Barker D G
Eur J Biochem. 1982 Jul;125(2):357-60. doi: 10.1111/j.1432-1033.1982.tb06691.x.
Two fragments of DNA which carry the genes coding for the tyrosyl-tRNA synthetases of Escherichia coli and Bacillus stearothermophilus have been cloned into the plasmid pBR322 and were selected by complementation of an E. coli temperature-sensitive mutant. Transformation of this strain with either of the recombinant plasmids results in a 100-fold increase in tyrosyl-tRNA synthetase activity measured in vitro and the protein products co-migrate with the corresponding purified enzymes on polyacrylamide gels.
携带着大肠杆菌和嗜热栖热放线菌酪氨酰 - tRNA合成酶编码基因的两段DNA片段已被克隆到质粒pBR322中,并通过对大肠杆菌温度敏感突变体的互补作用进行筛选。用任何一种重组质粒转化该菌株,都会使体外测得的酪氨酰 - tRNA合成酶活性增加100倍,并且蛋白质产物在聚丙烯酰胺凝胶上与相应的纯化酶共迁移。