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Plasmids for Independently Tunable, Low-Noise Expression of Two Genes

Some microbiology experiments and biotechnology applications can be improved if it is possible to tune the expression of two different genes at the same time with cell-to-cell variation at or below the level of genes constitutively expressed from the chromosome (the “extrinsic noise limit”). This wa...

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Autores principales: Silva, João P. N., Lopes, Soraia Vidigal, Grilo, Diogo J., Hensel, Zach
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541738/
https://www.ncbi.nlm.nih.gov/pubmed/31142623
http://dx.doi.org/10.1128/mSphere.00340-19
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author Silva, João P. N.
Lopes, Soraia Vidigal
Grilo, Diogo J.
Hensel, Zach
author_facet Silva, João P. N.
Lopes, Soraia Vidigal
Grilo, Diogo J.
Hensel, Zach
author_sort Silva, João P. N.
collection PubMed
description Some microbiology experiments and biotechnology applications can be improved if it is possible to tune the expression of two different genes at the same time with cell-to-cell variation at or below the level of genes constitutively expressed from the chromosome (the “extrinsic noise limit”). This was recently achieved for a single gene by exploiting negative autoregulation by the tetracycline repressor (TetR) and bicistronic gene expression to reduce gene expression noise. We report new plasmids that use the same principles to achieve simultaneous, low-noise expression for two genes in Escherichia coli. The TetR system was moved to a compatible plasmid backbone, and a system based on the lac repressor (LacI) was found to also exhibit gene expression noise below the extrinsic noise limit. We characterized gene expression mean and noise across the range of induction levels for these plasmids, applied the LacI system to tune expression for single-molecule mRNA detection under two different growth conditions, and showed that two plasmids can be cotransformed to independently tune expression of two different genes. IMPORTANCE Microbiologists often express foreign proteins in bacteria in order study them or to use bacteria as a microbial factory. Usually, this requires controlling the number of foreign proteins expressed in each cell, but for many common protein expression systems, it is difficult to “tune” protein expression without large cell-to-cell variation in expression levels (called “noise” in protein expression). This work describes two protein expression systems that can be combined in the same cell, with tunable expression levels and very low protein expression noise. One new system was used to detect single mRNA molecules by fluorescence microscopy, and the two systems were shown to be independent of each other. These protein expression systems may be useful in any experiment or biotechnology application that can be improved with low protein expression noise.
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spelling pubmed-65417382019-06-14 Plasmids for Independently Tunable, Low-Noise Expression of Two Genes Silva, João P. N. Lopes, Soraia Vidigal Grilo, Diogo J. Hensel, Zach mSphere Resource Report Some microbiology experiments and biotechnology applications can be improved if it is possible to tune the expression of two different genes at the same time with cell-to-cell variation at or below the level of genes constitutively expressed from the chromosome (the “extrinsic noise limit”). This was recently achieved for a single gene by exploiting negative autoregulation by the tetracycline repressor (TetR) and bicistronic gene expression to reduce gene expression noise. We report new plasmids that use the same principles to achieve simultaneous, low-noise expression for two genes in Escherichia coli. The TetR system was moved to a compatible plasmid backbone, and a system based on the lac repressor (LacI) was found to also exhibit gene expression noise below the extrinsic noise limit. We characterized gene expression mean and noise across the range of induction levels for these plasmids, applied the LacI system to tune expression for single-molecule mRNA detection under two different growth conditions, and showed that two plasmids can be cotransformed to independently tune expression of two different genes. IMPORTANCE Microbiologists often express foreign proteins in bacteria in order study them or to use bacteria as a microbial factory. Usually, this requires controlling the number of foreign proteins expressed in each cell, but for many common protein expression systems, it is difficult to “tune” protein expression without large cell-to-cell variation in expression levels (called “noise” in protein expression). This work describes two protein expression systems that can be combined in the same cell, with tunable expression levels and very low protein expression noise. One new system was used to detect single mRNA molecules by fluorescence microscopy, and the two systems were shown to be independent of each other. These protein expression systems may be useful in any experiment or biotechnology application that can be improved with low protein expression noise. American Society for Microbiology 2019-05-29 /pmc/articles/PMC6541738/ /pubmed/31142623 http://dx.doi.org/10.1128/mSphere.00340-19 Text en Copyright © 2019 Silva et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Resource Report
Silva, João P. N.
Lopes, Soraia Vidigal
Grilo, Diogo J.
Hensel, Zach
Plasmids for Independently Tunable, Low-Noise Expression of Two Genes
title Plasmids for Independently Tunable, Low-Noise Expression of Two Genes
title_full Plasmids for Independently Tunable, Low-Noise Expression of Two Genes
title_fullStr Plasmids for Independently Tunable, Low-Noise Expression of Two Genes
title_full_unstemmed Plasmids for Independently Tunable, Low-Noise Expression of Two Genes
title_short Plasmids for Independently Tunable, Low-Noise Expression of Two Genes
title_sort plasmids for independently tunable, low-noise expression of two genes
topic Resource Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541738/
https://www.ncbi.nlm.nih.gov/pubmed/31142623
http://dx.doi.org/10.1128/mSphere.00340-19
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