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Enzymatic hydrolysis of Norway spruce and sugarcane bagasse after treatment with 1-allyl-3-methylimidazolium formate
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå University, Faculty of Science and Technology, Department of Chemistry. Laboratory of Industrial Chemistry and Reaction Engineering, Department of Chemical Engineering, Process Chemistry Centre, Åbo Akademi University, Åbo-Turku, Finland.
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2013 (English)In: Journal of chemical technology and biotechnology (1986), ISSN 0268-2575, E-ISSN 1097-4660, Vol. 88, no 12, 2209-2215 p.Article in journal (Refereed) Published
Abstract [en]

BACKGROUND Enzymatic hydrolysis of cellulose in lignocellulosic materials suffers from slow reaction rates due to limited access to enzyme adsorption sites and to the high crystallinity of the cellulose. In this study, an attempt was made to facilitate enzymatic hydrolysis by pretreatment of cellulosic materials using the ionic liquid (IL) 1-allyl-3-methylimidazolium formate ([Amim][HCO2]) under mild reaction conditions. The effect of the IL was compared with that of thermochemical pretreatment under acidic conditions.

RESULTS The lignocellulosic substrates investigated were native and thermochemically pretreated Norway spruce and sugarcane bagasse. Microcrystalline cellulose (Avicel) was included for comparison. The IL treatments were performed in the temperature range 45–120 °C and, after regeneration and washing of the cellulosic substrates, enzymatic saccharification was carried out at 45 °C for 72 h. After 12 h of hydrolysis, the glucose yields from regenerated native spruce and sugarcane bagasse were up to nine times higher than for the corresponding untreated substrates. The results also show positive effects of pretreatment using [Amim][HCO2] on the hydrolysis of xylan and mannan.

Conclusion The present work demonstrates that both native wood and agricultural residues are readily soluble in [Amim][HCO2] under gentle conditions, and that pretreatment with ionic liquids such as [Amim][HCO2] warrants further attention as a potential alternative to conventional pretreatment techniques. © 2013 Society of Chemical Industry

