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A molecular genetic toolbox for Yarrowia lipolytica
BACKGROUND: Yarrowia lipolytica is an ascomycete yeast used in biotechnological research for its abilities to secrete high concentrations of proteins and accumulate lipids. Genetic tools have been made in a variety of backgrounds with varying similarity to a comprehensively sequenced strain. RESULTS...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210315/ https://www.ncbi.nlm.nih.gov/pubmed/28066508 http://dx.doi.org/10.1186/s13068-016-0687-7 |
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author | Bredeweg, Erin L. Pomraning, Kyle R. Dai, Ziyu Nielsen, Jens Kerkhoven, Eduard J. Baker, Scott E. |
author_facet | Bredeweg, Erin L. Pomraning, Kyle R. Dai, Ziyu Nielsen, Jens Kerkhoven, Eduard J. Baker, Scott E. |
author_sort | Bredeweg, Erin L. |
collection | PubMed |
description | BACKGROUND: Yarrowia lipolytica is an ascomycete yeast used in biotechnological research for its abilities to secrete high concentrations of proteins and accumulate lipids. Genetic tools have been made in a variety of backgrounds with varying similarity to a comprehensively sequenced strain. RESULTS: We have developed a set of genetic and molecular tools in order to expand capabilities of Y. lipolytica for both biological research and industrial bioengineering applications. In this work, we generated a set of isogenic auxotrophic strains with decreased non-homologous end joining for targeted DNA incorporation. Genome sequencing, assembly, and annotation of this genetic background uncovers previously unidentified genes in Y. lipolytica. To complement these strains, we constructed plasmids with Y. lipolytica-optimized superfolder GFP for targeted overexpression and fluorescent tagging. We used these tools to build the “Yarrowia lipolytica Cell Atlas,” a collection of strains with endogenous fluorescently tagged organelles in the same genetic background, in order to define organelle morphology in live cells. CONCLUSIONS: These molecular and isogenetic tools are useful for live assessment of organelle-specific protein expression, and for localization of lipid biosynthetic enzymes or other proteins in Y. lipolytica. This work provides the Yarrowia community with tools for cell biology and metabolism research in Y. lipolytica for further development of biofuels and natural products. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0687-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5210315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52103152017-01-06 A molecular genetic toolbox for Yarrowia lipolytica Bredeweg, Erin L. Pomraning, Kyle R. Dai, Ziyu Nielsen, Jens Kerkhoven, Eduard J. Baker, Scott E. Biotechnol Biofuels Research BACKGROUND: Yarrowia lipolytica is an ascomycete yeast used in biotechnological research for its abilities to secrete high concentrations of proteins and accumulate lipids. Genetic tools have been made in a variety of backgrounds with varying similarity to a comprehensively sequenced strain. RESULTS: We have developed a set of genetic and molecular tools in order to expand capabilities of Y. lipolytica for both biological research and industrial bioengineering applications. In this work, we generated a set of isogenic auxotrophic strains with decreased non-homologous end joining for targeted DNA incorporation. Genome sequencing, assembly, and annotation of this genetic background uncovers previously unidentified genes in Y. lipolytica. To complement these strains, we constructed plasmids with Y. lipolytica-optimized superfolder GFP for targeted overexpression and fluorescent tagging. We used these tools to build the “Yarrowia lipolytica Cell Atlas,” a collection of strains with endogenous fluorescently tagged organelles in the same genetic background, in order to define organelle morphology in live cells. CONCLUSIONS: These molecular and isogenetic tools are useful for live assessment of organelle-specific protein expression, and for localization of lipid biosynthetic enzymes or other proteins in Y. lipolytica. This work provides the Yarrowia community with tools for cell biology and metabolism research in Y. lipolytica for further development of biofuels and natural products. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0687-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-03 /pmc/articles/PMC5210315/ /pubmed/28066508 http://dx.doi.org/10.1186/s13068-016-0687-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Bredeweg, Erin L. Pomraning, Kyle R. Dai, Ziyu Nielsen, Jens Kerkhoven, Eduard J. Baker, Scott E. A molecular genetic toolbox for Yarrowia lipolytica |
title | A molecular genetic toolbox for Yarrowia lipolytica |
title_full | A molecular genetic toolbox for Yarrowia lipolytica |
title_fullStr | A molecular genetic toolbox for Yarrowia lipolytica |
title_full_unstemmed | A molecular genetic toolbox for Yarrowia lipolytica |
title_short | A molecular genetic toolbox for Yarrowia lipolytica |
title_sort | molecular genetic toolbox for yarrowia lipolytica |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210315/ https://www.ncbi.nlm.nih.gov/pubmed/28066508 http://dx.doi.org/10.1186/s13068-016-0687-7 |
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