Chakraburtty K
Nucleic Acids Res. 1975 Oct;2(10):1793-804. doi: 10.1093/nar/2.10.1793.
Escherichia coli tRNA Arg was treated with sodium bisulfite to convert exposed cytosine residues to uracil. This treatment resulted in the loss of amino acid acceptance of the tRNA Arg with pseudo first-order reaction kinetics. The active and inactive molecules were separated after about 60e active and inactive molecules were separated after about 60 percent inactivation and analyzed for U in various positions by finger-printing of the oligonucleotides produced by nucleases. The results show that C to U base transitions in the dihydrouridine loop and in the CCA terminus have no effect on the aminoacylation of this tRNA. Deamination of a cytosine residue at the second position of the anticodon resulted in the loss of amino acid acceptor activity of arginine transfer RNA.
用亚硫酸氢钠处理大肠杆菌tRNA精氨酸,将暴露的胞嘧啶残基转化为尿嘧啶。这种处理导致tRNA精氨酸的氨基酸接受能力以假一级反应动力学丧失。在约60%失活后分离活性和非活性分子,并通过对核酸酶产生的寡核苷酸进行指纹分析来分析各个位置的尿嘧啶。结果表明,二氢尿嘧啶环和CCA末端的C到U碱基转换对该tRNA的氨酰化没有影响。反密码子第二位的胞嘧啶残基脱氨基导致精氨酸转移RNA的氨基酸接受体活性丧失。