ライフサイエンスコーパス: Maillard reaction

1 much acrylamide as the reaction of glucose (Maillard reaction).

2 s and are formed alongside acrylamide in the Maillard reaction.

3 ns were found: oxidative degradation and the Maillard reaction.

4 ased as a function of time mainly due to the Maillard reaction.

5 and the presence of final products from the Maillard reaction.

6 saccharides (GOS) were synthesised using the Maillard reaction.

7 ermal treatment because of the triggering of Maillard reaction.

8 he formation of antioxidant compounds during Maillard reaction.

9 change and fluorescence, as expected for the Maillard reaction.

10 he first time, that UHP can be produced from Maillard reaction.

11 n vivo by several metabolic pathways and the Maillard reaction.

12 rmed, many of which result from the advanced Maillard reaction.

13 ing and cross-linking of proteins during the Maillard reaction.

14 olytic intermediates and produced during the Maillard reaction.

15 olite from sugar degradation obtained by the Maillard reaction.

16 nt directly, evaluating only products of the Maillard reaction.

17 d could be linked to lipid oxidation and the Maillard reaction.

18 g the perception of notes formed through the Maillard reaction.

19 including products from lipid oxidation and Maillard reaction.

20 during roasting, defined as end-products of Maillard reaction.

21 tofuranosyl cation to the early stage of the Maillard reaction.

22 ns and are inhibited by amino groups through Maillard reaction.

23 Conjugate was developed through Maillard reaction.

24 roteins, mainly generated as a result of the Maillard reaction.

25 gnificantly influence methylglyoxal-mediated Maillard reactions.

26 ent pathways in methylglyoxal metabolism and Maillard reactions.

27 nd were linked to mainly lipid oxidation and Maillard reactions.

28 ing thermal processing as an intermediate of Maillard reactions.

29 by thermal treatment inducing oxidation and Maillard reactions.

30 systems containing fish powder produced via Maillard reactions.

31 ther with indicators of the initial steps of Maillard reaction (2-furoylmethyl amino acids, 2-FM-AA)

32 min C retention (>65%) and scarce advance of Maillard reaction (2-furoylmethyl derivatives of Lys and

33 ized into recalcitrant forms by means of the Maillard reaction(5), although reaction kinetics at mari

34 The Maillard reaction, a chemical reaction between amino aci

35 The Maillard reaction, a non-enzymatic reaction of ketones a

36 The amount of the Maillard reaction advanced products was higher for WPI-l

37 However, the Maillard reaction also occurs in all cells, from prokary

38 However, the Maillard reaction also provides desirable sensory attrib

39 The Maillard reaction (also referred to as "glycation") take

40 tive Carbonyl Species (RCS) derived from the Maillard reaction and ascorbic acid degradation on brown

41 Multi-response kinetic modelling of Maillard reaction and caramelisation simultaneously indi

42 ts were highly prone to participating in the Maillard reaction and caramelization during baking, lead

43 tic model indicating the elementary steps of Maillard reaction and caramelization during hazelnut roa

44 GOSs) and galactan were produced through the Maillard reaction and characterised structurally and fun

45 d of carbohydrate-based intermediates of the Maillard reaction and defined as melanoidin precursors o

46 This mechanism is known as the Maillard reaction and is considered the main AA pathway.

47 The role of the Maillard reaction and the accumulation of non-enzymatic

48 avening agent for French bread making on the Maillard reaction and the bifidogenic effect.

49 ecular weights were first conjugated through Maillard reaction and the conjugates were exploited to e

50 osides and nucleobases in the context of the Maillard reaction and to identify the selectivity of pur

51 In summary, during storage, the Maillard reaction and/or its resulting products could de

52 d formation of volatile compounds related to Maillard reactions and oxidation of secondary lipid oxid

53 ins in vivo through non-enzymatic glycation (Maillard reaction) and formation of different products c

54 indicate that HHP treatments accelerated the Maillard reaction, and alcohol and fatty acid oxidation,

55 enous ribose and amino acids in meat through Maillard reaction, and facilitated the formation of dime

56 Sonication accelerated the Maillard reaction, and the glycosylation of GWP was sign

57 the innovative processing methods about the Maillard reaction are summarized to optimize the sensory

58 sor of RCS, indicating the important role of Maillard reaction as a mechanism of non-enzymatic browni

59 profile to that of roasted mullet roe, with Maillard reaction as the key flavor generator in roasted

60 on of vitamin C and the highest evolution of Maillard reaction, as evidenced by its high concentratio

61 or its antioxidant hydrolysate (WPH) through Maillard reaction at 90 degrees C.

