Harashima S, Sidhu R S, Toh-e A, Oshima Y
Gene. 1981 Dec;16(1-3):335-41. doi: 10.1016/0378-1119(81)90091-3.
A yeast DNA fragment complementing a yeast his5 mutation was cloned on a shuttle vector, YRp7, by transformation of the yeast host with plasmid DNA prepared from a gene bank constructed in the Escherichia coli host. That the DNA fragment contains the yeast HIS5 gene was confirmed by the integration of the cloned plasmid into the his5 region of the yeast chromosome. The cloned yeast HIS5 gene weakly complemented the E. coli hisC mutation and gave rise to a slow-growing E. coli transformant without addition of histidine. From the slow-growing culture, rapidly growing variants of E. coli were easily obtained by mutations either in the bacterial chromosome or in the plasmid.
通过用从大肠杆菌宿主构建的基因文库制备的质粒DNA转化酵母宿主,将一个互补酵母his5突变的酵母DNA片段克隆到穿梭载体YRp7上。通过将克隆的质粒整合到酵母染色体的his5区域,证实该DNA片段包含酵母HIS5基因。克隆的酵母HIS5基因对大肠杆菌hisC突变有微弱的互补作用,在不添加组氨酸的情况下产生生长缓慢的大肠杆菌转化体。从生长缓慢的培养物中,通过细菌染色体或质粒中的突变很容易获得快速生长的大肠杆菌变体。