Sreekrishna K, Dickson R C
Proc Natl Acad Sci U S A. 1985 Dec;82(23):7909-13. doi: 10.1073/pnas.82.23.7909.
We have constructed strains of Saccharomyces cerevisiae that grow on lactose (Lac+). S. cerevisiae strain YNN27, which, like all S. cerevisiae, is unable to grow on lactose, was transformed with pKR1B-LAC4-1. This plasmid has a selectable marker gene conferring resistance to the antibiotic G418 and carries a 13-kilobase region of the Kluyveromyces lactis genome including LAC4, a beta-galactosidase gene. Transformants were selected first for G418 resistance and then for growth on lactose. Southern hybridization experiments showed that Lac+ transformants had integrated 15-25 tandem copies of the vector into a host chromosome. Several lines of evidence indicate that the Lac+ phenotype in pKR1B-LAC4-1-transformed S. cerevisiae is due to expression of a K. lactis lactose permease gene that lies between 2 and 8.6 kilobase upstream of LAC4 and also to expression of LAC4. The permease gene has been designated LAC12.
我们构建了能在乳糖上生长(Lac+)的酿酒酵母菌株。酿酒酵母菌株YNN27与所有酿酒酵母一样,无法在乳糖上生长,用pKR1B-LAC4-1对其进行了转化。该质粒有一个赋予对抗生素G418抗性的选择标记基因,并携带克鲁维酵母基因组的一个13千碱基区域,包括β-半乳糖苷酶基因LAC4。首先选择对G418有抗性的转化体,然后选择能在乳糖上生长的转化体。Southern杂交实验表明,Lac+转化体已将15 - 25个串联拷贝的载体整合到宿主染色体中。几条证据表明,pKR1B-LAC4-1转化的酿酒酵母中的Lac+表型是由于位于LAC4上游2至8.6千碱基之间的克鲁维酵母乳糖通透酶基因的表达以及LAC4的表达。通透酶基因已被命名为LAC12。