62 in relation to the chemical markers for the Maillard reaction at the cooking, flaking and toasting s

63 nts during heat treatment as a result of the Maillard reaction between amino acids and reducing sugar

64 g cooking, focusing on the importance of the Maillard reaction between reducing sugar breakdown produ

65 erda van Ekenstein (LA) arrangement; (2) the Maillard reaction between the reducing sugar and lysine

66 vestigate the kinetics of early stage of the Maillard reaction by a reversible bimolecular reaction m

67 e ions and minerals abiotically catalyse the Maillard reaction by up to two orders of magnitude at te

68 on the formation of furans and acrylamide in Maillard reactions by the use of some plant extracts and

69 However, the Maillard reaction can be directed in favour of aroma for

70 The network of the Maillard reaction can be influenced by the presence of p

71 with their binary metal complexes during the Maillard reaction can initiate various processes, includ

72 Above 200 degrees C, the Maillard reaction can occur, inducing amino-acid losses.

73 ed in relation to compounds derived from the Maillard reaction, caramelisation and lipid oxidation.

74 mpounds are used to consider the mechanisms (Maillard reaction, caramelisation, pyrolysis) by which t

75 of lysine and arginine participation in the Maillard reaction-, carbohydrates, total polyphenols, pr

76 Thus, the Maillard reaction cascade appears to continue in food, i

77 es C) to participate in the interplay of the Maillard reaction cascade.

78 to have a large impact on the diversity the Maillard reaction causes.

79 tion showed that both the hydrolysis and the Maillard reactions changed the flavor description of the

80 ed the presence of phenolic and intermediate Maillard reaction compounds bound to the HT-BM structure

81 re effective in reducing lipid oxidation and Maillard reaction compounds formation, while improving t

82 ad without reducing agents contained typical Maillard reaction compounds such as aldehydes, alkyl pyr

83 (freeze-dried-extract)), and also containing Maillard reaction compounds, such as 5-hydroxymethylfurf

84 amino sugars are not easily accessible under Maillard reaction conditions and are only formed in the

85 e disclosed that the distinct pattern of the Maillard reaction could be attributed to different subst

86 The results suggested that the Maillard reaction could be used to generate beta-carboli

87 ne and dityrosine, identifying them as major Maillard reaction cross-links in lens proteins.

88 c beverages can, over longer periods, induce Maillard reaction, degrading nutritional components and

89 s allowed us to map the systematic nature of Maillard reaction derived compounds.

90 However, most cross-links of the Maillard reaction described so far are present in quanti

91 nt, antioxidative and reducing capacity, and Maillard reaction development in rye ginger cakes after

92 ples stored under glassy conditions that the Maillard reaction did not occur, independent of gelatin

93 o generate a broad class of compounds of the Maillard reaction during baking and linked to the typica

94 ccuracy, allowing reliable monitoring of the Maillard reaction during baking.

95 the leavening agent used, which affected the Maillard reaction during baking.

96 ds rich in carbohydrates or fats undergo the Maillard reaction during frying, which promotes the colo

97 ways (chlorogenic acid (CGA) degradation and Maillard reaction) during coffee roasting were investiga

98 r with our previous data indicating advanced Maillard reaction end products in RF, it seems that post

99 yl groups of side chains of proteins to form Maillard reaction end products, inducing a negative impa

100 Our findings help us to understand how Maillard reaction enhances the potential allergenicity o

101 s molecular dynamics, thereby modulating the Maillard reaction environment.

102 through Strecker degradation as part of the Maillard reaction, flavour precursors methionine and leu

103 peratures to make products such as ghee, the Maillard reaction forms a range of volatile flavour comp

104 ree APs and the protein-bound markers of the Maillard reaction (furosine, Nepsilon-(carboxymethyl)-l-

105 The Maillard reaction has been implicated in cross-linking a

106 es more modified by advanced products of the Maillard reaction, i.e., immunoreactive advanced glycati

107 Addition of salts inhibited Maillard reaction in favour of caramelisation, with diva

108 An assessment of the Maillard reaction in heated milk pointed out a higher fo

109 uld point to a new avenue for control of the Maillard reaction in high temperature food systems.

