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Lactic acid and biosurfactants production from hydrolyzed distilled grape marc
Institution:1. Department of Bioengineering and IBB-Institute for Biotechnology and Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal;2. MIT-Portugal Program, 77 Massachusetts Avenue, E40-221, Cambridge, MA 02139, USA;3. Laboratório Nacional de Energia e Geologia, I.P., Unidade de Bioenergia, Estrada do Paço do Lumiar 22, 1649-038 Lisboa, Portugal;4. Faculdade de Engenharia, Universidade Lusófona de Humanidades e Tecnologias, Av. Campo Grande 376, 1749-024 Lisboa, Portugal;5. Instituto de Tecnologia Química e Biológica (ITQB), Universidade Nova de Lisboa, 2780-156 Oeiras, Portugal;1. Department of Food Science, Faculty of Food Engineering, University of Campinas, P.O. Box 6121, 13083-862 Campinas, SP, Brazil;2. Chemical Engineering Department of Polytechnic School of the University of São Paulo, São Paulo, SP, Brazil;3. Brazilian Bioscience National Laboratory, Campinas, SP, Brazil;4. Department of Food and Nutritional Science, University of Reading, Reading, UK;1. Chemical Engineering Department, Faculty of Sciences, University of Granada, Spain;2. School of Biomedical Sciences, University of Ulster, Coleraine BT52 1SA, N. Ireland, UK
Abstract:Acid hydrolysis of distilled grape marc, an useless agricultural residue from wineries, was carried out using dilute sulfuric acid (1–5%) at several reaction times and 130 °C, in order to obtain monomeric sugars which after supplementation with corn steep liquor (10 g/L) and yeast extract (10 g/L) were used to carry out the fermentation into lactic acid by Lactobacillus pentosus without detoxification stage. Xylose was the main sugar generated followed by glucose and arabinose. Possible inhibitor compounds such as acetic acid liberated from acetyl groups, and furfural and hydroxymethylfurfural generated by sugars dehydration, were produced as degradation byproducts. The hydrolysis stage was optimized by using an incomplete factorial design where the independent variables were the percentage of catalyzer, the reaction time and the temperature. The optima conditions in terms of xylose concentration were 3.3% H2SO4, 125 min and 130 °C, but due to the high furfural concentration, two other conditions using lower reaction times (30 and 77.5 min) were also selected to assay the fermentation. Although any condition was feasible to fully utilize the relatively broad spectra of sugars released by the acid hydrolysis, under the shorter reaction time the best results were achieved (QP = 0.476 g/L h; YP/S = 0.71 g/g) which represents a theoretical yield of 97%. Furthermore, L. pentosus produced 4.8 mg/L of intracellular biosurfactants, measured as biosurfactin, representing a yield of 0.60 mg of intracellular biosurfactant per g of sugars consumed.
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