Structural comparison and enhanced enzymatic hydrolysis of the cellulosic preparation from Populus tomentosa Carr., by different cellulose-soluble solvent systems.
Identifieur interne : 002D04 ( Main/Exploration ); précédent : 002D03; suivant : 002D05Structural comparison and enhanced enzymatic hydrolysis of the cellulosic preparation from Populus tomentosa Carr., by different cellulose-soluble solvent systems.
Auteurs : Kun Wang [République populaire de Chine] ; Hai Yan Yang ; Feng Xu ; Run Cang SunSource :
- Bioresource technology [ 1873-2976 ] ; 2011.
Descripteurs français
- KwdFr :
- Cellulase (métabolisme), Cellulose (composition chimique), Cellulose (métabolisme), Cristallographie aux rayons X (MeSH), Glucose (analyse), Hydrolyse (MeSH), Polymérisation (MeSH), Populus (métabolisme), Solubilité (MeSH), Solvants (composition chimique), Spectroscopie infrarouge à transformée de Fourier (MeSH), Xylose (analyse).
- MESH :
- analyse : Glucose, Xylose.
- composition chimique : Cellulose, Solvants.
- métabolisme : Cellulase, Cellulose, Populus.
- Cristallographie aux rayons X, Hydrolyse, Polymérisation, Solubilité, Spectroscopie infrarouge à transformée de Fourier.
English descriptors
- KwdEn :
- MESH :
- chemical , analysis : Glucose, Xylose.
- chemical , chemistry : Cellulose, Solvents.
- chemical , metabolism : Cellulase, Cellulose.
- metabolism : Populus.
- Crystallography, X-Ray, Hydrolysis, Polymerization, Solubility, Spectroscopy, Fourier Transform Infrared.
Abstract
This study aims to establish an efficient pretreatment process using cellulose-dissolution solvents to enhance the enzymatic saccharification. LiOH/urea, LiCl/DMAc, concentrated phosphoric acid, ionic liquid (1-butyl-3-methylimidazolium chloride; [BMIM]Cl) and N-methyl-morpholine-N-oxide (NMMO) were selected as the cellulose dissolution agents. Except the cellulosic sample regenerated from LiCl/DMAc system, all the other treated samples exhibited lower cellulose crystallinity and degree of polymerization (DP), and consequently, exhibited a significant enhancement on enzymatic hydrolysis kinetic. Ionic liquid pretreatment offered unique advantages in the hydrolysis rate in the first 10h, probably due to the extensively structural transformation of cellulose from the crystalline to the amorphous region. Meanwhile, the regenerated cellulose from concentrated phosphoric acid almost completely consisted of cellulose II, and achieved the highest saccharification yield.
DOI: 10.1016/j.biortech.2010.12.088
PubMed: 21277776
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Yang, Hai Yan" sort="Yang, Hai Yan" uniqKey="Yang H" first="Hai Yan" last="Yang">Hai Yan Yang</name>
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<author><name sortKey="Xu, Feng" sort="Xu, Feng" uniqKey="Xu F" first="Feng" last="Xu">Feng Xu</name>
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<term>Glucose (analysis)</term>
<term>Hydrolysis (MeSH)</term>
<term>Polymerization (MeSH)</term>
<term>Populus (metabolism)</term>
<term>Solubility (MeSH)</term>
<term>Solvents (chemistry)</term>
<term>Spectroscopy, Fourier Transform Infrared (MeSH)</term>
<term>Xylose (analysis)</term>
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<term>Cellulose (composition chimique)</term>
<term>Cellulose (métabolisme)</term>
<term>Cristallographie aux rayons X (MeSH)</term>
<term>Glucose (analyse)</term>
<term>Hydrolyse (MeSH)</term>
<term>Polymérisation (MeSH)</term>
<term>Populus (métabolisme)</term>
<term>Solubilité (MeSH)</term>
<term>Solvants (composition chimique)</term>
<term>Spectroscopie infrarouge à transformée de Fourier (MeSH)</term>
<term>Xylose (analyse)</term>
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<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Glucose</term>
<term>Xylose</term>
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<term>Solvents</term>
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<term>Cellulose</term>
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<term>Xylose</term>
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<term>Solvants</term>
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<front><div type="abstract" xml:lang="en">This study aims to establish an efficient pretreatment process using cellulose-dissolution solvents to enhance the enzymatic saccharification. LiOH/urea, LiCl/DMAc, concentrated phosphoric acid, ionic liquid (1-butyl-3-methylimidazolium chloride; [BMIM]Cl) and N-methyl-morpholine-N-oxide (NMMO) were selected as the cellulose dissolution agents. Except the cellulosic sample regenerated from LiCl/DMAc system, all the other treated samples exhibited lower cellulose crystallinity and degree of polymerization (DP), and consequently, exhibited a significant enhancement on enzymatic hydrolysis kinetic. Ionic liquid pretreatment offered unique advantages in the hydrolysis rate in the first 10h, probably due to the extensively structural transformation of cellulose from the crystalline to the amorphous region. Meanwhile, the regenerated cellulose from concentrated phosphoric acid almost completely consisted of cellulose II, and achieved the highest saccharification yield.</div>
</front>
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<Abstract><AbstractText>This study aims to establish an efficient pretreatment process using cellulose-dissolution solvents to enhance the enzymatic saccharification. LiOH/urea, LiCl/DMAc, concentrated phosphoric acid, ionic liquid (1-butyl-3-methylimidazolium chloride; [BMIM]Cl) and N-methyl-morpholine-N-oxide (NMMO) were selected as the cellulose dissolution agents. Except the cellulosic sample regenerated from LiCl/DMAc system, all the other treated samples exhibited lower cellulose crystallinity and degree of polymerization (DP), and consequently, exhibited a significant enhancement on enzymatic hydrolysis kinetic. Ionic liquid pretreatment offered unique advantages in the hydrolysis rate in the first 10h, probably due to the extensively structural transformation of cellulose from the crystalline to the amorphous region. Meanwhile, the regenerated cellulose from concentrated phosphoric acid almost completely consisted of cellulose II, and achieved the highest saccharification yield.</AbstractText>
<CopyrightInformation>Copyright © 2011 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wang</LastName>
<ForeName>Kun</ForeName>
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<AffiliationInfo><Affiliation>Institute of Biomass Chemistry and Technology, Beijing Forestry University, Beijing 100083, China.</Affiliation>
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