110 The kinetics of Maillard reaction in lactose-hydrolysed skim milk powder

111 ne of the major consequences of the advanced Maillard reaction in proteins is the formation of covale

112 ailable lysine, as a means of monitoring the Maillard reaction in skim milk powders.

113 dori rearrangement products (ARP) during the Maillard reaction in solutions is well documented, but t

114 ative stress in protein cross-linking by the Maillard reaction in vitro and provides the first eviden

115 ne A/LM-1 is a novel product of the advanced Maillard reaction in vivo and a specific marker of a dia

116 bitor baking atmosphere may help prevent the Maillard reactions in bakery products.

117 sting conditions, implying the importance of Maillard reactions in CO2 formation.

118 ould effectively trap MGO and hereby inhibit Maillard reactions in UHT milk.

119 cursors of protein cross-links formed during Maillard reactions in vivo during aging and in disease.

120 -mediated protein modification occurs during Maillard reactions in vivo.

121 ten rely on a reduction in the extent of the Maillard reaction, in which acrylamide is formed from th

122 -related toxic compounds, mainly through the Maillard reaction, including some volatile organic compo

123 The inhibition of the Maillard reaction increased from 4.10% to 36.70% and 33.

124 of the studied IFs, which suggests that the Maillard reaction increases after opening the packets.

125 Phenolic acids (PA) and Maillard reaction indices (MRI) were quantified before a

126 The Maillard reaction, initiated by nonenzymatic glycosylati

127 ow that radicals are produced in vivo by the Maillard reaction, initiated by treating the skin of hai

128 In the meanwhile, Maillard reaction intermediates and advanced glycation e

129 In the meanwhile, the effects of Maillard reaction intermediates and AGEs on gut homeosta

130 suggested to be a common intermediate in the Maillard reaction involving glucose.

131 The Maillard reaction is a natural process in foods and wide

132 Glycation by the Maillard reaction is a naturally occurring process, whic

133 Maillard reaction is a promising and safe method to obta

134 ced formation of antioxidants throughout the Maillard reaction is known, this study was undertaken to

135 However, the more prominent Maillard reaction is mainly studied at a mechanistic lev

136 f the annotated compositions showed that the Maillard reaction is one of the driving forces of beer's

137 Maillard reaction is pH-responsive, the influence of sol

138 (AAs) and reducing sugars, also known as the Maillard reaction, is the primary source of free glycati

139 Nonenzymatic protein glycation (Maillard reaction) leads to heterogeneous, toxic, and an

140 ominant aroma compounds were derived via the Maillard reaction, lipid degradation/oxidation and sugar

141 ed that FSS has a rich volatilome (including Maillard reaction/lipid degradation products), increased

142 Aqueous extracted Maillard reaction markers (hydroxymethylfurfural, carbox

143 Results revealed that higher levels of Maillard reaction markers were present in PBMBAs in the

144 ithstand damage due to glycoxidation and the Maillard reaction may be under genetic control.

145 Mitigation procedures that modify the Maillard reaction may negatively affect flavour and colo

146 ults suggest that neoglycans obtained by the Maillard reaction may serve in the prophylaxis of ETEC K

147 the browning index and HMF level (formed via Maillard reaction) might be good tool for monitoring the

148 MRP fraction, extracted from a ribose/lysine Maillard reaction mixture by 85% ethanol, was monitored

149 pyrolytic conditions the acidity/basicity of Maillard reaction mixtures can be controlled through the

150 physical, and chemical properties of aqueous Maillard reaction mixtures of small aldehydes (glyoxal,

151 ecular pattern, validated by an experimental Maillard reaction model system, pervades over 2,800 (40%

152 -1 mmol) on acrylamide were evaluated in two Maillard reaction model systems (low-moisture and aqueou

153 -glycine and asparagine-fructose system as a Maillard reaction model, the effects of seven polyphenol

154 obiological safety of milk, but also induces Maillard reactions modifying for example proteins.

