Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Call, Toby P., Akhtar, M. Kalim, Baganz, Frank, Grant, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
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
_version_ 1782425763169959936
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
work_keys_str_mv AT calltobyp modulatingtheimportofmediumchainalkanesinecolithroughtunedexpressionoffadl
AT akhtarmkalim modulatingtheimportofmediumchainalkanesinecolithroughtunedexpressionoffadl
AT baganzfrank modulatingtheimportofmediumchainalkanesinecolithroughtunedexpressionoffadl
AT grantchris modulatingtheimportofmediumchainalkanesinecolithroughtunedexpressionoffadl