Alteration of enzymes and their application to nucleic acid amplification (Review)

被引:8
|
作者
Yasukawa, Kiyoshi [1 ]
Yanagihara, Itaru [2 ]
Fujiwara, Shinsuke [3 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto 6068502, Japan
[2] Osaka Womens & Childrens Hosp, Res Inst, Dept Dev Med, Izumi Ku, Osaka 5941101, Japan
[3] Kwansei Gakuin Univ, Sch Sci & Technol, Dept Biosci, Sanda, Hyogo 6691337, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
cDNA synthesis; DNA polymerase; fidelity; helicase; PCR; recombinase polymerase amplification; reverse transcriptase; sensitivity; specificity; VIRUS REVERSE-TRANSCRIPTASE; RECOMBINASE POLYMERASE AMPLIFICATION; AVIAN-MYELOBLASTOSIS VIRUS; THERMOSTABLE DNA-POLYMERASES; THERMAL STABILITIES; PCR AMPLIFICATION; KLENOW FRAGMENT; RAPID DETECTION; GENERATION; FIDELITY;
D O I
10.3892/ijmm.2020.4726
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Since the discovery of polymerase chain reaction (PCR) in 1985, several methods have been developed to achieve nucleic acid amplification, and are currently used in various fields including clinical diagnosis and life science research. Thus, a wealth of information has accumulated regarding nucleic acid-related enzymes. In this review, some nucleic acid-related enzymes were selected and the recent advances in their modification along with their application to nucleic acid amplification were described. The discussion also focused on optimization of the corresponding reaction conditions. Using newly developed enzymes under well-optimized reaction conditions, the sensitivity, specificity, and fidelity of nucleic acid tests can be improved successfully.
引用
收藏
页码:1633 / 1643
页数:11
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