McSwiggen J A, Cech T R
Howard Hughes Medical Institute, Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215.
Science. 1989 May 12;244(4905):679-83. doi: 10.1126/science.2470150.
The intervening sequence of the ribosomal RNA precursor of Tetrahymena is a catalytic RNA molecule, or ribozyme. Acting as a sequence-specific endoribonuclease, it cleaves single-stranded RNA substrates with concomitant addition of guanosine. The chemistry of the reaction has now been studied by introduction of a single phosphorothioate in the substrate RNA at the cleavage site. Kinetic studies show no significant effect of this substitution on kcat (rate constant) or Km (Michaelis constant), providing evidence that some step other than the chemical step is rate-limiting. Product analysis reveals that the reaction proceeds with inversion of configuration at phosphorus, consistent with an in-line, SN2 (P) mechanism. Thus, the ribozyme reaction is in the same mechanistic category as the individual displacement reactions catalyzed by protein nucleotidyltransferases, phosphotransferases, and nucleases.
四膜虫核糖体RNA前体的间隔序列是一种催化性RNA分子,即核酶。它作为一种序列特异性核糖核酸内切酶,在添加鸟苷的同时切割单链RNA底物。现在通过在底物RNA的切割位点引入单个硫代磷酸酯来研究该反应的化学过程。动力学研究表明,这种取代对催化常数(kcat,速率常数)或米氏常数(Km)没有显著影响,这证明除化学步骤外的某些步骤是限速步骤。产物分析表明,反应在磷原子处发生构型翻转,这与线性SN2(P)机制一致。因此,核酶反应与由蛋白质核苷酸转移酶、磷酸转移酶和核酸酶催化的个别取代反应属于同一机制类别。