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Team:EPF-Lausanne/2-step PCR
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The major advantage of this technique is time needed to create clone. A RBS, a promoter and a terminator can be added to an ORF in a few hours. The result of this 2-step PCR can be digest and ligated into a vector. In total, this operation needs approximately 30 hours. In comparison, creating the same clone using classical cloning would need six days. | The major advantage of this technique is time needed to create clone. A RBS, a promoter and a terminator can be added to an ORF in a few hours. The result of this 2-step PCR can be digest and ligated into a vector. In total, this operation needs approximately 30 hours. In comparison, creating the same clone using classical cloning would need six days. | ||
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==A primer library?== | ==A primer library?== | ||
Several cloning steps can be considered as standard in an IGEM project. Adding RBS, promoter or terminator to an ORF is a common feature of almost all project. For this reason, we suggest that a library containing primers designed for 2-steps PCR could be created. This would give an easier and quicker way to assembly component. The new parts created with this technique keep all the Biobricks properies, meaning that classical cloning can also be used afterwards to assemble big parts together. | Several cloning steps can be considered as standard in an IGEM project. Adding RBS, promoter or terminator to an ORF is a common feature of almost all project. For this reason, we suggest that a library containing primers designed for 2-steps PCR could be created. This would give an easier and quicker way to assembly component. The new parts created with this technique keep all the Biobricks properies, meaning that classical cloning can also be used afterwards to assemble big parts together. | ||
Revision as of 13:44, 29 October 2008
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2-steps PCR
The 2-steps PCR is a technique used to add small DNA sequences to a PCR product. In the IGEM context, this can be used as an alternative to classical cloning: instead of digesting and ligating each biobricks, small part can be directly added by PCR, saving a lot of time.
The 2-step PCR requires three pairs of primer and three PCR runs:
A first pair is used to amplify a sequence of interest (for example an ORF) and provides annealing sites for the second pair of primers:
The second pairs anneals with the first and contains the sequence wanted to be add to the PCR product. The third pairs of primer amplify the initial PCR product with the added sequence.
Results:
During our project, we used this technique to clone the ORF of the gene luxI (the corresponding Biobrick, F1610, seemed inconsistent). The first PCR was performed on a plasmid to amplify the ORF of LuxI. During the second step, a RBS and the prefix were added upstream, as a terminator and the suffix were added downstream. The result of the this 2-step PCR was digested and inserted in pSB1A, giving the Biobrick BBa_K092400)
Time saved
The major advantage of this technique is time needed to create clone. A RBS, a promoter and a terminator can be added to an ORF in a few hours. The result of this 2-step PCR can be digest and ligated into a vector. In total, this operation needs approximately 30 hours. In comparison, creating the same clone using classical cloning would need six days.
A primer library?
Several cloning steps can be considered as standard in an IGEM project. Adding RBS, promoter or terminator to an ORF is a common feature of almost all project. For this reason, we suggest that a library containing primers designed for 2-steps PCR could be created. This would give an easier and quicker way to assembly component. The new parts created with this technique keep all the Biobricks properies, meaning that classical cloning can also be used afterwards to assemble big parts together.
