
Antibacterial properties of Maillard reaction products: Molecular mechanisms and influencing factors (Review)
- Authors:
- Zhongshuang Hu
- Jiao Li
- Xianghuan Wu
- Yongzhong Wei
- Xudong Li
- Jing Ji
-
Affiliations: School of Food and Pharmacy, Shanghai Zhongqiao Vocational and Technical University, Shanghai 201514, P.R. China, School of Food and Pharmacy, Shanghai Zhongqiao Vocational and Technical University, Shanghai 201514, P.R. China, School of Agriculture and Biology, Shanghai Jiaotong University, Shanghai 200240, P.R. China - Published online on: June 17, 2025 https://doi.org/10.3892/br.2025.2019
- Article Number: 141
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Copyright: © Hu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
This article is mentioned in:
Abstract
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Nooshkam M, Varidi M and Verma DK: Functional and biological properties of Maillard conjugates and their potential application in medical and food: A review. Food Res Int. 131(109003)2020.PubMed/NCBI View Article : Google Scholar | |
Kathuria D, Hamid Gautam S and Thakur A: Maillard reaction in different food products: Effect on product quality, human health and mitigation strategies. Food Control. 153(109911)2023. | |
Khalid M, Petroianu G and Adem A: Advanced glycation end products and diabetes mellitus: Mechanisms and perspectives. Biomolecules. 12(542)2022.PubMed/NCBI View Article : Google Scholar | |
Ruggeri RM, Vicchio TM, Cristani M, Certo R, Caccamo D, Alibrandi A, Giovinazzo S, Saija A, Campennì A, Trimarchi F and Gangemi S: Oxidative stress and advanced glycation end products in Hashimoto's thyroiditis. Thyroid. 26:504–511. 2016.PubMed/NCBI View Article : Google Scholar | |
Fishman SL, Sonmez H, Basman C, Singh V and Poretsky L: The role of advanced glycation end-products in the development of coronary artery disease in patients with and without diabetes mellitus: A review. Mol Med. 24(59)2018.PubMed/NCBI View Article : Google Scholar | |
Shi A, Ji X, Li W, Dong L, Wu Y, Zhang Y, Liu X, Zhang Y and Wang S: The interaction between human microbes and advanced glycation end products: the role of Klebsiella X15 on advanced glycation end products' degradation. Nutrients. 16(754)2024.PubMed/NCBI View Article : Google Scholar | |
Phuong-Nguyen K, McNeill BA, Aston-Mourney K and Rivera LR: Advanced glycation end-products and their effects on gut health. Nutrients. 15(405)2023.PubMed/NCBI View Article : Google Scholar | |
Ke L, Luo S, Rao P, Bradshaw JP, Sa'adedin F, Rappolt M and Zhou J: An evidence for a novel antiviral mechanism: modulating effects of Arg-Glc Maillard reaction products on the phase transition of multilamellar vesicles. Front Cell Dev Biol. 8(629775)2021.PubMed/NCBI View Article : Google Scholar | |
Helou C, Marier D, Jacolot P, Abdennebi-Najar L, Niquet-Léridon C, Tessier FJ and Gadonna-Widehem P: Microorganisms and Maillard reaction products: A review of the literature and recent findings. Amino Acids. 46:267–277. 2014.PubMed/NCBI View Article : Google Scholar | |
Jiang T, Feng L and Li J: Changes in microbial and postharvest quality of shiitake mushroom (Lentinus edodes) treated with chitosan-glucose complex coating under cold storage. Food Chem. 131:780–786. 2012. | |
