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Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL
BACKGROUND: In recent years, there have been intensive efforts to develop synthetic microbial platforms for the production, biosensing and bio-remediation of fossil fuel constituents such as alkanes. Building predictable engineered systems for these applications will require the ability to tightly c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822313/ https://www.ncbi.nlm.nih.gov/pubmed/27053948 http://dx.doi.org/10.1186/s13036-016-0026-3 |
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author | Call, Toby P. Akhtar, M. Kalim Baganz, Frank Grant, Chris |
author_facet | Call, Toby P. Akhtar, M. Kalim Baganz, Frank Grant, Chris |
author_sort | Call, Toby P. |
collection | PubMed |
description | BACKGROUND: In recent years, there have been intensive efforts to develop synthetic microbial platforms for the production, biosensing and bio-remediation of fossil fuel constituents such as alkanes. Building predictable engineered systems for these applications will require the ability to tightly control and modulate the rate of import of alkanes into the host cell. The native components responsible for the import of alkanes within these systems have yet to be elucidated. To shed further insights on this, we used the AlkBGT alkane monooxygenase complex from Pseudomonas putida GPo1 as a reporter system for assessing alkane import in Escherichia coli. Two native E. coli transporters, FadL and OmpW, were evaluated for octane import given their proven functionality in the uptake of fatty acids along with their structural similarity to the P. putida GPo1 alkane importer, AlkL. RESULTS: Octane import was removed with deletion of fadL, but was restored by complementation with a fadL-encoding plasmid. Furthermore, tuned overexpression of FadL increased the rate of alkane import by up to 4.5- fold. A FadL deletion strain displayed a small but significant degree of tolerance toward hexane and octane relative to the wild type, while the responsiveness of the well-known alkane biosensor, AlkS, toward octane and decane was strongly reduced by 2.7- and 2.9-fold, respectively. CONCLUSIONS: We unequivocally show for the first time that FadL serves as the major route for medium-chain alkane import in E. coli. The experimental approaches used within this study, which include an enzyme-based reporter system and a fluorescent alkane biosensor for quantification and real-time monitoring of alkane import, could be employed as part of an engineering toolkit for optimizing biological systems that depend on the uptake of alkanes. Thus, the findings will be particularly useful for biological applications such as bioremediation and biomanufacturing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13036-016-0026-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4822313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48223132016-04-07 Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL Call, Toby P. Akhtar, M. Kalim Baganz, Frank Grant, Chris J Biol Eng Research BACKGROUND: In recent years, there have been intensive efforts to develop synthetic microbial platforms for the production, biosensing and bio-remediation of fossil fuel constituents such as alkanes. Building predictable engineered systems for these applications will require the ability to tightly control and modulate the rate of import of alkanes into the host cell. The native components responsible for the import of alkanes within these systems have yet to be elucidated. To shed further insights on this, we used the AlkBGT alkane monooxygenase complex from Pseudomonas putida GPo1 as a reporter system for assessing alkane import in Escherichia coli. Two native E. coli transporters, FadL and OmpW, were evaluated for octane import given their proven functionality in the uptake of fatty acids along with their structural similarity to the P. putida GPo1 alkane importer, AlkL. RESULTS: Octane import was removed with deletion of fadL, but was restored by complementation with a fadL-encoding plasmid. Furthermore, tuned overexpression of FadL increased the rate of alkane import by up to 4.5- fold. A FadL deletion strain displayed a small but significant degree of tolerance toward hexane and octane relative to the wild type, while the responsiveness of the well-known alkane biosensor, AlkS, toward octane and decane was strongly reduced by 2.7- and 2.9-fold, respectively. CONCLUSIONS: We unequivocally show for the first time that FadL serves as the major route for medium-chain alkane import in E. coli. The experimental approaches used within this study, which include an enzyme-based reporter system and a fluorescent alkane biosensor for quantification and real-time monitoring of alkane import, could be employed as part of an engineering toolkit for optimizing biological systems that depend on the uptake of alkanes. Thus, the findings will be particularly useful for biological applications such as bioremediation and biomanufacturing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13036-016-0026-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-05 /pmc/articles/PMC4822313/ /pubmed/27053948 http://dx.doi.org/10.1186/s13036-016-0026-3 Text en © Call et al. 2016 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 Call, Toby P. Akhtar, M. Kalim Baganz, Frank Grant, Chris Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL |
title | Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL |
title_full | Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL |
title_fullStr | Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL |
title_full_unstemmed | Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL |
title_short | Modulating the import of medium-chain alkanes in E. coli through tuned expression of FadL |
title_sort | modulating the import of medium-chain alkanes in e. coli through tuned expression of fadl |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822313/ https://www.ncbi.nlm.nih.gov/pubmed/27053948 http://dx.doi.org/10.1186/s13036-016-0026-3 |
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