Paluh J L, Zalkin H
J Bacteriol. 1983 Jan;153(1):345-9. doi: 10.1128/jb.153.1.345-349.1983.
Several plasmids, isolated from two plasmid pools, complemented a Saccharomyces cerevisiae trp3 mutant with defective indole-3-glycerol-phosphate synthase activity. Restriction mapping indicated that a 1.2-kilobase StuI segment was common to all complementing plasmids. Southern blot hybridization established that a cloned 5.2-kilobase BamHI fragment was derived intact from chromosomal DNA. A yeast trp3 mutant transformed with trp3-complementing plasmids contained approximately 40-fold elevated indole-3-glycerol-phosphate synthase activity. These plasmids also complemented an Escherichia coli trpC mutant, and transformants exhibited enzyme activity. Yeast trp3 is therefore associated with a 1.2-kilobase StuI DNA segment.
从两个质粒库中分离出的几种质粒,可对吲哚 - 3 - 甘油磷酸合酶活性有缺陷的酿酒酵母trp3突变体进行互补。限制性酶切图谱分析表明,所有互补质粒都有一个1.2千碱基的StuI片段。Southern印迹杂交证实,一个克隆的5.2千碱基BamHI片段完整地来源于染色体DNA。用trp3互补质粒转化的酵母trp3突变体中,吲哚 - 3 - 甘油磷酸合酶活性提高了约40倍。这些质粒也能互补大肠杆菌trpC突变体,转化体表现出酶活性。因此,酵母trp3与一个1.2千碱基的StuI DNA片段相关。