155 The Maillard reaction (MR) between the pretreated sample (UP

156 ur, sensory characteristics and formation of Maillard reaction (MR) compounds in lamb loins was studi

157 osine as indicator of lysine loss during the Maillard reaction (MR) has been also studied.

158 ion of lysine-glucose glycoconjugates during Maillard reaction (MR) has been studied, respectively, i

159 ethyl-amino acids (2-FM-AA) as indicators of Maillard reaction (MR) in black garlic elaboration, foll

160 The extent of Maillard reaction (MR) in control bread was confirmed by

161 This research delves into the Maillard reaction (MR) in high-solid gelatin-saccharide

162 s) formation is the key step to mitigate the Maillard reaction (MR) in milk.

163 est glycation of beta-lactoglobulin (BLG) in Maillard reaction (MR) induced by high-intensity ultraso

164 The control of Maillard reaction (MR) is a key point to ensure processe

165 Studies raise the notion that the Maillard reaction (MR) may be harnessed to modify the an

166 ng acetylation degree (AD), on the extent of Maillard reaction (MR) on chitosan-based films were stud

167 s components and to discern the influence of Maillard reaction (MR) on the overall reaction kinetics.

168 n of reducing sugars and free amino acids as Maillard reaction (MR) precursors change with grain spro

169 sound (US) pre-treatment on the evolution of Maillard reaction (MR), induced between low molecular we

170 The antioxidant capacity of Maillard reaction (MR)-modified gelatin (GE)-gum arabic

171 High intensity ultrasound (HIUS) can promote Maillard reaction (MR).

172 influence coffee flavour generation through Maillard reaction (MR).

173 roteins changing its behavior and may affect Maillard reaction (MR).

174 ures (180 to 310 degrees C), may undergo the Maillard reaction (MR).

175 key step determining the development of the Maillard reaction (MR).

176 The impacts of cross-linking through the Maillard reaction (MR, 3-5 h) and tannic acid (TA, 0.1-0

177 e intermediary radicals appearing during the Maillard reactions (MR), that take place during heating

178 The use of ultrasound in the Maillard reaction notably enhanced the solubility, foami

179 Baking triggered caramelization and Maillard reactions, notably with the pulse products whic

180 oresis (CE) was used to analyze the in vitro Maillard reaction of GlcN with glyceraldehyde (GA), gluc

181 in foods during the browning process by the Maillard reaction of glucose (GL) with asparagine (AS).

182 nuclease A identify proteins modified by the Maillard reaction of glucose, fructose, ribose, glyceral

183 ginine modification (argpyrimidine) from the Maillard reaction of MG.

184 uced lipid oxidation, lipid degradation, and Maillard reaction of these plant-based ingredients.

185 ethyl-3-furyl)-l-cysteine (MFT-S-Cys) in the Maillard reaction of xylose with cysteine at 100 degrees

186 Nonenzymatic glycation (Maillard reaction) of long-lived proteins is a major con

187 of Reactive Carbonyl Species (RCS) from the Maillard reaction on browning formation in apple juice d

188 study was to evaluate the occurrence of the Maillard reaction on gelatin-based films (bovine and sal

189 f gelatine because the intervals between the Maillard reaction parameters of the samples were far apa

190 Differentiation analysis of the Maillard reaction parameters was conducted using cluster

191 Amadori breakdown is considered as the main Maillard reaction pathway, other reactive intermediates,

192 d be modeled using transformations along the Maillard reaction pathway.

193 cific influence of emulsion structure on the Maillard reaction pathways that occur during the cooking

194 tion of divalent cations which affect pH and Maillard reaction pathways, addition of antioxidant comp

195 ose, fructose and maltose and based on known Maillard reaction pathways, was developed which showed t

196 ow major flavonoid classes in cereals affect Maillard reaction pathways.

197 t formation was shown to be reduced in model Maillard reactions performed in the presence of electrop

198 MGO and GO formed in the Maillard reaction play important roles as precursors of

199 oformed contaminant contents were related to Maillard reaction precursor levels (reducing sugars and

200 The levels of the Maillard reaction precursors were very different dependi

201 -hydroxymethylfurfural, a major intermediate Maillard reaction product was found in all treatments.

