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Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs
Synthetic sRNAs allow knockdown of target genes at translational level, but have been restricted to a limited number of bacteria. Here, we report the development of a broad-host-range synthetic sRNA (BHR-sRNA) platform employing the RoxS scaffold and the Hfq chaperone from Bacillus subtilis. BHR-sRN...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126203/ https://www.ncbi.nlm.nih.gov/pubmed/37095132 http://dx.doi.org/10.1038/s41467-023-38119-y |
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author | Cho, Jae Sung Yang, Dongsoo Prabowo, Cindy Pricilia Surya Ghiffary, Mohammad Rifqi Han, Taehee Choi, Kyeong Rok Moon, Cheon Woo Zhou, Hengrui Ryu, Jae Yong Kim, Hyun Uk Lee, Sang Yup |
author_facet | Cho, Jae Sung Yang, Dongsoo Prabowo, Cindy Pricilia Surya Ghiffary, Mohammad Rifqi Han, Taehee Choi, Kyeong Rok Moon, Cheon Woo Zhou, Hengrui Ryu, Jae Yong Kim, Hyun Uk Lee, Sang Yup |
author_sort | Cho, Jae Sung |
collection | PubMed |
description | Synthetic sRNAs allow knockdown of target genes at translational level, but have been restricted to a limited number of bacteria. Here, we report the development of a broad-host-range synthetic sRNA (BHR-sRNA) platform employing the RoxS scaffold and the Hfq chaperone from Bacillus subtilis. BHR-sRNA is tested in 16 bacterial species including commensal, probiotic, pathogenic, and industrial bacteria, with >50% of target gene knockdown achieved in 12 bacterial species. For medical applications, virulence factors in Staphylococcus epidermidis and Klebsiella pneumoniae are knocked down to mitigate their virulence-associated phenotypes. For metabolic engineering applications, high performance Corynebacterium glutamicum strains capable of producing valerolactam (bulk chemical) and methyl anthranilate (fine chemical) are developed by combinatorial knockdown of target genes. A genome-scale sRNA library covering 2959 C. glutamicum genes is constructed for high-throughput colorimetric screening of indigoidine (natural colorant) overproducers. The BHR-sRNA platform will expedite engineering of diverse bacteria of both industrial and medical interest. |
format | Online Article Text |
id | pubmed-10126203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101262032023-04-26 Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs Cho, Jae Sung Yang, Dongsoo Prabowo, Cindy Pricilia Surya Ghiffary, Mohammad Rifqi Han, Taehee Choi, Kyeong Rok Moon, Cheon Woo Zhou, Hengrui Ryu, Jae Yong Kim, Hyun Uk Lee, Sang Yup Nat Commun Article Synthetic sRNAs allow knockdown of target genes at translational level, but have been restricted to a limited number of bacteria. Here, we report the development of a broad-host-range synthetic sRNA (BHR-sRNA) platform employing the RoxS scaffold and the Hfq chaperone from Bacillus subtilis. BHR-sRNA is tested in 16 bacterial species including commensal, probiotic, pathogenic, and industrial bacteria, with >50% of target gene knockdown achieved in 12 bacterial species. For medical applications, virulence factors in Staphylococcus epidermidis and Klebsiella pneumoniae are knocked down to mitigate their virulence-associated phenotypes. For metabolic engineering applications, high performance Corynebacterium glutamicum strains capable of producing valerolactam (bulk chemical) and methyl anthranilate (fine chemical) are developed by combinatorial knockdown of target genes. A genome-scale sRNA library covering 2959 C. glutamicum genes is constructed for high-throughput colorimetric screening of indigoidine (natural colorant) overproducers. The BHR-sRNA platform will expedite engineering of diverse bacteria of both industrial and medical interest. Nature Publishing Group UK 2023-04-24 /pmc/articles/PMC10126203/ /pubmed/37095132 http://dx.doi.org/10.1038/s41467-023-38119-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cho, Jae Sung Yang, Dongsoo Prabowo, Cindy Pricilia Surya Ghiffary, Mohammad Rifqi Han, Taehee Choi, Kyeong Rok Moon, Cheon Woo Zhou, Hengrui Ryu, Jae Yong Kim, Hyun Uk Lee, Sang Yup Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs |
title | Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs |
title_full | Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs |
title_fullStr | Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs |
title_full_unstemmed | Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs |
title_short | Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs |
title_sort | targeted and high-throughput gene knockdown in diverse bacteria using synthetic srnas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126203/ https://www.ncbi.nlm.nih.gov/pubmed/37095132 http://dx.doi.org/10.1038/s41467-023-38119-y |
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