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Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins
Dissertation (MSc)--University of Pretoria, 2013.
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University of Pretoria
2013
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| _version_ | 1867613645557465088 |
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| access_status_str | Open Access |
| author2 | Apostolides, Zeno |
| author_browse | Apostolides, Zeno |
| author_facet | Apostolides, Zeno |
| collection | Thesis |
| dc_rights_str_mv | © 2013 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria E13/4/442/ |
| description | Dissertation (MSc)--University of Pretoria, 2013. |
| format | Thesis |
| id | oai:repository.up.ac.za:2263/30922 |
| institution | University of Pretoria (South Africa) |
| last_indexed | 2026-06-10T12:39:26.678Z |
| license_str | Other — see source repository |
| provenance_str_mv | Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository |
| publishDate | 2013 |
| publishDateRange | 2013 |
| publishDateSort | 2013 |
| publisher | University of Pretoria |
| publisherStr | University of Pretoria |
| record_format | dspace |
| source_str | UPSpace — University of Pretoria Institutional Repository |
| spelling | oai:repository.up.ac.za:2263/30922 Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins Apostolides, Zeno Steenkamp, L. Bannister, Magdalien UCTD Dissertation (MSc)--University of Pretoria, 2013. The reusability of active enzyme is important in industrial bio-catalysis applications. This is not readily accomplished with free enzymes. The project investigated a new enzyme immobilization matrix, ReSynTM, and compared it to three widely used matrixes, Eugergit C, Eupergit C 250 L and DEAE Sephadex A-25. Initial comparative immobilization performed with BSA, determined ReSynTM (covalent immobilization) to have an approximate 8 fold higher protein loading efficiency than the other support. The enzymes selected for immobilization were polyphenol oxidase (PPO) (first reported purification of PPO from Forelle pear) and laccase (Novozyme (Pty) Ltd) based upon their application potential. From the comparative assessment of immobilization based on BSA and the activity (units/mg support) attained by ReSynTM immobilized laccase, it was deduced that ReSynTM demonstrated performance superiority over the other supports. The project aim was the application of immobilized PPO in the ice tea industry to increase the value of black iced tea based upon an increased theaflavin content. The unusually rich sub-group of polyphenols known as flavanols or catechins, may constitute up to 30% of the dry tea leaf weight. The oxidation of green leaf polyphenols is precluded in the preparation of green tea in contrast to the promotion of oxidation in the production of black tea. PPO catalyzes the controlled aerobic oxidation of catechins producing various quinones which undergo condensation reactions resulting in dimeric compounds known as theaflavins, whereas a peroxidase (PO) enzyme produces polymeric substances, known as thearubigins, during the fermentation stage of black tea production (Graham 1992). The production of theaflavins from flavan-3-ols (catechins), is catalysed by PPO (Bonnely et al. 2003). The black tea theaflavins are a mixture of theaflavin, theaflavin-3-gallate, theaflavin-3'-gallate and theaflavin-3,3'-digallate. The project focussed on the bioconversion of green tea leaf catechins into theaflavins, as the original method employed to acquire theaflavins, the extraction of theaflavins from black tea (only 0.4-1.85% of the dry weight of black tea), doesn’t provide a cost-effective manner of recovering theaflavins, and amounts to an industrially unfeasible approach (Sharma et al. 2009, Wang & Li 2006). Preliminary exploratory investigation into the theaflavin synthesis capacity of Forelle pear and Yacon (Smallanthus sonchifolius) leaf homogenates, respectively determined a 136% and 98% theaflavin content to that present in Lipton® Yellow label black tea, after an hour of fermentation utilizing Lipton® Green tea as starting material. The homogenates of Forelle Biochemistry MSc Unrestricted 2013-09-09T07:51:45Z 2013-06-28 2013-09-09T07:51:45Z 2013-04-12 2013-06-28 2013-06-20 Dissertation Bannister, M 2013, Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins, MSc Dissertation, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/30922> E13/4/442/gm http://hdl.handle.net/2263/30922 http://upetd.up.ac.za/thesis/available/etd-06202013-115438/ © 2013 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria E13/4/442/ application/pdf University of Pretoria |
| spellingShingle | UCTD Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| title | Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| title_full | Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| title_fullStr | Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| title_full_unstemmed | Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| title_short | Comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| title_sort | comparison of free and immobilized polyphenol oxidase enzymes for the biocatalytic conversion of catechins into theaflavins |
| topic | UCTD |
| url | http://hdl.handle.net/2263/30922 http://upetd.up.ac.za/thesis/available/etd-06202013-115438/ |