“…Moreover, catechols, or more generally, phenols, are also prevalent in natural food products such as tea, wine, and tobacco. [5][6][7][8] Oxidized phenols can also react with free amino acids, peptides, proteins or quinonic compounds, resulting in a phenomenon called ''enzymatic browning''. The browning of food adversely affects the quality of the food, e.g., color, aroma and flavor.…”
Section: Martien a Cohen Stuartmentioning
confidence: 99%
“…Catechols are prevalent in many natural systems; playing an essential role in living organisms such as mussels, sandcastle worms and squids, [1][2][3][4] and in food processing such as cocoa fermentation and tea preparation. [5][6][7][8] A famous example is the mussel that secretes water-resistant adhesive proteins, containing significant amounts of the catechol-containing amino acid 3,4-dihydroxyphenylalanine (dopa). 9 In 1981, Waite and Tanzer identified dopa as a key element for the enduring fixation of mussels to various types of surfaces under harsh marine conditions.…”
Catechols play an important role in many natural systems. They are known to readily interact with both organic (e.g., amino acids) and inorganic (e.g., metal ions, metal oxides) compounds, thereby providing a powerful system for protein curing. Catechol crosslinked protein networks, such as sclerotized cuticle and byssal threads of the mussel, have been shown to exhibit excellent mechanical properties. A lot of effort has been devoted to mimicking the natural proteins using synthetic catechol-functionalized polymers. Despite the success in developing catechol-functionalized materials, the crosslinking chemistry of catechols is still a subject of debate. To develop materials with controlled and superior properties, a clear understanding of the crosslinking mechanism of catechols is of vital importance. This review describes the crosslinking pathways of catechol and derivatives in both natural and synthetic systems. We discuss existing pathways of catechol crosslinking and parameters that affect the catechol chemistry in detail. This overview will point towards a rational direction for further investigation of the complicated catechol chemistry.
“…Moreover, catechols, or more generally, phenols, are also prevalent in natural food products such as tea, wine, and tobacco. [5][6][7][8] Oxidized phenols can also react with free amino acids, peptides, proteins or quinonic compounds, resulting in a phenomenon called ''enzymatic browning''. The browning of food adversely affects the quality of the food, e.g., color, aroma and flavor.…”
Section: Martien a Cohen Stuartmentioning
confidence: 99%
“…Catechols are prevalent in many natural systems; playing an essential role in living organisms such as mussels, sandcastle worms and squids, [1][2][3][4] and in food processing such as cocoa fermentation and tea preparation. [5][6][7][8] A famous example is the mussel that secretes water-resistant adhesive proteins, containing significant amounts of the catechol-containing amino acid 3,4-dihydroxyphenylalanine (dopa). 9 In 1981, Waite and Tanzer identified dopa as a key element for the enduring fixation of mussels to various types of surfaces under harsh marine conditions.…”
Catechols play an important role in many natural systems. They are known to readily interact with both organic (e.g., amino acids) and inorganic (e.g., metal ions, metal oxides) compounds, thereby providing a powerful system for protein curing. Catechol crosslinked protein networks, such as sclerotized cuticle and byssal threads of the mussel, have been shown to exhibit excellent mechanical properties. A lot of effort has been devoted to mimicking the natural proteins using synthetic catechol-functionalized polymers. Despite the success in developing catechol-functionalized materials, the crosslinking chemistry of catechols is still a subject of debate. To develop materials with controlled and superior properties, a clear understanding of the crosslinking mechanism of catechols is of vital importance. This review describes the crosslinking pathways of catechol and derivatives in both natural and synthetic systems. We discuss existing pathways of catechol crosslinking and parameters that affect the catechol chemistry in detail. This overview will point towards a rational direction for further investigation of the complicated catechol chemistry.
“…Thermally initiated reactions of protein and its degradation products account for a significant number of the more than 300 compounds identified in the aroma fraction of chocolate (Keeney, 1972). Moreover, astringency associated with polyphenols is suppressed through complexes with protein and, under proper conditions of processing, undesirable flavor notes of protein are avoided (DeWitt, 1957;Purr et al, 1960;Bracco et al, 1969). Properties ultimately achieved represent the integrated effects of happenings in tropical regions where cacao grows and the subsequent processing in the chocolate factory.Key events in cocoa bean exporting countries include ripening of fruit, harvesting, fermentation, and drying of cocoa beans.…”
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