53 research outputs found

    Optimization of alkaline peroxide pretreatment of rice straw

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    Lignocellulose represents a promising starting material for conversion to fuels and chemicals in biorefinery; however, its efficient conversion to sugar requires a prerequisite pretreatment step. In the present research, the pretreatment of rice straw by alkaline peroxide pretreatment was studied aiming to enhance enzymatic digestibility of the cellulose-enriched solid. The alkaline hydrogen peroxide (AHP) pretreatment of rice straw using different concentration of hydrogen peroxide, reaction time, temperature, and solid loading were evaluated based on enzymatic digestibility and sugar recovery. The highest reducing sugar recovery was in the range of 499±6 mg/g native biomass after pretreatment using 2.5% H2O2 (v/v) at 35 ?C for 24 h and 7.5% biomass loading (w/v) after enzymatic hydrolysis using 20 FPU/g Accellerase® 1500. The work demonstrates the potential of the developed process for low temperature pretreatment of biomass for further conversion to value-added products.   Keywords: rice straw, biorefinery, alkaline peroxide pretreatmen

    Study of Liquid Alkanes Production from Biomass-Derived Carbohydrates by Aldol-Condensation and Hydrogenation Processes

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    This research aims to synthesis liquid alkanes from biomass-derived hydroxyl methyl furfural (HMF) and furfural by aldol-condensation and hydrogenation processes over several catalysts i.e. TiO2, TiO2-ZrO2, Pd/Al2O3 and Pd/CeO2. It was found that the catalysts make significant impact on the selectivity and yield of alkanes product. It is noted that Pd/Al2O3 provided the highest alkane yield and selectivity. The aldol-condensation and hydrogenation of HMF over Pd/Al2O3 provide high C12 selectivity whereas the aldol-condensation and hydrogenation of furfural over Pd/Al2O3 provide high C8 selectivity. The effects of reaction temperature, reaction pressure and reaction time were then studied. The effect of inlet furfural to acetone molar ratio was also determined. It was also found that the optimized conditions to maximize the yield of alkane production from the aldol-condensation/hydrogenation of HMF and furfural are (i) at 53oC and 24 hr for aldol-condenstation of HMF, (ii) 80oC and 24 hr for aldol-condenstation of furfural, and (iii) 120oC for 6 hr with HMF to acetone molar ratio of 3:1 and furfural to acetone molar ratio of 4:1 in the presence of Pd/Al2O3 (calcined at 500oC) for hydrogenation reaction

    Bioethanol Production from Glycerol by Mixed Culture System

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    AbstractGlycerol, a by-product from biodiesel industry, is a promising feedstock for subsequent bioconversion to higher-value products. Potential application of a mixed microbial consortium on the fermentative conversion of glycerol to ethanol was demonstrated in this study. Maximum ethanol concentration of 11.1 g l-1 was produced after 72 h fermentation from the initial pure glycerol concentration of 45 g l-1, at 30 ÌŠC, and pH 7 under anaerobic conditions, corresponding to the ethanol production rate and yield of 0.34 g l-1 h-1, and 0.81 mol ethanolmol-1 glycerol, respectively. The microbial consortium yielded lower ethanol concentration (6.5 g l-1) but similar ethanol yield (0.85 mol ethanol mol-1 glycerol) when crude glycerol of 45 g l-1 was fermented at the same condition. At the optimum fermentative condition of the pure glycerol, phylogenetic analysis of microbial consortium based on 16S rRNA gene sequences indicated that Gammaproteobacteria represented 95% of the microbial diversity in the consortium while the rest belonged to Betaproteobacteria. The consortium was dominated by bacteria closely related to genera Enterobacter and Klebsiella, which could play the role on conversion of glycerol to ethanol in this system

    Comparative analysis of bacterial communities associated with healthy and diseased corals in the Indonesian sea

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    Coral reef ecosystems are impacted by climate change and human activities, such as increasing coastal development, overfishing, sewage and other pollutant discharge, and consequent eutrophication, which triggers increasing incidents of diseases and deterioration of corals worldwide. In this study, bacterial communities associated with four species of corals: Acropora aspera, Acropora formosa, Cyphastrea sp., and Isopora sp. in the healthy and disease stages with different diseases were compared using tagged 16S rRNA sequencing. In total, 59 bacterial phyla, 190 orders, and 307 genera were assigned in coral metagenomes where Proteobacteria and Firmicutes were predominated followed by Bacteroidetes together with Actinobacteria, Fusobacteria, and Lentisphaerae as minor taxa. Principal Coordinates Analysis (PCoA) showed separated clustering of bacterial diversity in healthy and infected groups for individual coral species. Fusibacter was found as the major bacterial genus across all corals. The lower number of Fusibacter was found in A. aspera infected with white band disease and Isopora sp. with white plaque disease, but marked increases of Vibrio and Acrobacter, respectively, were observed. This was in contrast to A. formosa infected by a black band and Cyphastrea sp. infected by yellow blotch diseases which showed an increasing abundance of Fusibacter but a decrease in WH1-8 bacteria. Overall, infection was shown to result in disturbance in the complexity and structure of the associated bacterial microbiomes which can be relevant to the pathogenicity of the microbes associated with infected corals

    Elucidating cellular mechanisms of Saccharomyces cerevisiae tolerant to combined lignocellulosic-derived inhibitors using high-throughput phenotyping and multiomics analyses

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    A robust cell factory that can tolerate combined inhibitory lignocellulosic compounds is essential for the cost-effective lignocellulose-based production of second-generation bioethanol and other bulk chemicals. Following high-throughput phenotyping of a yeast genomic overexpression library, we identified a Saccharomyces cerevisiae mutant (denoted AFb.01) with improved growth and fermentation performance under combined toxicity of acetic acid and furfural. AFb.01 carries overexpression of TRX1, which encodes for thioredoxin, a cellular redox machinery. Through comparative proteomics and metabolomics, the resulting cell-wide changes in the mutant were elucidated and these primarily target on the maintenance of energy and redox homeostasis and the minimization of stress-induced cell damages. In particular, the upregulation of the stress-response proteins Hsp26p and Fmp16p conferred tolerance of AFb.01 against protein denaturation and DNA damage. Moreover, increased levels of protectant metabolites such as trehalose, fatty acids, GABA and putrescine provided additional defense mechanisms for the mutant against oxidative and redox stresses. Future studies will concentrate on targeted genetic engineering to validate these mechanisms as well as to support the creation of more robust yeast strains, applicable for industrial, cost-competitive biorefinery production
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