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Team:Alberta/Project/Primer Design
From 2009.igem.org
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Primer DesignWith our minimal essential gene list, it was now required to take these genes and insert them into the pAB and pBA plasmids which allow for BioByte Assembly (Please see the Standard Plasmids section under the DNA Assembly tab for more information on pAB/pBA and the BioBytes method). In order to do this, PCR was used to amplify the individual genes from MG1655 genomic DNA along with extensions to produce restriction sites. Prefix and Suffix to be Added For PCR Amplification These restriction sites were designed to be complementary to the restrictions sites found in pAB and pBA (PstI and XbaI). Due to the use of restriction enzymes, it was important to check each gene sequence for those same restriction sites. Genes which contained at least one PstI site, used the NsiI enzyme to be cloned into our standard plasmids (it produces the same overhang as PstI). Similarly if NsiI and PstI were in the gene sequence, SbfI was used. If all three of these sites were present in a gene sequence, other enzymes which produce the same overhang could be used. Genes which contained XbaI could use AvrII, NheI, as well as a multitude of others. In the attached file, 314 primers have been produced with their sequence information. 188 of these primers have been tested and amplified and their sequences uploaded onto the parts registry. These primers are additionally characterized by the restriction sites which they contain (the sites found in the primers were ensured to not appear in the gene sequence). In the wetlab we have used PCR to amplify over 150 of these gene already. To view our primer list please click here . |
Vector NTIVector NTI was used to produce all of the primers in the above list. Each primer's thermodynamic properties were examined using Vector NTI's hairpin and dimerzation programs. Primers were optimized to fit as many of the following criteria as possible:
The file which loads our Primer Settings into Vector NTI can be found here. |
