Peterson E T, Uhlenbeck O C
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215.
Biochemistry. 1992 Oct 27;31(42):10380-9. doi: 10.1021/bi00157a028.
The nucleotides in Escherichia coli tRNA(Phe) required for recognition by its cognate synthetase have been determined in vitro by measuring the kinetic parameters for aminoacylation using mutant tRNA(Phe) transcripts with purified E. coli tRNA(Phe) synthetase. The substitution of 11 nucleotides in E. coli tRNA(Phe) is shown to decrease the kcat/KM by as much as 1000-fold relative to the wild type. The most important recognition elements are the three anticodon nucleotides G34, A35, and A36. The recognition set also includes nucleotides in the variable pocket (U20 and U59), the acceptor end (A73), and the tRNA central core (G10, C25, A26, G44, and U45). Many of the recognition nucleotides are also among the residues comprising the identity set determined in vivo using an amber suppressor tRNA(Phe) [McClain, W. H., & Foss, K. (1988) J. Mol. Biol. 202, 697-709]. As could be anticipated from the very different methods used, some nucleotides in the identity set determined by the suppressor method were not among the recognition nucleotides and vice versa. The E. coli tRNA(Phe) recognition data can also be compared to the recognition sets for yeast and human tRNA(Phe) determined previously. The results indicate that the mechanism by which phenylalanyl-tRNA synthetases recognize their substrates seems to have diverged somewhat among different species. For example, nucleotide 20 in the D-loop, the anticodon nucleotides and the discriminator base 73 are important for the recognition by all three enzymes. However, recognition of the tRNA central core nucleotides is unique to E. coli FRS.(ABSTRACT TRUNCATED AT 250 WORDS)
通过使用纯化的大肠杆菌苯丙氨酰 - tRNA合成酶,测定突变体tRNA(Phe)转录本的氨酰化动力学参数,已在体外确定了大肠杆菌tRNA(Phe)中被其同源合成酶识别所需的核苷酸。结果表明,大肠杆菌tRNA(Phe)中11个核苷酸的取代,相对于野生型,使kcat/KM降低了多达1000倍。最重要的识别元件是三个反密码子核苷酸G34、A35和A36。识别位点还包括可变口袋中的核苷酸(U20和U59)、受体末端(A73)以及tRNA中央核心(G10、C25、A26、G44和U45)。许多识别核苷酸也包含在使用琥珀抑制tRNA(Phe)在体内确定的同一性位点残基中[麦克莱恩,W. H.,& 福斯,K.(1988年)《分子生物学杂志》202卷,697 - 709页]。从所使用的截然不同的方法可以预料到,通过抑制方法确定的同一性位点中的一些核苷酸不在识别核苷酸之中,反之亦然。大肠杆菌tRNA(Phe)的识别数据也可以与先前确定的酵母和人tRNA(Phe)的识别位点进行比较。结果表明,苯丙氨酰 - tRNA合成酶识别其底物的机制在不同物种之间似乎已经有所不同。例如,D环中的核苷酸20、反密码子核苷酸和鉴别碱基73对所有三种酶的识别都很重要。然而,对tRNA中央核心核苷酸的识别是大肠杆菌苯丙氨酰 - tRNA合成酶所特有的。(摘要截短于250字)