Agarwal K L, Caruthers M H, Fridkin M, Kumar A, van de Sande J H, Khorana H G
J Biol Chem. 1976 Feb 10;251(3):599-608.
The chemical syntheses of the dodecanucleotide, d(G-C-C-G-C-T-C-G-G-G-A-A), the decanucleotides, d(T-T-T-A-G-A-G-T-C-T), d(G-C-T-C-C-C-T-T-T-G), d(C-G-G-C-C-A-A-A-G-G), and the nonanucleotide, d(G-A-G-C-A-G-A-C-T), are described. The deoxypolynucleotides together represent the DNA duplex corresponding to the nucleotide sequence 47-78 of the gene for the tyrosine suppressor tRNA. Chemical syntheses used protected mono- and oligonucleotides and stepwise condensation methods. The detailed plans used are given in Diagrams 1 to 4 in the text. Two additional notable features in the present syntheses were: (a) solvent extraction procedures for the preparation of oligonucleotides as large as pentanucleotides and (b) the demonstration that a heptanucleotide containing 5'-phosphate group can be used successfully in condensation with the 3'-OH group of another oligonucleotide. The synthetic polynucleotides were purified and characterized at protected and unprotected levels.
描述了十二聚体d(G-C-C-G-C-T-C-G-G-G-A-A)、十聚体d(T-T-T-A-G-A-G-T-C-T)、d(G-C-T-C-C-C-T-T-T-G)、d(C-G-G-C-C-A-A-A-G-G)以及九聚体d(G-A-G-C-A-G-A-C-T)的化学合成。这些脱氧多核苷酸共同代表了与酪氨酸抑制tRNA基因核苷酸序列47 - 78相对应的DNA双链体。化学合成使用了受保护的单核苷酸和寡核苷酸以及逐步缩合方法。文中图1至图4给出了所采用的详细方案。本合成中的另外两个显著特点是:(a) 用于制备五聚体大小的寡核苷酸的溶剂萃取程序,以及(b) 证明含有5'-磷酸基团的七聚体可成功用于与另一个寡核苷酸3'-OH基团的缩合反应。对合成的多核苷酸在受保护和未受保护水平下进行了纯化和表征。