Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/3584
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dc.contributor.advisorBüyükkileci, Ali Oğuzen
dc.contributor.authorGenç, Berna-
dc.date.accessioned2014-07-22T13:51:52Z-
dc.date.available2014-07-22T13:51:52Z-
dc.date.issued2013en
dc.identifier.urihttp://hdl.handle.net/11147/3584-
dc.descriptionThesis (Master)--Izmir Institute of Technology, Biotechnology, Izmir, 2013en
dc.descriptionIncludes bibliographical references (leaves 66-71)en
dc.descriptionText in English; Abstract: Turkish and Englishen
dc.descriptionxi, 75 leavesen
dc.descriptionFull text release delayed at author's request until 2015.07.23en
dc.description.abstractPectinases are a group of hydrolytic enzymes that degrade pectic substances and produced by a variety of microorganisms including filamentous fungi. In previous studies orange peel especially in solid state fermentations was utilized as a source of additional sugars and nutrients. In this study, orange peel, an agro industrial residue was used for exo-polygalacturonase (exo-PG) production in submerged fermentation (SmF) by Aspergillus sojae which have been shown to be a potential exo-polygalacturonase producer. Solubilization of carbohydrates within orange peel was provided by water extraction and treatment with dilute phosphoric (at 0.4% acid concentration and 120 oC in 20 min.) and sulfuric (at 0.5% acid concentration and 116 oC in 13 min.) acid hydrolysis. Phosphoric acid hydrolysis was optimized selecting temperature (oC), time (min.) and acid concentration (v/v %) as variable factors, while reducing sugar concentration (gL-1) was the response factor. Two different dilute acid hydrolysis (at 0.4 % phosphoric acid concentration and 120 0C in 20 min and at 0.5 % sulfuric acid concentration and 116 0C in 13 min.) and water extraction were carried out to obtain media that were utilized for enzyme productions. A.sojae ATCC 20235 and mutant A.sojae strains were used to produce exo-PG in these hydrolysates and water extract of orange peel. To enhance exo-PG production, trace element solutions added as well as macro nutrients. Pellet size, number, density, pH and spore inoculation of fermentation were the other parameters that were controlled during fermentations. The highest exo-PG production was 18.4 UmL-1, which was obtained by mutant A.sojae in phosphoric acid hydrolysate but on the other hand mutant A.sojae produced 19.7 UmL-1 exo-PG activities in water extract of orange peel.en
dc.language.isoenen_US
dc.publisherIzmir Institute of Technologyen
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject.lcshFungi--Biotechnologyen
dc.subject.lcshFungal enzymesen
dc.subject.lcshFungal enzymes--Utilizationen
dc.titleUtilization of organce peel extract for fungal enzyme productionen_US
dc.typeMaster Thesisen_US
dc.authoridGenç, Berna-
dc.institutionauthorGenç, Berna-
dc.departmentThesis (Master)--İzmir Institute of Technology, Bioengineeringen_US
dc.relation.publicationcategoryTezen_US
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeMaster Thesis-
Appears in Collections:Master Degree / Yüksek Lisans Tezleri
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