Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553537
Title: In vitro evolution of aldolases : towards a Baylis-Hillmanase
Author: Swiatyj, Michael
Awarding Body: University of Manchester
Current Institution: University of Manchester
Date of Award: 2012
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Abstract:
The fructose 1,6-bisphosphate type I aldolase from the thermophilic organism Thermoproteus tenax has been expressed and purified by heat treatment. The aldolase aldehyde substrate scope was investigated using electrospray mass spectrometry to detect the formation of any aldol products. Parameters affecting aldolase activity, including temperature, buffer pH and solvent additive were investigated. The synthesis of an aldehyde with an attached fluorescent reporter group was performed for potential use in the screening of mutant aldolases for aldol or Baylis-Hillman activity. The synthesis of 1-hydroxy-3-buten-2-one phosphate, an analogue of dihydroxyacetone phosphate, capable of participating in Baylis-Hillman reactions, was achieved in 5 steps from 3-buten-1-ol. This analogue was used in the investigation of the wild type aldolase and several mutant aldolases for Baylis-Hillman activity. X-ray crystallographic data was obtained for the wild type enzyme and the Trp144Leu mutant aldolase with 1-hydroxy-3-buten-2-one phosphate bound at their active sites. In the wild type aldolase, the substrate was found to bind in a similar manner to dihydroxyacetone phosphate, with the formation of a Schiff base with the Lys177 amino acid residue at the enzyme active site. In the Trp144Leu mutant aldolase, Lys177 has added in Michael fashion to the enone functionality of the bound substrate forming an enolate instead of forming a Schiff base. Both forms of the bound substrate are potentially capable of participating in Baylis-Hillman reactions. The enzymes have yet to be fully investigated for Baylis-Hillman activity.
Supervisor: Berrisford, David Sponsor: CoEBio3 ; EPSRC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.553537  DOI: Not available
Keywords: Aldolase ; Baylis-Hillman
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