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Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes
BACKGROUND: Transcription factor-based biosensors are useful tools for the detection of metabolites and industrially valuable molecules, and present many potential applications in biotechnology and biomedicine. However, the most common approach to develop biosensors relies on employing a limited set...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882365/ https://www.ncbi.nlm.nih.gov/pubmed/31798685 http://dx.doi.org/10.1186/s13036-019-0214-z |
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author | F. M. Machado, Leopoldo Currin, Andrew Dixon, Neil |
author_facet | F. M. Machado, Leopoldo Currin, Andrew Dixon, Neil |
author_sort | F. M. Machado, Leopoldo |
collection | PubMed |
description | BACKGROUND: Transcription factor-based biosensors are useful tools for the detection of metabolites and industrially valuable molecules, and present many potential applications in biotechnology and biomedicine. However, the most common approach to develop biosensors relies on employing a limited set of naturally occurring allosteric transcription factors (aTFs). Therefore, altering the ligand specificity of aTFs towards the detection of new effectors is an important goal. RESULTS: Here, the PcaV repressor, a member of the MarR aTF family, was used to develop a biosensor for the detection of hydroxyl-substituted benzoic acids, including protocatechuic acid (PCA). The PCA biosensor was further subjected to directed evolution to alter its ligand specificity towards vanillin and other closely related aromatic aldehydes, to generate the Van2 biosensor. Ligand recognition of Van2 was explored in vitro using a range of biochemical and biophysical analyses, and extensive in vivo genetic-phenotypic analysis was performed to determine the role of each amino acid change upon biosensor performance. CONCLUSIONS: This is the first study to report directed evolution of a member of the MarR aTF family, and demonstrates the plasticity of the PCA biosensor by altering its ligand specificity to generate a biosensor for aromatic aldehydes. |
format | Online Article Text |
id | pubmed-6882365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68823652019-12-03 Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes F. M. Machado, Leopoldo Currin, Andrew Dixon, Neil J Biol Eng Research BACKGROUND: Transcription factor-based biosensors are useful tools for the detection of metabolites and industrially valuable molecules, and present many potential applications in biotechnology and biomedicine. However, the most common approach to develop biosensors relies on employing a limited set of naturally occurring allosteric transcription factors (aTFs). Therefore, altering the ligand specificity of aTFs towards the detection of new effectors is an important goal. RESULTS: Here, the PcaV repressor, a member of the MarR aTF family, was used to develop a biosensor for the detection of hydroxyl-substituted benzoic acids, including protocatechuic acid (PCA). The PCA biosensor was further subjected to directed evolution to alter its ligand specificity towards vanillin and other closely related aromatic aldehydes, to generate the Van2 biosensor. Ligand recognition of Van2 was explored in vitro using a range of biochemical and biophysical analyses, and extensive in vivo genetic-phenotypic analysis was performed to determine the role of each amino acid change upon biosensor performance. CONCLUSIONS: This is the first study to report directed evolution of a member of the MarR aTF family, and demonstrates the plasticity of the PCA biosensor by altering its ligand specificity to generate a biosensor for aromatic aldehydes. BioMed Central 2019-11-27 /pmc/articles/PMC6882365/ /pubmed/31798685 http://dx.doi.org/10.1186/s13036-019-0214-z Text en © The Author(s). 2019 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 | Research F. M. Machado, Leopoldo Currin, Andrew Dixon, Neil Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes |
title | Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes |
title_full | Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes |
title_fullStr | Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes |
title_full_unstemmed | Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes |
title_short | Directed evolution of the PcaV allosteric transcription factor to generate a biosensor for aromatic aldehydes |
title_sort | directed evolution of the pcav allosteric transcription factor to generate a biosensor for aromatic aldehydes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882365/ https://www.ncbi.nlm.nih.gov/pubmed/31798685 http://dx.doi.org/10.1186/s13036-019-0214-z |
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