Vander Horn P B, Davis M C, Cunniff J J, Ruan C, McArdle B F, Samols S B, Szasz J, Hu G, Hujer K M, Domke S T, Brummet S R, Moffett R B, Fuller C W
Amersham Life Science, Cleveland, OH, USA.
Biotechniques. 1997 Apr;22(4):758-62, 764-5. doi: 10.2144/97224pf02.
A combination of thermostable enzymes has been developed that produces higher quality cycle sequences. Thermo Sequenase DNA polymerase is a thermostable enzyme engineered to catalyze the incorporation of ddNTPs with an efficiency several thousandfold better than other thermostable DNA polymerases. Since the enzyme also catalyzes pyrophosphorolysis at dideoxy termini, a thermostable inorganic pyrophosphatase is needed to remove the pyrophosphate produced during sequencing reactions. Thermoplasma acidophilum inorganic pyrophosphatase (TAP) is thermostable and effective for converting pyrophosphate to orthophosphate. The use of the combination of Thermo Sequenase polymerase and TAP for cycle sequencing yields sequence data with uniform band intensities, allowing the determination of longer, more accurate sequence reads. Uniform band intensities also facilitate interpretation of sequence anomalies and the presence of mixed templates. Sequencing PCR products of DNA amplified from heterozygous diploid individuals results in signals of equal intensity from each allele.
已经开发出一种热稳定酶的组合,可产生更高质量的循环序列。热循环测序DNA聚合酶是一种经过工程改造的热稳定酶,其催化双脱氧核苷酸三磷酸(ddNTPs)掺入的效率比其他热稳定DNA聚合酶高出数千倍。由于该酶还催化双脱氧末端的焦磷酸解,因此需要一种热稳定的无机焦磷酸酶来去除测序反应过程中产生的焦磷酸。嗜热栖热菌无机焦磷酸酶(TAP)具有热稳定性,可有效将焦磷酸转化为正磷酸盐。将热循环测序聚合酶和TAP组合用于循环测序,可产生具有均匀条带强度的序列数据,从而能够确定更长、更准确的序列读数。均匀的条带强度也有助于解释序列异常和混合模板的存在。对从杂合二倍体个体扩增的DNA进行测序PCR产物,会产生来自每个等位基因的强度相等的信号。