2022
DOI: 10.1016/j.foodres.2022.111240
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Study of the reaction between genipin and amino acids, dairy proteins, and milk to form a blue colorant ingredient

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Cited by 12 publications
(10 citation statements)
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“…In the presence of oxygen, genipin can spontaneously react with primary amines of amino acids, peptides, proteins, or other polymers which contain amine groups through a crosslinking process used for some technological applications ( Neri-Numa et al, 2020 ). This reaction produces a blue pigment with a maximum absorbance at 590 nm ( Neves, Valdés, Silva, Meireles, Ibañéz, Cifuentes, 2022 ). Fig.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In the presence of oxygen, genipin can spontaneously react with primary amines of amino acids, peptides, proteins, or other polymers which contain amine groups through a crosslinking process used for some technological applications ( Neri-Numa et al, 2020 ). This reaction produces a blue pigment with a maximum absorbance at 590 nm ( Neves, Valdés, Silva, Meireles, Ibañéz, Cifuentes, 2022 ). Fig.…”
Section: Resultsmentioning
confidence: 99%
“…The crosslinking reaction between genipin and primary amines from amino acids, proteins or polymers produces a blue pigment ( Neves, Valdés, Silva, Meireles, Ibañéz, Cifuentes, 2022 ). The effect of NADES on the genipin crosslinking capacity was evaluated by determining the absorption modification of the solutions at 590 nm (wavelength corresponding to the blue).…”
Section: Methodsmentioning
confidence: 99%
“…Thus, it is an important reagent to produce future bio-based materials approved for human contact. [14][15][16][17][18][19] Genipin is an iridoid, a secondary plant metabolite that is part of the monoterpenoids and has hydroxyl groups in its structure that give it a polar character. Genipin can also form covalent bonds with amino groups, forming polysaccharide or protein crosslinking networks.…”
Section: Introductionmentioning
confidence: 99%
“…In 1987, genipin was observed to undergo a quick reaction with the simplest amino acid, glycine [6] . Later on, genipin has been commonly used to react with other amino acids, [7] and more complex amine‐containing structures such as chitosan, [8,9] collagen, [10] gelatin, [11] and enzymes [12] . Similar to other bifunctional crosslinkers, genipin can act as a “staple” of amine‐containing polymers to finally give stable crosslinked matrixes (Figure 1).…”
Section: Introductionmentioning
confidence: 99%