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Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid
BACKGROUND: Transposon mutagenesis is highly valuable for bacterial genetic and genomic studies. The transposons are usually delivered into host cells through conjugation or electroporation of a suicide plasmid. However, many bacterial species cannot be efficiently conjugated or transformed for tran...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201506/ https://www.ncbi.nlm.nih.gov/pubmed/30355324 http://dx.doi.org/10.1186/s12866-018-1319-0 |
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author | Naorem, Santa S. Han, Jin Zhang, Stephanie Y. Zhang, Junyi Graham, Lindsey B. Song, Angelou Smith, Cameron V. Rashid, Fariha Guo, Huatao |
author_facet | Naorem, Santa S. Han, Jin Zhang, Stephanie Y. Zhang, Junyi Graham, Lindsey B. Song, Angelou Smith, Cameron V. Rashid, Fariha Guo, Huatao |
author_sort | Naorem, Santa S. |
collection | PubMed |
description | BACKGROUND: Transposon mutagenesis is highly valuable for bacterial genetic and genomic studies. The transposons are usually delivered into host cells through conjugation or electroporation of a suicide plasmid. However, many bacterial species cannot be efficiently conjugated or transformed for transposon saturation mutagenesis. For this reason, temperature-sensitive (ts) plasmids have also been developed for transposon mutagenesis, but prolonged incubation at high temperatures to induce ts plasmid loss can be harmful to the hosts and lead to enrichment of mutants with adaptive genetic changes. In addition, the ts phenotype of a plasmid is often strain- or species-specific, as it may become non-ts or suicidal in different bacterial species. RESULTS: We have engineered several conditional suicide plasmids that have a broad host range and whose loss is IPTG-controlled. One construct, which has the highest stability in the absence of IPTG induction, was then used as a curable vector to deliver hyperactive miniTn5 transposons for insertional mutagenesis. Our analyses show that these new tools can be used for efficient and regulatable transposon mutagenesis in Escherichia coli, Acinetobacter baylyi and Pseudomonas aeruginosa. In P. aeruginosa PAO1, we have used this method to generate a Tn5 insertion library with an estimated diversity of ~ 10(8), which is ~ 2 logs larger than the best transposon insertional library of PAO1 and related Pseudomonas strains previously reported. CONCLUSION: We have developed a number of IPTG-controlled conditional suicide plasmids. By exploiting one of them for transposon delivery, a highly efficient and broadly useful mutagenesis system has been developed. As the assay condition is mild, we believe that our methodology will have broad applications in microbiology research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1319-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6201506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62015062018-10-31 Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid Naorem, Santa S. Han, Jin Zhang, Stephanie Y. Zhang, Junyi Graham, Lindsey B. Song, Angelou Smith, Cameron V. Rashid, Fariha Guo, Huatao BMC Microbiol Methodology Article BACKGROUND: Transposon mutagenesis is highly valuable for bacterial genetic and genomic studies. The transposons are usually delivered into host cells through conjugation or electroporation of a suicide plasmid. However, many bacterial species cannot be efficiently conjugated or transformed for transposon saturation mutagenesis. For this reason, temperature-sensitive (ts) plasmids have also been developed for transposon mutagenesis, but prolonged incubation at high temperatures to induce ts plasmid loss can be harmful to the hosts and lead to enrichment of mutants with adaptive genetic changes. In addition, the ts phenotype of a plasmid is often strain- or species-specific, as it may become non-ts or suicidal in different bacterial species. RESULTS: We have engineered several conditional suicide plasmids that have a broad host range and whose loss is IPTG-controlled. One construct, which has the highest stability in the absence of IPTG induction, was then used as a curable vector to deliver hyperactive miniTn5 transposons for insertional mutagenesis. Our analyses show that these new tools can be used for efficient and regulatable transposon mutagenesis in Escherichia coli, Acinetobacter baylyi and Pseudomonas aeruginosa. In P. aeruginosa PAO1, we have used this method to generate a Tn5 insertion library with an estimated diversity of ~ 10(8), which is ~ 2 logs larger than the best transposon insertional library of PAO1 and related Pseudomonas strains previously reported. CONCLUSION: We have developed a number of IPTG-controlled conditional suicide plasmids. By exploiting one of them for transposon delivery, a highly efficient and broadly useful mutagenesis system has been developed. As the assay condition is mild, we believe that our methodology will have broad applications in microbiology research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1319-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-24 /pmc/articles/PMC6201506/ /pubmed/30355324 http://dx.doi.org/10.1186/s12866-018-1319-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Naorem, Santa S. Han, Jin Zhang, Stephanie Y. Zhang, Junyi Graham, Lindsey B. Song, Angelou Smith, Cameron V. Rashid, Fariha Guo, Huatao Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid |
title | Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid |
title_full | Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid |
title_fullStr | Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid |
title_full_unstemmed | Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid |
title_short | Efficient transposon mutagenesis mediated by an IPTG-controlled conditional suicide plasmid |
title_sort | efficient transposon mutagenesis mediated by an iptg-controlled conditional suicide plasmid |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201506/ https://www.ncbi.nlm.nih.gov/pubmed/30355324 http://dx.doi.org/10.1186/s12866-018-1319-0 |
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