Team:Macquarie Australia/Project/background

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Pathway
Chlorophyll + Photosynthesis + Photosystem 2

Gibson Cloning

Gibson cloning is a powerful and innovative method of DNA polymer synthesis, devised by DG Gibson et al. in 2009 (Gibson et al., 2009). The technique comprises an isothermal, single-reaction experiment involving the concerted action of a 5’-exonuclease, a DNA polymerase and a DNA ligase. An overview of the Gibson assembly method is provided in Figure 1 below and involves the ligation of DNA oligos, or ‘gBlocks’, of varying size (upto 500 BP each). As can be seen in the figure, gBlocks contain overlapping DNA regions of at least 30 BP which are exposed upon the action of the exonuclease. This facilitates complimentary base pairing between gBlocks. The simultaneous action of a DNA polymerase (preferably with proof-reading activity) and Taq polymerase, respectively, then complete and seal the newly formed conjugate (Gibson et al., 2010, Gibson et al., 2009).

The technique has obvious advantages in terms of time efficiency and simplicity. It involves considerably less labour and steps to complete compared to traditional methods. In particular there are no polymerase cycling assembly; PCR, gel purification; restriction digestion and DNA ligation steps are necessary (Gibson et al., 2010). For these reasons we have chosen to apply this technique to the assembly our BioBricks.

Figure 1: An overview of the key steps in the Gibson assembly method for DNA polymer synthesis. (Figure adapted from DG Gibson et al.)