|標題:||Cloning, expression and characterization of beta-xylosidase from Aspergillus niger ASKU28|
Kongsaeree, Prachumporn T.
Department of Applied Chemistry
|關鍵字:||Aspergillus niger;Codon optimization;Glycoside hydrolase family 3;Pichia pastoris;Xylan hydrolysis;beta-Xylosidase|
|摘要:||beta-Xylosidases catalyze the breakdown of beta-1,4-xylooligosaccharides, which are produced from degradation of xylan by xylanases, to fermentable xylose. Due to their important role in xylan degradation, there is an interest in using these enzymes in biofuel production from lignocellulosic biomass. In this study, the coding sequence of a glycoside hydrolase family 3 beta-xylosidase from Aspergillus niger ASKU28 (AnBX) was cloned and expressed in Pichia pastoris as an N-terminal fusion protein with the alpha-mating factor signal sequence (alpha-MF) and a poly-histidine tag. The expression level was increased to 5.7 g/l in a fermenter system as a result of optimization of only five codons near the 5\' end of the alpha-MF sequence. The recombinant AnBX was purified to homogeneity through a single-step Phenyl Sepharose chromatography. The enzyme exhibited an optimal activity at 70 degrees C and at pH 4.0-4.5, and a very high kinetic efficiency toward a xyloside substrate. AnBX demonstrated an exo-type activity with retention of the beta-configuration, and a synergistic action with xylanase in hydrolysis of beechwood xylan. This study provides comprehensive data on characterization of a glycoside hydrolase family 3 beta-xylosidase that have not been determined in any prior investigations. Our results suggested that AnBX may be useful for degradation of lignocellulosic biomass in bioethanol production, pulp bleaching process and beverage industry. (C) 2015 Elsevier Inc. All rights reserved.|
|期刊:||PROTEIN EXPRESSION AND PURIFICATION|
|Appears in Collections:||Articles|