首页> 外文期刊>Journal of bacteriology >Bacillus subtilis phenylalanyl-tRNA synthetase genes: cloning and expression in Escherichia coli and B. subtilis.
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Bacillus subtilis phenylalanyl-tRNA synthetase genes: cloning and expression in Escherichia coli and B. subtilis.

机译:枯草芽孢杆菌苯丙氨酰-tRNA合成酶基因:在大肠杆菌和枯草芽孢杆菌中的克隆和表达。

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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.
机译:通过热互补性大肠杆菌pheS突变的特异性互补,从枯草芽孢杆菌DNA的alpha lambda文库中克隆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)都由一个6.6碱基对的PstI片段携带,该片段也与大肠杆菌pheT突变互补。该片段指导两个蛋白质的合成,其大小与枯草芽孢杆菌的苯丙氨酰-tRNA合成酶的纯化的α和β亚基相同,Mrs分别为42,000和97,000。携带该基因的重组穿梭质粒在枯草芽孢杆菌中导致功能性苯丙氨酰-tRNA合成酶过量生产10倍。

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