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Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics
Glycosyltransferase MurG catalyses the transfer of N-acetyl-d-glucosamine to lipid intermediate I on the bacterial peptidoglycan biosynthesis pathway, and is a target for development of new antibacterial agents. A transition state mimic was designed for MurG, containing a functionalised proline, lin...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3034214/ https://www.ncbi.nlm.nih.gov/pubmed/20226679 http://dx.doi.org/10.1016/j.bmc.2010.02.026 |
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author | Trunkfield, Amy E. Gurcha, Sudagar S. Besra, Gurdyal S. Bugg, Timothy D.H. |
author_facet | Trunkfield, Amy E. Gurcha, Sudagar S. Besra, Gurdyal S. Bugg, Timothy D.H. |
author_sort | Trunkfield, Amy E. |
collection | PubMed |
description | Glycosyltransferase MurG catalyses the transfer of N-acetyl-d-glucosamine to lipid intermediate I on the bacterial peptidoglycan biosynthesis pathway, and is a target for development of new antibacterial agents. A transition state mimic was designed for MurG, containing a functionalised proline, linked through the α-carboxylic acid, via a spacer, to a uridine nucleoside. A set of 15 functionalised prolines were synthesised, using a convergent dipolar cycloaddition reaction, which were coupled via either a glycine, proline, sarcosine, or diester linkage to the 5′-position of uridine. The library of 18 final compounds were tested as inhibitors of Escherichia coli glycosyltransferase MurG. Ten compounds showed inhibition of MurG at 1 mM concentration, the most active with IC(50) 400 μM. The library was also tested against Mycobacterium tuberculosis galactosyltransferase GlfT2, and one compound showed effective inhibition at 1 mM concentration. |
format | Text |
id | pubmed-3034214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30342142011-03-14 Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics Trunkfield, Amy E. Gurcha, Sudagar S. Besra, Gurdyal S. Bugg, Timothy D.H. Bioorg Med Chem Article Glycosyltransferase MurG catalyses the transfer of N-acetyl-d-glucosamine to lipid intermediate I on the bacterial peptidoglycan biosynthesis pathway, and is a target for development of new antibacterial agents. A transition state mimic was designed for MurG, containing a functionalised proline, linked through the α-carboxylic acid, via a spacer, to a uridine nucleoside. A set of 15 functionalised prolines were synthesised, using a convergent dipolar cycloaddition reaction, which were coupled via either a glycine, proline, sarcosine, or diester linkage to the 5′-position of uridine. The library of 18 final compounds were tested as inhibitors of Escherichia coli glycosyltransferase MurG. Ten compounds showed inhibition of MurG at 1 mM concentration, the most active with IC(50) 400 μM. The library was also tested against Mycobacterium tuberculosis galactosyltransferase GlfT2, and one compound showed effective inhibition at 1 mM concentration. Elsevier Science 2010-04-01 /pmc/articles/PMC3034214/ /pubmed/20226679 http://dx.doi.org/10.1016/j.bmc.2010.02.026 Text en © 2010 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Trunkfield, Amy E. Gurcha, Sudagar S. Besra, Gurdyal S. Bugg, Timothy D.H. Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics |
title | Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics |
title_full | Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics |
title_fullStr | Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics |
title_full_unstemmed | Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics |
title_short | Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics |
title_sort | inhibition of escherichia coli glycosyltransferase murg and mycobacterium tuberculosis gal transferase by uridine-linked transition state mimics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3034214/ https://www.ncbi.nlm.nih.gov/pubmed/20226679 http://dx.doi.org/10.1016/j.bmc.2010.02.026 |
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