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An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae

Thesis (MSc)--Stellenbosch University, 2020.

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Main Author: Wissing, Julian
Other Authors: Rohwer, Johann
Format: Thesis
Language:en_ZA
Published: Stellenbosch : Stellenbosch University 2020
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access_status_str Open Access
author Wissing, Julian
author2 Rohwer, Johann
author_browse Rohwer, Johann
Wissing, Julian
author_facet Rohwer, Johann
Wissing, Julian
author_sort Wissing, Julian
collection Thesis
dc_rights_str_mv Stellenbosch University
description Thesis (MSc)--Stellenbosch University, 2020.
format Thesis
id oai:scholar.sun.ac.za:10019.1/108251
institution Stellenbosch University (South Africa)
language en_ZA
last_indexed 2026-06-10T12:43:40.919Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from SUNScholar — Stellenbosch University Repository
publishDate 2020
publishDateRange 2020
publishDateSort 2020
publisher Stellenbosch : Stellenbosch University
publisherStr Stellenbosch : Stellenbosch University
record_format dspace
source_str SUNScholar — Stellenbosch University Repository
spelling oai:scholar.sun.ac.za:10019.1/108251 An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae Wissing, Julian Rohwer, Johann Stellenbosch University. Faculty of Science. Dept. of Biochemistry. UCTD Enzyme kinetics Glycolytic enzymes Saccharomyces cerevisiae Thesis (MSc)--Stellenbosch University, 2020. ENGLISH ABSTRACT: In order for mathematical models of metabolism to accurately emulate experimental data the conditions in which parameter values are obtained must be close to the actual in vivo environment. However, this is traditionally not the case, with enzyme kinetic studies usually taking place in conditions which are ideal for the enzyme being studied and can be far removed from the actual native conditions the enzyme would be found in. An aspect of the intracellular environment which has not been extensiely covered is the large quantity of different macromolecules which occupy it, known as macromolecular crowding. The space occupied by these macromolecules has thermodynamic and kinetic consequences which are not taken into consideration. In this study we mimicked a crowded environment by using the inert polymers PEG 8000 and Ficoll 70 and studied how they affected enzyme kinetic parameter estimates at different concentrations. NMR spectroscopy was used to obtain timecourse data for the upper glycolytic enzymes, phosphoglucose isomerase (PGI) and phosphofructokinase (PFK), in cell lysate. Parameter estimates were obtained by fitting NMR time-course data to a kinetic model based on rate equations for the two enzymes. The identifiability of each parameter was also determined and could be used to analyse the accuracy of parameter estimation. The aim of this study was to determine the effects of macromolecular crowding on enzyme kinetics and to explore if these effects should be considered when trying to simulate in vivo-like conditions when studying enzyme kinetics. In our results macromolecular crowding was shown to affect the parameter estimates for both enzymes, in particular decreasing their maximal activity, increasing the binding affinity of PFK for fructose-6-phosphate (F6P), and decreasing its affinity for adenosine tri-phosphate (ATP). AFRIKAANSE OPSOMMING: Geen opsomming beskikbaar. Masters 2020-02-26T07:33:32Z 2020-04-28T12:27:56Z 2020-02-26T07:33:32Z 2020-04-28T12:27:56Z 2020-03 Thesis http://hdl.handle.net/10019.1/108251 en_ZA Stellenbosch University 66 pages application/pdf Stellenbosch : Stellenbosch University
spellingShingle UCTD
Enzyme kinetics
Glycolytic enzymes
Saccharomyces cerevisiae
Wissing, Julian
An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae
title An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae
title_full An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae
title_fullStr An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae
title_full_unstemmed An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae
title_short An investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in Saccharomyces cerevisiae
title_sort investigation into the effects of macromolecular crowding on the kinetics of upper glycolytic enzymes in saccharomyces cerevisiae
topic UCTD
Enzyme kinetics
Glycolytic enzymes
Saccharomyces cerevisiae
url http://hdl.handle.net/10019.1/108251
work_keys_str_mv AT wissingjulian aninvestigationintotheeffectsofmacromolecularcrowdingonthekineticsofupperglycolyticenzymesinsaccharomycescerevisiae
AT wissingjulian investigationintotheeffectsofmacromolecularcrowdingonthekineticsofupperglycolyticenzymesinsaccharomycescerevisiae