Hiramoto S, Itoh K, Shizuuchi S, Kawachi Y, Morishita Y, Nagase M, Suzuki Y, Nobuta Y, Sudou Y, Nakamura O, et al: Melanoidin, a food protein-derived advanced maillard reaction product, suppresses helicobacter pylori in vitro and in vivo. Helicobacter. 9:429–435. 2004.PubMed/NCBI View Article : Google Scholar | |
Snelson M and Coughlan M: Dietary advanced glycatione end products: Digestion, metabolism and modulation of gut microbial ecology. Nutrients. 11(215)2019.PubMed/NCBI View Article : Google Scholar | |
Ni L, Shen R, Luo H, Li X, Zhang X, Huang L, Deng Y, Liao X, Wu Y, Duan C and Xie X: GlmS plays a key role in the virulence factor expression and biofilm formation ability of Staphylococcus aureus promoted by advanced glycation end products. Virulence. 15(2352476)2024.PubMed/NCBI View Article : Google Scholar | |
Hiramoto K, Sekiguchi K, Aso-O R, Ayuha K, Ni-Iyama H, Kato T and Kikugawa K: DNA strand breaks induced through active oxygen radicals by fragrant component 4-hydroxy-2-hydroxymethyl5-methyl-3(2H)-furanone in maillard reaction of hexose/amino acid. Food Chem Toxicol. 33:803–814. 1995.PubMed/NCBI View Article : Google Scholar | |
Sheikh-Zeinoddin M, Perehinec TM, Hill SE and Rees CED: Maillard reaction causes suppression of virulence gene expression in Listeria monocytogenes. Int J Food Microbiol. 61:41–49. 2000.PubMed/NCBI View Article : Google Scholar | |
Kundinger MM, Zabala-Díaz IB, Chalova VI and Ricke SC: Effects of Maillard reaction products on hilA expression in salmonella typhimurium. J Food Sci. 73:M32–5. 2008.PubMed/NCBI View Article : Google Scholar | |
Xie X, Liu X, Li Y, Luo L, Yuan W, Chen B, Liang G, Shen R, Li H, Huang S and Duan C: Advanced glycation end products enhance biofilm formation by promoting extracellular DNA release through sigB upregulation in Staphylococcus aureus. Front Microbiol. 11(1479)2020.PubMed/NCBI View Article : Google Scholar | |
Daglia M, Tarsi R, Papetti A, Grisoli P, Dacarro C, Pruzzo C and Gazzani G: Antiadhesive effect of green and roasted coffee on Streptococcus mutans adhesive properties on saliva-coated hydroxyapatite beads. J Agric Food Chem. 50:1225–1229. 2002.PubMed/NCBI View Article : Google Scholar | |
Lanciotti R, Anese M, Sinigaglia M, Severini C and Massini R: Effects of heated glucose-fructose-glutamic acid solutions on the growth of Bacillus stearothermophilus. LWT. 32:223–230. 1999. | |
Rurián-Henares JA and Morales FJ: Antimicrobial activity of melanoidins against Escherichia coli is mediated by a membrane-damage mechanism. J Agric Food Chem. 56:2357–2362. 2008.PubMed/NCBI View Article : Google Scholar | |
Silván JM, van de Lagemaat J, Olano A and Del Castillo MD: Analysis and biological properties of amino acid derivates formed by Maillard reaction in foods. J Pharm Biomed Anal. 41:1543–1551. 2006.PubMed/NCBI View Article : Google Scholar | |
Martins SIFS, Jongen WMF and Van Boekel MAJS: A review of Maillard reaction in food and implications to kinetic modelling. Trends Food Sci Technol. 11:364–373. 2000. | |
Wang HY, Qian H and Yao WR: Melanoidins produced by the Maillard reaction: Structure and biological activity. Food Chem. 128:573–584. 2011. | |
Kroh LW, Fiedler T and Wagner J: alpha- Dicarbonyl compounds-key intermediates for the formation of carbohydrate-based melanoidins. Ann N Y Acad Sci. 1126:210–215. 2008.PubMed/NCBI View Article : Google Scholar | |
Cämmerer B, Jalyschko W and Kroh LW: Intact carbohydrate structures as part of the melanoidin skeleton. J Agric Food Chem. 50:2083–2087. 2002.PubMed/NCBI View Article : Google Scholar | |
