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Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification

BACKGROUND: Plant biomass is a potentially important renewable source of energy and industrial products. The natural recalcitrance of the cell walls to enzymatic degradation (saccharification), which plants have evolved to defend themselves from biotic stresses, represents a major bottleneck for the...

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Autores principales: Francocci, Fedra, Bastianelli, Elisa, Lionetti, Vincenzo, Ferrari, Simone, De Lorenzo, Giulia, Bellincampi, Daniela, Cervone, Felice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843582/
https://www.ncbi.nlm.nih.gov/pubmed/24245704
http://dx.doi.org/10.1186/1754-6834-6-163
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author Francocci, Fedra
Bastianelli, Elisa
Lionetti, Vincenzo
Ferrari, Simone
De Lorenzo, Giulia
Bellincampi, Daniela
Cervone, Felice
author_facet Francocci, Fedra
Bastianelli, Elisa
Lionetti, Vincenzo
Ferrari, Simone
De Lorenzo, Giulia
Bellincampi, Daniela
Cervone, Felice
author_sort Francocci, Fedra
collection PubMed
description BACKGROUND: Plant biomass is a potentially important renewable source of energy and industrial products. The natural recalcitrance of the cell walls to enzymatic degradation (saccharification), which plants have evolved to defend themselves from biotic stresses, represents a major bottleneck for the industrial bioconversion of lignocellulosic biomasses. The identification of factors that influence the cell wall recalcitrance to saccharification may help to overcome the existing limitations that hamper the utilization of biomass. RESULTS: Here we have investigated in Arabidopsis thaliana the impact of homogalacturonan (HG) content and structure on tissue saccharification. We characterized mutants affected in genes encoding proteins involved in HG biosynthesis (quasimodo2-1; qua2-1) and methylesterification (pectin methylesterase 3; pme3). We also analyzed the natural variation of Arabidopsis through the characterization of a nested core collection of 24 accessions generated to maximize genetic variability. We found a negative correlation between the level of de-methyl-esterified HG (HGA) and cellulose degradability. CONCLUSIONS: We propose to use the level of HGA domains as a biochemical marker of the cell wall recalcitrance to saccharification. This may be utilized for selecting, on a large scale, natural variants or mutants with improved bioconversion features.
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spelling pubmed-38435822013-11-30 Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification Francocci, Fedra Bastianelli, Elisa Lionetti, Vincenzo Ferrari, Simone De Lorenzo, Giulia Bellincampi, Daniela Cervone, Felice Biotechnol Biofuels Research BACKGROUND: Plant biomass is a potentially important renewable source of energy and industrial products. The natural recalcitrance of the cell walls to enzymatic degradation (saccharification), which plants have evolved to defend themselves from biotic stresses, represents a major bottleneck for the industrial bioconversion of lignocellulosic biomasses. The identification of factors that influence the cell wall recalcitrance to saccharification may help to overcome the existing limitations that hamper the utilization of biomass. RESULTS: Here we have investigated in Arabidopsis thaliana the impact of homogalacturonan (HG) content and structure on tissue saccharification. We characterized mutants affected in genes encoding proteins involved in HG biosynthesis (quasimodo2-1; qua2-1) and methylesterification (pectin methylesterase 3; pme3). We also analyzed the natural variation of Arabidopsis through the characterization of a nested core collection of 24 accessions generated to maximize genetic variability. We found a negative correlation between the level of de-methyl-esterified HG (HGA) and cellulose degradability. CONCLUSIONS: We propose to use the level of HGA domains as a biochemical marker of the cell wall recalcitrance to saccharification. This may be utilized for selecting, on a large scale, natural variants or mutants with improved bioconversion features. BioMed Central 2013-11-18 /pmc/articles/PMC3843582/ /pubmed/24245704 http://dx.doi.org/10.1186/1754-6834-6-163 Text en Copyright © 2013 Francocci et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Francocci, Fedra
Bastianelli, Elisa
Lionetti, Vincenzo
Ferrari, Simone
De Lorenzo, Giulia
Bellincampi, Daniela
Cervone, Felice
Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
title Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
title_full Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
title_fullStr Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
title_full_unstemmed Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
title_short Analysis of pectin mutants and natural accessions of Arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
title_sort analysis of pectin mutants and natural accessions of arabidopsis highlights the impact of de-methyl-esterified homogalacturonan on tissue saccharification
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843582/
https://www.ncbi.nlm.nih.gov/pubmed/24245704
http://dx.doi.org/10.1186/1754-6834-6-163
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