Nameki N, Tamura K, Himeno H, Asahara H, Hasegawa T, Shimizu M
Institute of Space and Astronautical Science, Kanagawa, Japan.
Biochem Biophys Res Commun. 1992 Dec 15;189(2):856-62. doi: 10.1016/0006-291x(92)92282-3.
Various tRNA transcripts were constructed to study the identity elements of Escherichia coli tRNA(Asp). Base substitutions from G34 to U34 at the first position of the anticodon, and from U35 to A35 at the second, severely impaired the aspartate charging activity. The activity was also decreased, but in a more moderate fashion, by base changes at G2-C71, C36 and C38. Identity nucleotides of tRNA(Asp) are distributed in a different fashion between E. coli and yeast, which occur at the second base pair of the acceptor stem, G10-U25 base pair in the D-stem and 3' half of the anticodon loop.
构建了各种tRNA转录本以研究大肠杆菌tRNA(Asp)的识别元件。反密码子第一位从G34到U34以及第二位从U35到A35的碱基替换严重损害了天冬氨酸负载活性。G2-C71、C36和C38处的碱基变化也使活性降低,但程度较为适中。tRNA(Asp)的识别核苷酸在大肠杆菌和酵母之间的分布方式不同,它们出现在受体茎的第二个碱基对、D茎中的G10-U25碱基对以及反密码子环的3' 一半处。