Miethke M, Pieroni M, Weber T, Brönstrup M, Hammann P, Halby L, Arimondo PB, Glaser P, Aigle B, Bode HB, et al: Towards the sustainable discovery and development of new antibiotics. Nat Rev Chem. 5:726–749. 2021.PubMed/NCBI View Article : Google Scholar | |
Einarsson H, Snygg BG and Eriksson C: Inhibition of bacterial growth by Maillard reaction products. J Agric Food Chem. 31:1043–1047. 1983. | |
Bhattacharjee MK, Sugawara K and Ayandeji OT: Microwave sterilization of growth medium alleviates inhibition of Aggregatibacter actinomycetemcomitans by Maillard reaction products. J Microbiol Methods. 78:227–230. 2009.PubMed/NCBI View Article : Google Scholar | |
Rufián-Henares JA and Morales FJ: Microtiter plate-based assay for screening antimicrobial activity of melanoidins against E. coli and S. aureus. Food Chem. 111:1069–1074. 2008. | |
Bhattacharjee MK, Mehta BS and Akukwe B: Maillard reaction products inhibit the periodontal pathogen Aggregatibacter actinomycetemcomitans by chelating iron. Arch Oral Biol. 122(104989)2021.PubMed/NCBI View Article : Google Scholar | |
Aonishi K, Miyao S, Yokoi L, Kitaoka N, Koyama K, Matsuura H and Koseki S: Isolation and identification of the antibacterial compounds produced by Maillard reaction of xylose with phenylalanine or proline. J Agric Food Chem. 72:16010–16017. 2024.PubMed/NCBI View Article : Google Scholar | |
Kukuminato S, Koyama K and Koseki S: Antibacterial properties of melanoidins produced from various combinations of maillard reaction against pathogenic bacteria. Microbiol Spectr. 9(e0114221)2021.PubMed/NCBI View Article : Google Scholar | |
Maesaka E, Kukuminato S, Aonishi K, Koyama K and Koseki S: Antibacterial effect of melanoidins derived from xylose and phenylalanine against bacillus cereus and clostridium perfringens. J Food Prot. 86(100140)2023.PubMed/NCBI View Article : Google Scholar | |
Li SL, Lin J and Chen XM: Effect of chitosan molecular weight on the functional properties of chitosan-maltose Maillard reaction products and their application to fresh-cut Typha latifolia L. Carbohydr Polym. 102:682–690. 2014.PubMed/NCBI View Article : Google Scholar | |
Gottardi D, Hong PK, Ndagijimana M and Betti M: Conjugation of gluten hydrolysates with glucosamine at mild temperatures enhances antioxidant and antimicrobial properties. LWT-Food Sci Technol. 57:181–187. 2014. | |
Kraskouski A, Hileuskaya K, Nikalaichuk V, Ladutska A, Kabanava V, Yao W and You L: Chitosan-based Maillard self-reaction products: Formation, characterization, antioxidant and antimicrobial potential. Carbohydr Polym Technol Appl. 4(100257)2022. | |
Song R, Yang P, Wei R and Ruan G: Antioxidative, antibacterial, and food functional properties of the half-fin anchovy hydrolysates-glucose conjugates formed via Maillard reaction. Molecules. 21(795)2016.PubMed/NCBI View Article : Google Scholar | |
Jiang W, Liu Y, Yang X and Hu S: Antioxidant and antibacterial activities of modified crab shell bioactive peptides by Maillard reaction. Int J Food Prop. 21:2730–2743. 2018. | |
Kim Y, Kim S, Lee S, Ha J, Lee J, Choi Y, Oh H, Lee Y, Oh NS, Yoon Y and Lee H: Antimicrobial activity of fermented Maillard reaction products, novel milk-derived material, made by whey protein and Lactobacillus rhamnosus and Lactobacillus gasseri on Clostridium perfringens. Anim Biosci. 34:1525–1531. 2021.PubMed/NCBI View Article : Google Scholar | |
