Salhi S, Elie C, Jean-Jean O, Meunier-Rotival M, Forterre P, Rossignol J M, de Recondo A M
Laboratoire de Biologie Moléculaire de la Réplication, UPR 272-CNRS, BP n8, Villejuif, France.
Biochem Biophys Res Commun. 1990 Mar 30;167(3):1341-7. doi: 10.1016/0006-291x(90)90670-i.
A DNA polymerase purified from the thermoacidophilic archaebacterium Sulfolobus acidocaldarius was used to perform automated DNA amplification at 70 degrees C as well as site directed mutagenesis by Polymerase Chain Reaction (P.C.R.). The yield of amplification performed at optimum MgCl2 concentration for the Taq or the S. acidocaldarius DNA polymerase, for the same DNA target, was equivalent. The ability of S. acidocaldarius DNA polymerase to perform P.C.R. under less stringent requirement of MgCl2 concentration gives this enzyme a non-negligible advantage over the Taq DNA polymerase.
从嗜热嗜酸古细菌嗜酸热硫化叶菌中纯化得到的一种DNA聚合酶,被用于在70摄氏度下进行自动DNA扩增以及通过聚合酶链式反应(PCR)进行定点诱变。对于相同的DNA靶标,在Taq或嗜酸热硫化叶菌DNA聚合酶的最佳MgCl2浓度下进行扩增的产量是相当的。嗜酸热硫化叶菌DNA聚合酶在对MgCl2浓度要求不太严格的条件下进行PCR的能力,使其相对于Taq DNA聚合酶具有不可忽视的优势。