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Targeted mutagenesis: A sniper-like diversity generator in microbial engineering

Mutations, serving as the raw materials of evolution, have been extensively utilized to increase the chances of engineering molecules or microbes with tailor-made functions. Global and targeted mutagenesis are two main methods of obtaining various mutations, distinguished by the range of action they...

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Detalles Bibliográficos
Autores principales: Zheng, Xiang, Xing, Xin-Hui, Zhang, Chong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636951/
https://www.ncbi.nlm.nih.gov/pubmed/29062964
http://dx.doi.org/10.1016/j.synbio.2017.07.001
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author Zheng, Xiang
Xing, Xin-Hui
Zhang, Chong
author_facet Zheng, Xiang
Xing, Xin-Hui
Zhang, Chong
author_sort Zheng, Xiang
collection PubMed
description Mutations, serving as the raw materials of evolution, have been extensively utilized to increase the chances of engineering molecules or microbes with tailor-made functions. Global and targeted mutagenesis are two main methods of obtaining various mutations, distinguished by the range of action they can cover. While the former one stresses the mining of novel genetic loci within the whole genomic background, targeted mutagenesis performs in a more straightforward manner, bringing evolutionary escape and error catastrophe under control. In this review, we classify the existing techniques of targeted mutagenesis into two categories in terms of whether the diversity is generated in vitro or in vivo, and briefly introduce the mechanisms and applications of them separately. The inherent connections and development trends of the two classes are also discussed to provide an insight into the next generation evolution research.
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spelling pubmed-56369512017-10-23 Targeted mutagenesis: A sniper-like diversity generator in microbial engineering Zheng, Xiang Xing, Xin-Hui Zhang, Chong Synth Syst Biotechnol Article Mutations, serving as the raw materials of evolution, have been extensively utilized to increase the chances of engineering molecules or microbes with tailor-made functions. Global and targeted mutagenesis are two main methods of obtaining various mutations, distinguished by the range of action they can cover. While the former one stresses the mining of novel genetic loci within the whole genomic background, targeted mutagenesis performs in a more straightforward manner, bringing evolutionary escape and error catastrophe under control. In this review, we classify the existing techniques of targeted mutagenesis into two categories in terms of whether the diversity is generated in vitro or in vivo, and briefly introduce the mechanisms and applications of them separately. The inherent connections and development trends of the two classes are also discussed to provide an insight into the next generation evolution research. KeAi Publishing 2017-07-14 /pmc/articles/PMC5636951/ /pubmed/29062964 http://dx.doi.org/10.1016/j.synbio.2017.07.001 Text en © 2017 Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co. 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 Article
Zheng, Xiang
Xing, Xin-Hui
Zhang, Chong
Targeted mutagenesis: A sniper-like diversity generator in microbial engineering
title Targeted mutagenesis: A sniper-like diversity generator in microbial engineering
title_full Targeted mutagenesis: A sniper-like diversity generator in microbial engineering
title_fullStr Targeted mutagenesis: A sniper-like diversity generator in microbial engineering
title_full_unstemmed Targeted mutagenesis: A sniper-like diversity generator in microbial engineering
title_short Targeted mutagenesis: A sniper-like diversity generator in microbial engineering
title_sort targeted mutagenesis: a sniper-like diversity generator in microbial engineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636951/
https://www.ncbi.nlm.nih.gov/pubmed/29062964
http://dx.doi.org/10.1016/j.synbio.2017.07.001
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