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Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides
Rhodotorula toruloides is a potential chassis for microbial cell factories as this yeast can metabolise different substrates into a diverse range of natural products, but the lack of efficient synthetic biology tools hinders its applicability. In this study, the modular, versatile and efficient Gold...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157227/ https://www.ncbi.nlm.nih.gov/pubmed/35662893 http://dx.doi.org/10.1016/j.mec.2022.e00200 |
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author | Bonturi, Nemailla Pinheiro, Marina Julio de Oliveira, Paola Monteiro Rusadze, Eka Eichinger, Tobias Liudžiūtė, Gintare De Biaggi, Juliano Sabedotti Brauer, Age Remm, Maido Miranda, Everson Alves Ledesma-Amaro, Rodrigo Lahtvee, Petri-Jaan |
author_facet | Bonturi, Nemailla Pinheiro, Marina Julio de Oliveira, Paola Monteiro Rusadze, Eka Eichinger, Tobias Liudžiūtė, Gintare De Biaggi, Juliano Sabedotti Brauer, Age Remm, Maido Miranda, Everson Alves Ledesma-Amaro, Rodrigo Lahtvee, Petri-Jaan |
author_sort | Bonturi, Nemailla |
collection | PubMed |
description | Rhodotorula toruloides is a potential chassis for microbial cell factories as this yeast can metabolise different substrates into a diverse range of natural products, but the lack of efficient synthetic biology tools hinders its applicability. In this study, the modular, versatile and efficient Golden Gate DNA assembly system (RtGGA) was adapted to the first basidiomycete, an oleaginous yeast R. toruloides. R. toruloides CCT 0783 was sequenced, and used for the GGA design. The DNA fragments were assembled with predesigned 4-nt overhangs and a library of standardized parts was created containing promoters, genes, terminators, insertional regions, and resistance genes. The library was combined to create cassettes for the characterization of promoters strength and to overexpress the carotenoid production pathway. A variety of reagents, plasmids, and strategies were used and the RtGGA proved to be robust. The RtGGA was used to build three versions of the carotenoid overexpression cassette by using different promoter combinations. The cassettes were transformed into R. toruloides and the three new strains were characterized. Total carotenoid concentration increased by 41%. The dedicated GGA platform fills a gap in the advanced genome engineering toolkit for R. toruloides, enabling the efficient design of complex metabolic pathways. |
format | Online Article Text |
id | pubmed-9157227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91572272022-06-02 Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides Bonturi, Nemailla Pinheiro, Marina Julio de Oliveira, Paola Monteiro Rusadze, Eka Eichinger, Tobias Liudžiūtė, Gintare De Biaggi, Juliano Sabedotti Brauer, Age Remm, Maido Miranda, Everson Alves Ledesma-Amaro, Rodrigo Lahtvee, Petri-Jaan Metab Eng Commun Full Length Article Rhodotorula toruloides is a potential chassis for microbial cell factories as this yeast can metabolise different substrates into a diverse range of natural products, but the lack of efficient synthetic biology tools hinders its applicability. In this study, the modular, versatile and efficient Golden Gate DNA assembly system (RtGGA) was adapted to the first basidiomycete, an oleaginous yeast R. toruloides. R. toruloides CCT 0783 was sequenced, and used for the GGA design. The DNA fragments were assembled with predesigned 4-nt overhangs and a library of standardized parts was created containing promoters, genes, terminators, insertional regions, and resistance genes. The library was combined to create cassettes for the characterization of promoters strength and to overexpress the carotenoid production pathway. A variety of reagents, plasmids, and strategies were used and the RtGGA proved to be robust. The RtGGA was used to build three versions of the carotenoid overexpression cassette by using different promoter combinations. The cassettes were transformed into R. toruloides and the three new strains were characterized. Total carotenoid concentration increased by 41%. The dedicated GGA platform fills a gap in the advanced genome engineering toolkit for R. toruloides, enabling the efficient design of complex metabolic pathways. Elsevier 2022-05-23 /pmc/articles/PMC9157227/ /pubmed/35662893 http://dx.doi.org/10.1016/j.mec.2022.e00200 Text en © 2022 The Authors. Published by Elsevier B.V. on behalf of International Metabolic Engineering Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Full Length Article Bonturi, Nemailla Pinheiro, Marina Julio de Oliveira, Paola Monteiro Rusadze, Eka Eichinger, Tobias Liudžiūtė, Gintare De Biaggi, Juliano Sabedotti Brauer, Age Remm, Maido Miranda, Everson Alves Ledesma-Amaro, Rodrigo Lahtvee, Petri-Jaan Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides |
title | Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides |
title_full | Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides |
title_fullStr | Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides |
title_full_unstemmed | Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides |
title_short | Development of a dedicated Golden Gate Assembly Platform (RtGGA) for Rhodotorula toruloides |
title_sort | development of a dedicated golden gate assembly platform (rtgga) for rhodotorula toruloides |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157227/ https://www.ncbi.nlm.nih.gov/pubmed/35662893 http://dx.doi.org/10.1016/j.mec.2022.e00200 |
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