202 henyl)-2-butenal (BHPB), a tyrosine-fructose Maillard reaction product, as a small molecule with pote

203 Maillard reaction products (estimated with non-enzymatic

204 ontent (TPC), total flavonoid content (TFC), Maillard reaction products (MRP) and phenolic profile in

205 Maillard reaction products (MRP) contribute to sensory q

206 of home cooking methods on the generation of Maillard reaction products (MRP) in beef was investigate

207 antioxidant properties, phenolic profile and Maillard reaction products (MRP) of flaxseed flour (FF)

208 Formation of Maillard reaction products (MRP) of glucosamine (GlcN) w

209 maltodextrin (MD), to produce anti-oxidative Maillard reaction products (MRP) which was used to encap

210 The release of biscuit Maillard reaction products (MRP) with antioxidant capaci

211 inhibitory effect (46.8%) on acrylamide and Maillard reaction products (MRPs) (>52.6%), respectively

212 In parallel, the content of Maillard reaction products (MRPs) and antioxidant capaci

213 The Maillard reaction products (MRPs) are widely produced in

214 Maillard reaction products (MRPs) between chitosan and v

215 ypertensive effect and prebiotic activity of Maillard reaction products (MRPs) derived from biscuits

216 ong-term a diet containing commonly consumed Maillard reaction products (MRPs) from the glucose-lysin

217 ng on protein oxidation, lipid oxidation and Maillard reaction products (MRPs) generation was evaluat

218 The quantification of protein bound Maillard reaction products (MRPs) is still a challenge i

219 sifying properties due to the development of Maillard reaction products (MRPs) like reductones and me

220 Maillard reaction products (MRPs) show antimicrobial act

221 cts were richer in polyphenols and poorer in Maillard reaction products (MRPs) than were GPE200 extra

222 Formation of Maillard reaction products (MRPs) was monitored by mass

223 tents, antioxidant and reducing capacity and Maillard reaction products (MRPs) were determined in gin

224 e formation and the functional properties of Maillard reaction products (MRPs) were investigated in a

225 Maillard reaction products (MRPs) were prepared from aqu

226 ed that the oxidative stability index (OSI), Maillard reaction products (MRPs), chlorophyll and carot

227 The effect of Maillard reaction products (MRPs), formed during the pro

228 The changes in protein, reducing sugar, Maillard reaction products (MRPs), minerals, free and bo

229 ed dependent variables were the formation of Maillard reaction products (MRPs), protein hydrolysates

230 rowave powers on oil yield, pigment content, Maillard reaction products (MRPs), radical scavenging ac

231 es, coupled to the increase in colour of the Maillard reaction products (MRPs), were recorded.

232 Maillard reaction products (MRPs), which are common in p

233 lity index (OSI), fatty acid composition and Maillard reaction products (MRPs).

234 s can lead to the increased formation of the Maillard reaction products (MRPs).

235 ation temperatures promoted the formation of Maillard reaction products 3-methyl-1-butanol, pyrazine,

236 Changes in the formation of Maillard reaction products and antioxidant capacity of b

237 ed formation of furosine, advanced and final Maillard reaction products and caused changes in both re

238 ter crust and weaker aroma (lower amounts of Maillard reaction products and fusel alcohols).

239 rnels can be ascribed to both the new formed Maillard reaction products and the conditions adopted du

240 ned new insights in the relationship between Maillard reaction products and their precursors.

241 high content of volatile lipid oxidation and Maillard reaction products compared to the marinated sam

242 ore, the distribution of lipid oxidation and Maillard reaction products differed from those typically

243 Some phenolic acids were incorporated into Maillard reaction products during baking.

244 Emissions from phenolic compounds and Maillard reaction products exhibited the largest differe

245 This inhibition could be attributed to the Maillard reaction products formed during the microwave t

246 ydroxy-6-methyl-4(H)-pyran-4-one (pyranone), Maillard reaction products found in DC and CB ghee, rapi

247 formation of several protein-bound advanced Maillard reaction products identical with those of aging

248 on to H2O2 generation and the actual role of Maillard reaction products in collagen cross-linking in

249 of the plant protein affects the presence of Maillard reaction products in PBMBAs.

