4.3 Article

Study on Antioxidant Activity and Amino Acid Analysis of Rapeseed Protein Hydrolysates

期刊

INTERNATIONAL JOURNAL OF FOOD PROPERTIES
卷 19, 期 9, 页码 1899-1911

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/10942912.2015.1085397

关键词

Rapeseed protein hydrolysates (RPHs); Oxygen radical absorbance capacity (ORAC); Peroxyl radical-scavenging capacity (PSC); Cellular antioxidant activity (CAA); Reversed phase-high-performance liquid chromatography (RP-HPLC); Liquid chromatography-mass spectrometry (LC-MS)

资金

  1. National Natural Science Foundation of China [31571766]
  2. Natural Science Foundation of the Higher Education Institutions of Jiangsu Province, China [14KJB550004]
  3. Natural Science Foundation of Jiangsu Province, China [BK20141485]
  4. prospective Industry-Academy-Research cooperation projects of the Jiangsu province China [BY2015010-01]
  5. National High Technology Research and Development Program of China (863 Program) [2013AA102207-2]
  6. National agricultural achievements transformation projects, China [2014GB2C100318]
  7. National Science and Technology Pillar Program during the Twelfth Five-year Plan Period [2014BAD04B03]
  8. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

向作者/读者索取更多资源

Alkaline extraction followed by acid precipitation were employed to extract rapeseed protein and, Alcalase 2.4 L was used to obtain rapeseed protein hydrolysates. Three groups of rapeseed protein hydrolysates were obtained by purifying with membrane ultrafiltration and a Sephacryl S-100HR gel column. The antioxidant activities were then determined. Group 3 had the best antioxidant activities according to the oxygen radical absorbance capacity, peroxyl radical-scavenging capacity, and cellular antioxidant activity assays, with the following antioxidant values: an oxygen radical absorbance capacity value of 1610 +/- 113 mu mol TE/(g sample), a peroxyl radical-scavenging capacity value of 622 +/- 30 mg VC/(100 g sample), and a cellular antioxidant activity value of 25 +/- 2 mu mol QE/(g sample) and corresponding EC50 value of 58 +/- 3 mu g/mL. Six peaks of group 3 were collected and well separated by reversed phase-high-performance liquid chromatography. Peak 5 were identified to exhibit a higher antioxidant activity, the amino acid sequence of which was found to be Trp-Ile (Leu)-Tyr, as determined by liquid chromatography-mass spectrometry.

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