【摘要】 将来源于瘤胃真菌Neocallimastix frontalis的高比活木聚糖酶基因xyn-w整合到毕赤酵母表达载体pPIC9上,通过电击转化得到重组转化子。SDS-PAGE分析和表达产物的研究表明,木聚糖酶基因xyn-w得到了高效分泌表达,在5 L发酵罐中木聚糖酶蛋白表达量达到1 mg/mL,酶活性达到13 000 IU以上。XYN-W的C端57个氨基酸序列为连接序列和锚定区域,利用PCR方法将此段序列去除,得到截短的木聚糖酶序列xyn-m。用相同方法构建高效表达XYN-M蛋白的毕赤酵母工程菌株,表达产物经纯化后进行酶学性质测定,结果表明,其比活为19 856.6 IU/mg,Kcat值为4 433.8 s-1,与纯化的XYN-W蛋白(比活性13 795.3 IU/mg、Kcat值2 717.1 s-1)相比,分别提高了43.9%和63.2%。更多还原

【Abstract】 xyn-w gene encoding a xylanase with high specific activity from ruminal fungus Neocallimastix frontalis was inserted into pPIC9 with the yeast α-mating factor and transformed into Pichia pastoris by electroporation to obtain the recombinants.It was shown that the recombinant xylanase xyn-w was high efficiently expressed and secreted into the supernatant medium by SDS-PAGE and expression products analysis.In 5 liter fermentor,xylanase protein was expressed by the level of 1 mg/mL and its activity was more than 13 000 IU /mL.Using PCR method,a truncated xyn-m was obtained by deleting the 57 amino acids at the C-terminus of the xylanase XYN-W,which were binding domains and anchered domains.Similarly,the P.pastoris strains with high expression of xylanase XYN-M were constructed and the enzyme character of purified product was analyzed.The result showed that the specific activity and Kcat of XYN-M was 19 856.6 IU/mg and 4 433.8 s-1 respectively,increased 43.9% and 63.2% compared to those of XYN-W(13 795.3 IU/mg and 2 717.1 s-1),respectively.更多还原