Eisenbeis S J, Parker J
Mol Gen Genet. 1981;183(1):115-22. doi: 10.1007/BF00270148.
That portion of the Escherichia coli chromosome carried by a number of lambda transducing phages, all of which carry the gua operon, was mapped using restriction endonucleases. The DNA from one of these transducing phages was subcloned onto pBR322. We have identified two recombinant plasmids which carry the Escherichia coli gene hisS, the structural gene for histidyl-tRNA synthetase. The two plasmids, pSE301 and pSE401, have in common a 3,540 bp fragment of E. coli DNA which is bounded by BglII and SalI restriction endonuclease recognition sites. Strains carrying these plasmids overproduce histidyl-tRNA synthetase 20 to 30 fold. The growth rate of these strains is not affected although the histidine biosynthetic enzymes are derepressed. This derepression seems to be in addition to that caused by introduction of a hisT mutation on the chromosome.
利用限制性内切酶对许多携带gua操纵子的λ转导噬菌体所携带的大肠杆菌染色体部分进行了图谱绘制。其中一个转导噬菌体的DNA被亚克隆到pBR322上。我们鉴定出了两个携带大肠杆菌hisS基因(组氨酰-tRNA合成酶的结构基因)的重组质粒。这两个质粒pSE301和pSE401共有一段3540 bp的大肠杆菌DNA片段,其两端为BglII和SalI限制性内切酶识别位点。携带这些质粒的菌株组氨酰-tRNA合成酶的产量会超产20到30倍。尽管组氨酸生物合成酶被去阻遏,但这些菌株的生长速率并未受到影响。这种去阻遏似乎是除了染色体上引入hisT突变所导致的去阻遏之外的额外作用。