Sun T, Qin Y, Xu H, Xie J, Hu D, Xue B and Hua X: Antibacterial activities and preservative effect of chitosan oligosaccharide Maillard reaction products on Penaeus vannamei. Int J Biol Macromol. 105(Pt 1):764–768. 2017.PubMed/NCBI View Article : Google Scholar | |
Ji L, Zhang Y, Song W, Cai L, Wang Y and Guo J: Analysis on antibacterial activities and volatile compounds of Maillard reaction products derived from squid skin. E3S Web Conf. 145(01028)2020. | |
Wang J, Wei R and Song R: Novel antibacterial peptides isolated from the Maillard reaction products of half-fin anchovy (Setipinna taty) Hydrolysates/glucose and their mode of action in escherichia Coli. Mar Drugs. 17(47)2019.PubMed/NCBI View Article : Google Scholar | |
Goulas V, Nicolaou D, Botsaris G and Barbouti A: Straw wine melanoidins as potential multifunctional agents: Insight into antioxidant, antibacterial, and angiotensin-I-converting enzyme inhibition effects. Biomedicines. 6(83)2018.PubMed/NCBI View Article : Google Scholar | |
Mu K, Wang S and D Kitts DD: Evidence to indicate that maillard reaction products can provide selective antimicrobial activity. Integr Food Nutr Metab. 3:330–335. 2016. | |
Maletta AB and Were LM: Effect of coffee filtrate, methylglyoxal, glyoxal, and caffeine on Salmonella typhimurium and S. Enteritidis survival in ground chicken breasts. J Food Sci. 77:M135–41. 2012.PubMed/NCBI View Article : Google Scholar | |
Chen X, Jiang D, Xu P, Geng Z, Xiong G, Zou Y, Wang D and Xu W: Structural and antimicrobial properties of Maillard reaction products in chicken liver protein hydrolysate after sonication. Food Chem. 343(128417)2021.PubMed/NCBI View Article : Google Scholar | |
Trang VT, Takeuchi H, Kudo H, Aoki A, Katsuno S, Shimamura T, Sugiura T and Ukeda H: Antimicrobial activity of aminoreductone against Helicobacter pylori. J Agric Food Chem. 57:11343–11348. 2009.PubMed/NCBI View Article : Google Scholar | |
Trang VT, Son VH, Thanh LX, Sarter S, Shimamura T, Uked H and Takeuchi H: Functional properties of Maillard reaction products in food: antimicrobial activity of aminoreductone against pathogenic bacteria. Food Sci Technol Res. 19:833–841. 2013. | |
Trang VT, Takeuchi H, Kudo H, Katsuno S, Shimamura T, Kashiwagi T, Son VH, Sugiura T and Ukeda H: In Vitro Antimicrobial activity of aminoreductone against the pathogenic bacteria Methicillin-Resistant Staphylococcus aureus (MRSA). J Agric Food Chem. 59:8953–8960. 2011.PubMed/NCBI View Article : Google Scholar | |
Feng T, Zhou Y, Wang X, Wang X and Xia S: α-Dicarbonyl compounds related to antimicrobial and antioxidant activity of maillard reaction products derived from xylose, cysteine and corn peptide hydrolysate. Food Biosci. 41(100951)2021. | |
Mavric E, Wittmann S, Barth G and Henle T: Identification and quantification of methylglyoxal as the dominant antibacterial constituent of Manuka (Leptospermum scoparium) honeys from New Zealand. Mol Nutr Food Res. 52:483–489. 2008.PubMed/NCBI View Article : Google Scholar | |
Benattouche Z, Benamar K, Belkhodja H, Bouhadi D, Hariri A and Raho GB: Investigating the antimicrobial effect of Maillard products on pathogens microorganisms. Ro J Infect Dis. 27:290–295. 2024. | |
