Dickson R C, Markin J S
Cell. 1978 Sep;15(1):123-30. doi: 10.1016/0092-8674(78)90088-0.
The yeast Kluyveromyces lactis synthesizes a beta-galactosidase (EC 3.2.1.32) which is inducible by lactose. We have isolated the gene that codes for this enzyme using recombinant DNA techniques. K. lactis DNA was partially digested with the restriction endonuclease Eco R1 and joined to Eco R1-digested pBR322 plasmid DNA using DNA ligase. ligase. A lac-mutant of Escherichia coli lacking the structural gene for beta-galactosidase was transformed with ligated DNA. Three lac+ transformants containing recombinant plasmids were selected. Two of the plasmids (pK15 and pK17) contain four Eco R1-K. lactis DNA fragments having molecular weights of 2.2, 1.4, 0.55 and 0.5 x 10(6) daltons. The other plasmid (pK16) lacks the smallest fragment. E. coli carrying any of these plasmids produce beta-galactosidase activity that has a sedimentation coefficient and immunological determinants that are nearly identical to K. lactis beta-galactosidase and distinctly different from E. coli beta-galactosidase. DNA-DNA hybridization studies show that the four Eco R1 fragments in pK15 hybridize to K. lactis but not to E. coli DNA.
乳酸克鲁维酵母能合成一种β-半乳糖苷酶(EC 3.2.1.32),该酶可被乳糖诱导。我们利用重组DNA技术分离出了编码这种酶的基因。用限制性内切酶Eco R1对乳酸克鲁维酵母DNA进行部分消化,然后使用DNA连接酶将其与经Eco R1消化的pBR322质粒DNA连接。用连接后的DNA转化缺乏β-半乳糖苷酶结构基因的大肠杆菌lac突变体。筛选出了三个含有重组质粒的lac+转化体。其中两个质粒(pK15和pK17)含有四个Eco R1-乳酸克鲁维酵母DNA片段,分子量分别为2.2、1.4、0.55和0.5×10⁶道尔顿。另一个质粒(pK16)缺少最小的片段。携带这些质粒中的任何一种的大肠杆菌都会产生β-半乳糖苷酶活性,其沉降系数和免疫决定簇与乳酸克鲁维酵母β-半乳糖苷酶几乎相同,与大肠杆菌β-半乳糖苷酶明显不同。DNA-DNA杂交研究表明,pK15中的四个Eco R1片段与乳酸克鲁维酵母DNA杂交,但不与大肠杆菌DNA杂交。