Brakhage A A, Putzer H, Shazand K, Röschenthaler R J, Grunberg-Manago M
Institut für Mikrobiologie, Universität Münster, Federal Republic of Germany.
J Bacteriol. 1989 Feb;171(2):1228-32. doi: 10.1128/jb.171.2.1228-1232.1989.
The genes that encode the two subunits of Bacillus subtilis phenylalanyl-tRNA synthetase were cloned from alpha lambda library of chromosomal B. subtilis DNA by specific complementation of a thermosensitive Escherichia coli pheS mutation. Both genes (we named them pheS and pheT, analogous to the corresponding genes of E. coli) are carried by a 6.6-kilobase-pair PstI fragment which also complements E. coli pheT mutations. This fragment directs the synthesis of two proteins identical in size to the purified alpha and beta subunits of the phenylalanyl-tRNA synthetase of B. subtilis with Mrs of 42,000 and 97,000, respectively. A recombinant shuttle plasmid carrying the genes caused 10-fold overproduction of functional phenylalanyl-tRNA synthetase in B. subtilis.
通过对枯草芽孢杆菌DNA染色体αλ文库进行筛选,利用温度敏感型大肠杆菌pheS突变的特异性互补作用,克隆出了编码枯草芽孢杆菌苯丙氨酰 - tRNA合成酶两个亚基的基因。这两个基因(我们将它们命名为pheS和pheT,类似于大肠杆菌的相应基因)由一个6.6千碱基对的PstI片段携带,该片段也能互补大肠杆菌的pheT突变。这个片段指导合成两种大小与枯草芽孢杆菌苯丙氨酰 - tRNA合成酶纯化的α和β亚基相同的蛋白质,其相对分子质量分别为42,000和97,000。携带这些基因的重组穿梭质粒导致枯草芽孢杆菌中功能性苯丙氨酰 - tRNA合成酶过量产生10倍。