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Sequence analysis,cloning and over-expression of an endoxylanase from the alkaliphilic <Emphasis Type="BoldItalic">Bacillus halodurans</Emphasis>
Authors:Email author" target="_blank">M?Alejandra?MartínezEmail author  Osvaldo?D?Delgado  Mario?D?Baigorí  Faustino?Si?eriz
Institution:(1) PROIMI, Planta Piloto de Procesos Industriales Microbiológicos, Av. Belgrano y Pasaje Caseros, T-400 1MVB Tucumán, Argentina;(2) Department of Biotechnology, Centre for Chemistry & Chemical Engineering, Lund University, P.O. Box 124, , SE-221 00 Lund, Sweden
Abstract:The BhMIR32 xyn11A gene, encoding an extracellular endoxylanase of potential interest in bio-bleaching applications, was amplified from Bacillus halodurans MIR32 genomic DNA. The protein encoded is an endo-1,4-β-xylanase belonging to family 11 of glycosyl hydrolases. Its nucleotide sequence was analysed and the mature peptide was subcloned into pET22b(+) expression vector. The enzyme was over-expressed in a high density Escherichia coli culture as a soluble and active protein, and purified in a single step by immobilised metal ion affinity chromatography with a specific activity of 3073 IU mg−1.
Keywords:Bacillus halodurans MIR32  over-expression  purification  xylanase sequence
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