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1 ino acid and sucrose but a restricted amount reducing sugar.
2  producing ethanol at a competitive 0.45 g/g reducing sugar.
3 l, organo-metallic substituted aldehydes and reducing sugar.
4 er to those obtained by measuring the actual reducing sugars.
5 he Maillard reaction between amino acids and reducing sugars.
6 that compete with bound lysine to react with reducing sugars.
7 ture, soluble solids, fructose, glucose, and reducing sugars.
8 d meat with other dietary components such as reducing sugars.
9  fruits contained higher vitamin C and lower reducing sugars.
10 long-term stability and high selectivity for reducing sugars.
11 med from the reaction between asparagine and reducing sugars.
12 min C content could be ascribed to levels of reducing sugars.
13 ntained more water and less total sugars and reducing sugars.
14  treatment promoted a reduction in the total reducing sugars (46.7-84.5%), availability of free pheno
15 he highest yields of total carbohydrates and reducing sugars (6.14 and 3.15 mg/mL, respectively).
16 outing grains increases free amino acids and reducing sugars, accelerating the Maillard reaction to e
17 o vacuolar acid invertase gene VInv prevents reducing sugar accumulation in cold-stored tubers.
18 ato vacuolar invertase gene (VInv) and cause reducing sugar accumulation.
19 matic reaction between amino acids (AAs) and reducing sugars, also known as the Maillard reaction, is
20                   Moisture, total phenolics, reducing sugar and B vitamins (thiamine, riboflavin, and
21 ichia kluyveri showed greater changes in the reducing sugar and free amino acids in fermented cocoa b
22          Temperature, pH, titirable acidity, reducing sugar and free amino acids were evaluated durin
23 grees C respectively leading to formation of reducing sugar and lowering of viscosity.
24 ement; (2) the Maillard reaction between the reducing sugar and lysine residues.
25 ng revealed high percentage of carbohydrate, reducing sugar and phenolics in WFSP, whereas OFSP showe
26 able, as reaction clearly occurs between the reducing sugar and protein because of the potentially re
27                         The reaction between reducing sugar and protein in the dried state indicates
28 h, chlorophyll and carotenoid synthesis, and reducing sugar and soluble carbohydrate contents in dwar
29 eight loss, total sugar, reducing sugar, non-reducing sugar and total soluble solids (TSS) over the s
30 , 7mg/100g monomeric anthocyanins, 0.1g/100g reducing sugars and 0.12g/100g sucrose.
31 ilized biocatalyst, which released 3mg/mL of reducing sugars and allowed the highest product yield co
32 ation is the reaction of carbonyl compounds (reducing sugars and alpha-dicarbonyls) with amino acids,
33  by nonenzymatic glycation reactions between reducing sugars and amino acids, lipids, or DNA, are for
34      In the course of the Maillard reaction, reducing sugars and amino compounds are converted to col
35                      Chemical conversions of reducing sugars and amino compounds induce the formation
36 RPs) are widely produced in foods containing reducing sugars and amino-bearing compounds during therm
37 lated to Maillard reaction precursor levels (reducing sugars and asparagine) and secondary metabolite
38 l among them and were weakly correlated with reducing sugars and asparagine.
39  P2WS jams had lower carbohydrates contents, reducing sugars and calories, and higher fiber contents
40 n of protein amino and guanidino groups with reducing sugars and carbonyl products of their degradati
41                           Total polyphenols, reducing sugars and chlorophyll were the differential co
42 erred to as "glycation") takes place between reducing sugars and compounds with free amino groups dur
43 h GENT alone chitosanase did not produce any reducing sugars and did not affect GENT's antimicrobial
44 e duplicated by the nonenzymatic reaction of reducing sugars and extracellular matrix proteins.
45         The concentration and composition of reducing sugars and free amino acids as Maillard reactio
46 e chemistry to unprecedented applications to reducing sugars and in the synthesis of highly benzylate
47 on heat-induced reaction of amino acids with reducing sugars and include advanced glycation end produ
48              Reactive aldehydes derived from reducing sugars and lipid peroxidation play a critical r
49           The non-enzymatic reaction between reducing sugars and long-lived proteins in vivo results
50 olysis of the sisal root yielded 272 mg/g of reducing sugars and oligosaccharides.
51  Glycation is a process of protein damage by reducing sugars and other reactive carbonyl species lead
52              Reactive aldehydes derived from reducing sugars and peroxidation of lipids covalently mo
53                               The changes in reducing sugars and phenolic acids in different fraction
54  the reduction of the MTT reagent by honey's reducing sugars and phenolic compounds, and the lactate
55 d cocoa with similar pH, titratable acidity, reducing sugars and phenolic compounds.
