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|Title: ||Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism|
|Authors: ||Nasomjai, Pitak|
|Supervisors: ||O'Hagan, David, 1961-|
|Issue Date: ||2010|
|Abstract: ||This thesis is focused on an investigation of the mechanisms of three enzymatically mediated carbon skeleton isomerisation reactions.
Chapter 1 provides an overview of some representative examples of the carbon skeleton rearrangement reactions in enzymology.
Chapter 2 describes the preparation and use of fluorolittorines to explore the mechanism of the rearrangement of the tropane alkaloid littorine to hyoscyamine which is a reaction mediated by the cytochrome P450 enzyme.
Chapter 3 describes the synthesis of D-ribose-1-phosphonates and the cyclic phosphonates (phostone) that are candidate inhibitors of the enzymatic isomerisation of 5-fluoro-5-deoxy-ribose-1-phosphate (5-FDRP) to 5-fluoro-5-deoxy-ribulose-1-phosphate (5-FDRulP), an important step in fluorometabolite biosynthesis pathway in Streptomyces cattleya.
Chapter 4 describes the synthesis of 5-hydroxy-3,4-dioxohexylphosphonate and [5-13C]-5-hydroxy-3,4-dioxohexylphosphonate. These compounds are proposed as candidates for the transition state of the retro-aldol/aldol mechanism of the enzymatic isomerisation of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methylerythitol-phophate-2-phosphate (MEP) in the biosynthesis of isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP). The influence of pH on tautomerisation of [5-13C]-5-hydroxy-3,4-dioxohexylphosphonate is also described.
Chapter 5 describes the general chemical and biochemical methodologies utilised in this research project.|
|Other Identifiers: ||uk.bl.ethos.552357|
|Publisher: ||University of St Andrews|
|Appears in Collections:||Chemistry Theses|
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