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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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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