56       Maillard or browning reactions between reducing sugars and protein lead to formation of advance
57   Protein glycation may occur naturally when reducing sugars and proteins coexist, which is often the
58 ion products "glycotoxins." Like other known reducing sugars and reactive glycation products, glycoto
59 l chemical glycosylation method that employs reducing sugars and requires no protection or activation
60              Regarding Apis mellifera honey, reducing sugars and sucrose did not comply with the legi
61  a series of non-enzymatic reactions between reducing sugars and the amino groups of proteins and acc
62 king moieties that form from the reaction of reducing sugars and the amino groups of proteins, lipids
63 e of MR products, regardless the presence of reducing sugars and the cooking method.
64 dity and interfere with the reaction between reducing sugars and the DNS reagent.
65 ship between the ratio of free asparagine to reducing sugars and the levels of acrylamide identified
66 base reaction between the aldehyde groups of reducing sugars and the primary amines of proteins.
67 rson's correlation coefficient revealed that reducing sugars and titratable acidity can influence the
68 nteraction for acrylamide (p<0.003, F-test), reducing sugars and total sugars (p<0.001, F-test).
69 rthermore, the wort color, free amino acids, reducing sugars, and fatty acids compositions were deter
70 lysis revealed flavonoids, phenols, tannins, reducing sugars, and glycosides in both plants, while C.
71 s accurate spectrophotometric measurement of reducing sugars, and that fat removal restores quantitat
72 n firmness of banana tissue, the increase in reducing sugars, and the change in the indicator's color
73  amino and carbonyl groups of asparagine and reducing sugars are condensed into Schiff bases, they ar
74  long-term storage, and low tendency to form reducing sugars as acrylamide precursors.
75 grees C) processing cultivars maintained low reducing sugars as compared to non-processing cultivars.
76 ugates produced an equivalent amount of free reducing sugars as the unmodified control using insolubl
77 ces, weight loss, pH and titratable acidity, reducing sugars, ascorbic acid, total phenolics, DPPH an
78 iquid chromatography), dextrose equivalency (reducing sugar assays), and prevalence of branching (NMR
79        They readily undergo conjugation with reducing sugars at the desired 1:1 stoichiometry.
80                 The colorimetric sensors for reducing sugars based on a redox reaction between AuCl(4
81  importance of the Maillard reaction between reducing sugar breakdown products and 1-pyrroline derive
82 hat CML was not formed from oxidation of the reducing sugars, but from the Maillard reaction via the
83 s, this bioconjugate increased the amount of reducing sugars by 2.8-fold over three rounds of activit
84                Threonine, glycine, arginine, reducing sugar, caffeine, catechin (C), and epicatechin
85 Due to tautomeric equilibria, NMR spectra of reducing sugars can be complex with many overlapping res
86  lactose milk as the higher concentration of reducing sugars can lead to the increased formation of t
87                                              Reducing sugars can react with the free amino groups of
88 lumn reactors and according to turbidity and reducing sugar concentration values, batch reactor effic
89 action temperature and time on turbidity and reducing sugar concentration were optimized by Response
90 ht into the actual effectiveness of lowering reducing sugars concentration in par-fried potato strips
91 ong the parametric population, vitamin C and reducing sugar concentrations ranged between 2.54 to 50.
92  the batch reactor system, and turbidity and reducing sugar concentrations were monitored over time.
93 of all MR products because of an increase in reducing sugar concentrations.
94 s in French fries, although the variation in reducing sugars concentrations in low and normal types o
95  delivery of bottled water, was effective in reducing sugar consumption from beverages for Latina mot
96 ty, higher titratable acidity, and increased reducing sugar consumption, while SSIAF provided a more
97 ed, starch content (SC) decreased by 15.86%, reducing sugar content (RSC) increased by 32.71%, ascorb
98 s' was positively correlated to sweet taste, reducing sugar content and inversely correlated to acidi
99  loss, starch degradation, and increased the reducing sugar content of tubers without affecting the s
100 y used biochemical analyzer obtained a lower reducing sugar content than the deprotinization-SN assay
101 or having inferior flavors and aromas, had a reducing sugar content three times higher than the aged
102 oducts with darker color, higher solubility, reducing sugar content, total dietary fiber and proporti
103 e resulting extracts were examined for their reducing sugar content, total phenolic content (TPC), ox
104 rate, chromaticity a(*) and b(*) values, and reducing sugar content.
105 accuracy of 51 % for acrylamide and 76 % for reducing sugar content.
106 , orange and peach juices and enhanced their reducing sugar content.
