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Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran

BACKGROUND: Glyphosate is a non-selective systemic herbicide with a broad spectrum of weed control that inhibits a key enzyme, 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase, in the shikimate pathway. OBJECTIVES: Isolation and analysis of the epsps (aroA) gene responsible for glyphosate-toleranc...

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Autores principales: Ghaderitabar, Hadi, Mousavi, Amir, Hatef Salmanian, Ali, Hadi, Faranak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute of Genetic Engineering and Biotechnology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035420/
https://www.ncbi.nlm.nih.gov/pubmed/33850947
http://dx.doi.org/10.30498/IJB.2020.204133.2597
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author Ghaderitabar, Hadi
Mousavi, Amir
Hatef Salmanian, Ali
Hadi, Faranak
author_facet Ghaderitabar, Hadi
Mousavi, Amir
Hatef Salmanian, Ali
Hadi, Faranak
author_sort Ghaderitabar, Hadi
collection PubMed
description BACKGROUND: Glyphosate is a non-selective systemic herbicide with a broad spectrum of weed control that inhibits a key enzyme, 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase, in the shikimate pathway. OBJECTIVES: Isolation and analysis of the epsps (aroA) gene responsible for glyphosate-tolerance in bacteria from Roundup- contaminated soils was the aim of this study. MATERIALS AND METHODS: Sampling was done from the soil of the gardens which were heavily contaminated by Roundup herbicide and then bacterial screening was performed in the presence of high concentrations of glyphosate. The genus of bacterium was identified via molecular methods such as 16S rRNA sequencing. The aroA gene of this bacterium (aroA(HA-09)) was isolated using the primers designed-upon specific regions of aroA genes available in NCBI GenBank database. The PCR product was cloned, sequenced and subcloned into pET28a as an expression vector and transferred into E. coli strain BL21(DE3). The cells were inoculated in liquid M9 minimal medium containing IPTG and different concentrations of glyphosate. RESULTS: The genus of bacterium was identified as Pseudomonas sp. strain HA-09. The isolated aroA(HA-09) gene from this bacterium was approximately 2.2 kb in size. Bioassay of E. coli expressing this gene showed high tolerance to glyphosate (up to 300 mM). CONCLUSION: The aroA(HA-09) gene could be considered as a novel and efficient candidate for development of glyphosate-tolerant crop plants.
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spelling pubmed-80354202021-04-12 Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran Ghaderitabar, Hadi Mousavi, Amir Hatef Salmanian, Ali Hadi, Faranak Iran J Biotechnol Research Article BACKGROUND: Glyphosate is a non-selective systemic herbicide with a broad spectrum of weed control that inhibits a key enzyme, 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase, in the shikimate pathway. OBJECTIVES: Isolation and analysis of the epsps (aroA) gene responsible for glyphosate-tolerance in bacteria from Roundup- contaminated soils was the aim of this study. MATERIALS AND METHODS: Sampling was done from the soil of the gardens which were heavily contaminated by Roundup herbicide and then bacterial screening was performed in the presence of high concentrations of glyphosate. The genus of bacterium was identified via molecular methods such as 16S rRNA sequencing. The aroA gene of this bacterium (aroA(HA-09)) was isolated using the primers designed-upon specific regions of aroA genes available in NCBI GenBank database. The PCR product was cloned, sequenced and subcloned into pET28a as an expression vector and transferred into E. coli strain BL21(DE3). The cells were inoculated in liquid M9 minimal medium containing IPTG and different concentrations of glyphosate. RESULTS: The genus of bacterium was identified as Pseudomonas sp. strain HA-09. The isolated aroA(HA-09) gene from this bacterium was approximately 2.2 kb in size. Bioassay of E. coli expressing this gene showed high tolerance to glyphosate (up to 300 mM). CONCLUSION: The aroA(HA-09) gene could be considered as a novel and efficient candidate for development of glyphosate-tolerant crop plants. National Institute of Genetic Engineering and Biotechnology 2020-07-01 /pmc/articles/PMC8035420/ /pubmed/33850947 http://dx.doi.org/10.30498/IJB.2020.204133.2597 Text en Copyright: © 2020 The Author(s); Published by Iranian Journal of Biotechnology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 Unported License, ( http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ghaderitabar, Hadi
Mousavi, Amir
Hatef Salmanian, Ali
Hadi, Faranak
Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran
title Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran
title_full Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran
title_fullStr Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran
title_full_unstemmed Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran
title_short Novel aroA of Glyphosate-Tolerant Bacterium Pseudomonas sp. Strain HA-09 Isolated from Roundup-Contaminated Garden Soils in Iran
title_sort novel aroa of glyphosate-tolerant bacterium pseudomonas sp. strain ha-09 isolated from roundup-contaminated garden soils in iran
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035420/
https://www.ncbi.nlm.nih.gov/pubmed/33850947
http://dx.doi.org/10.30498/IJB.2020.204133.2597
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