Team:MoWestern Davidson/notebooks

WE NEED TO ADD A SITE MAP

We could try and somehow take the rolling stones' red lips picture and make the tongue green...or something.

This could tied to GFP and we need to incorprate an E. coli bacterium into the mix.

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Week 1 (May 25-May 29)

The Missouri Western students came to Davidson to finalize the research agenda for the summer. Both the biology and math aspects of the project were discussed in detail. By the end of the week, the team had unified around applications of the Satisfiability (SAT) problem to the genome of E.coli via the use of frameshift suppressor tRNAs.

We needed to design and engineer a reporter gene that the tRNA would suppress. Therefore, our research would consist of 2 main tracks: tRNA project and the 5mer Reporter Project.

Week 2 (June 1-June 5)

tRNA Project

We began to plan the construction of a 1-SAT model that would include a modified reporter gene suppressed by its respective tRNA.

The two campuses decided to split up the list of tRNAs according to percent suppression. Missouri Western took CUACC, AGGAC, CCAAU, CUAGC, CUACU, and CCACC. Davidson took CUAGU, CCACU, CGGUC, CCCUC, CCAUC-9 and CCAUC-10. We requested the sequence for our tRNAs from Dr. J. Christopher Anderson. After receiving them, we planned their construction via oligo assembly.

By the end of the week, we had planned to use 4 total oligos for our tRNAs.

5mer Reporter Project

In order to minimize major changes made to the protein structures and gene, we decided to place our 5 base pair addition upstream of our reporter protein. We accomplished this using PCR. We manipulated the PCR primers by designing our forward primer to include ATG, our 5mer, and the first half of the reporter protein up to a restriction site of our choice.

We wanted 1 fluorescence gene and 1 antibiotic resistance gene on each campus. After careful consideration of which reporters had the most "hardy" restriction sites, we decided upon RFP and tetracycline resistance protein on the Davidson campus; and GFP and chloramphenicol resistance on the Missouri campus.

Week 3 (June 8-June 12)

tRNA Project

After editing the first draft of 4 oligos, we devised a tRNA constructed of 7 oligos of shorter lengths to reduce the chance of mutations. We assembled our tRNA from these oligos and ligated/transformed the assembly. By the end of the week, we had obtained colonies from these transformations.

5mer Reporter Project

We chose NcoI as the restriction site in the RFP and BamHI as the site in Tet Resistance. We ordered the oligos of our primers. The forward primer was different for each of the 5 different 5mers on Davidson's campus and 6 different 5mer's on Missouri's campus. We only needed one reverse primer for each reporter gene we used. We carried our PCR using wild type RFP and Tet plasmids as our respective reporter templates.

We only used an aliquot amount to run a gel and verify that the sizes of the PCR fragments included the beginning of the reporter (with ATG and our 5mer) to the restriction site we chose.

Week 4 (June 15- June 19)

tRNA Project

We found that the variable to negative ratio of tRNA colonies was about 2 to 1. We saved liquid cultures of these and we re-ligated and re-transformed the tRNAs again.

Later that week, each lab member "adopted" a specific 5mer and tRNA for the rest of the summer. After verifying and plating tRNAs of correct insert size, we prepared samples of some tRNAs for sequencing.

5mer Reporter Project

We ligated cleaned and digested PCR inserts into vectors and transformed them. The vectors had been digested with EcoRI and either BamHI (Tet) or NcoI (RFP). Unfortunately, no colonies appeared on plates the next day. We repeated PCR to construct the first half of the reporter. We ended the week by verifying the insert sizes and cleaning the insert.

Week 5 (June 22-June 26)

tRNA Project

Sequencing for the tRNAs initially gave us 2 100% matches. The rest of the tRNAs had at least 1 ambigious nucleotide. We decided to resequence these tRNAs. We also decided that we would use pBad as the promoter for these tRNAs. We decided that to use the pBad promoter for the tRNAs because it maintains low expression of the tRNA in cells, which is best for the them. We also entered our tRNAs into the parts registry. Suppressor tRNA Parts

5mer Reporter Project

We re-verified our PCR inserts and after cleaning/digesting them, re-ligated and re-transformed them. We obtained colonies this second time. After PCR screening the colonies, we chose samples that looked the right size for sequencing. At the end of the week, we entered our 5mer reporters into the parts registry. 5mer Reporter Parts

Week 6 (June 29- July 3)

tRNA Project

We digested the tRNAs with XbaI and PstI to isolate the insert. We gel purified the insert, and ligated it to pBad vector. By the end of the week, we PCR screened the colonies from the ligations.

