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Quantifying heterologous gene expression during ectopic MazF production in Escherichia coli

Quantifying heterologous gene expression during ectopic MazF production in Escherichia coli
Quantifying heterologous gene expression during ectopic MazF production in Escherichia coli

OBJECTIVE: MazF is a sequence-specific endoribonuclease-toxin of the MazEF toxin-antitoxin system. MazF cleaves single-stranded ribonucleic acid (RNA) regions at adenine-cytosine-adenine (ACA) sequences in the bacterium Escherichia coli. The MazEF system has been used in various biotechnology and synthetic biology applications. In this study, we infer how ectopic mazF overexpression affects production of heterologous proteins. To this end, we quantified the levels of fluorescent proteins expressed in E. coli from reporters translated from the ACA-containing or ACA-less messenger RNAs (mRNAs). Additionally, we addressed the impact of the 5'-untranslated region of these reporter mRNAs under the same conditions by comparing expression from mRNAs that comprise (canonical mRNA) or lack this region (leaderless mRNA).

RESULTS: Flow cytometry analysis indicates that during mazF overexpression, fluorescent proteins are translated from the canonical as well as leaderless mRNAs. Our analysis further indicates that longer mazF overexpression generally increases the concentration of fluorescent proteins translated from ACA-less mRNAs, however it also substantially increases bacterial population heterogeneity. Finally, our results suggest that the strength and duration of mazF overexpression should be optimized for each experimental setup, to maximize the heterologous protein production and minimize the amount of phenotypic heterogeneity in bacterial populations, which is unfavorable in biotechnological processes.

5' Untranslated Regions, Adenine, DNA-Binding Proteins/genetics, Endoribonucleases/genetics, Escherichia coli/genetics, Escherichia coli Proteins/genetics, Gene Expression, RNA, Messenger/genetics
1756-0500
173
Nikolic, Nela
88a8f576-d9e2-4eb6-9219-39b7065963d3
Sauert, Martina
038a8905-c79f-4857-a286-5f8ee13e54b2
Albanese, Tanino G
a094abca-278a-452c-8d2b-2875bce87650
Moll, Isabella
6590eadb-b495-4ccf-b461-b68a4ea2e2b6
Nikolic, Nela
88a8f576-d9e2-4eb6-9219-39b7065963d3
Sauert, Martina
038a8905-c79f-4857-a286-5f8ee13e54b2
Albanese, Tanino G
a094abca-278a-452c-8d2b-2875bce87650
Moll, Isabella
6590eadb-b495-4ccf-b461-b68a4ea2e2b6

Nikolic, Nela, Sauert, Martina, Albanese, Tanino G and Moll, Isabella (2022) Quantifying heterologous gene expression during ectopic MazF production in Escherichia coli. BMC Research Notes, 15 (1), 173. (doi:10.1186/s13104-022-06061-9).

Record type: Article

Abstract

OBJECTIVE: MazF is a sequence-specific endoribonuclease-toxin of the MazEF toxin-antitoxin system. MazF cleaves single-stranded ribonucleic acid (RNA) regions at adenine-cytosine-adenine (ACA) sequences in the bacterium Escherichia coli. The MazEF system has been used in various biotechnology and synthetic biology applications. In this study, we infer how ectopic mazF overexpression affects production of heterologous proteins. To this end, we quantified the levels of fluorescent proteins expressed in E. coli from reporters translated from the ACA-containing or ACA-less messenger RNAs (mRNAs). Additionally, we addressed the impact of the 5'-untranslated region of these reporter mRNAs under the same conditions by comparing expression from mRNAs that comprise (canonical mRNA) or lack this region (leaderless mRNA).

RESULTS: Flow cytometry analysis indicates that during mazF overexpression, fluorescent proteins are translated from the canonical as well as leaderless mRNAs. Our analysis further indicates that longer mazF overexpression generally increases the concentration of fluorescent proteins translated from ACA-less mRNAs, however it also substantially increases bacterial population heterogeneity. Finally, our results suggest that the strength and duration of mazF overexpression should be optimized for each experimental setup, to maximize the heterologous protein production and minimize the amount of phenotypic heterogeneity in bacterial populations, which is unfavorable in biotechnological processes.

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More information

Accepted/In Press date: 28 April 2022
Published date: 13 May 2022
Additional Information: © 2022. The Author(s).
Keywords: 5' Untranslated Regions, Adenine, DNA-Binding Proteins/genetics, Endoribonucleases/genetics, Escherichia coli/genetics, Escherichia coli Proteins/genetics, Gene Expression, RNA, Messenger/genetics

Identifiers

Local EPrints ID: 488044
URI: http://eprints.soton.ac.uk/id/eprint/488044
ISSN: 1756-0500
PURE UUID: 01f9422b-248a-48a9-8889-3e89ca96b53f
ORCID for Nela Nikolic: ORCID iD orcid.org/0000-0001-9068-6090

Catalogue record

Date deposited: 12 Mar 2024 18:26
Last modified: 18 Mar 2024 04:18

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Contributors

Author: Nela Nikolic ORCID iD
Author: Martina Sauert
Author: Tanino G Albanese
Author: Isabella Moll

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