Structure elucidation of the kalimantacin antibiotics

In this thesis the production, isolation and purification of the kalimantacin antibiotics are described along with details of the elucidation of the structures including the relative and absolute stereochemistry. Kalimantacin A, isolated from Pseudomonas jluorescens strain BCCM_ ID9359, is biosynthe...

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Main Author: Thistlethwaite, Iain R. G.
Published: University of Bristol 2015
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685333
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spelling ndltd-bl.uk-oai-ethos.bl.uk-6853332017-03-16T16:23:30ZStructure elucidation of the kalimantacin antibioticsThistlethwaite, Iain R. G.2015In this thesis the production, isolation and purification of the kalimantacin antibiotics are described along with details of the elucidation of the structures including the relative and absolute stereochemistry. Kalimantacin A, isolated from Pseudomonas jluorescens strain BCCM_ ID9359, is biosynthesised by a trans-AT type I polyketide synthase (PKS) and exhibits strong and selective activity against multi-resistant Staphylococcus aureus (MRSA). Two mutant strains, ~batF and ~batM, have been produced from which 17- hydroxy analogue 20, 27-descarbamoyl analogue 21 and 17-hydroxy-27-descarbamoyl analogue 22 were isolated and fully characterised.615.1University of Bristolhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685333Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 615.1
spellingShingle 615.1
Thistlethwaite, Iain R. G.
Structure elucidation of the kalimantacin antibiotics
description In this thesis the production, isolation and purification of the kalimantacin antibiotics are described along with details of the elucidation of the structures including the relative and absolute stereochemistry. Kalimantacin A, isolated from Pseudomonas jluorescens strain BCCM_ ID9359, is biosynthesised by a trans-AT type I polyketide synthase (PKS) and exhibits strong and selective activity against multi-resistant Staphylococcus aureus (MRSA). Two mutant strains, ~batF and ~batM, have been produced from which 17- hydroxy analogue 20, 27-descarbamoyl analogue 21 and 17-hydroxy-27-descarbamoyl analogue 22 were isolated and fully characterised.
author Thistlethwaite, Iain R. G.
author_facet Thistlethwaite, Iain R. G.
author_sort Thistlethwaite, Iain R. G.
title Structure elucidation of the kalimantacin antibiotics
title_short Structure elucidation of the kalimantacin antibiotics
title_full Structure elucidation of the kalimantacin antibiotics
title_fullStr Structure elucidation of the kalimantacin antibiotics
title_full_unstemmed Structure elucidation of the kalimantacin antibiotics
title_sort structure elucidation of the kalimantacin antibiotics
publisher University of Bristol
publishDate 2015
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685333
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