首页> 外国专利> CELL OF MYCELIAL FUNGUS PENICILLIUM THE CANESCENS- PRODUCER OF XYLANASE AND LACCASE, METHOD OF OBTAINING COMBINED FERMENTATION PREPARATION OF XYLANASE AND LACCASE

CELL OF MYCELIAL FUNGUS PENICILLIUM THE CANESCENS- PRODUCER OF XYLANASE AND LACCASE, METHOD OF OBTAINING COMBINED FERMENTATION PREPARATION OF XYLANASE AND LACCASE

机译:木霉真菌青霉菌细胞木聚糖酶和漆酶的癌变产物,获得木聚糖酶和漆酶联合发酵制备的方法

摘要

1. Cage mycelial fungus Penicillium canescens, transformed with a plasmid containing the DNA fragment encoding the xylanase, and a plasmid containing the DNA fragment encoding the laccase, - producing xylanase and lakkazy.2. The cell of claim 1, characterized in that the said plasmids are plasmids and pBGlac pBGxylD sootvetstvenno.3. The cell of claim 1, which is a cell strain of Penicillium canescens PCA-10-4 / I-7/12 niaD, and transformed with plasmids pBGlac pBGxylD, - C1 ligninolytic laccase producer fungus Trametes hirsuta and xylanase XylD filamentous fungus Penicillium canescens.4. A method of producing a xylanase enzyme preparation and laccase, comprising the steps of growing the cells mycelial fungus Penicillium canescens according to claim 1 in a nutrient medium and isolating the xylanase enzyme preparation and zhidkosti.5 laccase from the culture. A method according to claim 4, characterized in that as a cell strain of filamentous fungus Penicillium canescens using cells of 2.6. A method according to claim 4, characterized in that the cultivation of cells of the strain of claim 1 carried out in the presence metalloproteinaz.7 inhibitors. A method according to claim 6, characterized in that the metalloproteinase inhibitor as used EDTA.8. A method according to claim 4, characterized in that the cultivation of cells of the strain of claim 1 carried out in a medium with a pH ranging 4,0-6,0.9. A method according to claim 4, characterized in that the selection enzyme preparations xylanase and laccase from the culture medium is carried out by concentrating using ultrafiltration membrane with a cutoff threshold of 5 KDa followed by vacuum evaporation of the filtrate of culture liquid at a temperature of 40-70 ° C.
机译:1.用含有编码木聚糖酶的DNA片段的质粒和含有编码漆酶的DNA片段的质粒转化笼养菌丝青霉,产生木聚糖酶和lakkazy。 2.根据权利要求1所述的细胞,其特征在于,所述质粒是质粒和pBGlac pBGxylD sootvetstvenno.3。 2.根据权利要求1所述的细胞,其是堪萨斯青霉PCA-10-4 / I-7 / 12 niaD的细胞株,并用质粒pBGlac pBGxylD,-C1木质素分解漆酶生产菌Trametes hirsuta和木聚糖酶XylD丝状真菌青枯菌转化。 4。一种生产木聚糖酶制剂和漆酶的方法,该方法包括以下步骤:在营养培养基中培养根据权利要求1的细胞菌丝体青霉菌,并从培养物中分离木聚糖酶制剂和zhidkosti.5漆酶。 5.根据权利要求4所述的方法,其特征在于,使用2.6的细胞作为丝状真菌Canescens的细胞株。 5.根据权利要求4的方法,其特征在于在金属蛋白az.7抑制剂存在下进行权利要求1的菌株的细胞培养。 7.根据权利要求6的方法,其特征在于金属蛋白酶抑制剂如EDTA.8所用。 5.根据权利要求4所述的方法,其特征在于,在pH为4.0-0.6的介质中进行权利要求1的菌株的细胞的培养。 5.根据权利要求4所述的方法,其特征在于,通过使用截止阈值为5KDa的超滤膜浓缩,然后在80℃的温度下真空蒸发培养液的滤液,来进行从培养基中选择酶制剂的木聚糖酶和漆酶的制备。 40-70℃。

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