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Engineering secondary cell wall deposition in plants

Lignocellulosic biomass was used for thousands of years as animal feed and is now considered a great sugar source for biofuels production. It is composed mostly of secondary cell walls built with polysaccharide polymers that are embedded in lignin to reinforce the cell wall structure and maintain it...

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Autores principales: Yang, Fan, Mitra, Prajakta, Zhang, Ling, Prak, Lina, Verhertbruggen, Yves, Kim, Jin-Sun, Sun, Lan, Zheng, Kejian, Tang, Kexuan, Auer, Manfred, Scheller, Henrik V, Loqué, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644865/
https://www.ncbi.nlm.nih.gov/pubmed/23140549
http://dx.doi.org/10.1111/pbi.12016
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author Yang, Fan
Mitra, Prajakta
Zhang, Ling
Prak, Lina
Verhertbruggen, Yves
Kim, Jin-Sun
Sun, Lan
Zheng, Kejian
Tang, Kexuan
Auer, Manfred
Scheller, Henrik V
Loqué, Dominique
author_facet Yang, Fan
Mitra, Prajakta
Zhang, Ling
Prak, Lina
Verhertbruggen, Yves
Kim, Jin-Sun
Sun, Lan
Zheng, Kejian
Tang, Kexuan
Auer, Manfred
Scheller, Henrik V
Loqué, Dominique
author_sort Yang, Fan
collection PubMed
description Lignocellulosic biomass was used for thousands of years as animal feed and is now considered a great sugar source for biofuels production. It is composed mostly of secondary cell walls built with polysaccharide polymers that are embedded in lignin to reinforce the cell wall structure and maintain its integrity. Lignin is the primary material responsible for biomass recalcitrance to enzymatic hydrolysis. During plant development, deep reductions of lignin cause growth defects and often correlate with the loss of vessel integrity that adversely affects water and nutrient transport in plants. The work presented here describes a new approach to decrease lignin content while preventing vessel collapse and introduces a new strategy to boost transcription factor expression in native tissues. We used synthetic biology tools in Arabidopsis to rewire the secondary cell network by changing promoter-coding sequence associations. The result was a reduction in lignin and an increase in polysaccharide depositions in fibre cells. The promoter of a key lignin gene, C4H, was replaced by the vessel-specific promoter of transcription factor VND6. This rewired lignin biosynthesis specifically for vessel formation while disconnecting C4H expression from the fibre regulatory network. Secondly, the promoter of the IRX8 gene, secondary cell wall glycosyltransferase, was used to express a new copy of the fibre transcription factor NST1, and as the IRX8 promoter is induced by NST1, this also created an artificial positive feedback loop (APFL). The combination of strategies—lignin rewiring with APFL insertion—enhances polysaccharide deposition in stems without over-lignifying them, resulting in higher sugar yields after enzymatic hydrolysis.
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spelling pubmed-36448652013-05-06 Engineering secondary cell wall deposition in plants Yang, Fan Mitra, Prajakta Zhang, Ling Prak, Lina Verhertbruggen, Yves Kim, Jin-Sun Sun, Lan Zheng, Kejian Tang, Kexuan Auer, Manfred Scheller, Henrik V Loqué, Dominique Plant Biotechnol J Research Articles Lignocellulosic biomass was used for thousands of years as animal feed and is now considered a great sugar source for biofuels production. It is composed mostly of secondary cell walls built with polysaccharide polymers that are embedded in lignin to reinforce the cell wall structure and maintain its integrity. Lignin is the primary material responsible for biomass recalcitrance to enzymatic hydrolysis. During plant development, deep reductions of lignin cause growth defects and often correlate with the loss of vessel integrity that adversely affects water and nutrient transport in plants. The work presented here describes a new approach to decrease lignin content while preventing vessel collapse and introduces a new strategy to boost transcription factor expression in native tissues. We used synthetic biology tools in Arabidopsis to rewire the secondary cell network by changing promoter-coding sequence associations. The result was a reduction in lignin and an increase in polysaccharide depositions in fibre cells. The promoter of a key lignin gene, C4H, was replaced by the vessel-specific promoter of transcription factor VND6. This rewired lignin biosynthesis specifically for vessel formation while disconnecting C4H expression from the fibre regulatory network. Secondly, the promoter of the IRX8 gene, secondary cell wall glycosyltransferase, was used to express a new copy of the fibre transcription factor NST1, and as the IRX8 promoter is induced by NST1, this also created an artificial positive feedback loop (APFL). The combination of strategies—lignin rewiring with APFL insertion—enhances polysaccharide deposition in stems without over-lignifying them, resulting in higher sugar yields after enzymatic hydrolysis. Blackwell Publishing Ltd 2013-04 2012-11-12 /pmc/articles/PMC3644865/ /pubmed/23140549 http://dx.doi.org/10.1111/pbi.12016 Text en Copyright © 2013 Society for Experimental Biology, Association of Applied Biologists and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research Articles
Yang, Fan
Mitra, Prajakta
Zhang, Ling
Prak, Lina
Verhertbruggen, Yves
Kim, Jin-Sun
Sun, Lan
Zheng, Kejian
Tang, Kexuan
Auer, Manfred
Scheller, Henrik V
Loqué, Dominique
Engineering secondary cell wall deposition in plants
title Engineering secondary cell wall deposition in plants
title_full Engineering secondary cell wall deposition in plants
title_fullStr Engineering secondary cell wall deposition in plants
title_full_unstemmed Engineering secondary cell wall deposition in plants
title_short Engineering secondary cell wall deposition in plants
title_sort engineering secondary cell wall deposition in plants
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644865/
https://www.ncbi.nlm.nih.gov/pubmed/23140549
http://dx.doi.org/10.1111/pbi.12016
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