Therefore, Bacillus subtilis was selected as xylanase gene expression host in this study.
因此本研究选择枯草芽孢杆菌为木聚糖酶基因表达宿主菌。
After the reading frame was confirmed correct by sequencing, the recombinant plasmid was transformed into expression host e.
测序表明读码框架正确后,将重组子分别转入表达宿主菌e。
The ABP1 and TIR1 prokaryotic expression vectors were transformed into expression host strain BL21 (DE3), then after, IPTG was added to induce expression.
将构建好的ABP1及TIR1原核表达载体,转化表达宿主菌bl21 (DE3),加入诱导物iptg进行诱导表达。
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