Pischetsrieder M, Schoetter C and Severin T: Formation of an aminoreductone during the Maillard reaction of lactose with Nr-acetyllysine or proteins. J Agric Food Chem. 46:928–931. 1998. | |
Nagarajan K, Taleuzzamman M, Kumar V, Singh S, Singh J, Panda BP and Ghosh LK: Antimicrobial glycopeptides: Synthesis and antibacterial activity of N-linked and O-linked smaller chain glycopeptides. Drug Res (Stuttg). 64:186–194. 2013.PubMed/NCBI View Article : Google Scholar | |
Trang VT: Effects of aminoreductone against the growth of food-borne bacteria in medium and in milk. Tạp Chí Khoa Học Và Công Nghệ. 53:606–614. 2015. | |
Shimamura T, Kurogi Y, Katsuno S, Kashiwagi T and Ukeda H: Demonstration of the presence of aminoreductone formed during the Maillard reaction in milk. Food Chem. 129:1088–1092. 2011.PubMed/NCBI View Article : Google Scholar | |
Kang HK and Park Y: Glycopeptide antibiotics: Structure and mechanisms of action. J Bacteriol Virol. 45(67)2015. | |
Hong PK, Gottardi D, Ndagijimana M and Betti M: Glycation and transglutaminase mediated glycosylation of fish gelatin peptides with glucosamine enhance bioactivity. Food Chem. 142:285–293. 2014.PubMed/NCBI View Article : Google Scholar | |
White JS: Misconceptions about high-fructose corn syrup: Is it uniquely responsible for obesity, reactive dicarbonyl compounds, and advanced glycation endproducts? J Nutr. 139:1219S–1227S. 2009.PubMed/NCBI View Article : Google Scholar | |
Shibamoto T: Diacetyl: Occurrence, analysis, and toxicity. J Agric Food Chem. 62:4048–4053. 2014.PubMed/NCBI View Article : Google Scholar | |
Papetti A, Mascherpa D and Gazzani G: Free α-dicarbonyl compounds in coffee, barley coffee and soy sauce and effects of in vitro digestion. Food Chem. 164:259–265. 2014.PubMed/NCBI View Article : Google Scholar | |
Brighina S, Restuccia C, Arena E, Palmeri R and Fallico B: Antibacterial activity of 1,2-dicarbonyl compounds and the influence of the in vitro assay system. Food Chem. 311(125905)2020.PubMed/NCBI View Article : Google Scholar | |
Adams CJ, Boult CH, Deadman BJ, Farr JM, Grainger MN, Manley-Harris M and Snow MJ: Isolation by HPLC and characterisation of the bioactive fraction of New Zealand manuka (Leptospermum scoparium) honey. Carbohydr Res. 343:651–659. 2008.PubMed/NCBI View Article : Google Scholar | |
Rabie E, Serem JC, Oberholzer HM, Gaspar AR and Bester MJ: How methylglyoxal kills bacteria: An ultrastructural study. Ultrastruct Pathol. 40:107–111. 2016.PubMed/NCBI View Article : Google Scholar | |
Kilty SJ, Duval M, Chan FT, Ferris W and Slinger R: Methylglyoxal: (active agent of manuka honey) in vitro activity against bacterial biofilms. Int Forum Allergy Rhinol. 1:348–350. 2011.PubMed/NCBI View Article : Google Scholar | |
Rufián-Henares JA and de la Cueva SP: Antimicrobial activity of coffee melanoidins-A study of their metal-chelating properties. J Agric Food Chem. 57:432–438. 2009.PubMed/NCBI View Article : Google Scholar | |
Zhong Y, Liu H, Chen F, He Q, Zhang X, Lan L and Yang C: Design, synthesis and biological evaluation of thiazolyl-halogenated pyrroles or pyrazoles as novel antibacterial and antibiofilm agents. Eur J Med Chem. 268(116221)2024.PubMed/NCBI View Article : Google Scholar | |
Liu Z, Zhang P, Qin Y, Zhang N, Teng Y, Venter H and Ma S: Design and synthesis of aryl-substituted pyrrolidone derivatives as quorum sensing inhibitors. Bioorganic Chem. 105(104376)2020.PubMed/NCBI View Article : Google Scholar | |
