Putzer H, Brakhage A A, Grunberg-Manago M
Institut de Biologie Physico-Chimique, Paris, France.
J Bacteriol. 1990 Aug;172(8):4593-602. doi: 10.1128/jb.172.8.4593-4602.1990.
With the exception of Escherichia coli lysyl-tRNA synthetase, the genes coding for the different aminoacyl-tRNA synthetases in procaryotes are always unique. Here we report on the occurrence and cloning of two genes (thrSv and thrS2), both encoding functional threonyl-tRNA synthetase in Bacillus subtilis. The two proteins share only 51.5% identical residues, which makes them almost as distinct from each other as each is from E. coli threonyl-tRNA synthetase (42 and 47%). Both proteins complement an E. coli thrS mutant and effectively charge E. coli threonyl tRNA in vitro. Their genes have been mapped to 250 degrees (thrSv) and 344 degrees (thrS2) on the B. subtilis chromosome. The regulatory regions of both genes are quite complex and show structural similarities. During vegetative growth, only the thrSv gene is expressed.
除了大肠杆菌赖氨酰 - tRNA合成酶外,原核生物中编码不同氨酰 - tRNA合成酶的基因总是唯一的。在此我们报道了枯草芽孢杆菌中两个均编码功能性苏氨酰 - tRNA合成酶的基因(thrSv和thrS2)的发现及克隆。这两种蛋白质只有51.5%的相同残基,这使得它们彼此之间的差异几乎与它们与大肠杆菌苏氨酰 - tRNA合成酶的差异一样大(分别为42%和47%)。这两种蛋白质都能互补大肠杆菌thrS突变体,并在体外有效地使大肠杆菌苏氨酰tRNA氨酰化。它们的基因已定位在枯草芽孢杆菌染色体的250°(thrSv)和344°(thrS2)处。这两个基因的调控区域相当复杂且显示出结构上的相似性。在营养生长期间,只有thrSv基因表达。