Journal
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 58, Issue 19, Pages 10697-10704Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jf102043k
Keywords
Protein oxidation; hydration; water-holding capacity; myofiber shrinkage
Funding
- NRI/CSREES/USDA, USA [2008-35503-18790]
- Natural Science Foundation, China [30972290]
- Ministry of Science and Technology, China [SKLF-MB-200803]
- China Scholarship Council
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Pork longissimus muscle was oxidized at 400 by mixed 10 mu M FeCl3/100 mu M ascorbate with 1, 5, 10, 20, 30, 40, or 50 mM H2O2 (pH 6.2). Oxidation with >1 mM H2O2 for 40 min significantly (P < 0.05) enhanced hydration of muscle samples, whereas oxidation with 40 and 50 mM H2O2 for 2 min or with 20 mM H2O2 for 40 min caused pronounced declines in water-holding capacity and product yield. The changes coincided with marked increases in the protein carbonyl content, TBARS formation, and cross-linking of both myofibrillar and sarcoplasmic proteins. Dye-tracing tests showed that the enhanced hydration at >1 mM H2O2 was due to facilitated water diffusion into muscle tissue. This result was strongly corroborated by microscopic images that illustrated enlargements of intercellular spacing, that is, gaps, in oxidized muscle tissue, which served as canals for water diffusion.
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