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Electrochemical analysis of template-free DNA synthesis: Lowering pH and the active component of the impedance spectrum

机译:无模板DNA合成的电化学分析:降低pH和阻抗谱的活性成分

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The process of template-free DNA synthesis was detected in two ways: by measuring the pH of the solution by a semiconductor sensor and by measuring the conductivity in the recording of impedance spectra. Synthesis was carried out without using template DNA, with only two enzymes being involved in the reaction: DNA polymerase and nicking endonuclease (nickase) in the presence of deoxynucleotide triphosphates. Previously, Purushothaman et al., by applying the recording of the results of template-directed synthesis with a pH-sensitive field-effect transistor, showed that protons are released into solution in the incorporation of nucleotides [4]. Regarding this, it was important to establish that the same release of protons into solution occurred in the template-free synthesis as in the template-directed synthesis and to identify the changes by measuring the conductivity of the solution using impedance spectra. It was found that the template-free synthesis was accompanied by the generation of protons (Delta pH is similar to 1.5 pH at an initial concentration of deoxynucleotide triphosphates of 150 A mu M) and a decrease in the value of active impedance component by similar to 25% of the initial value. The effect of a decrease in the active impedance component was explained as being due to an increasing conductivity of medium due to a growth in the concentration of protons.
机译:以两种方式检测到无模板DNA合成的方法:通过半导体传感器测量溶液的pH,并通过测量阻抗光谱的记录中的电导率。在不使用模板DNA的情况下进行合成,仅在反应中涉及两种酶:DNA聚合酶和在脱氧核苷酸三磷酸核苷酸存在下的切口内切核酸酶(酸脱酶)。以前,Purushothaman等人。通过使用pH敏感场效应晶体管施加模板引导合成的结果,显示质子在掺入核苷酸的溶液中[4]。关于这一点,重要的是在无模板的合成中确定在无模板合成中发生与溶液相同的质子释放,并通过阻抗光谱测量溶液的导电性来鉴定变化。发现,无模板的产生伴随着质子的产生(Delta pH在初始浓度为150μmm m的脱氧核苷酸三磷酸的初始浓度上的1.5 pH),并通过类似于的活性阻抗组分的值降低初始值的25%。由于培养基的浓度的生长而导致的培养基的导电性增加,解释了活性阻抗组分的效果。

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