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Developing a platform for production of the oxylipin KODA in plants
KODA (9-hydroxy-10-oxo-12(Z),15(Z)-octadecadienoic acid) is a plant oxylipin involved in recovery from stress. As an agrichemical, KODA helps maintain crop production under various environmental stresses. In plants, KODA is synthesized from α-linolenic acids via 9-lipoxygenase (9-LOX) and allene oxi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113317/ https://www.ncbi.nlm.nih.gov/pubmed/35560188 http://dx.doi.org/10.1093/jxb/erab557 |
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author | Ihara, Yuta Wakamatsu, Takayuki Yokoyama, Mineyuki Maezawa, Daisuke Ohta, Hiroyuki Shimojima, Mie |
author_facet | Ihara, Yuta Wakamatsu, Takayuki Yokoyama, Mineyuki Maezawa, Daisuke Ohta, Hiroyuki Shimojima, Mie |
author_sort | Ihara, Yuta |
collection | PubMed |
description | KODA (9-hydroxy-10-oxo-12(Z),15(Z)-octadecadienoic acid) is a plant oxylipin involved in recovery from stress. As an agrichemical, KODA helps maintain crop production under various environmental stresses. In plants, KODA is synthesized from α-linolenic acids via 9-lipoxygenase (9-LOX) and allene oxide synthase (AOS), although the amount is usually low, except in the free-floating aquatic plant Lemna paucicostata. To improve KODA biosynthetic yield in other plants such as Nicotiana benthamiana and Arabidopsis thaliana, we developed a system to overproduce KODA in vivo via ectopic expression of L. paucicostata 9-LOX and AOS. The transient expression in N. benthamiana showed that the expression of these two genes is sufficient to produce KODA in leaves. However, stable expression of 9-LOX and AOS (with consequent KODA production) in Arabidopsis plants succeeded only when the two proteins were targeted to plastids or the endoplasmic reticulum/lipid droplets. Although only small amounts of KODA could be detected in crude leaf extracts of transgenic Nicotiana or Arabidopsis plants, subsequent incubation of the extracts increased KODA abundance over time. Therefore, KODA production in transgenic plants stably expressing 9-LOX and AOS requires specific sub-cellular localization of these two enzymes and incubation of crude leaf extracts, which liberates α-linolenic acid via breakdown of endogenous lipids. |
format | Online Article Text |
id | pubmed-9113317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91133172022-05-18 Developing a platform for production of the oxylipin KODA in plants Ihara, Yuta Wakamatsu, Takayuki Yokoyama, Mineyuki Maezawa, Daisuke Ohta, Hiroyuki Shimojima, Mie J Exp Bot Research Papers KODA (9-hydroxy-10-oxo-12(Z),15(Z)-octadecadienoic acid) is a plant oxylipin involved in recovery from stress. As an agrichemical, KODA helps maintain crop production under various environmental stresses. In plants, KODA is synthesized from α-linolenic acids via 9-lipoxygenase (9-LOX) and allene oxide synthase (AOS), although the amount is usually low, except in the free-floating aquatic plant Lemna paucicostata. To improve KODA biosynthetic yield in other plants such as Nicotiana benthamiana and Arabidopsis thaliana, we developed a system to overproduce KODA in vivo via ectopic expression of L. paucicostata 9-LOX and AOS. The transient expression in N. benthamiana showed that the expression of these two genes is sufficient to produce KODA in leaves. However, stable expression of 9-LOX and AOS (with consequent KODA production) in Arabidopsis plants succeeded only when the two proteins were targeted to plastids or the endoplasmic reticulum/lipid droplets. Although only small amounts of KODA could be detected in crude leaf extracts of transgenic Nicotiana or Arabidopsis plants, subsequent incubation of the extracts increased KODA abundance over time. Therefore, KODA production in transgenic plants stably expressing 9-LOX and AOS requires specific sub-cellular localization of these two enzymes and incubation of crude leaf extracts, which liberates α-linolenic acid via breakdown of endogenous lipids. Oxford University Press 2021-12-27 /pmc/articles/PMC9113317/ /pubmed/35560188 http://dx.doi.org/10.1093/jxb/erab557 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 Papers Ihara, Yuta Wakamatsu, Takayuki Yokoyama, Mineyuki Maezawa, Daisuke Ohta, Hiroyuki Shimojima, Mie Developing a platform for production of the oxylipin KODA in plants |
title | Developing a platform for production of the oxylipin KODA in plants |
title_full | Developing a platform for production of the oxylipin KODA in plants |
title_fullStr | Developing a platform for production of the oxylipin KODA in plants |
title_full_unstemmed | Developing a platform for production of the oxylipin KODA in plants |
title_short | Developing a platform for production of the oxylipin KODA in plants |
title_sort | developing a platform for production of the oxylipin koda in plants |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113317/ https://www.ncbi.nlm.nih.gov/pubmed/35560188 http://dx.doi.org/10.1093/jxb/erab557 |
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