A Solid-Phase Platform for Combinatorial and Scarless Multipart Gene Assembly

被引:2
作者
de Raad, Markus [1 ]
Kooijmans, Sander A. A. [2 ]
Teunissen, Erik A. [1 ]
Mastrobattista, Enrico [1 ]
机构
[1] Univ Utrecht, Fac Sci, Utrecht Inst Pharmaceut Sci, Dept Pharmaceut, NL-3584 CG Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Clin Chem & Haematol, NL-3584 CX Utrecht, Netherlands
来源
ACS SYNTHETIC BIOLOGY | 2013年 / 2卷 / 06期
关键词
standardized; scarless; multipart DNA assembly; solid-phase; SEC; DNA; CLONING; SEPARATIONS; COMPLEX;
D O I
10.1021/sb300122q
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the emergence of standardized genetic modules as part of the synthetic biology toolbox, the need for universal and automatable assembly protocols increases. Although several methods and standards have been developed, these all suffer from drawbacks such as the introduction of scar sequences during ligation or the need for specific flanking sequences or a priori knowledge of the final sequence to be obtained. We have developed a method for scarless ligation of multipart gene segments in a truly sequence-independent fashion. The big advantage of this approach is that it is combinatorial, allowing the generation of all combinations of several variants of two or more modules to be ligated in less than a day. This method is based on the ligation of single stranded or double stranded oligodeoxynucleotides (ODN) and PCR products immobilized on a solid support. Different settings were tested to optimize the solid support ligation. Finally, to show proof cif concept for this novel multipart gene assembly platform a small library of all possible combinations of 4 BioBrick Modules was generated and tested.
引用
收藏
页码:316 / 326
页数:11
相关论文
共 28 条
  • [1] BglBricks: A flexible standard for biological part assembly
    Anderson J.C.
    Dueber J.E.
    Leguia M.
    Wu G.C.
    Arkin A.P.
    Keasling J.D.
    [J]. Journal of Biological Engineering, 4 (1)
  • [2] Pairwise selection assembly for sequence-independent construction of long-length DNA
    Blake, William J.
    Chapman, Brad A.
    Zindal, Anuradha
    Lee, Michael E.
    Lippow, Shaun M.
    Baynes, Brian M.
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 (08) : 2594 - 2602
  • [3] Gene assembly based on blunt-ended double-stranded DNA-modules
    Dietrich, R
    Wirsching, F
    Opitz, T
    Schwienhorst, A
    [J]. BIOTECHNOLOGY TECHNIQUES, 1998, 12 (01) : 49 - 54
  • [4] DNA assembly for synthetic biology: from parts to pathways and beyond
    Ellis, Tom
    Adie, Tom
    Baldwin, Geoff S.
    [J]. INTEGRATIVE BIOLOGY, 2011, 3 (02) : 109 - 118
  • [5] Golden Gate Shuffling: A One-Pot DNA Shuffling Method Based on Type IIs Restriction Enzymes
    Engler, Carola
    Gruetzner, Ramona
    Kandzia, Romy
    Marillonnet, Sylvestre
    [J]. PLOS ONE, 2009, 4 (05):
  • [6] Filipovska A., 2012, MOL BIOSYST, V8, P699
  • [7] Gibson DG, 2009, NAT METHODS, V6, P343, DOI [10.1038/NMETH.1318, 10.1038/nmeth.1318]
  • [8] Improved PCR-based gene synthesis method and its application to the Citrobacter freundii phytase gene codon modification
    Gordeeva, Tatiana L.
    Borschevskaya, Larisa N.
    Sineoky, Sergei P.
    [J]. JOURNAL OF MICROBIOLOGICAL METHODS, 2010, 81 (02) : 147 - 152
  • [9] HEGER BF, 2006, NAT BIOTECHNOL, V24, P1027
  • [10] Betaine improves the PCR amplification of GC-rich DNA sequences
    Henke, W
    Herdel, K
    Jung, K
    Schnorr, D
    Loening, SA
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (19) : 3957 - 3958