    Likewise, maceration techniques have produced increases in phenoli
191                                              Maceration techniques influenced colour parameters, and
192  study investigated the effects of different maceration techniques on the colour parameters, phenolic
193             In this study, the effect of two maceration techniques, traditional and oak chips-grape m
194 howed differences between the harvesting and maceration techniques.
195       This study investigates the effects of maceration temperature (24 or 29 degrees C) and duration
196 ected mostly by enzyme treatment followed by maceration temperature.
197 evaluated the influence blanching, freezing, maceration temperatures (2 degrees C, 50 degrees C) and
198  and non-toasted), dosage (4 and 12 g/L) and maceration time (1, 7, 21, 35 and 120 days) were tested.
199 with unripe grapes from February and shorter maceration time (p < 0.05).
200 ation and grouping of the wines according to maceration time and oak chips treatment.
201                                          The maceration time influenced strongly not only the content
202 d PLS-DA) to evaluate the grape maturity and maceration time on chemical composition of wines from tw
203 n contrast, increasing chip dose in extended maceration time resulted in wines with lighter and less
204 the ripeness degree and increasing the grape maceration time seems to result in higher concentrations
205 rtant factor in winemaking technology is the maceration time since the highest concentrations of tran
206                                A long pomace maceration time was also tested for non-treated wines.
207  chip dose, wood origin, toasting degree and maceration time) on the phenolic and chromatic profiles
208 chip doses, wood origin, toasting degree and maceration time) on the volatile profile of red wines du
209 ent of aroma compounds was related mostly to maceration time, observing increased relative amount of
210  lactones showed an increase with increasing maceration time.
211 tion degree (19, 21 and 23 degrees Brix) and maceration times (10, 20 and 30 days) on the volatile pr
212  study, Vranec wines produced with different maceration times (4, 7, 14 and 30 days) in presence of e
213   Two doses of oak chips (3 and 6g/L) at two maceration times (5 and 10days) during fermentation was
214                         Two different pomace maceration times (short and mid) were tested for sonicat
215 es (Vitis vinifera L.) obtained at different maceration times after pulsed electric fields (PEF) usin
216         The addition of oak chips at shorter maceration times enhanced phenolic extraction, colour an
217  of Tannat red wines produced by Traditional Maceration (TM), Prefermentative Cold Maceration (PCM),
218 nemaking, exogenous tannins are added before maceration to improve future wine color characteristics
219 mace was extracted using ultrasound-assisted maceration to obtain a polyphenol-rich extract.
220                           The effects of six maceration treatments on volatile aroma and phenol compo
221    capital TE, Cyrilliche effects of time of maceration, type of yeast and the level of sulphur dioxi
222 lgae Gracilaria gracilis was optimized using maceration, ultrasound-assisted extraction (ultrasonic w
223                                              Maceration using the binary system hexane/isopropanol (5
224 exhibited an increase in wines when carbonic maceration was applied.
225                     The study indicated that maceration was effective and simple technique for the ex
226 planta and its ability to cause plant tissue maceration was severely compromised.
227                                              Maceration was the most efficient extraction method yiel
228 ted higher esters level, while decoction and maceration were more abundant in sesquiterpenes and terp
229          Mechanical harvesting and cryogenic maceration were used in combination to produce a Sauvign
230 her recoveries of hydrophilic compounds than maceration whereas the highest amounts of lipophilic com
231 leaves) than maqui leaf extracts obtained by maceration, while the extract that prioritized purity ov
232 is possible to obtain a fraction of carbonic maceration wine (25-35% of the total) with a reduction i
233 -value enological compounds after 35 days of maceration with 12 g/L of toasted vine-shoots.
234                        Furthermore, oak chip maceration with and without HHP processing weakened the
235 eria parviflora rhizome extracts obtained by maceration with hexane, chloroform, methanol, and ethano
236 as a tool for monitoring the effects of wine maceration with oak chips was evaluated.
237 extracts clearly indicates that both SFE and maceration with water are the most selective techniques
238 minogen activator and thrombus aspiration or maceration, with or without stenting).

 
Page Top