DIA-based quantitative proteomic analysis on porcine meat quality at different chilling rates

The objective of this study was to evaluate the effects of chilling rate on porcine meat quality from the perspective of proteome using data independent acquisition (DIA)-based quantitative proteomic strategy. M. longissimus thoracis et lumborum (n = 9) was assigned randomly to the control group (3....

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Veröffentlicht in:Food science and human wellness 2024-09, Vol.13 (5), p.2573-2583
Hauptverfasser: Bai, Yuqiang, Yan, Tongjing, Fang, Fei, Li, Xin, Wang, Su, Li, Juan, Hou, Chengli, Zhang, Dequan
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Sprache:eng
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Zusammenfassung:The objective of this study was to evaluate the effects of chilling rate on porcine meat quality from the perspective of proteome using data independent acquisition (DIA)-based quantitative proteomic strategy. M. longissimus thoracis et lumborum (n = 9) was assigned randomly to the control group (3.72 °C/h), very fast chilling-I group (VFC-I, 9.31 °C/h) and VFC-II group (14.43 °C/h). The DIA was used to analyze the difference in proteins under different chilling rates. Results showed that tenderness was improved significantly in meat at the chilling rate of 14.43 °C/h. Seventy-nine differential abundant proteins (fold change > 1.5, P < 0.05), including 46 up-regulated and 33 down-regulated proteins, were identified and mainly involved in carbon metabolism, pyruvate metabolism and proteasome pathways. These pathways indicated that VFC delayed cell metabolism and glycolysis by down-regulating the expression of metabolic enzymes. The tenderness was improved by up-regulating the expression of proteasome and m-calpain. •The tenderness of pork meat was improved under chilling rate 14.43°C/h.•VFC improved tenderness from the aspects of glycolysis and proteasome.•VFC delayed glycolysis process by down-regulating enzyme expression.•VFC tenderized meat by promoting proteasome expression.•VFC promoted the degradation of skeletal proteins and maintained the integrity of sarcomere.
ISSN:2213-4530
2097-0765
2213-4530
DOI:10.26599/FSHW.2022.9250206