Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/41333
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Título : Probing the determinants of substrate specificity of a feruloyl esterase, AnFaeA, from Aspergillus niger
Autor : Faulds, Craig B., Molina, Rafael, González García, Ramón, Husband, Fiona, Juge, Nathalie, Sanz-Aparicio, J., Hermoso, Juan A.
Palabras clave : Active site specificity
Aspergillus niger
Fecha de publicación : 15-Aug-2005
Editor: John Wiley & Sons
Citación : FEBS Journal 272(17): 4362–4371 (2005)
Resumen: Feruloyl esterases hydrolyse phenolic groups involved in the cross-linking of arabinoxylan to other polymeric structures. This is important for opening the cell wall structure making material more accessible to glycoside hydrolases. Here we describe the crystal structure of inactive S133A mutant of type-A feruloyl esterase from Aspergillus niger (AnFaeA) in complex with a feruloylated trisaccharide substrate. Only the ferulic acid moiety of the substrate is visible in the electron density map, showing interactions through its OH and OCH3 groups with the hydroxyl groups of Tyr80. The importance of aromatic and polar residues in the activity of AnFaeA was also evaluated using site-directed mutagenesis. Four mutant proteins were heterologously expressed in Pichia pastoris, and their kinetic properties determined against methyl esters of ferulic, sinapic, caffeic and p-coumaric acid. The kcat of Y80S, Y80V, W260S and W260V was drastically reduced compared to that of the wild-type enzyme. However, the replacement of Tyr80 and Trp260 with smaller residues broadened the substrate specificity of the enzyme, allowing the hydrolysis of methyl caffeate. The role of Tyr80 and Trp260 in AnFaeA are discussed in light of the three-dimensional structure.
Versión del editor: http://dx.doi.org/10.1111/j.1742-4658.2005.04849.x
URI : http://hdl.handle.net/10261/41333
ISSN: 1742-464X
DOI: 10.1111/j.1742-4658.2005.04849.x
Citación : FEBS Journal 272(17): 4362–4371 (2005)
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