5mer Reporter Project

The sequencing that returned from our 5mer Reporter was quite messy. We decided to use a different mini prep kit (switched from Zyppy to Promega) to re-sequence our 5mers.

Week 7 (July 6-July 10)

tRNA Project

After mini prepping viable clones of the pBad-tRNA ligation, we decided that we wanted to see how the cells would function with more than one pBad-tRNA gene. During the week, digested pBad-tRNA plasmid with XbaI/PstI and SpeI/PstI to construct an insert and vector respectively.

5mer Reporter Project

We sent our 5mer Reporters for sequencing in glycerol stocks. Every member of our lab sent the different clones of their Tet and RFP 5mer reporters.

Week 8 (July 13-July 17)

tRNA Project

We entered pBad-tRNA into the registry and made their glycerol stocks for our freezer.

Over the past week we noted that the sizes of our plasmids appeared much larger than they actually were. Part of this incongruity resulted from the use of a different molecular weight marker with our gels. After sequencing our double pBad-tRNA ligation, however, we discovered a 32 bp insertion after the promoter. This insertion was palidromic and contained the NcoI restriction site. Further digestion with EcoRI and NcoI yielded the inserts expected from this mutation.

We traced the source of this mutation back to the pBad in our freezer stocks. We had to discard all minipreps and cells containing this promoter and start afresh.

5mer Reporter Project

We decided to test between pLac and pTet as the promoter for translation of our reporter. We digested and gel purified pLac, pTet, and RBS. Then, we ligated pLac to RBS and pTet to RBS. pLac+RBS produced colonies from the first ligation, but pTet+RBS produced colonies on the second ligation. These colonies were PCR screened and we found 3 pLac+RBS colonies to miniprep and digest for insert check.

We also recieved confirmation of sequencing for our 5mer reporters this week. We had 5 100% matches for RFP and 3 100% matches for Tet. However, all of the RFP sequences had a 25 bp insertion between the stop codon and the Bio Brick suffix. Because this insertion is not within the gene, we will continue to use this clone.

Week 9 (July 20-July 24)

5mer Reporter Project

We cut one of our good Tet clones and one good RFP clones with XbaI and PstI to make insert that will go downstream of the promoter and RBS. After we ran this on a gel, we gel purified the inserts.

We also digested (with EcoRI and PstI) and ran our viable pLac+RBS clones on a gel to check the insert size of the colonies from ligation. The insert looked about 50bp longer than we predicted, so we decided to send it off for sequencing.

Additionally, we ligated and transformed pTet with RBS. We PCR screened almost all the colonies that grew from this ligation and grew of up cultures of viable pTet+RBS.

Week 9 (July 27-July 31)

Davidson team traveled to St. Joseph, MO to summarize our findings, create the wiki and decide what we need to do next.

Olivia was working one more week by herself and she completed the final constructs for the summer.

We had to make a poster for the poster session on campus in early September.

Fall Semester

This Semester's work:
1) We started with the pBad Promoter

• Initially started with weaker promoter because we did not want to flood cells with suppressor tRNAs.
  
• Concerned about lethality and binding of suppressor tRNAs to non-target mRNAs.
  

2) pBad results

• 1 out of 5 clones gave visible fluorescence
  
• a second clone produced detectable fluorescence by fluorometer
  

3) We switched to a stronger promoter: pTet

• We hypothesized that stronger pTet promoter would increase suppression of 5mer, allowing increased transcription of RFP.
  
• We will compare successful frame shift suppression with pBad promoter and pTet promoter driving tRNA production.
  

4) Testing of second generation constructs

• Is there a difference in frame shift suppression if the promoter+tRNA construct is upstream or downstream of the 5mer-RFP reporter?
• Compare pTet and pBad promoters for frame shift suppressor phenotypes.