{"title":"Role of the Maillard Reaction Products in Affecting the Overall Antioxidant Properties of Processed Foods","authors":"M. Anese","doi":"10.1533/9781845698447.8.399A","DOIUrl":"https://doi.org/10.1533/9781845698447.8.399A","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"10 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129170090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Flavour Formation in Soy Hydrolysates Prepared Using Enzymes","authors":"Lene V Kotòd, M. Fischer","doi":"10.1533/9781845698447.8.417A","DOIUrl":"https://doi.org/10.1533/9781845698447.8.417A","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130717940","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"New Coloured Compounds from Model Systems: Xylose-Lysine","authors":"A. Arnoldi, L. Scaglioni, Emanuela Corain","doi":"10.1533/9781845698447.8.402A","DOIUrl":"https://doi.org/10.1533/9781845698447.8.402A","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"53 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126932896","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Influence of Maillard Browning on Cow and Buffalo Milk and Milk Proteins - A Comparative Study","authors":"A. Srinivasan, A. Gopalan, S. Ramabadran","doi":"10.1533/9781845698447.8.445A","DOIUrl":"https://doi.org/10.1533/9781845698447.8.445A","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"125 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121543063","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Correlations between Structure and Reactivity of Amadori Compounds: the Reactivity of Acyclic Forms","authors":"M. Feather, V. Mossine","doi":"10.1533/9781845698447.2.37","DOIUrl":"https://doi.org/10.1533/9781845698447.2.37","url":null,"abstract":"Summary Several Amadori compounds were prepared and solution (NMR) and, in some cases, solid-state structures (X-ray) were determined. Several of the compounds studied contain sugar units which exist predominantly in acyclic forms. Such compounds were used as model Amadori compounds and rates of reactivity with respect to C(1)H2 proton exchange, the ability to generate oxygen free radicals, and the type of dicarbonyl intermediates produced were evaluated. The results of the experiments enable direct, although qualitative, correlations to be made between the population of acyclic forms in solutions of Amadori compounds, the rates of their reversible enolization, and their reactivity in redox and degradation reactions.","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"36 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122268551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Separation of Coloured Components of Kecap Manis (an Indonesian Soy Sauce) by HPLC and Capillary Electrophoresis","authors":"A. Apriyantono, Santi Marianti","doi":"10.1533/9781845698447.8.400","DOIUrl":"https://doi.org/10.1533/9781845698447.8.400","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121143748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Novel Observations of the Effect of Aminoguanidine on Previously Glycated Protein: A Pro-Oxidant Activity that Increases Proteolytic Susceptibility","authors":"J. V. Hunt, D. Schultz","doi":"10.1533/9781845698447.8.413A","DOIUrl":"https://doi.org/10.1533/9781845698447.8.413A","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"311 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116760573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Modeling of Protein and Aminophospholipid Glycation Using Low Molecular Weight Analogs. A Comparative Study","authors":"O. Argirov, I. I. Kerina, J. Uzunova, M. Argirova","doi":"10.1533/9781845698447.7.245","DOIUrl":"https://doi.org/10.1533/9781845698447.7.245","url":null,"abstract":"Summary (2-aminoethyl)phenethylphosphate and (2-aminoethyl)ethylphosphate were synthesized as models of aminophospholipids. Their glycation by glucose and fructose was compared with that of appropriate peptides (Gly-Phe, Gly-Gly, Gly-Lys) and amino compounds (2-aminoethanol, β-alanine). Formation of glycation products was studied by electron spectroscopy and reversed-phase HPLC. The results obtained confirm that amino groups in aminophospholipids are reactive enough to form glycation products under physiological conditions.","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"47 4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116781374","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Maillard Products: Interference in Carbonyl Assay of Oxidized Protein","authors":"Peter J Coassons, M. Bagga, Stephanie Mulligan","doi":"10.1533/9781845698447.8.405","DOIUrl":"https://doi.org/10.1533/9781845698447.8.405","url":null,"abstract":"","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"92 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125184689","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Antioxidative Activity of Non-Enzymatically Browned Proteins by Reaction with Lipid Oxidation Products","authors":"F. Hidalgo, M. Alaiz, R. Zamora","doi":"10.1533/9781845698447.6.225","DOIUrl":"https://doi.org/10.1533/9781845698447.6.225","url":null,"abstract":"Summary Three oxidized lipid/amino acid reaction (OLAARP): (1-methyl-4-pentyl-1,4-dihydropyridine-3,5-dicarbaldehyde, 1-(5′-amino-1′-carboxypentyl)pyrrole, and N -(carbobenzyloxy)-1(3)-(1′-(formyl(methyl)-hexyl)-L-histidine dehydrate), and two browned proteins (the monomer and the dimmer produced in the reaction between BSA and 4,5( E )-epoxy-2- E )-hepatenal) were prepared and tested for antioxidative activity in a microsomal system in order to investigate the antioxidative function of OLAARP and non-enzymatically browned proteins in biological systems. The microsomal sytem consisted fo freshly prepared trout muscle microsomes, which were oxidized with Cu 2+ , Fe 3+ /ascorbate, or Cu 2+ /H 2 O 2 at 37 °C and in the presence of the compound to be tested as antioxidant. The three OLAARP (tested at 50 μM) and the two browned proteins (tested at 40 μg/mL) efficiently protected against lipid peroxidation, assessed by the formation of thiobarbituric acid-reactive substances, and protein damage, determined by amino acid analysis. These results suggest that the formation of non-enzymatically browned proteins by reaction with lipid oxidation products may constitute an antioxidative defense mechanism, which could play a significant role in vivo .","PeriodicalId":359473,"journal":{"name":"The Maillard Reaction in Foods and Medicine","volume":"16 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128034186","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}