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Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility

Plant biomass is a large source of fermentable sugars for the synthesis of bioproducts using engineered microbes. These sugars are stored as cell wall polymers, mainly cellulose and hemicellulose, and are embedded with lignin, which makes their enzymatic hydrolysis challenging. One of the strategies...

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Autores principales: Eudes, Aymerick, Zhao, Nanxia, Sathitsuksanoh, Noppadon, Baidoo, Edward E. K., Lao, Jeemeng, Wang, George, Yogiswara, Sasha, Lee, Taek Soon, Singh, Seema, Mortimer, Jenny C., Keasling, Jay D., Simmons, Blake A., Loqué, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949269/
https://www.ncbi.nlm.nih.gov/pubmed/27486577
http://dx.doi.org/10.3389/fbioe.2016.00058
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author Eudes, Aymerick
Zhao, Nanxia
Sathitsuksanoh, Noppadon
Baidoo, Edward E. K.
Lao, Jeemeng
Wang, George
Yogiswara, Sasha
Lee, Taek Soon
Singh, Seema
Mortimer, Jenny C.
Keasling, Jay D.
Simmons, Blake A.
Loqué, Dominique
author_facet Eudes, Aymerick
Zhao, Nanxia
Sathitsuksanoh, Noppadon
Baidoo, Edward E. K.
Lao, Jeemeng
Wang, George
Yogiswara, Sasha
Lee, Taek Soon
Singh, Seema
Mortimer, Jenny C.
Keasling, Jay D.
Simmons, Blake A.
Loqué, Dominique
author_sort Eudes, Aymerick
collection PubMed
description Plant biomass is a large source of fermentable sugars for the synthesis of bioproducts using engineered microbes. These sugars are stored as cell wall polymers, mainly cellulose and hemicellulose, and are embedded with lignin, which makes their enzymatic hydrolysis challenging. One of the strategies to reduce cell wall recalcitrance is the modification of lignin content and composition. Lignin is a phenolic polymer of methylated aromatic alcohols and its synthesis in tissues developing secondary cell walls is a significant sink for the consumption of the methyl donor S-adenosylmethionine (AdoMet). In this study, we demonstrate in Arabidopsis stems that targeted expression of AdoMet hydrolase (AdoMetase, E.C. 3.3.1.2) in secondary cell wall synthesizing tissues reduces the AdoMet pool and impacts lignin content and composition. In particular, both NMR analysis and pyrolysis gas chromatography mass spectrometry of lignin in engineered biomass showed relative enrichment of non-methylated p-hydroxycinnamyl (H) units and a reduction of dimethylated syringyl (S) units. This indicates a lower degree of methylation compared to that in wild-type lignin. Quantification of cell wall-bound hydroxycinnamates revealed a reduction of ferulate in AdoMetase transgenic lines. Biomass from transgenic lines, in contrast to that in control plants, exhibits an enrichment of glucose content and a reduction in the degree of hemicellulose glucuronoxylan methylation. We also show that these modifications resulted in a reduction of cell wall recalcitrance, because sugar yield generated by enzymatic biomass saccharification was greater than that of wild-type plants. Considering that transgenic plants show no important diminution of biomass yields, and that heterologous expression of AdoMetase protein can be spatiotemporally optimized, this novel approach provides a valuable option for the improvement of lignocellulosic biomass feedstock.
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spelling pubmed-49492692016-08-02 Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility Eudes, Aymerick Zhao, Nanxia Sathitsuksanoh, Noppadon Baidoo, Edward E. K. Lao, Jeemeng Wang, George Yogiswara, Sasha Lee, Taek Soon Singh, Seema Mortimer, Jenny C. Keasling, Jay D. Simmons, Blake A. Loqué, Dominique Front Bioeng Biotechnol Bioengineering and Biotechnology Plant biomass is a large source of fermentable sugars for the synthesis of bioproducts using engineered microbes. These sugars are stored as cell wall polymers, mainly cellulose and hemicellulose, and are embedded with lignin, which makes their enzymatic hydrolysis challenging. One of the strategies to reduce cell wall recalcitrance is the modification of lignin content and composition. Lignin is a phenolic polymer of methylated aromatic alcohols and its synthesis in tissues developing secondary cell walls is a significant sink for the consumption of the methyl donor S-adenosylmethionine (AdoMet). In this study, we demonstrate in Arabidopsis stems that targeted expression of AdoMet hydrolase (AdoMetase, E.C. 3.3.1.2) in secondary cell wall synthesizing tissues reduces the AdoMet pool and impacts lignin content and composition. In particular, both NMR analysis and pyrolysis gas chromatography mass spectrometry of lignin in engineered biomass showed relative enrichment of non-methylated p-hydroxycinnamyl (H) units and a reduction of dimethylated syringyl (S) units. This indicates a lower degree of methylation compared to that in wild-type lignin. Quantification of cell wall-bound hydroxycinnamates revealed a reduction of ferulate in AdoMetase transgenic lines. Biomass from transgenic lines, in contrast to that in control plants, exhibits an enrichment of glucose content and a reduction in the degree of hemicellulose glucuronoxylan methylation. We also show that these modifications resulted in a reduction of cell wall recalcitrance, because sugar yield generated by enzymatic biomass saccharification was greater than that of wild-type plants. Considering that transgenic plants show no important diminution of biomass yields, and that heterologous expression of AdoMetase protein can be spatiotemporally optimized, this novel approach provides a valuable option for the improvement of lignocellulosic biomass feedstock. Frontiers Media S.A. 2016-07-19 /pmc/articles/PMC4949269/ /pubmed/27486577 http://dx.doi.org/10.3389/fbioe.2016.00058 Text en Copyright © 2016 Eudes, Zhao, Sathitsuksanoh, Baidoo, Lao, Wang, Yogiswara, Lee, Singh, Mortimer, Keasling, Simmons and Loqué. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Eudes, Aymerick
Zhao, Nanxia
Sathitsuksanoh, Noppadon
Baidoo, Edward E. K.
Lao, Jeemeng
Wang, George
Yogiswara, Sasha
Lee, Taek Soon
Singh, Seema
Mortimer, Jenny C.
Keasling, Jay D.
Simmons, Blake A.
Loqué, Dominique
Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility
title Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility
title_full Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility
title_fullStr Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility
title_full_unstemmed Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility
title_short Expression of S-adenosylmethionine Hydrolase in Tissues Synthesizing Secondary Cell Walls Alters Specific Methylated Cell Wall Fractions and Improves Biomass Digestibility
title_sort expression of s-adenosylmethionine hydrolase in tissues synthesizing secondary cell walls alters specific methylated cell wall fractions and improves biomass digestibility
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949269/
https://www.ncbi.nlm.nih.gov/pubmed/27486577
http://dx.doi.org/10.3389/fbioe.2016.00058
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