I'm currently a sophomore in course 20. When I'm behaving myself, I'm allowed to work in the Endy Lab at MIT. I will be documenting my UROP projects here. I will put my 20.109 work directly below.
||2.27.07 Ligation and Transformation Data
|DNA Ligation Sample
||Expected Number of Transformants
||Observed Number of Transformants
| Control Plasmid
| BKB with cocktail but no ligase
| BKB with ligase and cocktail
| BKB with insert and ligase and cocktail #1
| BKB with insert and ligase and cocktail #2
2.27.06 Ligation and Transformation Data
We didn't determine the concentration of the prepped DNA from the ligation reactions, so we cannot calculate the transformation efficiency of these transformations. We do know, however, that 5 ng of vector was used to transform the control plasmid, so efficiency = (1184 colonies)/(5*10^-3 micrograms of DNA)= 5.92*10^6 colonies/microgram of DNA.
The control plasmid transformation serves as a positive control. It should work. If this transformation didn't work (along with some or all of the others), we might suspect an issue with the competency of the cells or with the transformation process. The appearance of colonies on this plate, however, demonstrates that this is not the case. The cells are indeed competent and our protocol worked.
The backbone with and without ligase mixed with the killcut cocktail serve as negative controls. They should not work. If a significant number of colonies were to show up on these plates, this would first mean that the restriction endonucleases weren't cutting. This could be because they had expired or because the sites no longer existed in the DNA. Assuming the latter for the ligated vector, this would mean that the vector sequence was somehow modified during the initial digest. For the linearized vector, the appearance of colonies would suggest that the DNA somehow became ligated and lost restriction sites, or the cell accepted cut vector.
The controls do not provide a definitive diagnosis of the problem should the experimental ligations fail, but they provide starting points for the inquiry into the failure.
2.27.09 Refactoring Work
My refactoring work generally followed the guidelines set out by Chan et al's "Refactoring T7". I started by designing [BBa_M31530] directly from the germane promoters, RBSs, and ORFs. As an exercise in abstraction, I then started defining more complex functional units. First I defined a gene with its transcriptional and translational regulatory regions as a part. In this way, I don't have to think about how the gene is expressed so much as the end result. An example is [Gene X (BBa_M31532)]. By the same token, I was able to create functional units of several genes related by their functions. For example, I created [BBa_M31538] which is made of all the genes responsible for gene amplification of M13K07 while in a host and I made [BBa_M31540] for phage coat proteins. Within each of these, I attempted to address the possibility of intergenetic cross-talk by introducing transcriptional terminators between the genes [BBa_0015]. From my work with Heather Keller, I also know that hair pins (5' and 3' UTRs) can play a role in stabilization of DNA and posit that they may be helpful in preventing recombination events. I was unable to locate hairpins as parts in the registry, but I would like to add and make use of them in my refactored M13K07.
Here are a few tables of my work.
||Extract from gene II.
||Separate from gene IX.
||Separate from gene IX.
|Abstraction (Functional Unit)
||Components of Functional Unit
| The Regulatory/Coding Region
||Strings of DNA
| The Gene
||The Promoter, RBS, and ORF
| A Portion of the Life Cycle
||The genes responsible for a certain part of the life cycle
4.3.07 Primer Designs