{"title":"不同二价阳离子对嗜热脂肪芽孢杆菌DNA聚合酶动力学和保真度的影响。","authors":"Ashwani Kumar Vashishtha, William H Konigsberg","doi":"10.3934/biophy.2018.2.125","DOIUrl":null,"url":null,"abstract":"<p><p>Although Mg<sup>2+</sup> is the metal ion that functions as the cofactor for DNA polymerases (DNA pols) <i>in vivo</i>, Mn<sup>2+</sup> can also serve in this capacity but it reduces base discrimination. Metal ions aside from Mg<sup>2+</sup> or Mn<sup>2+</sup> can act as cofactors for some DNA pols but not for others. Here we report on the ability of several divalent metal ions to substitute for Mg<sup>2+</sup> or Mn<sup>2+</sup> with BST DNA polymerase (BST pol), an A family DNA pol. We selected the metal ions based on whether they had previously been shown to be effective with other DNA pols. We found that Co<sup>2+</sup> and Cd<sup>2+</sup> were the only cations tested that could replace Mg<sup>2+</sup> or Mn<sup>2+</sup>. When Co<sup>2+</sup> was substituted for Mg<sup>2+</sup>, the incorporation efficiency for correct dNTPs increased 6-fold but for incorrect dNTPs there was a decrease which depended on the incoming dNTP. With Mn<sup>2+</sup>, base selectivity was impaired compared to Co<sup>2+</sup> and Cd<sup>2+</sup>. In addition, Co<sup>2+</sup> and Mn<sup>2+</sup> helped BST pol to catalyze primer-extension past a mismatch. Finally both Co<sup>2+</sup> and Mn<sup>2+</sup> enhanced ground-state binding of both correct and incorrect dNTPs to BST pol: Dideoxy terminated primer-template complexes.</p>","PeriodicalId":7529,"journal":{"name":"AIMS Biophysics","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992921/pdf/","citationCount":"10","resultStr":"{\"title\":\"The effect of different divalent cations on the kinetics and fidelity of <i>Bacillus stearothermophilus</i> DNA polymerase.\",\"authors\":\"Ashwani Kumar Vashishtha, William H Konigsberg\",\"doi\":\"10.3934/biophy.2018.2.125\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Although Mg<sup>2+</sup> is the metal ion that functions as the cofactor for DNA polymerases (DNA pols) <i>in vivo</i>, Mn<sup>2+</sup> can also serve in this capacity but it reduces base discrimination. Metal ions aside from Mg<sup>2+</sup> or Mn<sup>2+</sup> can act as cofactors for some DNA pols but not for others. Here we report on the ability of several divalent metal ions to substitute for Mg<sup>2+</sup> or Mn<sup>2+</sup> with BST DNA polymerase (BST pol), an A family DNA pol. We selected the metal ions based on whether they had previously been shown to be effective with other DNA pols. We found that Co<sup>2+</sup> and Cd<sup>2+</sup> were the only cations tested that could replace Mg<sup>2+</sup> or Mn<sup>2+</sup>. When Co<sup>2+</sup> was substituted for Mg<sup>2+</sup>, the incorporation efficiency for correct dNTPs increased 6-fold but for incorrect dNTPs there was a decrease which depended on the incoming dNTP. With Mn<sup>2+</sup>, base selectivity was impaired compared to Co<sup>2+</sup> and Cd<sup>2+</sup>. In addition, Co<sup>2+</sup> and Mn<sup>2+</sup> helped BST pol to catalyze primer-extension past a mismatch. Finally both Co<sup>2+</sup> and Mn<sup>2+</sup> enhanced ground-state binding of both correct and incorrect dNTPs to BST pol: Dideoxy terminated primer-template complexes.</p>\",\"PeriodicalId\":7529,\"journal\":{\"name\":\"AIMS Biophysics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992921/pdf/\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"AIMS Biophysics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3934/biophy.2018.2.125\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2018/4/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"BIOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIMS Biophysics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3934/biophy.2018.2.125","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/4/25 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOPHYSICS","Score":null,"Total":0}
The effect of different divalent cations on the kinetics and fidelity of Bacillus stearothermophilus DNA polymerase.
Although Mg2+ is the metal ion that functions as the cofactor for DNA polymerases (DNA pols) in vivo, Mn2+ can also serve in this capacity but it reduces base discrimination. Metal ions aside from Mg2+ or Mn2+ can act as cofactors for some DNA pols but not for others. Here we report on the ability of several divalent metal ions to substitute for Mg2+ or Mn2+ with BST DNA polymerase (BST pol), an A family DNA pol. We selected the metal ions based on whether they had previously been shown to be effective with other DNA pols. We found that Co2+ and Cd2+ were the only cations tested that could replace Mg2+ or Mn2+. When Co2+ was substituted for Mg2+, the incorporation efficiency for correct dNTPs increased 6-fold but for incorrect dNTPs there was a decrease which depended on the incoming dNTP. With Mn2+, base selectivity was impaired compared to Co2+ and Cd2+. In addition, Co2+ and Mn2+ helped BST pol to catalyze primer-extension past a mismatch. Finally both Co2+ and Mn2+ enhanced ground-state binding of both correct and incorrect dNTPs to BST pol: Dideoxy terminated primer-template complexes.
期刊介绍:
AIMS Biophysics is an international Open Access journal devoted to publishing peer-reviewed, high quality, original papers in the field of biophysics. We publish the following article types: original research articles, reviews, editorials, letters, and conference reports. AIMS Biophysics welcomes, but not limited to, the papers from the following topics: · Structural biology · Biophysical technology · Bioenergetics · Membrane biophysics · Cellular Biophysics · Electrophysiology · Neuro-Biophysics · Biomechanics · Systems biology