Elneairy MAA, Youssef EGN, Ebrahim SAA, Mohammad NEM, Abd El-Rahman NMS, Elhewaty ASM, Sanad SMH and Mekky AEM: MRSA inhibitory activity of some new pyrazolo[1,5-a]pyrimidines linked to arene and/or furan or thiophene units. Chem Biodivers. 22(e202402031)2025.PubMed/NCBI View Article : Google Scholar | |
Noda K, Kishimoto M, Shimamura Y and Murata M: Conditions and mechanism of formation of the Maillard reaction pigment, furpenthiazinate, in a model system and in some acid hydrolyzates of foods and its biological properties. J Agric Food Chem. 72:6593–6600. 2024.PubMed/NCBI View Article : Google Scholar | |
Zou T, Liu J, Song H and Liu Y: Discovery of Amadori-type conjugates in a peptide Maillard reaction and their corresponding influence on the formation of pyrazines. J Food Sci. 83:1588–1595. 2018.PubMed/NCBI View Article : Google Scholar | |
Bekedam EK, Roos E, Schols HA, Van Boekel MA and Smit G: Low molecular weight melanoidins in coffee brew. J Agric Food Chem. 56:4060–4067. 2008.PubMed/NCBI View Article : Google Scholar | |
Mondaca-Navarro BA, Ávila-Villa LA, González-Córdova AF, López-Cervantes J, Sánchez-Machado DI, Campas-Baypoli ON and Rodríguez-Ramírez R: Antioxidant and chelating capacity of Maillard reaction products in amino acid-sugar model systems: Applications for food processing. J Sci Food Agric. 97:3522–3529. 2017.PubMed/NCBI View Article : Google Scholar | |
Qiu DH, Huang ZL, Zhou T, Shen C and Hider RC: In vitro inhibition of bacterial growth by iron chelators. FEMS Microbiol Lett. 314:107–111. 2011.PubMed/NCBI View Article : Google Scholar | |
Morales F: Iron-binding ability of melanoidins from food and model systems? Food Chem. 90:821–827. 2005. | |
Lang A, Lan W and Xie J: Preparation and antimicrobial mechanism of Maillard reaction products derived from ε-polylysine and chitooligosaccharides. Biochem Biophys Res Commun. 650:30–38. 2023.PubMed/NCBI View Article : Google Scholar | |
Liang C, Yuan F, Liu F, Wang Y and Gao Y: Structure and antimicrobial mechanism of ɛ-polylysine-chitosan conjugates through Maillard reaction. Int J Biol Macromol. 70:427–434. 2014.PubMed/NCBI View Article : Google Scholar | |
Hauser C, Müller U, Sauer T, Augner K and Pischetsrieder M: Maillard reaction products as antimicrobial components for packaging films. Food Chem. 145:608–613. 2014.PubMed/NCBI View Article : Google Scholar | |
Ugye JT, Uzairu A, Idris SO and Kwanashie HO: The mechanism of the biochemical activity of 3,5-diphenylamine-1,4 dihydro-2,6-dimethylpyridine dicarboxylate adduct of formaldehyde and plasma albumin cross link. Int J Chem Biomed Sci. 3:73–78. 2017. | |
Mueller U, Sauer T, Weigel I, Pichner R and Pischetsrieder M: Identification of H2O2 as a major antimicrobial component in coffee. Food Funct. 2:265–272. 2011.PubMed/NCBI View Article : Google Scholar | |
Hofmann T: Studies on the relationship between molecular weight and the color potency of fractions obtained by thermal treatment of glucose/amino acid and glucose/protein solutions by using ultracentrifugation and color dilution techniques. J Agric Food Chem. 46:3891–3895. 1998. | |
Kim JS and Lee YS: The Influence of pH on the color development of melanoidins formed from fructose/amino acid enantiomer model systems. Prev Nutr Food Sci. 13:306–312. 2008. | |
