1) endo-xylanase
内切木聚糖酶
1.
The multiplicity of Trichoderma reesei xylanase,and the effects of carbon source,pH value and ratio of carbon to nitrogen on synthesis of endo-xylanase and xylosidase are systematically reviewed,and the methods to controll these cultivation conditions to synthesize xylosidase-poor xylanases are put forward in order to make the xylanases better application in .
系统地介绍了里氏木霉木聚糖酶的的多样性以及碳源、pH和碳氮比等培养条件对合成内切木聚糖酶和木糖苷酶的影响,提出了调控这些培养条件选择性合成低木糖苷酶活的木聚糖酶的方法。
2.
A model describing the solubilization of arabinoxylans and degradation by endo-xylanase random attacking during mashing was developed.
建立了糖化过程中阿拉伯木聚糖溶解及内切木聚糖酶随机进攻的预测模型,希望通过此模型能预测在不同初始条件和参数设置下糖化过程中阿拉伯木聚糖的浓度,以减少其在酿造过程中的负面作用。
2) endo-β-xylanase
内切-β-木聚糖酶
1.
Effects of feed velocity, operational pressure and enzyme activity of xylanases on ultrafiltration separation of endo-β-xylanase and β-xylosidase were investigated.
研究了进料速度、操作压力、木聚糖酶活大小对内切-β-木聚糖酶和β-木糖苷酶超滤分离的影响。
3) 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)。
4) cellulase Cex
内切-β-1,4-木聚糖酶
5) endoglucanase Ⅰ
瑞氏木霉内切葡聚糖酶
1.
Phage display of endoglucanase Ⅰ from Trichoderma reesei and its cellulose-binding domain;
瑞氏木霉内切葡聚糖酶Ⅰ及其CBD的噬菌体表面展示系统的构建
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.
ＢＴ７克隆内切木聚糖酶基因的结果。
补充资料：木聚糖酶
分子式：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
分子量：暂无
CAS号：暂无
性质：暂无
制备方法：暂无
用途：暂无
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条