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| | [[Boston_UniversityPrimerDesign | Primer Design]] | | [[Boston_UniversityPrimerDesign | Primer Design]] |
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| - | == Week's (Ambitious) Goals ==
| + | [[Boston_UniversityCompTransf | Making Shewanella Competent and Transforming Plasmid]] |
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| - | Week of 6/4:
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| - | 1. Evaluate the transformation that was done on Friday.
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| - | 2. Confirm the correct plasmid (pJQ200)
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| - | 3. Find appropriate restriction enzymes that cut by BLASTing all the plasmid's restriction enzyme sites onto the global transcription factors.
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| - | 4. Re-design primers for the global transcription factors based on the restriction enzymes we have selected.
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| - | 5. Order primers.
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| - | 6. Practice regular (non-error prone) PCR with the primers to check that they work.
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| - | 7. Incorporate the global transcription factors into the plasmid and transform this plasmid into the E.coli.
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| - | 8. Conjugate this plasmid into Shewy.
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| | == Materials We Need == | | == Materials We Need == |
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| - | Error-Prone PCR: Need to Buy | + | Error-Prone PCR: From CAB(?) |
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| - | Ligases: Need to Buy? | + | Ligases: Need to Buy |
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| | == Short-Term To-Do List == | | == Short-Term To-Do List == |
| - | | + | EDIT THE WIIIIKIIII |
| - | Ordering of Error-Prone PCR Materials: Not completed
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| - | Thank-You Letters sent to Pfizer: Not Completed
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| - | Thank-You Letters sent to BU ppl: Not completed
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| | == Protocols == | | == Protocols == |
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| | [[Boston_UniversityTOPO | pTrcHis TOPO TA Expression Kit Cloning Protocol]] | | [[Boston_UniversityTOPO | pTrcHis TOPO TA Expression Kit Cloning Protocol]] |
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| - | == Question and Answer ==
| + | [[Boston_UniversityNEBCutter| Using NEBCutter for checking specific restriction enzymes against a sequence]] |
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| - | '''Bold'''=new question/answer
| + | [[Boston_UniversityGel | Making an Electrophoresis Gel]] |
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| - | Q: Can we get the kanR gene with appropriate sticky ends for BsaI and Tth111I? (DB)
| + | [[Boston_UniversityZymo/SOB | Procedure for 50 mL E. Coli mixture in Zymo Broth or SOB |
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| - | A: yeah, we can get the DNA template for the kanR gene from the lab. we'll need to design some primers to PCR amplify it out with the BsaI and Tth111I cut sites. after cutting with the restriction enzymes, the kanR will have the appropriate sticky ends. frank suggested that we try ligating the kanR gene to the global regulator gene. (ie. kanR ligated to hlyU) and then stick that into the pJQ200. this way we can select for succesfull hlyU transformations with kanamycin
| + | == Question and Answer == |
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| - | Q: Ok, good. Do those primers still need to be ordered? And if we follow Frank's suggestion, what will go in place of the gtmR gene?
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| - | A: the hlyU-kanR gene will be inserted into gmtR. the sacB will be left untouched if this method is used. the other method we can do is to just kill the gmtR gene, then insert hlyU into sacB. we will then add sucrose so any bacteria with a sacB site will die. since hlyU will be interrupting the sacB site, successfull transformations with hlyU will survive the sucrose selection
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| - | '''Q: So according to the first method, you'd have to never expose the bacteria to sucrose. Are we sure this is possible (some of the media might contain sucrose). According to the second method, won't bacteria without plasmids survive? I suppose we could expose them to more antibiotics then. Is there a problem with the plan I think I got out of our talks on Friday (ie the one on this wiki--inserting kanR into gtmR and hlyU into sacB?)'''
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| - | Q: Also, can someone update the primer design section? Also also, have thank you letters been sent?
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| - | A: i'll get on both of those by monday's end
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| - | == Relevant Publications and Links== | + | |
| - | http://www.shewybase.bu.edu
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| - | https://www.atcc.org/common/catalog/numSearch/numResults.cfm?collection=mb-vector&atccNum=77482
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| | [https://2007.igem.org/Boston_University Back] | | [https://2007.igem.org/Boston_University Back] |
