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Metabologenomics: Correlation of Microbial Gene Clusters with Metabolites Drives Discovery of a Nonribosomal Peptide with an Unusual Amino Acid Monomer
[Image: see text] For more than half a century the pharmaceutical industry has sifted through natural products produced by microbes, uncovering new scaffolds and fashioning them into a broad range of vital drugs. We sought a strategy to reinvigorate the discovery of natural products with distinctive...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827660/ https://www.ncbi.nlm.nih.gov/pubmed/27163034 http://dx.doi.org/10.1021/acscentsci.5b00331 |
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author | Goering, Anthony W. McClure, Ryan A. Doroghazi, James R. Albright, Jessica C. Haverland, Nicole A. Zhang, Yongbo Ju, Kou-San Thomson, Regan J. Metcalf, William W. Kelleher, Neil L. |
author_facet | Goering, Anthony W. McClure, Ryan A. Doroghazi, James R. Albright, Jessica C. Haverland, Nicole A. Zhang, Yongbo Ju, Kou-San Thomson, Regan J. Metcalf, William W. Kelleher, Neil L. |
author_sort | Goering, Anthony W. |
collection | PubMed |
description | [Image: see text] For more than half a century the pharmaceutical industry has sifted through natural products produced by microbes, uncovering new scaffolds and fashioning them into a broad range of vital drugs. We sought a strategy to reinvigorate the discovery of natural products with distinctive structures using bacterial genome sequencing combined with metabolomics. By correlating genetic content from 178 actinomycete genomes with mass spectrometry-enabled analyses of their exported metabolomes, we paired new secondary metabolites with their biosynthetic gene clusters. We report the use of this new approach to isolate and characterize tambromycin, a new chlorinated natural product, composed of several nonstandard amino acid monomeric units, including a unique pyrrolidine-containing amino acid we name tambroline. Tambromycin shows antiproliferative activity against cancerous human B- and T-cell lines. The discovery of tambromycin via large-scale correlation of gene clusters with metabolites (a.k.a. metabologenomics) illuminates a path for structure-based discovery of natural products at a sharply increased rate. |
format | Online Article Text |
id | pubmed-4827660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48276602016-05-09 Metabologenomics: Correlation of Microbial Gene Clusters with Metabolites Drives Discovery of a Nonribosomal Peptide with an Unusual Amino Acid Monomer Goering, Anthony W. McClure, Ryan A. Doroghazi, James R. Albright, Jessica C. Haverland, Nicole A. Zhang, Yongbo Ju, Kou-San Thomson, Regan J. Metcalf, William W. Kelleher, Neil L. ACS Cent Sci [Image: see text] For more than half a century the pharmaceutical industry has sifted through natural products produced by microbes, uncovering new scaffolds and fashioning them into a broad range of vital drugs. We sought a strategy to reinvigorate the discovery of natural products with distinctive structures using bacterial genome sequencing combined with metabolomics. By correlating genetic content from 178 actinomycete genomes with mass spectrometry-enabled analyses of their exported metabolomes, we paired new secondary metabolites with their biosynthetic gene clusters. We report the use of this new approach to isolate and characterize tambromycin, a new chlorinated natural product, composed of several nonstandard amino acid monomeric units, including a unique pyrrolidine-containing amino acid we name tambroline. Tambromycin shows antiproliferative activity against cancerous human B- and T-cell lines. The discovery of tambromycin via large-scale correlation of gene clusters with metabolites (a.k.a. metabologenomics) illuminates a path for structure-based discovery of natural products at a sharply increased rate. American Chemical Society 2016-01-20 2016-02-24 /pmc/articles/PMC4827660/ /pubmed/27163034 http://dx.doi.org/10.1021/acscentsci.5b00331 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Goering, Anthony W. McClure, Ryan A. Doroghazi, James R. Albright, Jessica C. Haverland, Nicole A. Zhang, Yongbo Ju, Kou-San Thomson, Regan J. Metcalf, William W. Kelleher, Neil L. Metabologenomics: Correlation of Microbial Gene Clusters with Metabolites Drives Discovery of a Nonribosomal Peptide with an Unusual Amino Acid Monomer |
title | Metabologenomics: Correlation of Microbial Gene Clusters
with Metabolites Drives Discovery of a Nonribosomal Peptide with an
Unusual Amino Acid Monomer |
title_full | Metabologenomics: Correlation of Microbial Gene Clusters
with Metabolites Drives Discovery of a Nonribosomal Peptide with an
Unusual Amino Acid Monomer |
title_fullStr | Metabologenomics: Correlation of Microbial Gene Clusters
with Metabolites Drives Discovery of a Nonribosomal Peptide with an
Unusual Amino Acid Monomer |
title_full_unstemmed | Metabologenomics: Correlation of Microbial Gene Clusters
with Metabolites Drives Discovery of a Nonribosomal Peptide with an
Unusual Amino Acid Monomer |
title_short | Metabologenomics: Correlation of Microbial Gene Clusters
with Metabolites Drives Discovery of a Nonribosomal Peptide with an
Unusual Amino Acid Monomer |
title_sort | metabologenomics: correlation of microbial gene clusters
with metabolites drives discovery of a nonribosomal peptide with an
unusual amino acid monomer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827660/ https://www.ncbi.nlm.nih.gov/pubmed/27163034 http://dx.doi.org/10.1021/acscentsci.5b00331 |
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