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Automated structure prediction of trans-acyltransferase polyketide synthase products
Bacterial trans-acyltransferase polyketide synthases (trans-AT PKSs) are among the most complex known enzymes from secondary metabolism and are responsible for the biosynthesis of highly diverse bioactive polyketides. However, most of these metabolites remain uncharacterized, since trans-AT PKSs fre...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642696/ https://www.ncbi.nlm.nih.gov/pubmed/31308532 http://dx.doi.org/10.1038/s41589-019-0313-7 |
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author | Helfrich, Eric J. N. Ueoka, Reiko Dolev, Alon Rust, Michael Meoded, Roy A. Bhushan, Agneya Califano, Gianmaria Costa, Rodrigo Gugger, Muriel Steinbeck, Christoph Moreno, Pablo Piel, Jörn |
author_facet | Helfrich, Eric J. N. Ueoka, Reiko Dolev, Alon Rust, Michael Meoded, Roy A. Bhushan, Agneya Califano, Gianmaria Costa, Rodrigo Gugger, Muriel Steinbeck, Christoph Moreno, Pablo Piel, Jörn |
author_sort | Helfrich, Eric J. N. |
collection | PubMed |
description | Bacterial trans-acyltransferase polyketide synthases (trans-AT PKSs) are among the most complex known enzymes from secondary metabolism and are responsible for the biosynthesis of highly diverse bioactive polyketides. However, most of these metabolites remain uncharacterized, since trans-AT PKSs frequently Occur in poorly studied microbes and feature a remarkable array of non-canonical biosynthetic components with poorly understood functions. As a consequence, genome-guided natural product identification has been challenging. To enable de novo structural predictions for trans-AT PKS-derived polyketides, we developed the Trans-AT PKS Polyketide Predictor (TransATor). TransATor is a versatile bio- and chemoinformatics web application that suggests informative chemical structures for even highly aberrant trans-AT PKS biosynthetic gene clusters, thus permitting hypothesis-based, targeted biotechnological discovery and biosynthetic studies. We demonstrate the applicative scope in several examples, including the characterization of new variants of bioactive natural products as well as structurally novel polyketides from unusual bacterial sources. |
format | Online Article Text |
id | pubmed-6642696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-66426962020-01-15 Automated structure prediction of trans-acyltransferase polyketide synthase products Helfrich, Eric J. N. Ueoka, Reiko Dolev, Alon Rust, Michael Meoded, Roy A. Bhushan, Agneya Califano, Gianmaria Costa, Rodrigo Gugger, Muriel Steinbeck, Christoph Moreno, Pablo Piel, Jörn Nat Chem Biol Article Bacterial trans-acyltransferase polyketide synthases (trans-AT PKSs) are among the most complex known enzymes from secondary metabolism and are responsible for the biosynthesis of highly diverse bioactive polyketides. However, most of these metabolites remain uncharacterized, since trans-AT PKSs frequently Occur in poorly studied microbes and feature a remarkable array of non-canonical biosynthetic components with poorly understood functions. As a consequence, genome-guided natural product identification has been challenging. To enable de novo structural predictions for trans-AT PKS-derived polyketides, we developed the Trans-AT PKS Polyketide Predictor (TransATor). TransATor is a versatile bio- and chemoinformatics web application that suggests informative chemical structures for even highly aberrant trans-AT PKS biosynthetic gene clusters, thus permitting hypothesis-based, targeted biotechnological discovery and biosynthetic studies. We demonstrate the applicative scope in several examples, including the characterization of new variants of bioactive natural products as well as structurally novel polyketides from unusual bacterial sources. 2019-06-17 2019-07-15 /pmc/articles/PMC6642696/ /pubmed/31308532 http://dx.doi.org/10.1038/s41589-019-0313-7 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Helfrich, Eric J. N. Ueoka, Reiko Dolev, Alon Rust, Michael Meoded, Roy A. Bhushan, Agneya Califano, Gianmaria Costa, Rodrigo Gugger, Muriel Steinbeck, Christoph Moreno, Pablo Piel, Jörn Automated structure prediction of trans-acyltransferase polyketide synthase products |
title | Automated structure prediction of trans-acyltransferase polyketide synthase products |
title_full | Automated structure prediction of trans-acyltransferase polyketide synthase products |
title_fullStr | Automated structure prediction of trans-acyltransferase polyketide synthase products |
title_full_unstemmed | Automated structure prediction of trans-acyltransferase polyketide synthase products |
title_short | Automated structure prediction of trans-acyltransferase polyketide synthase products |
title_sort | automated structure prediction of trans-acyltransferase polyketide synthase products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642696/ https://www.ncbi.nlm.nih.gov/pubmed/31308532 http://dx.doi.org/10.1038/s41589-019-0313-7 |
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