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Key saltiness-enhancing substances in Maillard reaction products derived from chicken breast hydrolysate: Identification, saltiness-enhancing ability and mechanism
被引:0
|作者:
Zheng, Ruiyi
[1
,2
,3
]
Zhang, Lili
[1
,2
,3
]
Sun, Xingming
[1
,2
,3
]
Qiao, Kaina
[1
,2
,3
]
Sun, Baoguo
[2
]
Zhang, Yuyu
[1
,2
,3
]
机构:
[1] Beijing Technol & Business Univ, Food Lab Zhongyuan, Beijing 100048, Peoples R China
[2] Beijing Technol & Business Univ, Minist Educ, Key Lab Geriatr Nutr & Hlth, Beijing 100048, Peoples R China
[3] Beijing Technol & Business Univ, Key Lab Flavor Sci China Gen Chamber Commerce, Beijing 100048, Peoples R China
来源:
基金:
中国国家自然科学基金;
中国博士后科学基金;
关键词:
Chicken breast hydrolysate;
Maillard reaction;
Saltiness-enhancing ability;
TMC4;
Molecular docking;
SOY-SAUCE;
TASTE;
SALT;
PERCEPTION;
PEPTIDES;
FLAVOR;
ACID;
D O I:
10.1016/j.foodchem.2024.140881
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
This work employs a saltiness-guided separation combined with UPLC-QTOF-MS to identify the key saltinessenhancing substances in Maillard reaction products derived from chicken breast hydrolysate (CBH-MRPs). Thirteen compounds in the U3 fraction exhibited significant saltiness-enhancing abilities, which increased the saltiness intensity of NaCl (3 g/L) from 2.80 to 3.35-3.88. Interactions between the compounds and NaCl were evaluated using the S-curve method. The results showed that five compounds (5 '-GMP, 5 '-IMP, L-glutamic acid, Llactic acid, and L-carnosine) and one compound (glutamine) exhibited synergistic and additive effects with NaCl, respectively, at tested concentrations. Notably, 5 '-GMP/5 '-IMP/glutamine and L-carnosine/L-lactic acid demonstrated better saltiness-enhancing abilities at their suprathreshold and subthreshold levels, respectively. Molecular docking results showed that hydrogen bonding was the key force for docking. Residues Cys475, Glu378, and Trp236 were the primary binding sites of the transmembrane channel-like protein 4 (TMC4). These results contribute to a better understanding of the saltiness modulating mechanisms of CBH-MRPs.
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页数:10
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