250 The role of Maillard reaction products isolated from barley malt by

251 lecular properties and volatile compounds of Maillard reaction products obtained from chicken bone ex

252 he thermal formation of early ribose-glycine Maillard reaction products over time by ion cyclotron re

253 nstrate that the formation of acrylamide and Maillard reaction products was lower with glucose than w

254 Microwave treatment induced the formation of Maillard reaction products with a high antioxidant activ

255 Maillard reaction products with intense meat aroma, such

256 potentially toxic food contaminants, called Maillard reaction products, found in processed foods.

257 The formation of Maillard reaction products, including Amadori compounds

258 in Strecker aldehydes (6-23 fold) and other Maillard reaction products, including pyrroles, furans,

259 glycoxidation (pentosidine, PEN), glycation (Maillard reaction products, MRP), lipid oxidation (4-hyd

260 ormation of acrylamide by 98% and also other Maillard reaction products, specifically alkylpyrazines.

261 impact on the development of characteristic Maillard reaction products, such as pyrazines and some a

262 DC and CB ghee contained volatile Maillard reaction products, whereas PS ghee did not.

263 iates with proteins lead to the formation of Maillard reaction products, which subsequently leads to

264 tents as well as markers of barrel aging and Maillard reaction products.

265 rst time that CS-conjugates are described as Maillard reaction products.

266 as advanced glycation endproducts (AGEs) or Maillard reaction products.

267 etermination of several markers arising from Maillard reaction proved pyrraline (PYR) and hydroxymeth

268 h alkaline hydrolysis and enhanced using the Maillard reaction, reaching a maximum concentration of 7

269 In the course of the Maillard reaction, reducing sugars and amino compounds a

270 It also provides the pros and cons of the Maillard reaction, some available antioxidant assays to

271 The formation of acrylamide in model Maillard reaction systems containing phenolic compounds

272 During such treatment, the Maillard reaction takes place, generating brown polymers

273 occurs in parboiled rice as a result of the Maillard reaction that negatively affects consumers' acc

274 (more than six times) but also the extent of Maillard reaction that resulted in three times lower amo

275 Methylglyoxal-mediated Maillard reactions that occur in the human lens may play

276 ons are known to influence the course of the Maillard reaction through formation of various complexes

277 acids and reducing sugars, accelerating the Maillard reaction to enhance flavour in baked goods, but

278 igh mass accuracy proved the contribution of Maillard reaction to non-enzymatic reactions in fruit pr

279 amined different indicators of each stage of Maillard reaction under adverse storage conditions in a

280 CS/SSPS conjugates were prepared through the Maillard reaction using dry heating.

281 4-b]indol-1-l)phenol), were prepared via the Maillard reaction using food flavours and 5-methoxytrypt

282 n was linked to available information on the Maillard reaction via multiresponse modelling.

283 idation of the reducing sugars, but from the Maillard reaction via the Amadori rearrangement product.

284 Higher amount of Maillard reaction volatile products, associated with mor

285 The occurrence of the Maillard reaction was demonstrated by the lowering of pH

286 long-term glycemic control and the advanced Maillard reaction was investigated in dura mater collage

287 e, free amino acids, and certain products of Maillard reaction was monitored during roasting of sunfl

288 kers of the early and advanced stages of the Maillard reaction were also followed in the crumb and th

289 The products of the Maillard reaction were compared with the products of int

290 (glucose, asparagine, and tryptophan) of the Maillard reaction were partitioned either inside the dro

291 agave syrups (HFASs) as intermediates of the Maillard reaction, were determined.

292 it grows and is also formed, as part of the Maillard reaction, when rice is heated.

293 rated from glucose via caramelization and/or Maillard reaction, whereas the formation of Strecker ald

294 This measurement is crucial for studying the Maillard reaction, which affects the sensorial quality o

295 values for odour-active aroma compounds from Maillard reaction, which are related to roast flavour an

296 We hypothesized that the Maillard reaction, which leads browning and aroma develo

297 sin, chymotrypsin or subtilisin, and finally Maillard reaction with glucose or xylose of resulting hy

298 ofunctional properties were modified through Maillard reaction with maltodextrin (MD).

299 ils (AFs) was investigated by performing the Maillard reaction with the free anomeric carbon of the m

300 ils (AFs) was investigated by performing the Maillard reaction with the free anomeric carbon of the m