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• W1976041330 abstract "Cyanobacteria are an attractive host for biofuel production because they can produce valuable chemical compounds from CO2 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." @default.
• W1976041330 created "2016-06-24" @default.
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• W1976041330 date "2015-04-10" @default.
• W1976041330 modified "2023-09-27" @default.
• W1976041330 title "Scaffold‐fused riboregulators for enhanced gene activation in <i>Synechocystis</i> sp. <scp>PCC</scp> 6803" @default.
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• W1976041330 doi "https://doi.org/10.1002/mbo3.257" @default.
• W1976041330 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4554450" @default.
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