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BETA-GLUCOSIDASE GENE ISOLATED FROM RUMINOCOCCUS ALBUS

机译:从白夜蛾中分离出β-葡糖苷酶基因

摘要

PURPOSE: A beta-glucosidase gene sequence to be isolated from Ruminococcus albums is identified, and the expression vector inserting such gene and transformants thereby that are able to grow on the selective medium are obtained by using the genetic engineering techniques to produce a large amount of beta-glucosidase being useful in degrading cellulose. CONSTITUTION: A chromosomal DNA of Ruminococcus albums is cleaved with several restriction enzymes, so that its DNA library is prepared. The interest DNA fragments within the DNA library are inserted into a vector plasmid pUC 19. The gene is cloned through incubation of E. coli transformed by the pUC 19 vector. E. coli transformants by the pUC 19 vector containing the beta-glucosidase gene are isolated, which is determined by blue-colored colonization. After incubation of such isolated vector, the beta-glucosidase activity within the culture is measured.
机译:目的:鉴定出要从Ruminococcus Albums中分离的β-葡萄糖苷酶基因序列,并通过使用基因工程技术生产大量可克隆的β-葡萄糖苷酶基因的表达载体,从而使该基因和转化子能够在选择培养基上生长。 β-葡萄糖苷酶可用于降解纤维素。组成:Ruminococcus albums的染色体DNA被几种限制性内切酶切割,从而制备了其DNA文库。将DNA文库内的目的DNA片段插入载体质粒pUC 19中。通过孵育由pUC 19载体转化的大肠杆菌来克隆该基因。通过含有β-葡糖苷酶基因的pUC 19载体分离大肠杆菌转化体,其通过蓝色定殖确定。孵育这种分离的载体后,测量培养物中的β-葡糖苷酶活性。

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