DNA ligases from thermophilic bacteria enhance PCR amplification of long DNA sequences

被引:5
作者
Ignatov, K. B. [1 ]
Kramarov, V. M. [1 ]
机构
[1] Russian Acad Sci, Vavilov Inst Gen Genet, Moscow 119991, Russia
关键词
long PCR; Taq DNA polymerase; Taq DNA ligase; NUCLEOTIDE-SEQUENCE; REPLICATION INVITRO; POLYMERASES; PURIFICATION; EXPRESSION; FIDELITY; HOMOLOG; PROTEIN; CLONING;
D O I
10.1134/S0006297909050113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial NAD-dependent Taq and Tth DNA ligases are capable of significantly increasing the yield of long PCR products when the amplification is carried out using bacterial family A DNA polymerases, e.g. Taq or Tth DNA polymerases, or with enzymatic blends containing these polymerases. We also show that Taq and Tth DNA ligases improve the results of PCR in the absence of NAD and therefore in the absence of DNA ligase activity. These observations suggest that bacterial DNA ligases can interact with these DNA polymerases, presumably as accessory proteins, thereby enhancing the efficiency of DNA polymerization.
引用
收藏
页码:557 / 561
页数:5
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