Johanson K O, McHenry C S
J Biol Chem. 1984 Apr 10;259(7):4589-95.
Adenosine 5'-O-(3-thiotriphosphate) (ATP gamma S) will substitute for ATP in the formation of an initiation complex between the DNA polymerase III holoenzyme of Escherichia coli and primed DNA. The initiation complex formed in the presence of ATP gamma S between the DNA polymerase III holoenzyme and single-stranded DNA-binding protein-encoated primed M13 Gori DNA is stabile and isolable by gel filtration at room temperature. Upon addition of the four required deoxynucleoside triphosphates, this complex is rapidly converted to the duplex replicative form without dissociation of the polymerase. Initiation complexes formed in the presence of either ATP gamma S or ATP are indistinguishable by their resistance to antibody directed against the beta subunit of the holoenzyme and by their ability to elongate without further activation. A 2-fold difference was observed, however, in both the extent of initiation complex formation and in the dissociation of initiation complexes once formed. This difference is discussed in the light of previous proposals regarding a dimeric polymerase capable of replicating both strands at a replication fork concurrently.
腺苷 5'-O-(3-硫代三磷酸)(ATPγS)在大肠杆菌 DNA 聚合酶 III 全酶与引发 DNA 形成起始复合物的过程中可替代 ATP。在 ATPγS 存在下,DNA 聚合酶 III 全酶与单链 DNA 结合蛋白包被的引发 M13 Gori DNA 形成的起始复合物是稳定的,在室温下可通过凝胶过滤分离。加入四种所需的脱氧核苷三磷酸后,该复合物迅速转化为双链复制形式,而聚合酶不会解离。在 ATPγS 或 ATP 存在下形成的起始复合物,通过它们对针对全酶β亚基的抗体的抗性以及无需进一步激活即可延伸的能力来看是无法区分的。然而,在起始复合物形成的程度以及一旦形成后的起始复合物解离方面都观察到了 2 倍的差异。根据先前关于能够在复制叉处同时复制两条链的二聚体聚合酶的提议,对这种差异进行了讨论。