1) endo-1,4-xylanase gene
内切-1,4-木聚糖酶基因
1.
The endo-1,4-xylanase gene from Aspergillus usamii E001 was cloned into the Pichia pastoris expression vector,pPIC9K,the recombinant plasmid was named pPXYNII.
将宇佐美曲霉E001的内切-1,4-木聚糖酶基因克隆到毕赤酵母表达载体pPIC9K中,得到重组质粒pPXY-NII,将其经SalⅠ线性化后分别转化2株毕赤酵母GS115和KM71,xynⅡ基因通过同源重组被整合到毕赤酵母染色体上,并处于酵母α因子的下游,经筛选获得阳性重组菌PXGL98(Mut+)和PXKL29(Muts)。
2) β-1,4-endo-glucanase gene
β-1,4-内切葡聚糖酶基因
3) endo-β-1,4-glucanase gene
内切-β-1,4-葡聚糖酶基因
4) endo xylanase genes
内切木聚糖酶基因
1.
The analyses by restriction mapping and Southern hybridization proved that they were three different endo xylanase genes.
ＢＴ７克隆内切木聚糖酶基因的结果。
5) cellulase Cex
内切-β-1,4-木聚糖酶
6) endo-1,4-beta-xylanase
内切-1,4-β-木聚糖酶
1.
Two clones expressing endo-1,4-beta-xylanase activity were isolated and one clone designated UMXYL2 was characterized by subcloning and sequencing.
6×10~8bp,筛选得到2个表达内切-1,4-β-木聚糖酶活性的克隆。
补充资料：木聚糖酶
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分子量：暂无
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性质：暂无
制备方法：暂无
用途：暂无
分子量：暂无
CAS号：暂无
性质：暂无
制备方法：暂无
用途：暂无
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