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Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum

Our ability to genetically manipulate living organisms is usually constrained by the efficiency of the genetic tools available for the system of interest. In this report, we present the design, construction and characterization of a set of four new modular vectors, the pHsal series, for engineering...

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Autores principales: Silva-Rocha, Rafael, Pontelli, Marjorie Cornejo, Furtado, Gilvan Pessoa, Zaramela, Livia Soares, Koide, Tie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465625/
https://www.ncbi.nlm.nih.gov/pubmed/26061363
http://dx.doi.org/10.1371/journal.pone.0129215
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author Silva-Rocha, Rafael
Pontelli, Marjorie Cornejo
Furtado, Gilvan Pessoa
Zaramela, Livia Soares
Koide, Tie
author_facet Silva-Rocha, Rafael
Pontelli, Marjorie Cornejo
Furtado, Gilvan Pessoa
Zaramela, Livia Soares
Koide, Tie
author_sort Silva-Rocha, Rafael
collection PubMed
description Our ability to genetically manipulate living organisms is usually constrained by the efficiency of the genetic tools available for the system of interest. In this report, we present the design, construction and characterization of a set of four new modular vectors, the pHsal series, for engineering Halobacterium salinarum, a model halophilic archaeon widely used in systems biology studies. The pHsal shuttle vectors are organized in four modules: (i) the E. coli’s specific part, containing a ColE1 origin of replication and an ampicillin resistance marker, (ii) the resistance marker and (iii) the replication origin, which are specific to H. salinarum and (iv) the cargo, which will carry a sequence of interest cloned in a multiple cloning site, flanked by universal M13 primers. Each module was constructed using only minimal functional elements that were sequence edited to eliminate redundant restriction sites useful for cloning. This optimization process allowed the construction of vectors with reduced sizes compared to currently available platforms and expanded multiple cloning sites. Additionally, the strong constitutive promoter of the fer2 gene was sequence optimized and incorporated into the platform to allow high-level expression of heterologous genes in H. salinarum. The system also includes a new minimal suicide vector for the generation of knockouts and/or the incorporation of chromosomal tags, as well as a vector for promoter probing using a GFP gene as reporter. This new set of optimized vectors should strongly facilitate the engineering of H. salinarum and similar strategies could be implemented for other archaea.
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spelling pubmed-44656252015-06-25 Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum Silva-Rocha, Rafael Pontelli, Marjorie Cornejo Furtado, Gilvan Pessoa Zaramela, Livia Soares Koide, Tie PLoS One Research Article Our ability to genetically manipulate living organisms is usually constrained by the efficiency of the genetic tools available for the system of interest. In this report, we present the design, construction and characterization of a set of four new modular vectors, the pHsal series, for engineering Halobacterium salinarum, a model halophilic archaeon widely used in systems biology studies. The pHsal shuttle vectors are organized in four modules: (i) the E. coli’s specific part, containing a ColE1 origin of replication and an ampicillin resistance marker, (ii) the resistance marker and (iii) the replication origin, which are specific to H. salinarum and (iv) the cargo, which will carry a sequence of interest cloned in a multiple cloning site, flanked by universal M13 primers. Each module was constructed using only minimal functional elements that were sequence edited to eliminate redundant restriction sites useful for cloning. This optimization process allowed the construction of vectors with reduced sizes compared to currently available platforms and expanded multiple cloning sites. Additionally, the strong constitutive promoter of the fer2 gene was sequence optimized and incorporated into the platform to allow high-level expression of heterologous genes in H. salinarum. The system also includes a new minimal suicide vector for the generation of knockouts and/or the incorporation of chromosomal tags, as well as a vector for promoter probing using a GFP gene as reporter. This new set of optimized vectors should strongly facilitate the engineering of H. salinarum and similar strategies could be implemented for other archaea. Public Library of Science 2015-06-10 /pmc/articles/PMC4465625/ /pubmed/26061363 http://dx.doi.org/10.1371/journal.pone.0129215 Text en © 2015 Silva-Rocha et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Silva-Rocha, Rafael
Pontelli, Marjorie Cornejo
Furtado, Gilvan Pessoa
Zaramela, Livia Soares
Koide, Tie
Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum
title Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum
title_full Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum
title_fullStr Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum
title_full_unstemmed Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum
title_short Development of New Modular Genetic Tools for Engineering the Halophilic Archaeon Halobacterium salinarum
title_sort development of new modular genetic tools for engineering the halophilic archaeon halobacterium salinarum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465625/
https://www.ncbi.nlm.nih.gov/pubmed/26061363
http://dx.doi.org/10.1371/journal.pone.0129215
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