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1)  xylanase sequence
木聚糖酶基因序列
2)  xylanase gene
木聚糖酶基因
1.
Using the method of transparent circle to the positive clones, the identical xylanase genes was identified.
采用改良鸟枪法构建了草本纤维精制高效菌种CXJZ11-01的基因组文库,通过透明圈法筛选到了2个木聚糖酶基因阳性克隆。
2.
In the past decades over hundred on xylanase genes have been cloned into homogenous and heterogenetic hosts to super-express the xylanase and to change .
在过去几十年里,有超过100个木聚糖酶基因被克隆进同源或异源宿主中,其目的是为了超表达木聚糖酶和改变它们的特性以适应商业应用。
3.
The xylanase genes on the two clones were subcloned,sequenced and analysed.
从自制堆肥样品中提取未培养细菌的总DNA,用柯斯质粒pW EB∷TNC为载体构建宏基因组文库,对文库进行筛选获得表达木聚糖酶活性的克隆,再进行亚克隆、测序分析以及B lastx搜索G enB ank分析木聚糖酶基因。
3)  xylanase gene(xyn I)
木聚糖酶基因(xynⅠ)
4)  xyn B gene
木聚糖酶B基因
5)  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)。
6)  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.
BT7克隆内切木聚糖酶基因的结果。
补充资料:木聚糖酶
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