ATP对大肠杆菌DNA聚合酶整合三磷酸脱氧核糖核苷的影响

Tatjana Spasokukotskaja, Mária Staub, Mária Sasvári-Székely, Ference Antoni
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引用次数: 3

摘要

研究了ATP对大肠杆菌DNA聚合酶I的影响,并将其作为底物和二价金属离子浓度的函数进行了研究。在饱和Mg2+浓度下,当只有一种底物(dGTP)存在时,1.5 mM ATP刺激了2.5倍的[3H]dGTP的掺入,并且在所有四种dntp存在时没有显著影响,而在类似条件下,饱和浓度的dATP仅使反应速率提高了1.5倍。在最佳Mn2+浓度下,ATP也仅在反应中存在一种底物(dGTP)的情况下显示出类似的显著效果。当四种底物同时存在时,ATP将Mn2+的最佳浓度转移到更高的浓度。ATP对dGTP的表观Km没有影响,而V增加了约2.5倍。通过同位素稀释分析,排除了ATP中可能存在的不纯dNTP。因此,ATP仅在有限的条件下才会刺激聚合反应,即当反应中存在一种底物时。
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The effect of ATP on the incorporation of deoxyribonucleoside triphosphates by Escherichia coli DNA polymerase I

The effect of ATP on Escherichia coli DNA polymerase I has been investigated as a function of the concentration of substrates and divalent metal ions in the presence of activated DNA as template. At saturating Mg2+ concentration 1.5 mM ATP stimulated 2.5-times the incorporation of [3H]dGTP when only one substrate (dGTP) was present, and had no significant effect in the presence of all four dNTPs, whereas under similar conditions, a saturating concentration of dATP increased the reaction rate only 1.5-times. At optimal Mn2+ concentrations ATP also showed a similarly marked effect only in the case when one substrate (dGTP) was present in the reaction. The optimal concentration of Mn2+ was shifted by ATP to higher concentrations both in the presence of one and of all four substrates. ATP did not influence the apparent Km for dGTP, while V was increased by a factor of about 2.5. The possible presence of dNTP in ATP, as inpurity, was ruled out by isotope dilution analysis. Thus, ATP stimulated the polymerization reaction only under limited conditions, i.e., when one substrate was present in the reaction.

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