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Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases†
[Image: see text] Construction of a genomic DNA library from Pantoea agglomerans strain CU0119 and screening against the plant pathogen Erwinia amylovora yielded a new family of antibiotics, dapdiamides A−E (1−5). The structures were established through 2D-NMR experiments and mass spectrometry, as w...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society and American Society of Pharmacognosy
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846032/ https://www.ncbi.nlm.nih.gov/pubmed/20041689 http://dx.doi.org/10.1021/np900685z |
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author | Dawlaty, Jessica Zhang, Xiaorong Fischbach, Michael A. Clardy, Jon |
author_facet | Dawlaty, Jessica Zhang, Xiaorong Fischbach, Michael A. Clardy, Jon |
author_sort | Dawlaty, Jessica |
collection | PubMed |
description | [Image: see text] Construction of a genomic DNA library from Pantoea agglomerans strain CU0119 and screening against the plant pathogen Erwinia amylovora yielded a new family of antibiotics, dapdiamides A−E (1−5). The structures were established through 2D-NMR experiments and mass spectrometry, as well as the synthesis of dapdiamide A (1). Transposon mutagenesis of the active cosmid allowed identification of the biosynthetic gene cluster. The dapdiamide family’s promiscuous biosynthetic pathway contains two unconventional amide ligases that are predicted to couple its constituent monomers. |
format | Text |
id | pubmed-2846032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | American Chemical Society and American Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
spelling | pubmed-28460322010-03-26 Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† Dawlaty, Jessica Zhang, Xiaorong Fischbach, Michael A. Clardy, Jon J Nat Prod [Image: see text] Construction of a genomic DNA library from Pantoea agglomerans strain CU0119 and screening against the plant pathogen Erwinia amylovora yielded a new family of antibiotics, dapdiamides A−E (1−5). The structures were established through 2D-NMR experiments and mass spectrometry, as well as the synthesis of dapdiamide A (1). Transposon mutagenesis of the active cosmid allowed identification of the biosynthetic gene cluster. The dapdiamide family’s promiscuous biosynthetic pathway contains two unconventional amide ligases that are predicted to couple its constituent monomers. American Chemical Society and American Society of Pharmacognosy 2009-12-30 2010-03-26 /pmc/articles/PMC2846032/ /pubmed/20041689 http://dx.doi.org/10.1021/np900685z Text en Copyright © 2009 American Chemical Society and American Society of Pharmacognosy and American Society of Pharmacognosy http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Dawlaty, Jessica Zhang, Xiaorong Fischbach, Michael A. Clardy, Jon Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† |
title | Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† |
title_full | Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† |
title_fullStr | Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† |
title_full_unstemmed | Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† |
title_short | Dapdiamides, Tripeptide Antibiotics Formed by Unconventional Amide Ligases† |
title_sort | dapdiamides, tripeptide antibiotics formed by unconventional amide ligases† |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846032/ https://www.ncbi.nlm.nih.gov/pubmed/20041689 http://dx.doi.org/10.1021/np900685z |
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