107 ices were successfully clarified, increasing reducing sugars content and markedly decreasing turbidit
108 ccumulation of reducing sugar (RS), high non-reducing sugars content, low invertase activity and high
109 imal sample processing for the prediction of reducing sugar contents in the tubers or acrylamide cont
110 ng inhibitors led to higher starch and lower reducing sugar contents, and the tubers retained the rec
111 elated to its relatively high asparagine and reducing sugars contents, respect the other local cultiv
112 esent that aerosolizing aqueous solutions of reducing sugars (d-glucose and l-fructose) spontaneously
113 late, citrate, fruit acids, amino acids, and reducing sugars did not interfere with the proposed sens
114 ylamide is produced from free asparagine and reducing sugars during high-temperature cooking and food
115 bit low levels of glycation from exposure to reducing sugars during production.
116 ir relationship with the fungal community by reducing sugar efflux carriers and enhancing defense pro
117 haff released 21.76+/-1.42 and 32.3+/-0.75mg reducing sugars equivalents/g after 24h when applied at
118                             Final content of reducing sugars, ethanol, acetic acid, and amino nitroge
119 d sprouting by modulation of accumulation of reducing sugars, ethylene, and expression of genes invol
120                                    Different reducing sugars exhibited distinct reaction rates for Au
121          The current study demonstrates that reducing sugars form advanced glycation endproducts (AGE
122                                              Reducing sugars formed due to inversion hinder crystal g
123                      The changes in sucrose, reducing sugars, free amino acids, asparagine, acrylamid
124 oposed method is based on the correlation of reducing sugars generated during the enzymatic process w
125      The precursors of acrylamide formation, reducing sugars (glucose and fructose) and ten major ami
126 ical analysis yielded data on the content of reducing sugars (glucose and fructose) that dominate the
127     The reaction of long lived proteins with reducing sugars has been implicated in the pathophysiolo
128 glycosylation of amino groups on proteins by reducing sugars, has been studied for its potential role
129 reactions of an amino group of proteins with reducing sugars, have been identified and detected in vi
130 ymatic glycation of proteins and lipids with reducing sugars, have been implicated in many diabetic c
131                                              Reducing sugar in packaged foods and beverages could hel
132 s proposed for colorimetric determination of reducing sugars in cachaca employing digital image and a
133 iour of the reaction between amino acids and reducing sugars in emulsions during thermal treatments i
134 se than with fructose when they were used as reducing sugars in food model systems.
135 lectrochemical sensors for the monitoring of reducing sugars in foods has great potential as a rapid
136  vitamin C content and its relationship with reducing sugars in fruit pericarp.
137 patterns of C3 to C6 free and phosphorylated reducing sugars in heart tissues from (13)C-labeled wild
138 itation of the major free and phosphorylated reducing sugars in mouse heart tissue.
139 ccessfully applied to the rapid detection of reducing sugars in potatoes, without the need for sample
140 ese findings should indicate that the use of reducing sugars in the formulation of an excipient for t
141 ly, cold storage triggers an accumulation of reducing sugars in tubers.
142  temperatures, incubation times and types of reducing sugars, including glucose and different low mol
143                                The amount of reducing sugar increased form 2.0% in the control sample
144    Titrable acidity total soluble sugars and reducing sugars increased too.
145 ning of chips was more influenced by the non-reducing sugars, instead of RS.
146 inked to a 2-carbon aglycon derived from the reducing sugar, irrespective of the linkage position bet
147                                    Measuring reducing sugar is a common practice in carbohydrate rese
148              A likely intranuclear source of reducing sugar is ADP-ribose, which is generated followi
149  chain linked to the C-3 position of the non-reducing sugar known to undergo cleavage impacting stabi
150 roduction of inhibitory phytohormones and by reducing sugar levels and energy balance.
151                      The changes in protein, reducing sugar, Maillard reaction products (MRPs), miner
152 nic acids (tartaric acid and succinic acid), reducing sugars (maltose, glucose, and fructose), and as
153 o anthron and phenol-sulphuric acid methods, reducing sugars method after EPS hydrolysis with glucose
154 ofile are also reported for each of the GlcN reducing sugar model systems.
155                                              Reducing sugars, most of organic acid, pH and TSS increa
156 increased per cent weight loss, total sugar, reducing sugar, non-reducing sugar and total soluble sol
157      The pro-oxidant molecular mechanisms of reducing sugars on this environment are unknown.
158 ent reaction between proteins and endogenous reducing sugars or dicarbonyls (methylglyoxal, glyoxal)
159            The effect of the addition of non-reducing sugars or methylcellulose on the matrix physica
160 ignificantly affected the moisture (p<0.01), reducing sugar (p<0.05), ash (p<0.05) and HMF (p<0.05) c
161 ontrol, enabled to release up to 1.21 g/L of reducing sugars (p < 0.001), led to an eight-fold increa
162 ct demonstrated the presence of amino acids, reducing sugar, phenolic compounds, anthraquinone, and s
163  total carbohydrates, total polysaccharides, reducing sugars, phenolics and protein content were high
164 for acrylamide and between 1.64 and 2.23 for reducing sugar prediction rendered low medium to medium
165           The ratios of soluble to insoluble reducing sugar produced after filter paper hydrolysis by
166 unctional groups, antioxidant, phenolics and reducing sugar properties.
