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    Please use this identifier to cite or link to this item: http://140.128.103.80:8080/handle/310901/24785


    Title: Purification and identification of lipolysis-stimulating peptides derived from enzymatic hydrolysis of soy protein
    Authors: Tsou, M.-J.;Kao, F.-J.;Lu, H.-C.;Kao, H.-C.;Chiang, W.-D.
    Contributors: Department of Food Science, Tunghai University
    Keywords: 3T3-L1 adipocytes;Glycerol release;Lipolysis-stimulating peptides;Purification;Soy protein isolate
    Date: 2013
    Issue Date: 2014-05-30T02:31:07Z (UTC)
    Abstract: The aim of this study was to purify and identify lipolysis-stimulating peptides derived from Flavourzyme?-soy protein isolate (SPI) hydrolysate (F-SPIH). Glycerol release was employed as a marker for lipolysis in 3T3-L1 adipocytes. A higher glycerol release represents a better lipolysis-stimulating activity. The peptide fraction with highest glycerol release obtained from F-SPIH fractionated by sequential ultrafiltration membranes was further purified using gel filtration chromatography and two steps of reverse-phase high-performance liquid chromatography. The peptides were identified using liquid chromatography-tandem mass spectrometry (LC/MS/MS). Three lipolysis-stimulating peptides were obtained, and the amino acid sequences were ILL, LLL and VHVV, respectively. The in vitro effect of gastrointestinal proteases on lipolysis-stimulating activity of synthetic ILL, LLL and VHVV, respectively, was also investigated. The result suggested that the gastrointestinal protease did not affect lipolysis-stimulating activity of the three novel peptides, which reveals their potential to act as anti-obesity ingredients. ? 2012 Elsevier Ltd. All rights reserved.
    Relation: Food Chemistry,Vol.138,P.1454-1460
    Appears in Collections:[食品科學系所] 期刊論文

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