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Functional analysis of alternative castor bean DGAT enzymes
The diversity of diacylglycerol acyltransferases (DGATs) indicates alternative roles for these enzymes in plant metabolism besides triacylglycerol (TAG) biosynthesis. In this work, we functionally characterized castor bean (Ricinus communis L.) DGATs assessing their subcellular localization, express...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747089/ https://www.ncbi.nlm.nih.gov/pubmed/36512712 http://dx.doi.org/10.1590/1678-4685-GMB-2022-0097 |
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author | Trenz, Thomaz Stumpf Turchetto-Zolet, Andreia Carina Margis, Rogério Margis-Pinheiro, Marcia Maraschin, Felipe dos Santos |
author_facet | Trenz, Thomaz Stumpf Turchetto-Zolet, Andreia Carina Margis, Rogério Margis-Pinheiro, Marcia Maraschin, Felipe dos Santos |
author_sort | Trenz, Thomaz Stumpf |
collection | PubMed |
description | The diversity of diacylglycerol acyltransferases (DGATs) indicates alternative roles for these enzymes in plant metabolism besides triacylglycerol (TAG) biosynthesis. In this work, we functionally characterized castor bean (Ricinus communis L.) DGATs assessing their subcellular localization, expression in seeds, capacity to restore triacylglycerol (TAG) biosynthesis in mutant yeast and evaluating whether they provide tolerance over free fatty acids (FFA) in sensitive yeast. RcDGAT3 displayed a distinct subcellular localization, located in vesicles outside the endoplasmic reticulum (ER) in most leaf epidermal cells. This enzyme was unable to restore TAG biosynthesis in mutant yeast; however, it was able to outperform other DGATs providing higher tolerance over FFA. RcDAcTA subcellular localization was associated with the ER membranes, resembling RcDGAT1 and RcDGAT2, but it failed to rescue the long-chain TAG biosynthesis in mutant yeast, even with fatty acid supplementation. Besides TAG biosynthesis, our results suggest that RcDGAT3 might have alternative functions and roles in lipid metabolism. |
format | Online Article Text |
id | pubmed-9747089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Sociedade Brasileira de Genética |
record_format | MEDLINE/PubMed |
spelling | pubmed-97470892022-12-20 Functional analysis of alternative castor bean DGAT enzymes Trenz, Thomaz Stumpf Turchetto-Zolet, Andreia Carina Margis, Rogério Margis-Pinheiro, Marcia Maraschin, Felipe dos Santos Genet Mol Biol Plant Molecular Genetics - Special Issue The diversity of diacylglycerol acyltransferases (DGATs) indicates alternative roles for these enzymes in plant metabolism besides triacylglycerol (TAG) biosynthesis. In this work, we functionally characterized castor bean (Ricinus communis L.) DGATs assessing their subcellular localization, expression in seeds, capacity to restore triacylglycerol (TAG) biosynthesis in mutant yeast and evaluating whether they provide tolerance over free fatty acids (FFA) in sensitive yeast. RcDGAT3 displayed a distinct subcellular localization, located in vesicles outside the endoplasmic reticulum (ER) in most leaf epidermal cells. This enzyme was unable to restore TAG biosynthesis in mutant yeast; however, it was able to outperform other DGATs providing higher tolerance over FFA. RcDAcTA subcellular localization was associated with the ER membranes, resembling RcDGAT1 and RcDGAT2, but it failed to rescue the long-chain TAG biosynthesis in mutant yeast, even with fatty acid supplementation. Besides TAG biosynthesis, our results suggest that RcDGAT3 might have alternative functions and roles in lipid metabolism. Sociedade Brasileira de Genética 2022-12-09 /pmc/articles/PMC9747089/ /pubmed/36512712 http://dx.doi.org/10.1590/1678-4685-GMB-2022-0097 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, istribution and reproduction in any medium, provided the original article is properly cited. |
spellingShingle | Plant Molecular Genetics - Special Issue Trenz, Thomaz Stumpf Turchetto-Zolet, Andreia Carina Margis, Rogério Margis-Pinheiro, Marcia Maraschin, Felipe dos Santos Functional analysis of alternative castor bean DGAT enzymes |
title | Functional analysis of alternative castor bean DGAT enzymes |
title_full | Functional analysis of alternative castor bean DGAT enzymes |
title_fullStr | Functional analysis of alternative castor bean DGAT enzymes |
title_full_unstemmed | Functional analysis of alternative castor bean DGAT enzymes |
title_short | Functional analysis of alternative castor bean DGAT enzymes |
title_sort | functional analysis of alternative castor bean dgat enzymes |
topic | Plant Molecular Genetics - Special Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747089/ https://www.ncbi.nlm.nih.gov/pubmed/36512712 http://dx.doi.org/10.1590/1678-4685-GMB-2022-0097 |
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