Cargando…
Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis
BACKGROUND: Mutational technology has been used to achieve genome-wide variations in laboratory and industrial microorganisms. Genetic polymorphisms of natural genome evolution include nucleotide variations and structural variations, which inspired us to suggest that both types of genotypic variatio...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082887/ https://www.ncbi.nlm.nih.gov/pubmed/35527251 http://dx.doi.org/10.1186/s12934-022-01793-6 |
_version_ | 1784703301135106048 |
---|---|
author | Jin, Jin Jia, Bin Yuan, Ying-Jin |
author_facet | Jin, Jin Jia, Bin Yuan, Ying-Jin |
author_sort | Jin, Jin |
collection | PubMed |
description | BACKGROUND: Mutational technology has been used to achieve genome-wide variations in laboratory and industrial microorganisms. Genetic polymorphisms of natural genome evolution include nucleotide variations and structural variations, which inspired us to suggest that both types of genotypic variations are potentially useful in improving the performance of chassis cells for industrial applications. However, highly efficient approaches that simultaneously generate structural and nucleotide variations are still lacking. RESULTS: The aim of this study was to develop a method of increasing biosynthesis of astaxanthin in yeast by Combining Nucleotide variations And Structure variations (CNAS), which were generated by combinations of Atmospheric and room temperature plasma (ARTP) and Synthetic Chromosome Recombination and Modification by LoxP-Mediated Evolution (SCRaMbLE) system. CNAS was applied to increase the biosynthesis of astaxanthin in yeast and resulted in improvements of 2.2- and 7.0-fold in the yield of astaxanthin. Furthermore, this method was shown to be able to generate structures (deletion, duplication, and inversion) as well as nucleotide variations (SNPs and InDels) simultaneously. Additionally, genetic analysis of the genotypic variations of an astaxanthin improved strain revealed that the deletion of YJR116W and the C2481G mutation of YOL084W enhanced yield of astaxanthin, suggesting a genotype-to-phenotype relationship. CONCLUSIONS: This study demonstrated that the CNAS strategy could generate both structure variations and nucleotide variations, allowing the enhancement of astaxanthin yield by different genotypes in yeast. Overall, this study provided a valuable tool for generating genomic variation diversity that has desirable phenotypes as well as for knowing the relationship between genotypes and phenotypes in evolutionary processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01793-6. |
format | Online Article Text |
id | pubmed-9082887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90828872022-05-10 Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis Jin, Jin Jia, Bin Yuan, Ying-Jin Microb Cell Fact Research BACKGROUND: Mutational technology has been used to achieve genome-wide variations in laboratory and industrial microorganisms. Genetic polymorphisms of natural genome evolution include nucleotide variations and structural variations, which inspired us to suggest that both types of genotypic variations are potentially useful in improving the performance of chassis cells for industrial applications. However, highly efficient approaches that simultaneously generate structural and nucleotide variations are still lacking. RESULTS: The aim of this study was to develop a method of increasing biosynthesis of astaxanthin in yeast by Combining Nucleotide variations And Structure variations (CNAS), which were generated by combinations of Atmospheric and room temperature plasma (ARTP) and Synthetic Chromosome Recombination and Modification by LoxP-Mediated Evolution (SCRaMbLE) system. CNAS was applied to increase the biosynthesis of astaxanthin in yeast and resulted in improvements of 2.2- and 7.0-fold in the yield of astaxanthin. Furthermore, this method was shown to be able to generate structures (deletion, duplication, and inversion) as well as nucleotide variations (SNPs and InDels) simultaneously. Additionally, genetic analysis of the genotypic variations of an astaxanthin improved strain revealed that the deletion of YJR116W and the C2481G mutation of YOL084W enhanced yield of astaxanthin, suggesting a genotype-to-phenotype relationship. CONCLUSIONS: This study demonstrated that the CNAS strategy could generate both structure variations and nucleotide variations, allowing the enhancement of astaxanthin yield by different genotypes in yeast. Overall, this study provided a valuable tool for generating genomic variation diversity that has desirable phenotypes as well as for knowing the relationship between genotypes and phenotypes in evolutionary processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01793-6. BioMed Central 2022-05-09 /pmc/articles/PMC9082887/ /pubmed/35527251 http://dx.doi.org/10.1186/s12934-022-01793-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Jin, Jin Jia, Bin Yuan, Ying-Jin Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
title | Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
title_full | Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
title_fullStr | Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
title_full_unstemmed | Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
title_short | Combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
title_sort | combining nucleotide variations and structure variations for improving astaxanthin biosynthesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082887/ https://www.ncbi.nlm.nih.gov/pubmed/35527251 http://dx.doi.org/10.1186/s12934-022-01793-6 |
work_keys_str_mv | AT jinjin combiningnucleotidevariationsandstructurevariationsforimprovingastaxanthinbiosynthesis AT jiabin combiningnucleotidevariationsandstructurevariationsforimprovingastaxanthinbiosynthesis AT yuanyingjin combiningnucleotidevariationsandstructurevariationsforimprovingastaxanthinbiosynthesis |