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。
Therefore, Bacillus subtilis was selected as xylanase gene expression host in this study.
表达载体和宿主的选择对于木聚糖酶基因的表达起着至关重要的作用。
The choice of expression vector and host strain plays an important role in expression of xylanase.
采用PCR方法对短小芽孢杆菌A - 30菌株的耐碱性木聚糖酶基因进行克隆。
The alkali-tolerant xylanase gene of Bacillus pumilus A-30 was cloned by PCR.
在进行基因组步行PCR克隆真菌木聚糖酶基因的研究中，探索并建立了一套可在普通分子生物学实验室采用的高得率、高质量真菌染色体DNA的抽提方法。
When we cloned fungal xylanase gene with the method of Genomic walking PCR, we constructed a simple and cheap protocol for extraction of fungal chromosomal DNA.
在进行基因组步行PCR克隆真菌木聚糖酶基因的研究中，探索并建立了一套可在普通分子生物学实验室采用的高得率、高质量真菌染色体DNA的抽提方法。
When we cloned fungal xylanase gene with the method of Genomic walking PCR, we constructed a simple and cheap protocol for extraction of fungal chromosomal DNA.
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