Preparation of marine silage of swordfish, ray and shark visceral waste by lactic acid bacteria

The goal of the present work was to study the efficacy of several lactic acid bacteria (LAB) as bio-silage inoculants of swordfish, ray and shark viscera by-products. A sterilised medium was initially used as a model system for assessing the potential of these microorganisms in batch and fed-batch c...

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Detalles Bibliográficos
Autores: Vázquez, José Antonio, Nogueira, Margarita, Durán, Ana, Prieto, Miguel Ángel, Rodríguez-Amado, I., Rial, Diego, González Fernández, Pilar, Murado García, Miguel Anxo
Tipo de recurso: artículo
Fecha de publicación:2011
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/44450
Acceso en línea:http://hdl.handle.net/10261/44450
Access Level:acceso abierto
Palabra clave:Visceral waste upgrading
Lactic acid bacteria
Bio-silage
Marine peptones
Fish-by products
Environmental pollution
Descripción
Sumario:The goal of the present work was to study the efficacy of several lactic acid bacteria (LAB) as bio-silage inoculants of swordfish, ray and shark viscera by-products. A sterilised medium was initially used as a model system for assessing the potential of these microorganisms in batch and fed-batch cultures with re-neutralisation. In all cases, batch cultivations without re-neutralisation led to the highest production and yields of the main metabolites of LAB fermentation (lactic and acetic acids). The dynamics of these metabolites followed a conversion pattern from lactic to acetic acid with a final joint concentration over 16 g/L and final pH lower than 4.5. Both productions were modelled by means of logistic modified equations. In addition, the capability of LAB to ferment the fish visceral wastes was always high and easily reproducible. Finally, the results obtained for non-sterilised fermentations with Lactobacillus casei CECT 4043 were similar to those obtained for sterilised media, and a stable material was obtained after 72 h of culture.