Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
ECB-ART-50626
Food Chem 2022 May 01;375:131722. doi: 10.1016/j.foodchem.2021.131722.
Show Gene links Show Anatomy links

Cleavage sites and non-enzymatic self-degradation mechanism of ready-to-eat sea cucumber during storage.

Sun X , Zhu L , Qi X , Zhang H , Wu L , Wang J , Hou H .


???displayArticle.abstract???
The non-enzymatic degradation of ready-to-eat sea cucumber (RSC) was closely related to the quality of sea cucumber products. When stored at 37 °C for 0-30 d, the hardness of RSC decreased by 86.7% and the proportion of free water increased by 12.71%. The content of free hydroxyproline increased from 8.33 μg/g to 24.12 μg/g. Label-free quantitative proteomics analysis showed that protein was prone to break at the sites of G, Q, N, D, and L, and the peptide bonds in QI, DL, NL, RI, EF and SY were much more liable to break. Edman degradation method showed that the breakage sites of RSC were at S, D, H, E, and V. NL, NA and NG calculated by B3LYP/6-31G(d) showed that the relative free energies in the initial cyclization step were 53.20, 143.53 and 78.10 kcal/mol, respectively, which may be the rate-determining step for peptide bond cleavage.

???displayArticle.pubmedLink??? 34922275
???displayArticle.link??? Food Chem