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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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| - | [[Image:shorttermgoal.jpg|thumb|Our month's goal]] | + | |
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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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| | == Protocols == | | == Protocols == |
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| | [[Boston_UniversityGel | Making an Electrophoresis Gel]] | | [[Boston_UniversityGel | Making an Electrophoresis Gel]] |
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| - | [[Boston_UniversityZymoorSOB | E. Coli mixture in Zymo Broth or SOB]] | + | [[Boston_UniversityZymo/SOB | Procedure for 50 mL E. Coli mixture in Zymo Broth or SOB |
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| - | [[Boston_UniversityTransformZComp | Transformation of Z-competent cells]]
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| | == Question and Answer == | | == Question and Answer == |
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| - | '''Bold'''=new question/answer
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| - | Q: Can we get the kanR gene with appropriate sticky ends for BsaI and Tth111I? (DB)
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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
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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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| - | A: so if we insert kan into gmtr and hlyu into sacb we could have several possible plasmids:
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| - | (1)(ideally) kan inserts into gmtr and hlyu inserts into sacb. so this is conjugated into shewy which has a gent resistance already. a double selection with the antibiotic kan and gent will select for this plasmid (and add some sucrose too to get rid of the unwanted plasmid (2)
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| - | (2)kan inserts into gmtr, hlyU insertion doesnt happen. so we have kan resistance and sacB in this plasmid. adding sucrose will kill this plasmid cuz of the presence of sacB
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| - | (3)hlyU inserts into sacB but kan doesn't insert into gmtr. so we have gent resistance and have no sacB. a double selection plate will kill this because there's no kan resistance.
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| - | (4)hlyU does not insert into sacB, kan does not insert into gmtr. so this is just plasmid pJQ200. kan and sucrose will kill this guy.
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| - | shewy that don't have plasmid will not survive in the presence of kanamicin.
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| - | the e.coli S17-1 has no kan resistance so it will die in the double selection methods'''
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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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| - | Q: hey danny not quite sure how to make the image i just uploaded fit well (the figure with what we plan to do over the next month)
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| - | A: Looks pretty good to me
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| - | Q: Can I move the Lab Design and Notes sections to the What We've Accomplished section?'''
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| - | A: yeah
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| - | '''Q: OK, I think that all three things from the Lab Design and Notes sections are now put in other places--the first section under What We've Accomplishd, the final two under Protocols. Just verify that before we get rid of that page.'''
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| - | '''A: looks good. delete away!'''
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| - | == Relevant Publications and Links==
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| - | 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] |
