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Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803

Cyanobacteria are an attractive host for biofuel production because they can produce valuable chemical compounds from CO(2) fixed by photosynthesis. However, the available genetic tools that enable precise gene regulation for the applications of synthetic biology are insufficient. Previously, we eng...

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Detalles Bibliográficos
Autores principales: Sakai, Yuta, Abe, Koichi, Nakashima, Saki, Ellinger, James J, Ferri, Stefano, Sode, Koji, Ikebukuro, Kazunori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554450/
https://www.ncbi.nlm.nih.gov/pubmed/25865486
http://dx.doi.org/10.1002/mbo3.257
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author Sakai, Yuta
Abe, Koichi
Nakashima, Saki
Ellinger, James J
Ferri, Stefano
Sode, Koji
Ikebukuro, Kazunori
author_facet Sakai, Yuta
Abe, Koichi
Nakashima, Saki
Ellinger, James J
Ferri, Stefano
Sode, Koji
Ikebukuro, Kazunori
author_sort Sakai, Yuta
collection PubMed
description Cyanobacteria are an attractive host for biofuel production because they can produce valuable chemical compounds from CO(2) fixed by photosynthesis. However, the available genetic tools that enable precise gene regulation for the applications of synthetic biology are insufficient. Previously, we engineered an RNA-based posttranscriptional regulator, termed riboregulator, for the control of target gene expression in cyanobacterium Synechocystis sp. PCC 6803. Moreover, we enhanced the gene regulation ability of the riboregulators in Escherichia coli by fusing and engineering a scaffold sequence derived from naturally occurring E. coli noncoding small RNAs. Here, we demonstrated that the scaffold sequence fused to the riboregulators improved their gene regulation ability in Synechocystis sp. PCC 6803. To further improve gene regulation, we expressed an exogenous RNA chaperone protein that is responsible for noncoding small RNA-mediated gene regulation, which resulted in higher target gene expression. The scaffold sequence derived from natural E. coli noncoding small RNAs is effective for designing RNA-based genetic tools and scaffold-fused riboregulators are a strong RNA-tool to regulate gene expression in cyanobacteria.
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spelling pubmed-45544502015-09-03 Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803 Sakai, Yuta Abe, Koichi Nakashima, Saki Ellinger, James J Ferri, Stefano Sode, Koji Ikebukuro, Kazunori Microbiologyopen Original Research Cyanobacteria are an attractive host for biofuel production because they can produce valuable chemical compounds from CO(2) fixed by photosynthesis. However, the available genetic tools that enable precise gene regulation for the applications of synthetic biology are insufficient. Previously, we engineered an RNA-based posttranscriptional regulator, termed riboregulator, for the control of target gene expression in cyanobacterium Synechocystis sp. PCC 6803. Moreover, we enhanced the gene regulation ability of the riboregulators in Escherichia coli by fusing and engineering a scaffold sequence derived from naturally occurring E. coli noncoding small RNAs. Here, we demonstrated that the scaffold sequence fused to the riboregulators improved their gene regulation ability in Synechocystis sp. PCC 6803. To further improve gene regulation, we expressed an exogenous RNA chaperone protein that is responsible for noncoding small RNA-mediated gene regulation, which resulted in higher target gene expression. The scaffold sequence derived from natural E. coli noncoding small RNAs is effective for designing RNA-based genetic tools and scaffold-fused riboregulators are a strong RNA-tool to regulate gene expression in cyanobacteria. John Wiley & Sons, Ltd 2015-08 2015-04-10 /pmc/articles/PMC4554450/ /pubmed/25865486 http://dx.doi.org/10.1002/mbo3.257 Text en © 2015 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sakai, Yuta
Abe, Koichi
Nakashima, Saki
Ellinger, James J
Ferri, Stefano
Sode, Koji
Ikebukuro, Kazunori
Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803
title Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803
title_full Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803
title_fullStr Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803
title_full_unstemmed Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803
title_short Scaffold-fused riboregulators for enhanced gene activation in Synechocystis sp. PCC 6803
title_sort scaffold-fused riboregulators for enhanced gene activation in synechocystis sp. pcc 6803
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554450/
https://www.ncbi.nlm.nih.gov/pubmed/25865486
http://dx.doi.org/10.1002/mbo3.257
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