In biology, the kynurenine pathway is the major degradation pathway of tryptophan (L-Trp). The first and rate-limiting step is the oxidation of L-Trp to N-formylkynurenine (NFK). The mechanism of this oxygen-dependent reaction has not been established, but is catalysed by two heme-containing dioxygenase enzymes: indoleamine 2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO). Early proposals suggested a base-catalysed abstraction mechanism, but most of the recent studies argue against that. Instead, formation of a ferryl (Compound II intermediate) seems more likely. In this thesis, aspects of the reaction mechanism have been investigated. A Compound II intermediate was detected during the oxidation of L-Trp by hIDO using stopped flow photodiode array spectroscopy. A Compound II intermediate was also detected during the oxidation of a number of different tryptophan analogues. The results suggest a common mechanism of oxidation between L-Trp and other substrates of hIDO. The difference in reactivity between the tryptophan analogues 5-hydroxy-tryptophan and 5-methoxy-tryptophan with hIDO have been interpreted to indicate that initial oxygen atom insertion occurs by radical rather than electrophilic addition. An intermediate was detected during the oxidation of L-Trp by hTDO and XcTDO. The spectrum of this intermediate did not appear to be characteristic of a Compound II based on comparison with the spectrum of Compound II from hIDO. Weaker binding of L-Trp to both hTDO and XcTDO has been used to interpret these results. It is suggested that Compound II in TDO has a different spectrum or that the rate-limiting step is altered and an alternative catalytic intermediate accumulates. Crystal trials have been conducted for hIDO and hTDO, with some conditions producing micro-crystals. The structure of XcTDO in complex with potassium cyanide and L-Trp was solved. The binding mode of L-Trp within the distal pocket does not correlate with the L-Trp binding mode in the published ferrous XcTDO- L-Trp binary complex structure. Oxidation of L-Trp by ferric TDO without the addition of reducing agent was investigated. The results suggest the recruitment of hydrogen peroxide from solution to activate ferric heme. A summary of the mechanistic information gathered from all of the above experiments is presented.
| Identifer | oai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:682409 |
| Date | January 2016 |
| Creators | Booth, Elizabeth Suzanne |
| Contributors | Raven, Emma ; Handa, Sandeep |
| Publisher | University of Leicester |
| Source Sets | Ethos UK |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Source | http://hdl.handle.net/2381/37091 |
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