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Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules

BACKGROUND: Monolignol-like molecules can be integrated into lignin along with conventional monolignol units, and it has been shown that the incorporation of non-canonical subunits can be used to generate hydrolysable lignin by introduction of ester linkages into the polymer and that this type of li...

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Autores principales: Lee, Shinyoung, Mo, Huaping, Kim, Jeong Im, Chapple, Clint
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316160/
https://www.ncbi.nlm.nih.gov/pubmed/28239412
http://dx.doi.org/10.1186/s13068-017-0725-0
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author Lee, Shinyoung
Mo, Huaping
Kim, Jeong Im
Chapple, Clint
author_facet Lee, Shinyoung
Mo, Huaping
Kim, Jeong Im
Chapple, Clint
author_sort Lee, Shinyoung
collection PubMed
description BACKGROUND: Monolignol-like molecules can be integrated into lignin along with conventional monolignol units, and it has been shown that the incorporation of non-canonical subunits can be used to generate hydrolysable lignin by introduction of ester linkages into the polymer and that this type of lignin is more easily removable. Disinapoyl esters (DSEs), which to some degree resemble the monolignol sinapyl alcohol, may be promising lignin modifying units for this purpose. As a first step toward determining whether this goal is achievable, we manipulated metabolic flux in Arabidopsis to increase the amounts of DSEs by overexpressing sinapoylglucose:sinapoylglucose sinapoyltransferase (SST) which produces two main DSEs, 1,2-disinapoylglucose, and another compound we identify in this report as 3,4-disinapoyl-fructopyranose. RESULTS: We succeeded in overproducing DSEs by introducing an SST-overexpression construct into the sinapoylglucose accumulator1 (sng1-6) mutant (SST-OE sng1-6) which lacks several of the enzymes that would otherwise compete for the SST substrate, sinapoyglucose. Introduction of cinnamyl alcohol dehydrogenase-c (cad-c) and cad-d mutations into the SST-OE sng1-6 line further increased DSEs. Surprisingly, a reduced epidermal fluorescence (ref) phenotype was observed when SST-OE sng1-6 plants were evaluated under UV light, which appears to have been induced by the sequestration of DSEs into subvacuolar compartments. Although we successfully upregulated the accumulation of the target DSEs, we did not find any evidence showing the integration of DSEs into the cell wall. CONCLUSIONS: Our results suggest that although phenylpropanoid metabolic engineering is possible, a deeper understanding of sequestration and transport mechanisms will be necessary for successful lignin engineering through this route. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0725-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-53161602017-02-24 Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules Lee, Shinyoung Mo, Huaping Kim, Jeong Im Chapple, Clint Biotechnol Biofuels Research BACKGROUND: Monolignol-like molecules can be integrated into lignin along with conventional monolignol units, and it has been shown that the incorporation of non-canonical subunits can be used to generate hydrolysable lignin by introduction of ester linkages into the polymer and that this type of lignin is more easily removable. Disinapoyl esters (DSEs), which to some degree resemble the monolignol sinapyl alcohol, may be promising lignin modifying units for this purpose. As a first step toward determining whether this goal is achievable, we manipulated metabolic flux in Arabidopsis to increase the amounts of DSEs by overexpressing sinapoylglucose:sinapoylglucose sinapoyltransferase (SST) which produces two main DSEs, 1,2-disinapoylglucose, and another compound we identify in this report as 3,4-disinapoyl-fructopyranose. RESULTS: We succeeded in overproducing DSEs by introducing an SST-overexpression construct into the sinapoylglucose accumulator1 (sng1-6) mutant (SST-OE sng1-6) which lacks several of the enzymes that would otherwise compete for the SST substrate, sinapoyglucose. Introduction of cinnamyl alcohol dehydrogenase-c (cad-c) and cad-d mutations into the SST-OE sng1-6 line further increased DSEs. Surprisingly, a reduced epidermal fluorescence (ref) phenotype was observed when SST-OE sng1-6 plants were evaluated under UV light, which appears to have been induced by the sequestration of DSEs into subvacuolar compartments. Although we successfully upregulated the accumulation of the target DSEs, we did not find any evidence showing the integration of DSEs into the cell wall. CONCLUSIONS: Our results suggest that although phenylpropanoid metabolic engineering is possible, a deeper understanding of sequestration and transport mechanisms will be necessary for successful lignin engineering through this route. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0725-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-17 /pmc/articles/PMC5316160/ /pubmed/28239412 http://dx.doi.org/10.1186/s13068-017-0725-0 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
Lee, Shinyoung
Mo, Huaping
Kim, Jeong Im
Chapple, Clint
Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
title Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
title_full Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
title_fullStr Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
title_full_unstemmed Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
title_short Genetic engineering of Arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
title_sort genetic engineering of arabidopsis to overproduce disinapoyl esters, potential lignin modification molecules
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316160/
https://www.ncbi.nlm.nih.gov/pubmed/28239412
http://dx.doi.org/10.1186/s13068-017-0725-0
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