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Team:Tsinghua/Result1
From 2009.igem.org
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[[Image:j24.png|200px|center|j24]] | [[Image:j24.png|200px|center|j24]] | ||
| - | After constructing the GenSniper genome with the structral proteins we need, we further incorporated the lysis genes into pACYCDuet-1+C+D+E+FI+FII. | + | After constructing the GenSniper genome with the structral proteins we need, we further incorporated the lysis genes (S+R+Rz) into pACYCDuet-1+C+D+E+FI+FII. |
[[Image:j26.png|600px|center|j26]] | [[Image:j26.png|600px|center|j26]] | ||
| + | Enzyme digestion identification confirmed that the cloning of pACYCDuet-1+S+R+Rz+C+D+E+FI+FII is corrected. | ||
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[[Image:j27.png|600px|center|j27]] | [[Image:j27.png|600px|center|j27]] | ||
Revision as of 04:59, 12 October 2009
Contents |
Synthesis of the Genome of GenSniper
Bottom-Up Approach
Showed above are the maps of the GenSniper using bottom-up approach. The genes of Nu1, A, W, B and lysis genes (S, R, Rz) are incorporated into pET-28a, while C, D, E, FI and FII are synthesized into pACYCDuet-1. In other word, the GenSniper will have two linkage groups.
We have successfully cloned the Nu1-A, W-B, C and D-E-FI-FII gene segments from the bacteriophage lambda genome.
Positive clones of the two linkage groups of the GenSniper genome have been achieved (termed pACYCDuet-1+C+D+E+FI+FII and pET-28a+Nu1+A+W+B). After PCR of the purified recombinant plasmids, we can get the desired bands on the gels. Nonspecific bands are due to the low annealing temperature.
After constructing the GenSniper genome with the structral proteins we need, we further incorporated the lysis genes (S+R+Rz) into pACYCDuet-1+C+D+E+FI+FII.
Enzyme digestion identification confirmed that the cloning of pACYCDuet-1+S+R+Rz+C+D+E+FI+FII is corrected.
Top-Down Approach
GenSniper Production Evaluation
