Journal
FRONTIERS IN NUTRITION
Volume 7, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2020.00151
Keywords
pork; chill storage; in vitrodigestion; Raman spectroscopy; LC-MS; MS
Categories
Funding
- NSFC [31530054]
- SXGC [[(2017])212]
- [CARS-35]
- [SZ-XZ2017029]
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In this work, we investigated changes in protein structures in vacuum-packed pork during chill storage and its impact on thein vitroprotein digestion.Longissimus dorsimuscles were vacuum packed and stored at 4 degrees C for 3 days. Samples were subjected to Raman spectroscopy,in vitrodigestion and nano LC-MS/MS. The 3 d samples had lower alpha-helix content, but higher beta-sheet, beta-turn, and random coil contents than the 0 d samples (P< 0.05). SDS-PAGE revealed significant protein degradation in the 3 d samples and the differences in digested products across the storage time. Proteome analysis indicated that the 3 d samples had the higher susceptibility to digestion. Increasing protein digestibility was mainly attributed to the degradation of myofibrillar proteins. Thus, exposure of more enzymatic sites in loose protein structure during chill storage could increase protein degradation in meat.
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