Antioxidant activity of hydrolysates derived from porcine plasma

被引:30
|
作者
Xu, Xueming [1 ,2 ]
Cao, Ruyan [2 ]
He, Liu [3 ]
Yang, Na [2 ]
机构
[1] Jiangnan Univ, Sch Food Sci & Technol, State Key Lab Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
[2] So Yangtze Univ, Sch Food Sci & Technol, Wuxi 274122, Jiangsu, Peoples R China
[3] Bohai Univ, Sch Biol & Food Sci, Liaoning 121000, Jinzhou, Peoples R China
关键词
porcine; plasma; antioxidant activity; hydrolysis separation; PEPTIDES;
D O I
10.1002/jsfa.3670
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUND: In China alone, more than 400 million pigs are slaughtered each year to provide meat. Porcine blood is rich in proteins but is usually discarded, which can cause environmental contamination. Recovering porcine blood and converting it to high-value products is therefore economically and environmentally desirable. However, very little information on antioxidant peptides from porcine blood by-products is currently available. In this study the antioxidant properties of porcine plasma hydrolysates PPE and PPA prepared with pepsin and papain respectively were investigated. RESULTS: Both PPE and PPA showed excellent antioxidant activity in a linoleic acid system (AL) compared with alpha-tocopherol (VE) at the same concentration (P < 0.01). Their activities were respectively 3.33 and 1.83 times stronger than that of VE at a concentration of 10 mu g mL(-1) and 5.4 and 5.6 times stronger at 100 mu g mL(-1). The 2,2-diphenyl-1-picryihydrazyl (DPPH) radical-scavenging activity (DRSA) reached 48.4 and 43.1% for PPE and PPA respectively at 500 mu g mL(-1) The ferrous ion-chelating power (FICP) of PPE at 100 mu g mL(-1) was about 1.5 times stronger than that of 10 mu mol L-1 ethylene diamine tetraacetic acid (EDTA) in a 50 mu mol L-1 Fe2+ system, whereas the FICP of PPA at 100 mu g mL(-1) was 61% that of 10 mu mol L-1 EDTA. Furthermore, PPE was separated on Resource 15RPC and Superdex peptide 10/300GL columns, and the antioxidant activity of the peptides and its relationship to their polarity and molecular weight (MW) were analysed. The hydrolysate was divided into four groups (R1-R4) with hydrophobicities ranging from weak to strong by Resource 15RPC, while it was divided into three groups (S1, MW 7-12 kDa; S2, MW 3-7 kDa; S3, MW 1-3 kDa) by Superdex peptide 10/300GL. CONCLUSION: The results showed that AL was significantly and positively correlated with the relative amounts of R1, S2 and S3 and that DRSA was dependent on R3 and S1. The fractions of PPE were not responsible for FICP. (C) 2009 Society of Chemical Industry
引用
收藏
页码:1897 / 1903
页数:7
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