167 ructures containing N,N-dimethylamine at the reducing sugar prove that are more cytotoxic than their
168 hermore, the highest soluble carbohydrate to reducing sugars ratio was observed in treatments of 100
169                                  The sucrose/reducing sugar ratios (sugar index - SI) of the original
170                                              Reducing sugars react with amino groups in proteins, lip
171 follows the specific amino acid route, i.e., reducing sugars react with asparagine to form the Schiff
172                            Glucose and other reducing sugars react with proteins by a nonenzymatic, p
173  Raftiline(R) GR and 7.5% oat bran flour) in reducing sugars released and standardised AUC values com
174 in a single reaction increased the amount of reducing sugars released from native chitin to 140% abov
175  yielded a twofold increase in the amount of reducing sugars released from wheat straw compared with
176 dation of terminally linked sialic acids and reducing sugar residues.
177                      Exposure of proteins to reducing sugars results in nonenzymatic glycation with t
178 ing opening, the structural integrity of the reducing sugar ring (pyranose or furanose) is lost durin
179  The disaccharide is bound to calcium by the reducing sugar ring, and a stabilizing H-bond is formed
180 tions in particle size (PS), DS content, and reducing sugar (RS) levels among the flours.
181                                              Reducing sugar (RS) quantification is essential in the p
182 uia was characterized by low accumulation of reducing sugar (RS), high non-reducing sugars content, l
183 ring glucose (G), fructose (F), sucrose (S), reducing sugars (RS), total sugars (TS), amino acids, an
184 fect by elevating HXK catalytic activity but reducing sugar sensitivity in transgenic plants.
185 rch does not interfere in the measurement of reducing sugars, so that the diastase activity is easily
186 argest variation was found for plant weight, reducing sugars, starch at the end of the night, and sev
187 ally arise from the nonenzymatic addition of reducing sugars (such as glucose) to protein amino group
188 ymatic modification of protein and lipids by reducing sugars, such as glucose, is thought to contribu
189  was assessed in the presence/absence of non-reducing sugars (sucrose and trehalose) and polyols (gly
190 infection leads to a significant increase in reducing sugar, sucrose, amino acid and protein in potat
191           The Harenna forest honey moisture, reducing sugar, sucrose, water insoluble solids, ash, fr
192 s chlorophyll a fluorescence indices, total, reducing sugars, sucrose, ethylene, ascorbic acid, lipid
193                                              Reducing sugar-sweetened beverage (SSB) consumption is a
194                                              Reducing sugar-sweetened beverages (SSB) is a worldwide
195 television, increasing physical activity and reducing sugar-sweetened beverages.
196 d potato strips with lower concentrations of reducing sugars than the commonly used potato strips was
197 ose concentration and lower concentration of reducing sugars than the standard of Apis mellifera hone
198 tation, rs/rs, conditions a shift from these reducing sugars to sucrose.
199 ccharide revealed a decrease in the ratio of reducing sugars to total sugar content, indicating a lon
200 00 degrees C) and chemical (acid, alkali and reducing sugar) treatments on the IgY binding of peanut
201  could be reacted with aldehyde bearing/free reducing sugars under the heating condition to afford N-
202                                              Reducing sugar values determined were in good agreement
203                              The increase in reducing sugar was also associated with subsequent incre
204  in actual frying time; no obvious effect of reducing sugars was found.
205               The contents of dietary fiber, reducing sugar, water-extractable arabinoxylans, phytic
206 ed higher contents of soluble dietary fiber, reducing sugar, water-extractable arabinoxylans, total p
207 ethanol, extract proteins, anthraquinone and reducing sugar were not detected.
208                                     Although reducing sugars were lowered due to their consumption by
209 lamide, frying time, frying temperature, and reducing sugars were measured and characteristics of fry
210 lamide, frying time, frying temperature, and reducing sugars were measured and the actual practices a
211 ages (RT0-5), and their free amino acids and reducing sugars were profiled and quantitated.
212 ing the strong positive correlations between reducing sugars with Mn and total acidity with Fe.
213 o acids competing with asparagine, replacing reducing sugars with non-reducing alternatives, applicat
214 on in this initial report of the reaction of reducing sugars with the amino group of GlcN.
215 ration of a 1:1 mixture of (12)C(6)/(13)C(6) reducing sugars with the assumption that the same sites
216 ive determination of free and phosphorylated reducing sugars without the interferences from their non

 
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