Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens

Vibrio natriegens constitutes one of the fastest-growing nonpathogenic bacteria and a potential novel workhorse for many biotechnological applications. Here, we report the development of a Vibrio-based cell-free protein synthesis system (CFPS). Specifically, up to 0.4 g L-1 eGFP could be successfull...

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Main Authors: Jurek Failmezger, Steffen Scholz, Bastian Blombach, Martin Siemann-Herzberg
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-06-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2018.01146/full
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spelling doaj-1210ef623a1b4354b9d8f7dcd594cc762020-11-25T00:55:50ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2018-06-01910.3389/fmicb.2018.01146389251Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegensJurek FailmezgerSteffen ScholzBastian BlombachMartin Siemann-HerzbergVibrio natriegens constitutes one of the fastest-growing nonpathogenic bacteria and a potential novel workhorse for many biotechnological applications. Here, we report the development of a Vibrio-based cell-free protein synthesis system (CFPS). Specifically, up to 0.4 g L-1 eGFP could be successfully synthesized in small-scale batch reactions using cell-free extract obtained from fast-growing V. natriegens cultures. Versatile CFPS system characterization attained by combining the analyses of key metabolites for translation and ribosomes revealed limitations regarding rRNA stability and critical substrate consumption (e.g., amino acids). Alternatively, rRNA showed increased stability by inducing Mg2+homeostasis in the reaction. Although the enormous translation capacity of the CFPS system based on the available ribosome concentration could not yet be fully exploited, its potential was successfully demonstrated by activating an endogenous transcription unit with V. natriegensRNA polymerase (RNAP) for protein expression. This allowed the use of in vitro screening for promoter strength, a critical factor for efficient gene expression in vitro and in vivo. Three different promoters were tested and output signals corresponded well with the expected affinity for V. natriegens RNAP. This established CFPS toolbox may provide a foundation to establish V. natriegens as a valuable platform in biotechnology as well as synthetic biology.https://www.frontiersin.org/article/10.3389/fmicb.2018.01146/fullin vitro translationVibrio natriegensribosomesrRNAcell-free extract
collection DOAJ
language English
format Article
sources DOAJ
author Jurek Failmezger
Steffen Scholz
Bastian Blombach
Martin Siemann-Herzberg
spellingShingle Jurek Failmezger
Steffen Scholz
Bastian Blombach
Martin Siemann-Herzberg
Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens
Frontiers in Microbiology
in vitro translation
Vibrio natriegens
ribosomes
rRNA
cell-free extract
author_facet Jurek Failmezger
Steffen Scholz
Bastian Blombach
Martin Siemann-Herzberg
author_sort Jurek Failmezger
title Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens
title_short Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens
title_full Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens
title_fullStr Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens
title_full_unstemmed Cell-Free Protein Synthesis From Fast-Growing Vibrio natriegens
title_sort cell-free protein synthesis from fast-growing vibrio natriegens
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2018-06-01
description Vibrio natriegens constitutes one of the fastest-growing nonpathogenic bacteria and a potential novel workhorse for many biotechnological applications. Here, we report the development of a Vibrio-based cell-free protein synthesis system (CFPS). Specifically, up to 0.4 g L-1 eGFP could be successfully synthesized in small-scale batch reactions using cell-free extract obtained from fast-growing V. natriegens cultures. Versatile CFPS system characterization attained by combining the analyses of key metabolites for translation and ribosomes revealed limitations regarding rRNA stability and critical substrate consumption (e.g., amino acids). Alternatively, rRNA showed increased stability by inducing Mg2+homeostasis in the reaction. Although the enormous translation capacity of the CFPS system based on the available ribosome concentration could not yet be fully exploited, its potential was successfully demonstrated by activating an endogenous transcription unit with V. natriegensRNA polymerase (RNAP) for protein expression. This allowed the use of in vitro screening for promoter strength, a critical factor for efficient gene expression in vitro and in vivo. Three different promoters were tested and output signals corresponded well with the expected affinity for V. natriegens RNAP. This established CFPS toolbox may provide a foundation to establish V. natriegens as a valuable platform in biotechnology as well as synthetic biology.
topic in vitro translation
Vibrio natriegens
ribosomes
rRNA
cell-free extract
url https://www.frontiersin.org/article/10.3389/fmicb.2018.01146/full
work_keys_str_mv AT jurekfailmezger cellfreeproteinsynthesisfromfastgrowingvibrionatriegens
AT steffenscholz cellfreeproteinsynthesisfromfastgrowingvibrionatriegens
AT bastianblombach cellfreeproteinsynthesisfromfastgrowingvibrionatriegens
AT martinsiemannherzberg cellfreeproteinsynthesisfromfastgrowingvibrionatriegens
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