A wild-growing glucose-rich (i.e. 56.7% glucose content) brown seaweed species Laminaria digitata, collected from the North Coast of Denmark in August 2012, was used as the feedstock for an integrated bioethanol and protein production. Glutamic acid and aspartic acid are the two most abundant amino acids in the algal protein, both with proportional content of 10% in crude protein. Only minor pretreatment of milling was used on the biomass to facilitate the subsequent enzymatic hydrolysis and fermentation. The Separate Hydrolysis and Fermentation (SHF) resulted in obviously higher ethanol yield than the Simultaneous Saccharification and Fermentation (SSF). High conversion rate at maximum of 84.1% glucose recovery by enzymatic hydrolysis and overall ethanol yield at maximum of 77.7% theoretical were achieved. Protein content in the solid residues after fermentation was enriched by 2.7 fold, with similar distributions of amino acids, due to the hydrolysis of polymers in the seaweed cell wall matrix.
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http://dx.doi.org/10.1016/j.biortech.2015.08.091 | DOI Listing |
RSC Adv
December 2024
Laboratoire des Silicates, Polymères et des Nanocomposites (LSPN), Université 8 Mai 1945, Guelma BP 401 Guelma 24000 Algeria.
Pollution by heavy metals is a major global issue. The biosorptive removal of Cd and Cu by () was evaluated in this work. FTIR and XRD analysis were performed to determine the characteristics of the biosorbent.
View Article and Find Full Text PDFChemSusChem
December 2024
Department of Energy, Environmental, and Chemical Engineering, McKelvey School of Engineering, Washington University in St. Louis, St Louis, MO 63130, USA.
Chemical depolymerization of lignin is a non-selective process that often generates a wide distribution of product compounds, denoted herein as lignin breakdown products (LBPs). To address this limitation, we developed a hybrid lignin conversion process that employs a lignin-first catalytic approach on biomass and subsequent microbial upgrading. A Pd/C catalyst was used for reductive catalytic fractionation (RCF) of poplar biomass, and Rhodococcus opacus PD630 (R.
View Article and Find Full Text PDFBioresour Technol
December 2024
Waste to Bioproducts-Lab, Department of Agronomy Food Natural resources Animals and Environment (DAFNAE), Università degli Studi di Padova, Agripolis, Viale dell'Università 16, 35020 Legnaro PD, Italy; Department of Microbiology, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa. Electronic address:
This study utilized a circular economy approach to convert unripe rice, a low-cost by-product of the rice milling industry, into biofuels using a biorefinery process. The recombinant yeast Saccharomyces cerevisiae ER T12.7 strain was tested for its ability to produce ethanol from unripe rice.
View Article and Find Full Text PDFSci Total Environ
December 2024
Energy Systems Engineering Group, Department of Energy Engineering, Sharif University of Technology, Azadi Ave, P.O. Box 14565-114, Tehran, Islamic Republic of Iran. Electronic address:
This study presents an integrated model that addresses the complex interplay between water, land, food, and human health for the optimal design of a BioEnergy Supply Chain (BESC), with a focus on future climate challenges. The model is designed to balance key objectives such as minimizing economic costs, reducing human health impacts, and optimizing water use. By employing a weighted-sum approach, the model identifies the best land allocation for various crops and the most efficient biofuel production pathways.
View Article and Find Full Text PDFBioprocess Biosyst Eng
November 2024
College of Life Sciences, Northeast Forestry University, No. 26, Hexing Road, Harbin, 150040, China.
The efficient and eco-friendly removal of lignin is a critical challenge for bioethanol production from lignocellulosic biomass. Herein, we report the integration of laccase with deep eutectic solvents (DESs) for the pretreatment of corn stover to enhance the production of reducing sugars. Three betaine-based DESs were prepared and tested for their effects on the activity and stability of a bacterial laccase from Bacillus amyloliquefaciens LC02.
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