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Comparison of glucose/xylose cofermentation of poplar hydrolysates processed by different pretreatment technologies.

Identifieur interne : 003413 ( Main/Exploration ); précédent : 003412; suivant : 003414

Comparison of glucose/xylose cofermentation of poplar hydrolysates processed by different pretreatment technologies.

Auteurs : Yulin Lu [États-Unis] ; Ryan Warner ; Miroslav Sedlak ; Nancy Ho ; Nathan S. Mosier

Source :

RBID : pubmed:19319980

Descripteurs français

English descriptors

Abstract

The inhibitory effects of furfural and acetic acid on the fermentation of xylose and glucose to ethanol in YEPDX medium by a recombinant Saccharomyces cerevisiae strain (LNH-ST 424A) were investigated. Initial furfural concentrations below 5 g/L caused negligible inhibition to glucose and xylose consumption rates in batch fermentations with high inoculum (4.5-6.0 g/L). At higher initial furfural concentrations (10-15 g/L) the inhibition became significant with xylose consumption rates especially affected. Interactive inhibition between acetic acid and pH were observed and quantified, and the results suggested the importance of conditioning the pH of hydrolysates for optimal fermentation performance. Poplar biomass pretreated by various CAFI processes (dilute acid, AFEX, ARP, SO(2)-catalyzed steam explosion, and controlled-pH) under respective optimal conditions was enzymatically hydrolyzed, and the mixed sugar streams in the hydrolysates were fermented. The 5-hydroxymethyl furfural (HMF) and furfural concentrations were low in all hydrolysates and did not pose negative effects on fermentation. Maximum ethanol productivity showed that 0-6.2 g/L initial acetic acid does not substantially affect the ethanol fermentation with proper pH adjustment, confirming the results from rich media fermentations with reagent grade sugars.

DOI: 10.1002/btpr.158
PubMed: 19319980


Affiliations:


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Le document en format XML

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<term>Acetic Acid (chemistry)</term>
<term>Biomass (MeSH)</term>
<term>Biotechnology (methods)</term>
<term>Energy-Generating Resources (MeSH)</term>
<term>Ethanol (metabolism)</term>
<term>Fermentation (MeSH)</term>
<term>Furaldehyde (chemistry)</term>
<term>Glucose (metabolism)</term>
<term>Hydrolysis (MeSH)</term>
<term>Populus (chemistry)</term>
<term>Populus (metabolism)</term>
<term>Saccharomyces cerevisiae (genetics)</term>
<term>Saccharomyces cerevisiae (metabolism)</term>
<term>Xylose (metabolism)</term>
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<term>Acide acétique (composition chimique)</term>
<term>Biomasse (MeSH)</term>
<term>Biotechnologie (méthodes)</term>
<term>Fermentation (MeSH)</term>
<term>Furfural (composition chimique)</term>
<term>Glucose (métabolisme)</term>
<term>Hydrolyse (MeSH)</term>
<term>Populus (composition chimique)</term>
<term>Populus (métabolisme)</term>
<term>Ressources de production d'énergie (MeSH)</term>
<term>Saccharomyces cerevisiae (génétique)</term>
<term>Saccharomyces cerevisiae (métabolisme)</term>
<term>Xylose (métabolisme)</term>
<term>Éthanol (métabolisme)</term>
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<term>Acetic Acid</term>
<term>Furaldehyde</term>
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<term>Ethanol</term>
<term>Glucose</term>
<term>Xylose</term>
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<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Populus</term>
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<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>Acide acétique</term>
<term>Furfural</term>
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<term>Saccharomyces cerevisiae</term>
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<term>Xylose</term>
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<term>Hydrolysis</term>
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<div type="abstract" xml:lang="en">The inhibitory effects of furfural and acetic acid on the fermentation of xylose and glucose to ethanol in YEPDX medium by a recombinant Saccharomyces cerevisiae strain (LNH-ST 424A) were investigated. Initial furfural concentrations below 5 g/L caused negligible inhibition to glucose and xylose consumption rates in batch fermentations with high inoculum (4.5-6.0 g/L). At higher initial furfural concentrations (10-15 g/L) the inhibition became significant with xylose consumption rates especially affected. Interactive inhibition between acetic acid and pH were observed and quantified, and the results suggested the importance of conditioning the pH of hydrolysates for optimal fermentation performance. Poplar biomass pretreated by various CAFI processes (dilute acid, AFEX, ARP, SO(2)-catalyzed steam explosion, and controlled-pH) under respective optimal conditions was enzymatically hydrolyzed, and the mixed sugar streams in the hydrolysates were fermented. The 5-hydroxymethyl furfural (HMF) and furfural concentrations were low in all hydrolysates and did not pose negative effects on fermentation. Maximum ethanol productivity showed that 0-6.2 g/L initial acetic acid does not substantially affect the ethanol fermentation with proper pH adjustment, confirming the results from rich media fermentations with reagent grade sugars.</div>
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<AbstractText>The inhibitory effects of furfural and acetic acid on the fermentation of xylose and glucose to ethanol in YEPDX medium by a recombinant Saccharomyces cerevisiae strain (LNH-ST 424A) were investigated. Initial furfural concentrations below 5 g/L caused negligible inhibition to glucose and xylose consumption rates in batch fermentations with high inoculum (4.5-6.0 g/L). At higher initial furfural concentrations (10-15 g/L) the inhibition became significant with xylose consumption rates especially affected. Interactive inhibition between acetic acid and pH were observed and quantified, and the results suggested the importance of conditioning the pH of hydrolysates for optimal fermentation performance. Poplar biomass pretreated by various CAFI processes (dilute acid, AFEX, ARP, SO(2)-catalyzed steam explosion, and controlled-pH) under respective optimal conditions was enzymatically hydrolyzed, and the mixed sugar streams in the hydrolysates were fermented. The 5-hydroxymethyl furfural (HMF) and furfural concentrations were low in all hydrolysates and did not pose negative effects on fermentation. Maximum ethanol productivity showed that 0-6.2 g/L initial acetic acid does not substantially affect the ethanol fermentation with proper pH adjustment, confirming the results from rich media fermentations with reagent grade sugars.</AbstractText>
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