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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...

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Autores principales: García‐Gutiérrez, Coral, Aparicio, Tomás, Torres‐Sánchez, Lucía, Martínez‐García, Esteban, de Lorenzo, Víctor, Villar, Claudio J., Lombó, Felipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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