Guan YG, Wang SL, Yu SJ, Yu SM and Zhao ZG: Changes in the initial stages of a glucose-proline Maillard reaction model system influences dairy product quality during thermal processing. J Dairy Sci. 95:590–601. 2012.PubMed/NCBI View Article : Google Scholar | |
Tamanna N and Mahmood N: Food processing and maillard reaction products: Effect on human health and nutrition. Int J Food Sci. 2015(526762)2015.PubMed/NCBI View Article : Google Scholar | |
Lund MN and Ray CA: Control of maillard reactions in foods: Strategies and chemical mechanisms. J Agric Food Chem. 65:4537–4552. 2017.PubMed/NCBI View Article : Google Scholar | |
Ajandouz EH, Tchiakpe LS, Ore FD, Benajiba A and Puigserver A: Effects of pH on caramelization and Maillard reaction kinetics in fructose-lysine model systems. J Food Sci. 66:926–931. 2001. | |
Wijewickreme AN, Kitts DD and Durance TD: Reaction conditions influence the elementary composition and metal chelating affinity of nondialyzable model Maillard reaction products. J Agric Food Chem. 45:4577–4583. 1997. | |
Hrynets Y, Bhattacherjee A, Ndagijimana M, Hincapie Martinez DJ and Betti M: Iron (Fe2+)-catalyzed glucosamine browning at 50˚C: Identification and quantification of major flavor compounds for antibacterial activity. J Agric Food Chem. 64:3266–3275. 2016.PubMed/NCBI View Article : Google Scholar | |
Yoshimura Y, Iijima T, Watanabe T and Nakazawa H: Antioxidative effect of Maillard reaction products using glucose-glycine model system. J Agric Food Chem. 45:4106–4109. 1997. | |
Le AQ, Dang VP, Nguyen ND, Nguyen QH and Ngo DN: Preparation of chitosan-glucosamine derivatives (Maillard reaction products) by gamma Co-60 irradiation method and investigation of antibacterial activity. Nucl Sci Technol (Hanoi). 7:44–50. 2017. | |
Chevalier F, Chobert JM, Genot C and Haertlé T: Scavenging of free radicals, antimicrobial, and cytotoxic activities of the maillard reaction products of beta-lactoglobulin glycated with several sugars. J Agric Food Chem. 49:5031–5038. 2001.PubMed/NCBI View Article : Google Scholar | |
Yu X, Jing Y and Yan F: Chitooligosaccharide-Lysine Maillard reaction products: Preparation and potential application on fresh-cut Kiwifruit. Food Bioprocess Technol. 12:1133–1143. 2019. | |
Hancock RE, Brown KL and Mookherjee N: Host defence peptides from invertebrates - emerging antimicrobial strategies. Immunobiology. 211:315–322. 2006.PubMed/NCBI View Article : Google Scholar | |
Su G, Zheng L, Cui C, Yang B, Ren J and Zhao M: Characterization of antioxidant activity and volatile compounds of Maillard reaction products derived from different peptide fractions of peanut hydrolysate. Food Res Int. 44:3250–3258. 2011. | |
Dolashka P, Moshtanska V, Borisova V, Dolashki A, Stevanovic S, Dimanov T and Voelter W: Antimicrobial proline-rich peptides from the hemolymph of marine snail Rapana venosa. Peptides. 32:1477–1483. 2011.PubMed/NCBI View Article : Google Scholar | |
Patrignani M, Rinaldi GJ, Rufián-Henares JÁ and Lupano CE: Antioxidant capacity of Maillard reaction products in the digestive tract: An in vitro and in vivo study. Food Chem. 276:443–450. 2019.PubMed/NCBI View Article : Google Scholar | |
Nagaoka I, Hirota S, Yomogida S, Ohwada A and Hirata M: Synergistic actions of antibacterial neutrophil defensins and cathelicidins. Inflamm Res. 49:73–79. 2000.PubMed/NCBI View Article : Google Scholar | |
