What is  Gibson Assembly?

Gibson assembly is a useful molecular cloning technique published in 2009 by Dr. Daniel Gibson and his colleagues(Gibson, D.G., et al. (2009) Nat. Methods 6, 343-345). This technique allows for the assembly of up to 15 different DNA fragments in a single in vitro reaction. Despite its efficient process, Gibson assembly is an expensive cloning procedure because it requires high amounts of Taq DNA ligase.

What are we aiming to do?

Due to its ease of genetic manipulation and its high replication rate, Escherichia coli has developed into a useful tool for researchers to express genes of interest. We believe that we can use engineered E. coli to overcome the high cost of using Gibson assembly method. The gene for Phusion DNA polymerase and Taq DNA ligase, two of the three proteins needed for Gibson assembly, could each be inserted into a high expression vector backbone.

These construct backbones are assembled via Gibson Assembly and transformed into E. coli. The E. coli strains containing the assembled plasmids will use the local machinery to naturally express the proteins encoded in the genes inserts. The third protein required for Gibson assembly, the T5 5’ exonuclease, will be used from the natural amounts of exonuclease produced in the E. coli cell.

Cell lysate of the E. coli cells containing Phusion DNA polymerase enzyme and the cell lysate for the E. coli cells containing Taq DNA ligase will be added in ratios to a single tube and assemble the insert and vector into an a plasmid construct.