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Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli

A significant challenge in the field of in vitro synthetic biology is the construction of a self-reproducing cell-free translation system, which reproduces its components, such as translation proteins, through translation and transcription by itself. As a first step for such construction, in this st...

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Detalles Bibliográficos
Autores principales: Awai, Takako, Ichihashi, Norikazu, Yomo, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668874/
https://www.ncbi.nlm.nih.gov/pubmed/29124177
http://dx.doi.org/10.1016/j.bbrep.2015.08.006
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author Awai, Takako
Ichihashi, Norikazu
Yomo, Tetsuya
author_facet Awai, Takako
Ichihashi, Norikazu
Yomo, Tetsuya
author_sort Awai, Takako
collection PubMed
description A significant challenge in the field of in vitro synthetic biology is the construction of a self-reproducing cell-free translation system, which reproduces its components, such as translation proteins, through translation and transcription by itself. As a first step for such construction, in this study we expressed and evaluated the activity of 20 aminoacyl-tRNA synthetases (aaRSs), a major component of a translation system, in a reconstituted translation system (PURE system). We found that 19 aaRS with the exception of phenylalanyl-tRNA synthetase (PheRS) are expressed as soluble proteins and their activities are comparable to those expressed in Escherichia coli . This study provides basic information on the properties of aaRSs expressed in the PURE system, which will be helpful for the future reconstitution of a self-reproducing translation system.
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spelling pubmed-56688742017-11-09 Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli Awai, Takako Ichihashi, Norikazu Yomo, Tetsuya Biochem Biophys Rep Research Article A significant challenge in the field of in vitro synthetic biology is the construction of a self-reproducing cell-free translation system, which reproduces its components, such as translation proteins, through translation and transcription by itself. As a first step for such construction, in this study we expressed and evaluated the activity of 20 aminoacyl-tRNA synthetases (aaRSs), a major component of a translation system, in a reconstituted translation system (PURE system). We found that 19 aaRS with the exception of phenylalanyl-tRNA synthetase (PheRS) are expressed as soluble proteins and their activities are comparable to those expressed in Escherichia coli . This study provides basic information on the properties of aaRSs expressed in the PURE system, which will be helpful for the future reconstitution of a self-reproducing translation system. Elsevier 2015-08-08 /pmc/articles/PMC5668874/ /pubmed/29124177 http://dx.doi.org/10.1016/j.bbrep.2015.08.006 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Awai, Takako
Ichihashi, Norikazu
Yomo, Tetsuya
Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli
title Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli
title_full Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli
title_fullStr Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli
title_full_unstemmed Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli
title_short Activities of 20 aminoacyl-tRNA synthetases expressed in a reconstituted translation system in Escherichia coli
title_sort activities of 20 aminoacyl-trna synthetases expressed in a reconstituted translation system in escherichia coli
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668874/
https://www.ncbi.nlm.nih.gov/pubmed/29124177
http://dx.doi.org/10.1016/j.bbrep.2015.08.006
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