Lowdon M, Goddard J P
Nucleic Acids Res. 1976 Dec;3(12):3383-96. doi: 10.1093/nar/3.12.3383.
E coli tRNA2Phe was modified at 25 degrees C with 3M sodium bisulphite, pH6.0, for periods of up to 48 hours, Three cytadinine residues, at position 17, 74 and 75 from the 5' end were each deaminated to uridine. The 2-methylthio-N6-isopentenyl adenosine at position 37 formed a 1:1 bi-sulphite addition product which was stable to alkaii. No other residues were permanently modified. The rate of modification of each residue was first order with respect to remaining unmodified nucleotide, the time of half reaction, t1/2, being different for each residue. C17 reaction reacted at twice the rate of cytidine in PolyC, indicating that it occupied a very exposed position in the tRNA.
大肠杆菌苯丙氨酸转运核糖核酸(E coli tRNA2Phe)在25摄氏度下用pH6.0的3M亚硫酸氢钠处理长达48小时。从5'端起第17、74和75位的三个胞嘧啶残基各自脱氨形成尿苷。37位的2-甲硫基-N6-异戊烯基腺苷形成了一种对碱稳定的1:1亚硫酸氢盐加成产物。没有其他残基被永久性修饰。每个残基的修饰速率相对于剩余未修饰的核苷酸是一级反应,每个残基的半衰期(t1/2)不同。C17反应的速率是聚胞嘧啶(PolyC)中胞嘧啶反应速率的两倍,这表明它在转运核糖核酸中占据非常暴露的位置。