Haynie S L, Whitesides G M
Department of Chemistry, Massachusetts Institute of Technology, Cambridge 02139.
Appl Biochem Biotechnol. 1990 Mar;23(3):205-20. doi: 10.1007/BF02942055.
This paper (1) describes the enzymatic synthesis of a mixture of adenosine, guanosine, cytidine, and uridine triphosphates (ATP, GTP, CTP, and UTP) from ribonucleic acid (RNA). RNA was hydrolyzed by nuclease P1 to a mixture of 5'-nucleoside monophosphates. This mixture was converted to the nucleoside triphosphates using a mixture of nucleoside monophosphate kinases and acetate kinase, with acetyl phosphate as the ultimate phosphoryl donor. The nucleoside monophosphokinases were extracted from brewer's yeast in a four-step procedure. The specific activity of the yeast enzyme preparation after gel permeation chromatography was sufficiently high that the yeast kinases could be immobilized in volumes that were practical for laboratory scale syntheses. Conversions from NMP to NTP in a mixture containing 0.34 mol of total nucleoside phosphates were: ATP, 90%; GTP, 90%; CTP, 60%; and UTP, 40%.
本文(1)描述了由核糖核酸(RNA)通过酶促合成腺苷三磷酸、鸟苷三磷酸、胞苷三磷酸和尿苷三磷酸(ATP、GTP、CTP和UTP)混合物的方法。RNA被核酸酶P1水解为5'-单磷酸核苷混合物。使用单磷酸核苷激酶和乙酸激酶的混合物,以乙酰磷酸作为最终磷酰基供体,将该混合物转化为三磷酸核苷。单磷酸核苷激酶通过四步程序从啤酒酵母中提取。凝胶渗透色谱后酵母酶制剂的比活性足够高,以至于酵母激酶可以固定在适合实验室规模合成的体积中。在含有0.34摩尔总核苷磷酸的混合物中从NMP到NTP的转化率为:ATP,90%;GTP,90%;CTP,60%;UTP,40%。