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YALÇIN, AHMET SUHA

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YALÇIN

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AHMET SUHA

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2008 - 200912010 - 20141
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    Comparison of antioxidant capacity, protein profile and carbohydrate content of whey protein fractions
    (ELSEVIER SCI LTD, 2014) YALÇIN, AHMET SUHA; Onay-Ucar, Evren; Arda, Nazli; Pekmez, Murat; Yilmaz, Ayse Mine; Boke-Sarikahya, Nazli; Kirmizigul, Suheyla; Yalcin, A. Suha
    Whey is used as an additive in food industry and a dietary supplement in nutrition. Here we report a comparative analysis of antioxidant potential of whey and its fractions. Fractions were obtained by size exclusion chromatography, before and after enzymatic digestion with pepsin or trypsin. Superoxide radical scavenging, lipid peroxidation inhibition and cupric ion reducing activities of different fractions were checked. Peptides were detected by SDS-PAGE and GC-MS was used to determine carbohydrate content of the fractions. All samples showed antioxidant activity and the second fraction of the trypsin hydrolysate showed the highest superoxide radical scavenging activity. CUPRAC value of this fraction was two-times higher than that of whey filtrate. The first fraction of the pepsin hydrolysate was the most effective inhibitor of lipid peroxidation. Each sample exhibited a different polypeptide profile. Different percentages of carbohydrates were identified in whey filtrate and in all second fractions, where galactose was the major component. (C) 2013 Elsevier Ltd. All rights reserved.
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    Antioxidant activity of whey protein fractions isolated by gel exclusion chromatography an protease treatment
    (ELSEVIER SCIENCE BV, 2008) YALÇIN, AHMET SUHA; Bayram, Tugba; Pekmez, Murat; Arda, Nazli; Yalcin, A. Sueha
    Whey proteins were isolated from whey powder by a combination of gel exclusion chromatography and protease (pepsin or trypsin) treatment. Whey solution (6 g/dl) was applied to Sephadex G-200 column chromatography and three fractions were obtained. Gel electrophoresis (SDS-PAGE) was used to identify the fractions; the first one contained immunooglobulins and bovine serum albumin, the second contained P-lactoglobulin and a-lactalbumin whereas the third fraction contained small peptides. We have also subjected the whey filtrate to proteases (pepsin and trypsin). Treatment with proteases showed that P-lactoglobulin can be obtained after hydrolysis of the second fraction with pepsin. When the whey filtrate was treated with pepsin and then applied to Sephadex G-200 column chromatography three fractions were obtained; the first one was bovine serum albumin, the second was beta-lactoglobulin and the third fraction contained small peptides. After trypsin treatment only two fractions were obtained; the first one was serum albumin and the second fraction was an alpha-lactalbumin rich fraction. We have determined the antioxidant activity of the fractions using an assay based on the measurement of superoxide radical scavenging activity. Our results showed that among the three fractions, the first fraction had the highest superoxide radical scavenging activity. Also, protease treatment of the second fraction resulted in an increase in the antioxidant activity. (c) 2007 Elsevier B.V. All rights reserved.