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Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria
Actinomycetales, such as the genus Streptomyces, are well‐known cell factories employed to produce a wide variety of secondary metabolites for industrial use. However, not only is the genetic engineering of Streptomyces more complicated and tedious than other model laboratory species, such as Escher...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294301/ https://www.ncbi.nlm.nih.gov/pubmed/32170856 http://dx.doi.org/10.1002/mbo3.1024 |
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author | García‐Gutiérrez, Coral Aparicio, Tomás Torres‐Sánchez, Lucía Martínez‐García, Esteban de Lorenzo, Víctor Villar, Claudio J. Lombó, Felipe |
author_facet | García‐Gutiérrez, Coral Aparicio, Tomás Torres‐Sánchez, Lucía Martínez‐García, Esteban de Lorenzo, Víctor Villar, Claudio J. Lombó, Felipe |
author_sort | García‐Gutiérrez, Coral |
collection | PubMed |
description | Actinomycetales, such as the genus Streptomyces, are well‐known cell factories employed to produce a wide variety of secondary metabolites for industrial use. However, not only is the genetic engineering of Streptomyces more complicated and tedious than other model laboratory species, such as Escherichia coli, there is also a considerable lack of genetic tools, hindering its adoption as a common chassis for synthetic biology. In this work, 23 novel shuttle vectors are presented that follow the canonical SEVA (Standard European Vector Architecture) common architecture with the goal of increasing the genetic toolbox repertoire for Streptomyces and other actinomycetes. The ORI module of these plasmids is composed of the combination of two origins of replication, one for Gram‐negative bacteria and the other for Streptomyces, a Gram‐positive bacteria. Origins of replication have been included in the collection for integrative, low‐copy number, and medium‐to‐high‐copy number vectors for Streptomyces. Also, a new selection marker has been developed that confers resistance to apramycin. The functionality of these plasmids was tested via the heterologous expression of GFP and the heterologous production of the plant flavonoid apigenin in Streptomyces albus J1074, with successful results in both cases, therefore expanding the current repertoire of genetic manipulation tools in Streptomyces species. |
format | Online Article Text |
id | pubmed-7294301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72943012020-06-15 Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria García‐Gutiérrez, Coral Aparicio, Tomás Torres‐Sánchez, Lucía Martínez‐García, Esteban de Lorenzo, Víctor Villar, Claudio J. Lombó, Felipe Microbiologyopen Original Articles Actinomycetales, such as the genus Streptomyces, are well‐known cell factories employed to produce a wide variety of secondary metabolites for industrial use. However, not only is the genetic engineering of Streptomyces more complicated and tedious than other model laboratory species, such as Escherichia coli, there is also a considerable lack of genetic tools, hindering its adoption as a common chassis for synthetic biology. In this work, 23 novel shuttle vectors are presented that follow the canonical SEVA (Standard European Vector Architecture) common architecture with the goal of increasing the genetic toolbox repertoire for Streptomyces and other actinomycetes. The ORI module of these plasmids is composed of the combination of two origins of replication, one for Gram‐negative bacteria and the other for Streptomyces, a Gram‐positive bacteria. Origins of replication have been included in the collection for integrative, low‐copy number, and medium‐to‐high‐copy number vectors for Streptomyces. Also, a new selection marker has been developed that confers resistance to apramycin. The functionality of these plasmids was tested via the heterologous expression of GFP and the heterologous production of the plant flavonoid apigenin in Streptomyces albus J1074, with successful results in both cases, therefore expanding the current repertoire of genetic manipulation tools in Streptomyces species. John Wiley and Sons Inc. 2020-03-14 /pmc/articles/PMC7294301/ /pubmed/32170856 http://dx.doi.org/10.1002/mbo3.1024 Text en © 2020 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles García‐Gutiérrez, Coral Aparicio, Tomás Torres‐Sánchez, Lucía Martínez‐García, Esteban de Lorenzo, Víctor Villar, Claudio J. Lombó, Felipe Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria |
title | Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria |
title_full | Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria |
title_fullStr | Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria |
title_full_unstemmed | Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria |
title_short | Multifunctional SEVA shuttle vectors for actinomycetes and Gram‐negative bacteria |
title_sort | multifunctional seva shuttle vectors for actinomycetes and gram‐negative bacteria |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294301/ https://www.ncbi.nlm.nih.gov/pubmed/32170856 http://dx.doi.org/10.1002/mbo3.1024 |
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