Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257799
Title: The biochemistry of phosphonate analogues of naturally occurring phosphates
Author: Roach, D. J. W.
ISNI:       0000 0001 3520 4626
Awarding Body: University of Bath
Current Institution: University of Bath
Date of Award: 1980
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Abstract:
6,7 dideoxy-alpha-D-gluco-heptose 7-phosphonic acid, the isosteric phosphonate analogue of naturally-occurring glucose 6-phosphate was synthesised via a novel route, involving the use of an easily-prepared and stable ethyl ester, followed by a facile dealkylation procedure. 6,7 dideoxy alpha-D-gluco-heptose 7-phosphonic acid was shown to behave as a product inhibitor of purified bovine brain hexokinase I, being a competitive inhibitor of MgATP2- and a noncompetitive inhibitor of glucose. 6,7 dideoxy alpha-D-gluco-heptonic 7-phosphonic acid, the isoteric phosphonate analogue of gluconate 6-phosphate was enzymically synthesised from 6,7 dideoxy alpha-D-gluco heptose 7-phosphonic acid and was shown to be a poor substrate for yeast gluconate 6-phosphate dehydrogenase at pH 7.5 and 8.0. 6,7 dideoxy alpha-D-gluco-heptose 7-phosphonic acid had no effect on cell proliferation of mouse lymphoma cells (at mM concentrations) but was found to be more stable then the natural phosphate in their presence. alpha-D-glucose fluorophosphate was tested as an active-site-directed irreversible inhibitor of yeast glucose 6-phosphate dehydrogenase with a view to eventual use of the corresponding phosphonate analogue in similar systems. The fluorophosphate was found to be inactive in this respect.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.257799  DOI: Not available
Keywords: Biochemistry
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