Weymouth L A, Loeb L A
Proc Natl Acad Sci U S A. 1978 Apr;75(4):1924-8. doi: 10.1073/pnas.75.4.1924.
The error frequency of in vitro DNA synthesis using a natural DNA template has been measured with a biological assay for nucleotide substitutions. phiX174 DNA containing an amber mutation was copied in vitro by Escherichia coli DNA polymerase I, and the reversion frequency of the progeny DNA was determined by transfection of E. coli spheroplasts. E. coli polymerase I makes less than 1 mistake at the am3 locus for every 7700 nucleotides incorporated under standard reaction conditions. Substitution of Mn2+ for Mg2+ and unequal concentrations of deoxynucleoside triphosphate substrates raises this mutation frequency to greater than 1 in 1000. Thus, E. coli DNA polymerase I can copy natural DNA templates with high fidelity and its accuracy can be affected by alterations in reaction conditions.
利用核苷酸取代的生物学检测方法,已对使用天然DNA模板进行体外DNA合成的错误频率进行了测定。含有琥珀突变的phiX174 DNA在体外由大肠杆菌DNA聚合酶I进行复制,子代DNA的回复频率通过大肠杆菌原生质球的转染来确定。在标准反应条件下,大肠杆菌聚合酶I每掺入7700个核苷酸,在am3位点的错误少于1个。用Mn2+取代Mg2+以及脱氧核苷三磷酸底物浓度不等会使这种突变频率提高到千分之一以上。因此,大肠杆菌DNA聚合酶I能够以高保真度复制天然DNA模板,其准确性会受到反应条件改变的影响。