Phi29 DNA polymerase-based methods for genomics applications

被引:0
|
作者
Nelson, JR [1 ]
机构
[1] Amersham Biosci, Dept Res, Piscataway, NJ 08855 USA
来源
JOURNAL OF CLINICAL LIGAND ASSAY | 2002年 / 25卷 / 03期
关键词
DNA amplification; DNA sequencing; phi29;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The DNA polymerase from Bacillus subtilis phage phi29 is unique in that, in addition to DNA polymerase and proofreading exonuclease activities, this single subunit enzyme has extremely high processivity and strand displacement activities. Recently, a number of techniques have been developed which utilize this enzyme to perform novel isothermal DNA amplifications that are not possible with other enzymes. Two methods, one designed to produce DNA sequencing templates from bacterial colonies or cultures and the other designed to representatively amplify entire genomic DNA samples for genetic testing, have recently emerged as novel technologies which will have a significant impact in the genomics community. Other potential applications that may utilize this enzyme are discussed.
引用
收藏
页码:276 / 279
页数:4
相关论文
共 50 条
  • [21] Amplification of plant genomic DNA by Phi29 DNA polymerase for use in physical mapping of the hypermethylated genomic region
    Adachi, E
    Shimamura, K
    Wakamatsu, S
    Kodama, H
    PLANT CELL REPORTS, 2004, 23 (03) : 144 - 147
  • [22] Amplification of plant genomic DNA by Phi29 DNA polymerase for use in physical mapping of the hypermethylated genomic region
    E. Adachi
    K. Shimamura
    S. Wakamatsu
    H. Kodama
    Plant Cell Reports, 2004, 23 : 144 - 147
  • [23] Improved single-cell genome amplification by a high-efficiency phi29 DNA polymerase
    Single-Cell Center, CAS Key Laboratory of Biofuels, Shandong Key Laboratory of Energy Genetics, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Shandong, Qingdao, China
    不详
    不详
    不详
    不详
    不详
    Front. Bioeng. Biotechnol.,
  • [24] Improved single-cell genome amplification by a high-efficiency phi29 DNA polymerase
    Zhang, Jia
    Su, Xiaolu
    Wang, Yefei
    Wang, Xiaohang
    Zhou, Shiqi
    Jia, Hui
    Jing, Xiaoyan
    Gong, Yanhai
    Wang, Jichao
    Xu, Jian
    FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, 2023, 11
  • [25] Structures of phi29 DNA polymerase complexed with substrate:: The mechanism of translocation in B-family polymerases
    Berman, Andrea J.
    Kamtekar, Satwik
    Goodman, Jessica L.
    Lazaro, José M.
    de Vega, Miguel
    Blanco, Luis
    Salas, Margarita
    Steitz, Thomas A.
    EMBO JOURNAL, 2007, 26 (14): : 3494 - 3505
  • [26] TRANSCRIPTION INVITRO OF PHI29 DNA AND ECORI FRAGMENTS BY BACILLUS-SUBTILIS RNA-POLYMERASE
    INCIARTE, MR
    VINUELA, E
    SALAS, M
    EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 71 (01): : 77 - 83
  • [27] Bacteriophage Phi29 Negatively Twists DNA During Packaging
    Hetherington, Craig L.
    Karunakaran, Aathavan
    Schnitzbauer, Jorg
    Jardine, Paul
    Grimes, Shelley
    Anderson, Dwight
    Bustamante, Carlos
    BIOPHYSICAL JOURNAL, 2009, 96 (03) : 416A - 416A
  • [28] Unidirectional Translocation of DNA Through the Phi29 Connector Channel
    Jing, Peng
    Harque, Farzin
    Shu, Dan
    Montemagno, Carlo
    Guo, Peixuan
    BIOPHYSICAL JOURNAL, 2011, 100 (03) : 167 - 167
  • [29] Isothermal multiple displacement amplification of DNA templates in minimally buffered conditions using phi29 polymerase
    Tenaglia, Enrico
    Imaizumi, Yuki
    Miyahara, Yuji
    Guiducci, Carlotta
    CHEMICAL COMMUNICATIONS, 2018, 54 (17) : 2158 - 2161
  • [30] DNA amplification using phi29 DNA polymerase validates gene polymorphism analysis from buccal mucosa samples
    Taniguchi, R.
    Masaki, C.
    Murashima, Y.
    Makino, M.
    Kojo, T.
    Nakamoto, T.
    Hosokawa, R.
    JOURNAL OF PROSTHODONTIC RESEARCH, 2011, 55 (03) : 165 - 170