Martin B R, Voorheis H P
Biochem J. 1977 Mar 1;161(3):555-9. doi: 10.1042/bj1610555.
A simple, rapid and inexpensive method is described for the enzymic synthesis of [alpha-32P]ATP from [32P]Pi on a preparative scale with an overall yield of 53%. The final product contained all of the detectable radioactivity (less than 99.9%) in the alpha position and has been shown to behave identically with commerically availabe [alpha-32P]ATP during the synthesis of 3':5'-cyclic AMP in the reaction catalysed by adenylate cyclase.
本文描述了一种简单、快速且廉价的方法,可用于从[32P]Pi以制备规模酶促合成[α-32P]ATP,总产率为53%。最终产物在α位含有所有可检测到的放射性(小于99.9%),并且已证明在腺苷酸环化酶催化的反应中合成3':5'-环AMP时,其行为与市售的[α-32P]ATP相同。