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dc.contributor.author
del Gobbo, Luciana Melisa  
dc.contributor.author
Villegas, Liliana Beatriz  
dc.contributor.author
Colin, Veronica Leticia  
dc.date.available
2022-12-15T17:21:22Z  
dc.date.issued
2021  
dc.identifier.citation
Study of the protein production of Aspergillus sp. V1 using sugarcane vinasse as substrate; IV Joint Meeting of the Biology Societies of Argentina; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 117  
dc.identifier.uri
http://hdl.handle.net/11336/181357  
dc.description.abstract
Vinasse is an acidic effluent with a high organic load, which result from ethyl alcohol production. This residue represents a potential hazard for theenvironment if not responsibly managed. Filamentous fungi can adapt to a wide variety of substrates and grow in large quantities on organic wastes.In turn, bioconversion of residues into protein-rich fungal biomass is of great interest since it can be used as an alternative nutrient source to theexpensive aquafeeds such as fishmeal and soybean meal. In a prior study, a filamentous fungus isolated from northwest of the Argentine, Aspergillussp. V1, was able to grow on sugarcane vinasse. The objective of the present work was to evaluate the protein content of Aspergillus sp. V1 biomasscultivated on vinasse, with and without supplement of exogenous nutrients. The optimal vinasse concentration for the growth of Aspergillus sp. V1was determined making dilutions of the residue in distilled water (10% to 100%, v/v) at a final volume of 10 mL. Each dilution was inoculated with1×106spores/mL and incubated at 30ºC (150 rpm) for 96 h under sterile conditions; then dry weight of biomass at 105°C was determined. Biomassproduction was carried out in 200 mL of sterile vinasse at the selected concentration, with and without supplementation of nitrogen and phosphorousin the following combinations: vinasse without nutrient supplementation (B1); vinasse supplemented with 2 g/L of (NH4)2SO4 (B2), or 2 g/L ofCO(NH2)2 (B3); vinasse supplemented with 2 g/L of (NH4)2SO4 and 1 g/L of KH2PO4 (B4), or 2 g/L of CO(NH2)2 and 1 g/L of KH2PO4 (B5). Thebiomass produced was separated by filtration, lyophilized, and weighed. In each case, percentage of total proteins (Kjeldahl-Arnold-Gunning methodusing the universal factor of conversion to protein 6.25) and productivity (in terms of milligrams of protein per liter of culture per h) was determined.The highest growth of Aspergillus sp. V1 was observed in 100% vinasse, with a biomass production of 41.55 g/L thereby following assays wereconducted witn undiluted vinasse. The weight of lyophilized biomasses was 0.89; 0.61; 2.84; 1.00 and 2.99 g/L, with protein percentages of 33%;49%; 41%; 38% and 36%, and a productivity of 3.0; 3.1; 12.0; 4.0 and 11.1 mg/L h for B1, B2, B3, B4 and B5, respectively. According to literature,aquafeeds should contain between 26% to 55% protein. In all cases, protein percentages of Aspergillus sp. V1 biomass were within the desirablerange. However, B3 was selected as the most promising biomass for future assays due to its higher productivity (12.0 mg/L h). Our findingsdemonstrate that the mycelium of Aspergillus sp. V1 grown in vinasse could be a promising and inexpensive protein source to be used as aquafeed.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Tech Science Press  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
ASPERGILLUS SP. V1  
dc.subject
SUGARCANE VINASSE  
dc.subject
AQUAFEEDS  
dc.subject
PROTEIN-RICH FUNGAL BIOMASS  
dc.subject.classification
Otras Ingeniería del Medio Ambiente  
dc.subject.classification
Ingeniería del Medio Ambiente  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Study of the protein production of Aspergillus sp. V1 using sugarcane vinasse as substrate  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.type
info:eu-repo/semantics/conferenceObject  
dc.type
info:ar-repo/semantics/documento de conferencia  
dc.date.updated
2022-12-12T23:15:20Z  
dc.journal.volume
45  
dc.journal.number
Suplemento 3  
dc.journal.pagination
117  
dc.journal.pais
Argentina  
dc.journal.ciudad
Tucuman  
dc.description.fil
Fil: del Gobbo, Luciana Melisa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Planta Piloto de Procesos Industriales Microbiológicos; Argentina  
dc.description.fil
Fil: Villegas, Liliana Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina  
dc.description.fil
Fil: Colin, Veronica Leticia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Planta Piloto de Procesos Industriales Microbiológicos; Argentina  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.techscience.com/biocell/v45nSuppl.3/44000/pdf  
dc.conicet.rol
Autor  
dc.conicet.rol
Autor  
dc.conicet.rol
Autor  
dc.coverage
Internacional  
dc.type.subtype
Reunión  
dc.description.nombreEvento
IV Joint Meeting of the Biology Societies of Argentina  
dc.date.evento
2020-09-09  
dc.description.ciudadEvento
Ciudad Autónoma de Buenos Aires  
dc.description.paisEvento
Argentina  
dc.type.publicacion
Journal  
dc.description.institucionOrganizadora
Asociación de Biología de Tucumán  
dc.description.institucionOrganizadora
Sociedad de Biología de Cuyo  
dc.description.institucionOrganizadora
Sociedad de Biología de Córdoba  
dc.description.institucionOrganizadora
Sociedad de Biología de Córdoba  
dc.description.institucionOrganizadora
Sociedad de Biología de Rosario  
dc.description.institucionOrganizadora
Sociedad Argentina de Biología  
dc.source.revista
Biocell  
dc.date.eventoHasta
2020-09-15  
dc.type
Reunión