Hennecke H, Böck A
Eur J Biochem. 1975 Jul 1;55(2):431-7. doi: 10.1111/j.1432-1033.1975.tb02179.x.
Three different phenylalanyl-tRNA synthetases have been purified to near homogeneity, one from a wild-type strain of Escherichia coli and the others from two independently isolated p-fluorophenyalanine-resistant strains. The mutant enzymes were not able to use p-fluorophenylalanine as a substrate for activation and attachment to tRNA. They proved to be indistinguishable from the wild-type enzyme by several electrophoretic and immunological criteria. The alpha and beta subunits of all three enzymes have been prepared by a method described in this paper. The isolated subunits per se did not reveal any significant enzyme activity, but combined they were able to form active phenylalanyl tRNA synthetase after a defined reconstitution process. Mixed reconstitution experiments between wild-type and mutant subunits indicate that the mutant alpha subunit is responsible for p-fluorophenylalanine resistance and therefore seems to carry the phenylalanine-binding site or to participate in its formation.
三种不同的苯丙氨酰 - tRNA合成酶已被纯化至接近均一,一种来自大肠杆菌野生型菌株,另外两种来自两个独立分离的对氟苯丙氨酸抗性菌株。突变酶不能使用对氟苯丙氨酸作为底物进行激活并连接到tRNA上。通过几种电泳和免疫学标准证明它们与野生型酶没有区别。所有三种酶的α和β亚基已通过本文所述方法制备。分离出的亚基本身没有显示出任何显著的酶活性,但在经过特定的重组过程后,它们组合在一起能够形成活性苯丙氨酰tRNA合成酶。野生型和突变亚基之间的混合重组实验表明,突变的α亚基是对氟苯丙氨酸抗性的原因,因此似乎携带苯丙氨酸结合位点或参与其形成。