Nagahari K, Koshikawa T, Sakaguchi K
Mol Gen Genet. 1979 Mar 20;171(2):115-9. doi: 10.1007/BF00269997.
RP4-trp hybrid plasmid containing Escherichia coli whole tryptophan operon was conjugatively transferred from E. coli to Rhizobium leguminosarum strains carrying mutations in different trp genes, converting their Trp- phenotype to Trp+. That the phenotype change of the R. leguminosarum cells was due to the presence of the E. coli tryptophan operon was verified by the isolation of RP4-trp hybrid plasmid from the R. leguminosarum conjugant cells, and by re-transfer of RP4-trp plasmid by conjugation back to E. coli trp and Pseudomonas putida trp strains. Enzymatic activities of anthranilate synthetase and beta subunit of tryptophan synthetase in crude extracts of R. leguminosarum cells containing RP4-trp plasmid were much higher than that of the wild-type cells and were not repressed by the presence of tryptophan in the culture medium.
含有大肠杆菌完整色氨酸操纵子的RP4 - trp杂种质粒通过接合作用从大肠杆菌转移到在不同色氨酸基因中携带突变的豆科根瘤菌菌株中,将它们的色氨酸缺陷型表型转变为色氨酸原养型。通过从豆科根瘤菌接合子细胞中分离出RP4 - trp杂种质粒,以及通过接合作用将RP4 - trp质粒重新转移回大肠杆菌色氨酸缺陷型菌株和恶臭假单胞菌色氨酸缺陷型菌株,证实了豆科根瘤菌细胞的表型变化是由于存在大肠杆菌色氨酸操纵子。含有RP4 - trp质粒的豆科根瘤菌细胞粗提物中邻氨基苯甲酸合成酶和色氨酸合成酶β亚基的酶活性比野生型细胞高得多,并且不受培养基中色氨酸存在的抑制。