Place, publisher, year, edition, pages
Wiley-Blackwell, 2013. Vol. 88, no 12, 2209-2215 p.
Keyword [en]
ionic liquid; 1-allyl-3-methylimidazolium formate; lignocellulose; pretreatment; enzymatic hydrolysis
National Category
Chemical Sciences
URN: urn:nbn:se:umu:diva-79641DOI: 10.1002/jctb.4089ISI: 000326462900012OAI: diva2:643570
Swedish Research Council Formas
Available from: 2013-08-27 Created: 2013-08-27 Last updated: 2015-05-05Bibliographically approved
In thesis
1. Biochemical conversion of biomass to biofuels: pretreatment–detoxification–hydrolysis–fermentation
Open this publication in new window or tab >>Biochemical conversion of biomass to biofuels: pretreatment–detoxification–hydrolysis–fermentation
2015 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The use of lignocellulosic materials to replace fossil resources for the industrial production of fuels, chemicals, and materials is increasing. The carbohydrate composition of lignocellulose (i.e. cellulose and hemicellulose) is an abundant source of sugars. However, due to the feedstock recalcitrance, rigid and compact structure of plant cell walls, access to polysaccharides is hindered and release of fermentable sugars has become a bottle-neck. Thus, to overcome the recalcitrant barriers, thermochemical pretreatment with an acid catalyst is usually employed for the physical or chemical disruption of plant cell wall. After pretreatment, enzymatic hydrolysis is the preferred option to produce sugars that can be further converted into liquid fuels (e.g. ethanol) via fermentation by microbial biocatalysts. However, during acid pretreatment, several inhibitory compounds namely furfural, 5-hydroxymethyl furfural, phenols, and aliphatic acids are released from the lignocellulose components. The presence of these compounds can greatly effect both enzymatic hydrolysis and microbial fermentation. For instance, when Avicel cellulose and acid treated spruce wood hydrolysate were mixed, 63% decrease in the enzymatic hydrolysis efficiency was observed compared to when Avicel was hydrolyzed in aqueous citrate buffer. In addition, the acid hydrolysates were essentially non-fermentable. Therefore, the associated problems of lignocellulose conversion can be addressed either by using feedstocks that are less recalcitrant or by developing efficient pretreatment techniques that do not cause formation of inhibitory byproducts and simultaneously give high sugar yields. A variety of lignocellulose materials including woody substrates (spruce, pine, and birch), agricultural residues (sugarcane bagasse and reed canary grass), bark (pine bark), and transgenic aspens were evaluated for their saccharification potential. Apparently, woody substrates were more recalcitrant than the rest of the species and bark was essentially amorphous. However, the saccharification efficiency of these substrates varied based on the pretreatment method used. For instance, untreated reed canary grass was more recalcitrant than woody materials whereas the acid treated reed canary grass gave a higher sugar yield (64%) than the woody substrates (max 34%). Genetic modification of plants was beneficial, since under similar pretreatment and enzymatic hydrolysis conditions, up to 28% higher sugar production was achieved from the transgenic plants compare to the wild type. As an alternative to the commonly used acid catalysed pretreatments (prior to enzymatic hydrolysis) lignocellulose materials were treated with four ionic liquid solvents (ILs): two switchable ILs (SILs) -SO2DBUMEASIL and CO2DBUMEASIL, and two other ILs [Amim][HCO2] and [AMMorp][OAc]. viii After enzymatic hydrolysis of IL treated substrates, a maximum amount of glucan to glucose conversion of between 75% and 97% and a maximum total sugar yields of between 71% and 94% were obtained. When using acid pretreatment these values varied between 13-77% for glucan to glucose conversion and 26-83% for total sugar yield. For woody substrates, the hemicellulose recovery (max 92%) was higher for the IL treated substrates than compared to acid treated samples. However, in case of reed canary grass and pine bark the hemicellulose recovery (90% and 88%, respectively) was significantly higher for the acid treated substrates than the IL treated samples. To overcome the inhibitory problems associated with the lignocellulose hydrolysates, three chemical conditioning methods were used 1. detoxification with ferrous sulfate (FeSO4) and hydrogen peroxide (H2O2) 2. application of reducing agents (sulfite, dithionite, or dithiothreitol) and 3. treatment with alkali: Ca(OH)2, NaOH, and NH4OH. The concentrations of inhibitory compounds were significantly lower after treatments with FeSO4 and H2O2 or alkali. Using reducing agents did not cause any decrease in the concentration of inhibitors, but detoxification of spruce acid hydrolysates resulted in up to 54% improvement of the hydrolysis efficiency (in terms of sugar release) compared to untreated samples. On the other hand, application of detoxification procedures to the aqueous buffer resulted in up to 39% decrease in hydrolysis efficiency, thus confirming that the positive effect of detoxification was due to the chemical alteration of inhibitory compounds. In addition, the fermentability of detoxified hydrolysates were investigated using the yeast Saccharomyces cerevisiae. The detoxified hydrolysates were readily fermented to ethanol yielding a maximum ethanol concentration of 8.3 g/l while the undetoxified hydrolysates were basically non-fermentable.

Place, publisher, year, edition, pages
Umeå: Umeå universitet, 2015. 90 p.
Lignocellulosic materials, Ionic liquids, Pretreatment, Inhibitors, Detoxification, Ferrous sulfate and hydrogen peroxide, reducing agents, alkaline treatments, Hydrolysis, Fermentation, Biofuels
National Category
Environmental Biotechnology
Research subject
urn:nbn:se:umu:diva-102722 (URN)978-91-7601-268-0 (ISBN)
Public defence
2015-05-28, KB, Chalmers University of Technology, Göteborg, 13:30 (English)
Available from: 2015-05-07 Created: 2015-04-30 Last updated: 2015-06-01Bibliographically approved

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Soudham, Venkata PrabhakarGräsvik, JohnMikkola, Jyri-PekkaJönsson, Leif J
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