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Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster
Comparative transcriptional profiling of a ΔbldM mutant of Streptomyces venezuelae with its unmodified progenitor revealed that the expression of a cryptic biosynthetic gene cluster containing both type I and type III polyketide synthase genes is activated in the mutant. The 29.5 kb gene cluster, wh...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132015/ https://www.ncbi.nlm.nih.gov/pubmed/27605017 http://dx.doi.org/10.1002/cbic.201600396 |
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author | Thanapipatsiri, Anyarat Gomez‐Escribano, Juan Pablo Song, Lijiang Bibb, Maureen J. Al‐Bassam, Mahmoud Chandra, Govind Thamchaipenet, Arinthip Challis, Gregory L. Bibb, Mervyn J. |
author_facet | Thanapipatsiri, Anyarat Gomez‐Escribano, Juan Pablo Song, Lijiang Bibb, Maureen J. Al‐Bassam, Mahmoud Chandra, Govind Thamchaipenet, Arinthip Challis, Gregory L. Bibb, Mervyn J. |
author_sort | Thanapipatsiri, Anyarat |
collection | PubMed |
description | Comparative transcriptional profiling of a ΔbldM mutant of Streptomyces venezuelae with its unmodified progenitor revealed that the expression of a cryptic biosynthetic gene cluster containing both type I and type III polyketide synthase genes is activated in the mutant. The 29.5 kb gene cluster, which was predicted to encode an unusual biaryl metabolite, which we named venemycin, and potentially halogenated derivatives, contains 16 genes including one—vemR—that encodes a transcriptional activator of the large ATP‐binding LuxR‐like (LAL) family. Constitutive expression of vemR in the ΔbldM mutant led to the production of sufficient venemycin for structural characterisation, confirming its unusual biaryl structure. Co‐expression of the venemycin biosynthetic gene cluster and vemR in the heterologous host Streptomyces coelicolor also resulted in venemycin production. Although the gene cluster encodes two halogenases and a flavin reductase, constitutive expression of all three genes led to the accumulation only of a monohalogenated venemycin derivative, both in the native producer and the heterologous host. A competition experiment in which equimolar quantities of sodium chloride and sodium bromide were fed to the venemycin‐producing strains resulted in the preferential incorporation of bromine, thus suggesting that bromide is the preferred substrate for one or both halogenases. |
format | Online Article Text |
id | pubmed-5132015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51320152016-12-02 Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster Thanapipatsiri, Anyarat Gomez‐Escribano, Juan Pablo Song, Lijiang Bibb, Maureen J. Al‐Bassam, Mahmoud Chandra, Govind Thamchaipenet, Arinthip Challis, Gregory L. Bibb, Mervyn J. Chembiochem Full Papers Comparative transcriptional profiling of a ΔbldM mutant of Streptomyces venezuelae with its unmodified progenitor revealed that the expression of a cryptic biosynthetic gene cluster containing both type I and type III polyketide synthase genes is activated in the mutant. The 29.5 kb gene cluster, which was predicted to encode an unusual biaryl metabolite, which we named venemycin, and potentially halogenated derivatives, contains 16 genes including one—vemR—that encodes a transcriptional activator of the large ATP‐binding LuxR‐like (LAL) family. Constitutive expression of vemR in the ΔbldM mutant led to the production of sufficient venemycin for structural characterisation, confirming its unusual biaryl structure. Co‐expression of the venemycin biosynthetic gene cluster and vemR in the heterologous host Streptomyces coelicolor also resulted in venemycin production. Although the gene cluster encodes two halogenases and a flavin reductase, constitutive expression of all three genes led to the accumulation only of a monohalogenated venemycin derivative, both in the native producer and the heterologous host. A competition experiment in which equimolar quantities of sodium chloride and sodium bromide were fed to the venemycin‐producing strains resulted in the preferential incorporation of bromine, thus suggesting that bromide is the preferred substrate for one or both halogenases. John Wiley and Sons Inc. 2016-10-13 2016-11-17 /pmc/articles/PMC5132015/ /pubmed/27605017 http://dx.doi.org/10.1002/cbic.201600396 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Thanapipatsiri, Anyarat Gomez‐Escribano, Juan Pablo Song, Lijiang Bibb, Maureen J. Al‐Bassam, Mahmoud Chandra, Govind Thamchaipenet, Arinthip Challis, Gregory L. Bibb, Mervyn J. Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster |
title | Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster |
title_full | Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster |
title_fullStr | Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster |
title_full_unstemmed | Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster |
title_short | Discovery of Unusual Biaryl Polyketides by Activation of a Silent Streptomyces venezuelae Biosynthetic Gene Cluster |
title_sort | discovery of unusual biaryl polyketides by activation of a silent streptomyces venezuelae biosynthetic gene cluster |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132015/ https://www.ncbi.nlm.nih.gov/pubmed/27605017 http://dx.doi.org/10.1002/cbic.201600396 |
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