Marchfelder A, Brennicke A
Institut für Genbiologische Forschung, Berlin, FRG.
Biochem Mol Biol Int. 1993 Mar;29(4):621-33.
Substrate specificity requirements of the plant mitochondrial RNase P were investigated with different natural and mutated substrates. Heterologous precursors with intact tRNAs from plant and fungal mitochondria, from bacteria, archaebacteria and of eukaryotic origins were processed faithfully, albeit with different efficiencies. Alteration of the acceptor stem length did not disturb correct processing, while activity is completely inhibited by deletion of the pseudouridine loop. Such and other minimal substrates processed by the E. coli RNase P are not recognized as substrates by the plant mitochondrial enzyme, suggesting different requirements for substrate recognition.
利用不同的天然和突变底物研究了植物线粒体核糖核酸酶P的底物特异性要求。来自植物和真菌线粒体、细菌、古细菌以及真核生物来源的带有完整tRNA的异源前体均能被准确加工,尽管加工效率有所不同。受体茎长度的改变并不影响正确加工,而假尿苷环的缺失则会完全抑制活性。大肠杆菌核糖核酸酶P能够加工的此类及其他最小底物不能被植物线粒体酶识别为底物,这表明底物识别的要求不同。