Приказ основних података о документу

dc.creatorKnežević-Jugović, Zorica
dc.creatorJovanović, Jelena
dc.creatorStefanović, Andrea
dc.creatorGrbavčić, Sanja
dc.creatorŠekuljica, Nataša
dc.creatorElmalimadi, Mohamed B.
dc.creatorBugarski, Branko
dc.date.accessioned2023-03-21T14:43:57Z
dc.date.available2023-03-21T14:43:57Z
dc.date.issued2015
dc.identifier.isbn978-80-89475-14-8
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/6271
dc.description.abstractWheat gluten is a relatively inexpensive industrial byproduct from wheat starch processing, and in Europe also from manufacturing of bioethanol fuel. Egg producers are also faced with problems of excess of egg white because mayonnaise industry and bakery industry use relatively high egg yolk amounts and egg white is the remainder. Of high importance is the production of new value-added products based on gluten and/or egg white proteins with improved properties and specialized functionality to be used in food and biobased consumer products. The objective of this research was a production of both wheat gluten and egg white protein hydrolysates with improved antioxidant properties. For this purpose, both substrates were pretreated by thermal treatment and then intensively hydrolysed with a commercial food-grade bacterial protease, Alcalase. Thus, the obtained hydrolysates were further separated by sequential ultrafiltration into four peptide fraction viz. Fraction I (> 30kDa), II (10 - 30 kDa), III (1 - 10 kDa) and IV (< 1kDa) which were investigated in terms of their antioxidant activity. The antioxidant activity of hydrolysates and peptide fractions were evaluated using 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2′-azinobis(3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt (ABTS) radical scavenging assays and measuring ferric reducing antioxidant power assay. Scavenging of 2,2′- diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azinobis(3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt (ABTS) by Fraction III, prepared with gluten protein was found to be significantly higher than other gluten or egg white fractions. The results show that the fractionated hydrolysates were superior to the original hydrolysate in the antioxidative activity tested in all cases and can be concluded that by combining thermal pretreatment and controlled enzymatic hydrolysis, the hydrolysates with improved antioxidant properties can be produced enhancing utilization of egg white and gluten in food products.sr
dc.language.isoensr
dc.publisherBratislava, SK : Slovak Society of Chemical Engineeringsr
dc.relationEUREKA project / ENZEGG E!6750 - Development of enzyme processes for production of egg white protein hydrolysatessr
dc.relationInnovation Project / Production of new dietary formulations based on natural protein with antioxidant and antitumor effectsr
dc.rightsopenAccesssr
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceProceedings / 42nd International Conference of SSCHE Tatranské Matliaresr
dc.subjectAntioxidant peptidessr
dc.subjectMembrane ultrafiltrationsr
dc.subjectEgg white proteinssr
dc.subjectGlutensr
dc.subjectEnzymatic hydrolysissr
dc.titleHydrolysis of egg white and wheat proteins with protease from bacillus licheniformis: fractionation and identification of bioactive peptidessr
dc.typeconferenceObjectsr
dc.rights.licenseBY-NC-NDsr
dc.citation.spage753
dc.identifier.fulltexthttp://TechnoRep.tmf.bg.ac.rs/bitstream/id/16561/SSCHE2015-proceedings-abstract-Knezevic-Jugovic.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_technorep_6271
dc.type.versionpublishedVersionsr


Документи

Thumbnail

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу