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Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium
Strains of Clostridium genus are used for production of various value-added products including fuels and chemicals. Development of any commercially viable production process requires a combination of both strain and fermentation process development strategies. The strain development in Clostridium s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181999/ https://www.ncbi.nlm.nih.gov/pubmed/32363182 http://dx.doi.org/10.3389/fbioe.2020.00282 |
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author | Kwon, Seong Woo Paari, Kuppusamy Alagesan Malaviya, Alok Jang, Yu-Sin |
author_facet | Kwon, Seong Woo Paari, Kuppusamy Alagesan Malaviya, Alok Jang, Yu-Sin |
author_sort | Kwon, Seong Woo |
collection | PubMed |
description | Strains of Clostridium genus are used for production of various value-added products including fuels and chemicals. Development of any commercially viable production process requires a combination of both strain and fermentation process development strategies. The strain development in Clostridium sp. could be achieved by random mutagenesis, and targeted gene alteration methods. However, strain improvement in Clostridium sp. by targeted gene alteration method was challenging due to the lack of efficient tools for genome and transcriptome engineering in this organism. Recently, various synthetic biology tools have been developed to facilitate the strain engineering of solventogenic Clostridium. In this review, we consolidated the recent advancements in toolbox development for genome and transcriptome engineering in solventogenic Clostridium. Here we reviewed the genome-engineering tools employing mobile group II intron, pyrE alleles exchange, and CRISPR/Cas9 with their application for strain development of Clostridium sp. Next, transcriptome engineering tools such as untranslated region (UTR) engineering and synthetic sRNA techniques were also discussed in context of Clostridium strain engineering. Application of any of these discussed techniques will facilitate the metabolic engineering of clostridia for development of improved strains with respect to requisite functional attributes. This might lead to the development of an economically viable butanol production process with improved titer, yield and productivity. |
format | Online Article Text |
id | pubmed-7181999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71819992020-05-01 Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium Kwon, Seong Woo Paari, Kuppusamy Alagesan Malaviya, Alok Jang, Yu-Sin Front Bioeng Biotechnol Bioengineering and Biotechnology Strains of Clostridium genus are used for production of various value-added products including fuels and chemicals. Development of any commercially viable production process requires a combination of both strain and fermentation process development strategies. The strain development in Clostridium sp. could be achieved by random mutagenesis, and targeted gene alteration methods. However, strain improvement in Clostridium sp. by targeted gene alteration method was challenging due to the lack of efficient tools for genome and transcriptome engineering in this organism. Recently, various synthetic biology tools have been developed to facilitate the strain engineering of solventogenic Clostridium. In this review, we consolidated the recent advancements in toolbox development for genome and transcriptome engineering in solventogenic Clostridium. Here we reviewed the genome-engineering tools employing mobile group II intron, pyrE alleles exchange, and CRISPR/Cas9 with their application for strain development of Clostridium sp. Next, transcriptome engineering tools such as untranslated region (UTR) engineering and synthetic sRNA techniques were also discussed in context of Clostridium strain engineering. Application of any of these discussed techniques will facilitate the metabolic engineering of clostridia for development of improved strains with respect to requisite functional attributes. This might lead to the development of an economically viable butanol production process with improved titer, yield and productivity. Frontiers Media S.A. 2020-04-16 /pmc/articles/PMC7181999/ /pubmed/32363182 http://dx.doi.org/10.3389/fbioe.2020.00282 Text en Copyright © 2020 Kwon, Paari, Malaviya and Jang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Kwon, Seong Woo Paari, Kuppusamy Alagesan Malaviya, Alok Jang, Yu-Sin Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium |
title | Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium |
title_full | Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium |
title_fullStr | Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium |
title_full_unstemmed | Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium |
title_short | Synthetic Biology Tools for Genome and Transcriptome Engineering of Solventogenic Clostridium |
title_sort | synthetic biology tools for genome and transcriptome engineering of solventogenic clostridium |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181999/ https://www.ncbi.nlm.nih.gov/pubmed/32363182 http://dx.doi.org/10.3389/fbioe.2020.00282 |
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