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Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074
Streptomyces albus J1074 is a streptomycete strain widely used as a host for expression of secondary metabolite gene clusters. Bioinformatic analysis of the genome of this organism predicts the presence of 27 gene clusters for secondary metabolites. We have used three different strategies for the ac...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992020/ https://www.ncbi.nlm.nih.gov/pubmed/24593309 http://dx.doi.org/10.1111/1751-7915.12116 |
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author | Olano, Carlos García, Ignacio González, Aranzazu Rodriguez, Miriam Rozas, Daniel Rubio, Julio Sánchez-Hidalgo, Marina Braña, Alfredo F Méndez, Carmen Salas, José A |
author_facet | Olano, Carlos García, Ignacio González, Aranzazu Rodriguez, Miriam Rozas, Daniel Rubio, Julio Sánchez-Hidalgo, Marina Braña, Alfredo F Méndez, Carmen Salas, José A |
author_sort | Olano, Carlos |
collection | PubMed |
description | Streptomyces albus J1074 is a streptomycete strain widely used as a host for expression of secondary metabolite gene clusters. Bioinformatic analysis of the genome of this organism predicts the presence of 27 gene clusters for secondary metabolites. We have used three different strategies for the activation of some of these silent/cryptic gene clusters in S. albus J1074: two hybrid polyketide-non-ribosomal peptides (PK-NRP) (antimycin and 6-epi-alteramides), a type I PK (candicidin), a non-ribosomal peptides (NRP) (indigoidine) and glycosylated compounds (paulomycins). By insertion of a strong and constitutive promoter in front of selected genes of two clusters, production of the blue pigment indigoidine and of two novel members of the polycyclic tetramate macrolactam family (6-epi-alteramides A and B) was activated. Overexpression of positive regulatory genes from the same organism also activated the biosynthesis of 6-epi-alteramides and heterologous expression of the regulatory gene pimM of the pimaricin cluster activated the simultaneous production of candicidins and antimycins, suggesting some kind of cross-regulation between both clusters. A cluster for glycosylated compounds (paulomycins) was also identified by comparison of the high-performance liquid chromatography profiles of the wild-type strain with that of a mutant in which two key enzymes of the cluster were simultaneously deleted. |
format | Online Article Text |
id | pubmed-3992020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley & Sons Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39920202014-05-01 Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 Olano, Carlos García, Ignacio González, Aranzazu Rodriguez, Miriam Rozas, Daniel Rubio, Julio Sánchez-Hidalgo, Marina Braña, Alfredo F Méndez, Carmen Salas, José A Microb Biotechnol Research Articles Streptomyces albus J1074 is a streptomycete strain widely used as a host for expression of secondary metabolite gene clusters. Bioinformatic analysis of the genome of this organism predicts the presence of 27 gene clusters for secondary metabolites. We have used three different strategies for the activation of some of these silent/cryptic gene clusters in S. albus J1074: two hybrid polyketide-non-ribosomal peptides (PK-NRP) (antimycin and 6-epi-alteramides), a type I PK (candicidin), a non-ribosomal peptides (NRP) (indigoidine) and glycosylated compounds (paulomycins). By insertion of a strong and constitutive promoter in front of selected genes of two clusters, production of the blue pigment indigoidine and of two novel members of the polycyclic tetramate macrolactam family (6-epi-alteramides A and B) was activated. Overexpression of positive regulatory genes from the same organism also activated the biosynthesis of 6-epi-alteramides and heterologous expression of the regulatory gene pimM of the pimaricin cluster activated the simultaneous production of candicidins and antimycins, suggesting some kind of cross-regulation between both clusters. A cluster for glycosylated compounds (paulomycins) was also identified by comparison of the high-performance liquid chromatography profiles of the wild-type strain with that of a mutant in which two key enzymes of the cluster were simultaneously deleted. John Wiley & Sons Ltd 2014-05 2014-03-04 /pmc/articles/PMC3992020/ /pubmed/24593309 http://dx.doi.org/10.1111/1751-7915.12116 Text en © 2014 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Olano, Carlos García, Ignacio González, Aranzazu Rodriguez, Miriam Rozas, Daniel Rubio, Julio Sánchez-Hidalgo, Marina Braña, Alfredo F Méndez, Carmen Salas, José A Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 |
title | Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 |
title_full | Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 |
title_fullStr | Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 |
title_full_unstemmed | Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 |
title_short | Activation and identification of five clusters for secondary metabolites in Streptomyces albus J1074 |
title_sort | activation and identification of five clusters for secondary metabolites in streptomyces albus j1074 |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992020/ https://www.ncbi.nlm.nih.gov/pubmed/24593309 http://dx.doi.org/10.1111/1751-7915.12116 |
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