Department of Microbiology, University of Delhi South Campus, Benito Juarez Road, New Delhi 110021, India.
Bioresour Technol. 2015 Mar;179:382-389. doi: 10.1016/j.biortech.2014.12.049. Epub 2014 Dec 18.
The recombinant Pichia pastoris harboring the endoxylanase gene (TSEV1xyl) of Bacillus halodurans TSEV1 yielded a high titer of extracellular xylanase (502±23 U ml(-1)) on induction with methanol. The purified recombinant xylanase (TSEV1xyl) displayed optimal activity at 80°C and pH 9.0. The glycosylated recombinant xylanase exhibited higher thermostability (T1/2 of 45 min at 80°C) than the native enzyme (T1/2 of 35 min at 80°C). The agroresidues subjected to pretreatment (soaking in alkali followed by microwave irradiation) liberated xylooligosaccharides (XOS) upon hydrolysis with the recombinant xylanase. The removal of unhydrolyzed agroresidues, xylanase and xylose from the hydrolysate by two-step ultrafiltration led to the purification of XOS as confirmed by TLC as well as HPLC analysis.
含有嗜盐杆菌 TSEV1 内切木聚糖酶基因(TSEV1xyl)的重组毕赤酵母在甲醇诱导下产生了高浓度的胞外木聚糖酶(502±23 U ml(-1))。纯化的重组木聚糖酶(TSEV1xyl)在 80°C 和 pH 9.0 下表现出最佳活性。与天然酶相比,糖基化的重组木聚糖酶(T1/2 为 45 min 在 80°C)表现出更高的热稳定性。经预处理(碱浸泡后微波辐射)的农业残余物在用重组木聚糖酶水解时释放出木二糖寡糖(XOS)。通过两步超滤从水解物中去除未水解的农业残余物、木聚糖酶和木糖,通过薄层色谱和高效液相色谱分析证实了 XOS 的纯化。