Yang H, Zhang Y, Zhou F, Guo J, Tang J, Han Y, Li Z and Fu C: Preparation, bioactivities and applications in food industry of chitosan-based Maillard products: A review. Molecules. 26(166)2020.PubMed/NCBI View Article : Google Scholar | |
Kitaura A, Nishinaka T, Hamasaki S, Hatipoglu OF, Wake H, Nishibori M, Mori S, Nakao S and Takahashi H: Advanced glycation end-products reduce lipopolysaccharide uptake by macrophages. PLoS One. 16(e0245957)2021.PubMed/NCBI View Article : Google Scholar | |
Baisier WM and Labuza TP: Maillard browning kinetics in a liquid model system. J Agric Food Chem. 40:707–713. 1992. | |
Liu X, Xia B, Hu L, Ni Z, Thakur K and Wei Z: Maillard conjugates and their potential in food and nutritional industries: A review. Food Front. 1:382–397. 2020. | |
Kim ES and Yaylayan V: Identification of the Maillard reaction intermediates as divalent iron complexes in alanine/glucose/FeCl2 model system using ESI/qTOF/MS/MS and isotope labelling technique. Curr Res Food Sci. 4:287–294. 2021.PubMed/NCBI View Article : Google Scholar | |
Yang N, Yang S and Zheng X: Inhibition of Maillard reaction during alkaline thermal hydrolysis of sludge. Sci Total Environ. 814(152497)2022.PubMed/NCBI View Article : Google Scholar | |
Ye X, Zhang M, Gong Z, Jiao W, Li L, Dong M, Xiang T, Feng N and Wu Q: Inhibition of polyphenols on Maillard reaction products and their induction of related diseases: A comprehensive review. Phytomedicine. 128(155589)2024.PubMed/NCBI View Article : Google Scholar | |
Panja S, Rankenberg J, Michel C, Cooksley G, Glomb MA and Nagaraj RH: Proximal cysteine residues in proteins promote Nε-carboxyalkylation of lysine residues by α-dicarbonyl compounds. J Biol Chem. 301(108377)2025.PubMed/NCBI View Article : Google Scholar | |
Ecevit K, Barros AA, Silva JM and Reis RL: Preventing microbial infections with natural phenolic compounds. Future Pharmacol. 2:460–498. 2022. | |
Dahlem Junior MA, Nguema Edzang RW, Catto AL and Raimundo JM: Quinones as an efficient molecular scaffold in the antibacterial/antifungal or antitumoral arsenal. Int J Mol Sci. 23(14108)2022.PubMed/NCBI View Article : Google Scholar | |
Bork LV, Haase PT, Rohn S and Kanzler C: Structural characterization of polar melanoidins deriving from Maillard reaction intermediates-A model approach. Food Chem. 395(133592)2022.PubMed/NCBI View Article : Google Scholar | |
Yang JQ, Chen HJ, Huang CR, Chen CS and Chen YF: Antibacterial activities of functional groups on the benzene rings in nucleic acid nanocarriers. Mater Today Chem. 38(102106)2024. | |
Rusu A, Moga IM, Uncu L and Hancu G: The role of five-membered heterocycles in the molecular structure of antibacterial drugs used in therapy. Pharmaceutics. 15(2554)2023.PubMed/NCBI View Article : Google Scholar | |
Zhang W, Chen Z, Yang R, Hua X, Zhao W and Guan S: Application of caseinate modified with maillard reaction for improving physicochemical properties of high load flaxseed oil microcapsules. Eur J Lipid Sci Technol. 123(2000172)2021. | |
Khubiev OM, Egorov AR, Kirichuk AA, Khrustalev VN, Tskhovrebov AG and Kritchenkov AS: Chitosan-based antibacterial films for biomedical and food applications. Int J Mol Sci. 24(10738)2023.PubMed/NCBI View Article : Google Scholar | |
Simões D, Miguel SP and Correia IJ: Biofunctionalization of electrospun poly(caprolactone) fibers with Maillard reaction products for wound dressing applications. React Funct Polym. 131:191–202. 2018. |