Production of Bioactive Peptides from Ovotransferrin Using two Enzyme Combinations and Determining the Functional Properties of Its Hydrolysates

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dc.contributor.authorWickramasinghe, H.S.I.
dc.date.accessioned2022-10-07T08:28:33Z
dc.date.available2022-10-07T08:28:33Z
dc.date.issued2016
dc.description.abstractPeptides from food sources possess numerous bioactivities, which make them useful in improving human health. Although many studies related to egg protein hydrolysis are present, less work has been carried out with the production of bioactive peptides from ovotransferrin using a two-step enzyme combination. The research objectives were to produce bioactive peptides from ovotransferrin using two enzyme combinations and determine the firnctional properties of its hydrolysates. Lipolyzed ovotransferrin solution (20 mg/mL) was treated with protease (3hr/55oC), papain (3hr/37oC), elastase (24hr37oC), and a-chymotrypsin (3hr/37oC) as the first treatment identified previously. Produced hydrolysates were treated with the above enzymes in different combinations and incubated for 0-24 hours at the optimal pH and temperatures, followed by heat inactivation at 100oC for 15 min. 15% SDS-PAGE was used to select the best conditions and analyze antioxidant, metal chelating, and antimicrobial activities. Protease + Papain (ProPap), Protease + a- chymotrypsin (ProChy), a-chymotrypsin + Protease (ChyPro), a-chymotrypsin + Papain (ChyPap), Elastase + a-chymotrypsin (ElaChy), Elastase + Papain (ElaPap), Elastase + Protease (ElaPro) treatments as Oh (since all band patterns in the gel were same), Papain + Protease (PapPro), Papain + a-chymotrypsin (PapChy) treatments for 3h were selected as the best conditions. Hydrolysates produced with ChyPap treatment showed some level of metal chelating activity (4.11±0.28%), and Ela (-2.88±0.16%), ElaChy (-7.80±0.28%), and ElaChy (6.38±0.14) showed metal releasing activities. ChyPap (0.59±0.08 MDA mg/kg) treatment followed by ProChy (0.74±0.07 MDA mg/kg), ProPap (0.78±0.04 MDA mg/kg) and ChyPap treatments showed strongest antioxidant activity than ovotransferrin (0.98±0.07 MDA mg/kg) and hydrolysates produced with single enzyme treatments (p<0.05). However, none of the hydrolysates showed any antimicrobial activities against locally isolated E. coli and in Total Plate Count agar. Accordingly, hydrolysates produced with two enzyme combinations as ChyPap, ProChy, and ProPap showed strong antioxidant and some metal chelating activities. Keywords: Enzyme combination, Hydrolysates, Ovotransferrin, TBARen_US
dc.identifier.otherUWU/ANS/16/0029
dc.identifier.urihttp://www.erepo.lib.uwu.ac.lk/bitstream/handle/123456789/9766/ans%2c16%2c0029-02092022101611.pdf?sequence=1&isAllowed=y
dc.language.isoenen_US
dc.publisherUva Wellassa University of Sri Lankaen_US
dc.relation.ispartofseries;UWU/ANS/16/0029
dc.subjectAnimal Science Degree Programmeen_US
dc.titleProduction of Bioactive Peptides from Ovotransferrin Using two Enzyme Combinations and Determining the Functional Properties of Its Hydrolysatesen_US
dc.title.alternativeResearch Article – ANS 2016en_US
dc.typeThesisen_US
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