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dc.creatorBanjanac, Katarina
dc.creatorMilivojević, Ana
dc.creatorĆorović, Marija
dc.creatorCarević, Milica
dc.creatorPrlainović, Nevena
dc.creatorMarinković, Aleksandar
dc.creatorBezbradica, Dejan
dc.date.accessioned2023-03-09T11:24:33Z
dc.date.available2023-03-09T11:24:33Z
dc.date.issued2018
dc.identifier.isbn978-86-7994-056-8
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/6021
dc.description.abstractThe objective of this research was to study the production of sunflower meal protein hydrolysate (SMPH) from sunflower meal protein isolate (SMPI) prepared by sedimentation/flotation and isoelectric precipitation of sunflower meal (SM). SM is the main co-product formed during the industrial process of extracting oil from sunflower seed. By fractionation of SM, the crude protein content was increased from approximately 37.4 % in SM to 80.8 % in SMPI and represent a good source of protein for human consumption. The percentages of fiber, soluble sugars, polyphenols, lignocellulose fibers and residual lipids which may reduce the chemical and nutritive value of proteins in the SMPI were reduced to more than 92 % with respect to the SM. Since functional properties of SMPI can be improved by enzymatic hydrolysis under controlled conditions, the hydrolysis of SMPI was carry out using endo-protease Alcalase covalently immobilized on epoxy modified silica nanoparticles (Alcalase-GFNS) and/or exo-protease Flavourzyme covalently immobilized on cyanuric chloride activated amino modified silica nanoparticles (Flavourzume-CCAFNS). Results showed that enzymatic hydrolysis of the SMPI should be performed using sequentially Alcalase-GFNS and Flavourzyme-CCAFNS since the achieved hydrolysis yield was greater by 1.5 and 3 times in comparison to the use of only Alcalase-GFNS or Flavourzyme-CCAFNS, respectively, during the same time. Also, it should be mentioned that Flavourzyme-CCAFNS was added in reaction mixture 2 h after the start of hydrolysis with Alcalase-GFNS. With the predigestion with Alcalase- GFNS, the number of N-terminal sites for the exoprotease activity of Flavourzyme-CCAFNS was increased which directly led to the increment of SMPI hydrolysis degree. Finally, it can be concluded that Alcalase-GFNS and Flavourzyme-CCAFNS have great prospects for usage in the hydrolysis of SMPI to produce SMPH with high nutritional value that can be used directly, for example, in the fortification of liquid foods or high energetic beverages.sr
dc.language.isoensr
dc.publisherUniversity of Novi Sad, Institute of Food Technologysr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/46010/RS//sr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172013/RS//sr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45019/RS//sr
dc.rightsopenAccesssr
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceIV International congress of Food Technology, Quality and Safety, Proceedingssr
dc.subjectsunflower meal protein hydrolysatesr
dc.subjectsilica nanoparticlessr
dc.subjectproteasesr
dc.subjectimmobilizationsr
dc.subjectenzymatic hydrolysissr
dc.titleProduction of sunflower meal protein hydrolysate by sequential hydrolysis with alcalase and flavourzyme immobilized on functionalized silica nanoparticlessr
dc.typeconferenceObjectsr
dc.rights.licenseBYsr
dc.citation.epage252
dc.citation.spage247
dc.identifier.fulltexthttp://TechnoRep.tmf.bg.ac.rs/bitstream/id/15956/bitstream_15956.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_technorep_6021
dc.type.versionpublishedVersionsr


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