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Catalytic Plasticity of the Aspartate/Glutamate Racemase Superfamily

Fisch, Florian A (2009) Catalytic Plasticity of the Aspartate/Glutamate Racemase Superfamily. PhD thesis, University of York.

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The bacterial and archaeal Asp/Glu racemase enzyme superfamily contains a variety of catalytic functions that have great potential for use in industrial biocatalysis. Members of this superfamily include aspartate racemases (AspRs), glutamate racemases (GluRs), hydantoin racemases (HydRs), arylmalonate decarboxylases (AMDs) and maleate cis-trans isomerases (MIs). Despite their catalytic diversity, all characterised members share the same protein fold, catalytic cysteine residues and reaction intermediate. Attempts to exploit this evolutionary flexibility for new processes have had limited success so far, showing that the employed mechanisms are not yet fully understood. For example, the well-characterised Bordetella bronchiseptica AMD (BbAMD) enantiospecifically decarboxylates a range of arylmalonates was but is not able to decarboxylate alkylmalonates despite considerable efforts made by site directed mutagenesis. In this work an investigation of the sequence diversity of the superfamily was undertaken and a range of BbAMD sequence homologues was tested for both aryl- and alkylmalonate decarboxylation (Chapter 3). However, none of the homologues exhibited decarboxylation activity. Targeted mutation of active site residues in an attempt to introduce decarboxylase activity was also unsuccessful. In an alternative approach to identify new alkylmalonate decarboxylating enzymes, a range of bacterial strains capable of processing alkylmalonates was isolated using selective enrichment from soil samples (Appendix D). The only characterised superfamily enzymes without a described three dimensional protein structure are MIs. In order to illuminate the distinct mechanism of MIs, the activity of the superfamily member Nocardia farcinica MI (NfMI) was characterised (Chapter 4) and its structure was determined by X-ray crystallography (Chapter 5). A potent inhibitor and substrate analogue bromomaleate was found. Mutagenesis of the active site cysteine dyad confirmed its catalytic role and Cys76 was found to be more important than Cys194. The data support a mechanism initiated by nucleophilic attack by Cys76 on the double bond of maleate. Although alternative mechanisms cannot be excluded at present, these findings indicate that the mechanistic chemistry in the superfamily is more adaptable than previously thought.

Item Type: Thesis (PhD)
Keywords: arylmalonate decarboxylase; maleate cis-trans isomerases; aspartate/glutamate racemase superfamily; industrial biocatalysis; enzyme mechanism; crystal-structure; Nocardia farcinica
Academic Units: The University of York > Biology (York)
Identification Number/EthosID: uk.bl.ethos.516589
Depositing User: Mr Florian A Fisch
Date Deposited: 20 Aug 2010 07:08
Last Modified: 08 Sep 2016 12:16
URI: http://etheses.whiterose.ac.uk/id/eprint/799

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