Cargando…
Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations
Glucose-1-phosphate uridylyltransferase in conjunction with UDP-glucose pyrophosphorylase was found to catalyse the conversion of a range of 5-substituted UTP derivatives into the corresponding UDP-galactose derivatives in poor yield. Notably the 5-iodo derivative was not converted to UDP-sugar. In...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340641/ https://www.ncbi.nlm.nih.gov/pubmed/25662737 http://dx.doi.org/10.1016/j.carres.2014.12.005 |
_version_ | 1782359046398935040 |
---|---|
author | Wagstaff, Ben A. Rejzek, Martin Pesnot, Thomas Tedaldi, Lauren M. Caputi, Lorenzo O’Neill, Ellis C. Benini, Stefano Wagner, Gerd K. Field, Robert A. |
author_facet | Wagstaff, Ben A. Rejzek, Martin Pesnot, Thomas Tedaldi, Lauren M. Caputi, Lorenzo O’Neill, Ellis C. Benini, Stefano Wagner, Gerd K. Field, Robert A. |
author_sort | Wagstaff, Ben A. |
collection | PubMed |
description | Glucose-1-phosphate uridylyltransferase in conjunction with UDP-glucose pyrophosphorylase was found to catalyse the conversion of a range of 5-substituted UTP derivatives into the corresponding UDP-galactose derivatives in poor yield. Notably the 5-iodo derivative was not converted to UDP-sugar. In contrast, UDP-glucose pyrophosphorylase in conjunction with inorganic pyrophosphatase was particularly effective at converting 5-substituted UTP derivatives, including the iodo compound, into a range of gluco-configured 5-substituted UDP-sugar derivatives in good yields. Attempts to effect 4″-epimerization of these 5-substituted UDP-glucose with UDP-glucose 4″-epimerase from yeast were unsuccessful, while use of the corresponding enzyme from Erwinia amylovora resulted in efficient epimerization of only 5-iodo-UDP-Glc, but not the corresponding 5-aryl derivatives, to give 5-iodo-UDP-Gal. Given the established potential for Pd-mediated cross-coupling of 5-iodo-UDP-sugars, this provides convenient access to the galacto-configured 5-substituted-UDP-sugars from gluco-configured substrates and 5-iodo-UTP. |
format | Online Article Text |
id | pubmed-4340641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-43406412015-03-03 Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations Wagstaff, Ben A. Rejzek, Martin Pesnot, Thomas Tedaldi, Lauren M. Caputi, Lorenzo O’Neill, Ellis C. Benini, Stefano Wagner, Gerd K. Field, Robert A. Carbohydr Res Article Glucose-1-phosphate uridylyltransferase in conjunction with UDP-glucose pyrophosphorylase was found to catalyse the conversion of a range of 5-substituted UTP derivatives into the corresponding UDP-galactose derivatives in poor yield. Notably the 5-iodo derivative was not converted to UDP-sugar. In contrast, UDP-glucose pyrophosphorylase in conjunction with inorganic pyrophosphatase was particularly effective at converting 5-substituted UTP derivatives, including the iodo compound, into a range of gluco-configured 5-substituted UDP-sugar derivatives in good yields. Attempts to effect 4″-epimerization of these 5-substituted UDP-glucose with UDP-glucose 4″-epimerase from yeast were unsuccessful, while use of the corresponding enzyme from Erwinia amylovora resulted in efficient epimerization of only 5-iodo-UDP-Glc, but not the corresponding 5-aryl derivatives, to give 5-iodo-UDP-Gal. Given the established potential for Pd-mediated cross-coupling of 5-iodo-UDP-sugars, this provides convenient access to the galacto-configured 5-substituted-UDP-sugars from gluco-configured substrates and 5-iodo-UTP. Elsevier 2015-03-02 /pmc/articles/PMC4340641/ /pubmed/25662737 http://dx.doi.org/10.1016/j.carres.2014.12.005 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wagstaff, Ben A. Rejzek, Martin Pesnot, Thomas Tedaldi, Lauren M. Caputi, Lorenzo O’Neill, Ellis C. Benini, Stefano Wagner, Gerd K. Field, Robert A. Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations |
title | Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations |
title_full | Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations |
title_fullStr | Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations |
title_full_unstemmed | Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations |
title_short | Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations |
title_sort | enzymatic synthesis of nucleobase-modified udp-sugars: scope and limitations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340641/ https://www.ncbi.nlm.nih.gov/pubmed/25662737 http://dx.doi.org/10.1016/j.carres.2014.12.005 |
work_keys_str_mv | AT wagstaffbena enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT rejzekmartin enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT pesnotthomas enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT tedaldilaurenm enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT caputilorenzo enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT oneillellisc enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT beninistefano enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT wagnergerdk enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations AT fieldroberta enzymaticsynthesisofnucleobasemodifiedudpsugarsscopeandlimitations |