Characterization of a versatile arylesterase from Lactobacillus plantarum active on wine esters

The gene lp-1002 from Lactobacillus plantarum WCFS1 encoding a putative lipase/esterase was cloned and overexpressed in Escherichia coli BL21(DE3). The purified Lp-1002 protein was biochemically characterized. Lp-1002 is an arylesterase which showed high hydrolytic activity on phenyl acetate. Althou...

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Detalles Bibliográficos
Autores: Esteban-Torres, María, Barcenilla Moraleda, José María, De Las Rivas, Blanca, Muñoz, Rosario
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2014
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/99870
Acceso en línea:http://hdl.handle.net/10261/99870
Access Level:acceso abierto
Palabra clave:Wine aroma
Lactic acid bacteria
flavor
Esterase
Ethyl acetate
Descripción
Sumario:The gene lp-1002 from Lactobacillus plantarum WCFS1 encoding a putative lipase/esterase was cloned and overexpressed in Escherichia coli BL21(DE3). The purified Lp-1002 protein was biochemically characterized. Lp-1002 is an arylesterase which showed high hydrolytic activity on phenyl acetate. Although to a lesser extent, Lp-1002 also hydrolyzed most of the esters assayed including relevant wine aroma compounds. Importantly, Lp-1002 exhibited hydrolytic activity at winemaking conditions, although optimal catalytic activity is observed at 40 °C and pH 5-7. The effect of wine compounds on Lp-1002 activity was assayed. From the compounds assayed (ethanol, sodium metabisulfite, and malic, tartaric, lactic and citric acids), only malic acid slightly inhibited Lp-1002 activity. Lp-1002 is the first arylesterase described in a wine lactic acid bacteria and possessed suitable biochemical properties to be used during winemaking. © 2014 American Chemical Society.