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Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids

The high-value carotenoid astaxanthin (3,3′-dihydroxy-β,β-carotene-4,4′-dione) is one of the most potent antioxidants in nature. In addition to its large-scale use in fish farming, the pigment has applications as a food supplement and an active ingredient in cosmetics and in pharmaceuticals for the...

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Autores principales: Agrawal, Shreya, Karcher, Daniel, Ruf, Stephanie, Erban, Alexander, Hertle, Alexander P, Kopka, Joachim, Bock, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774745/
https://www.ncbi.nlm.nih.gov/pubmed/34623449
http://dx.doi.org/10.1093/plphys/kiab428
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author Agrawal, Shreya
Karcher, Daniel
Ruf, Stephanie
Erban, Alexander
Hertle, Alexander P
Kopka, Joachim
Bock, Ralph
author_facet Agrawal, Shreya
Karcher, Daniel
Ruf, Stephanie
Erban, Alexander
Hertle, Alexander P
Kopka, Joachim
Bock, Ralph
author_sort Agrawal, Shreya
collection PubMed
description The high-value carotenoid astaxanthin (3,3′-dihydroxy-β,β-carotene-4,4′-dione) is one of the most potent antioxidants in nature. In addition to its large-scale use in fish farming, the pigment has applications as a food supplement and an active ingredient in cosmetics and in pharmaceuticals for the treatment of diseases linked to reactive oxygen species. The biochemical pathway for astaxanthin synthesis has been introduced into seed plants, which do not naturally synthesize this pigment, by nuclear and plastid engineering. The highest accumulation rates have been achieved in transplastomic plants, but massive production of astaxanthin has resulted in severe growth retardation. What limits astaxanthin accumulation levels and what causes the mutant phenotype is unknown. Here, we addressed these questions by making astaxanthin synthesis in tobacco (Nicotiana tabacum) plastids inducible by a synthetic riboswitch. We show that, already in the uninduced state, astaxanthin accumulates to similarly high levels as in transplastomic plants expressing the pathway constitutively. Importantly, the inducible plants displayed wild-type–like growth properties and riboswitch induction resulted in a further increase in astaxanthin accumulation. Our data suggest that the mutant phenotype associated with constitutive astaxanthin synthesis is due to massive metabolite turnover, and indicate that astaxanthin accumulation is limited by the sequestration capacity of the plastid.
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spelling pubmed-87747452022-01-21 Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids Agrawal, Shreya Karcher, Daniel Ruf, Stephanie Erban, Alexander Hertle, Alexander P Kopka, Joachim Bock, Ralph Plant Physiol Research Articles The high-value carotenoid astaxanthin (3,3′-dihydroxy-β,β-carotene-4,4′-dione) is one of the most potent antioxidants in nature. In addition to its large-scale use in fish farming, the pigment has applications as a food supplement and an active ingredient in cosmetics and in pharmaceuticals for the treatment of diseases linked to reactive oxygen species. The biochemical pathway for astaxanthin synthesis has been introduced into seed plants, which do not naturally synthesize this pigment, by nuclear and plastid engineering. The highest accumulation rates have been achieved in transplastomic plants, but massive production of astaxanthin has resulted in severe growth retardation. What limits astaxanthin accumulation levels and what causes the mutant phenotype is unknown. Here, we addressed these questions by making astaxanthin synthesis in tobacco (Nicotiana tabacum) plastids inducible by a synthetic riboswitch. We show that, already in the uninduced state, astaxanthin accumulates to similarly high levels as in transplastomic plants expressing the pathway constitutively. Importantly, the inducible plants displayed wild-type–like growth properties and riboswitch induction resulted in a further increase in astaxanthin accumulation. Our data suggest that the mutant phenotype associated with constitutive astaxanthin synthesis is due to massive metabolite turnover, and indicate that astaxanthin accumulation is limited by the sequestration capacity of the plastid. Oxford University Press 2021-09-07 /pmc/articles/PMC8774745/ /pubmed/34623449 http://dx.doi.org/10.1093/plphys/kiab428 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Agrawal, Shreya
Karcher, Daniel
Ruf, Stephanie
Erban, Alexander
Hertle, Alexander P
Kopka, Joachim
Bock, Ralph
Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
title Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
title_full Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
title_fullStr Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
title_full_unstemmed Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
title_short Riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
title_sort riboswitch-mediated inducible expression of an astaxanthin biosynthetic operon in plastids
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774745/
https://www.ncbi.nlm.nih.gov/pubmed/34623449
http://dx.doi.org/10.1093/plphys/kiab428
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