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Towards developing a new host-vector system for high-level protein expression

Dissertation (MSc)--University of Pretoria, 2015.

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Other Authors: Cowan, Don A.
Format: Thesis
Language:English
Published: University of Pretoria 2016
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access_status_str Open Access
author2 Cowan, Don A.
author_browse Cowan, Don A.
author_facet Cowan, Don A.
collection Thesis
dc_rights_str_mv © 2016, 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.
description Dissertation (MSc)--University of Pretoria, 2015.
format Thesis
id oai:repository.up.ac.za:2263/53551
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:37:27.405Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
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:2263/53551 Towards developing a new host-vector system for high-level protein expression Cowan, Don A. sandraphoma@gmail.com Berger, E. Phoma, Boitumelo Nana Sandra UCTD Dissertation (MSc)--University of Pretoria, 2015. Filamentous fungi are critical for the production of many commercial enzymes and organic compounds. Due to their decomposer lifestyle, they have a natural potential for large scale production of proteins, many of these extracellular. The concept of this project was to exploit the protein synthesis and secretory capability of a large number of indigenous fungi as the basis to generate a new fungal expression platform. Filamentous fungi were obtained from the culture collection (CMW) of the Forestry and Agricultural Biotechnology Institute (FABI) University of Pretoria, South Africa. Screening of the isolates for extracellular protein expression in malt extract liquid medium shake flasks, led to the identification of a Clonostachys rosea 17970 isolate after internal transcribed spacer (ITS) sequencing and morphological studies. A ~35 kDa protein secreted at high levels was identified through LC-MS/MS as a cuticle-degrading serine protease (Cdsp). The optimum pH and temperature for protein production were found to be 9.0 and 32°C respectively, after 96 h of incubation on malt extract liquid media. Designed primers were used for the PCR amplification of an internal fragment of the cdsp gene from chromosomal DNA. Sequence data was used for further PCR-amplification of the up and downstream regions through chromosome walking using Inverse and SiteFinding PCR technology. Analysis of the assembled cdsp gene fragment (2,923 bp) revealed that the gene harbours a 5 upstream region (1,141 bp), coding region (1,300 bp) and 3 downstream region (509 bp). The coding region contains three introns. Reverse transcriptase-PCR of the coding region revealed a 1,140 bp open reading frame that encodes Cdsp. The putative cdsp signal peptide, promoter and terminator regions were identified in silico and are predicted to be important elements for the construction of an expression vector. Overall, these results demonstrate that C. rosea 17970 could be a good source for extracellular protein production and is a potential candidate for development as a new host-vector system based on its secretory capability and identified regulatory regions via in silico analysis. Microbiology and Plant Pathology MSc Unrestricted 2016-07-01T10:33:44Z 2016-07-01T10:33:44Z 2016-04-18 2015 Dissertation Phoma, BNS 2016, Towards developing a new host-vector system for high-level protein expression, MSc Dissertation, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/53551> A2016 http://hdl.handle.net/2263/53551 en © 2016, 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. application/pdf University of Pretoria
spellingShingle UCTD
Towards developing a new host-vector system for high-level protein expression
title Towards developing a new host-vector system for high-level protein expression
title_full Towards developing a new host-vector system for high-level protein expression
title_fullStr Towards developing a new host-vector system for high-level protein expression
title_full_unstemmed Towards developing a new host-vector system for high-level protein expression
title_short Towards developing a new host-vector system for high-level protein expression
title_sort towards developing a new host vector system for high level protein expression
topic UCTD
url http://hdl.handle.net/2263/53551