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Team:Bielefeld-Germany/Labjournal/week4
From 2012.igem.org
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===Saturday May 26th=== | ===Saturday May 26th=== | ||
===Sunday May 27th=== | ===Sunday May 27th=== | ||
Revision as of 19:49, 12 September 2012
Contents |
Labjournal
Week1 Week2 Week3 Week4 Week5 Week6 Week7 Week8 Week9 Week10 Week11 Week12 Week13 Week14 Week15 Week16 Week17 Week18 Week19 Week20 Week21
Week 4 (05/21 - 05/27/12)
weekly seminar:
- Lab service: Isabel
- We try to establish a collaboration with the iGEM team from SDU-Denmark
- Got our distribution kits
- First successful cloning and cultivations
- Who wants to be a summer school teacher?
- We will not travel to the ACHEMA because only local teams are invited
- Do we want to participate in the Biolympics? (It's a sports party with fun organized by the [http://bts-ev.de/ bts])
Monday May 21st
- Team Modeling: Our aims for modeling:
- model the expression of the laccases in the organisms.
- model the aktivity of our enzyms.
- model the interesing parts of a clarification plant (the part witch are interesing for our cleaner.
- Team Bacterial Laccases: We did some restriction digests to clone our laccase PCR products from Xanthomonas campestris and E. coli in pSB1C3 backbone. Therefore we we transformed [http://partsregistry.org/Part:BBa_J04450 BBa_J04450] (pSB1C3 with RFP) in competent KRX cells.
Tuesday May 22nd
Team Bacterial Laccases: We picked colonies from transformed BBa_J04450 and plated them on new LB plates with chloramphenicol.
Wednesday May 23rd
- Team Student Academy: Repetition of the transformation of [http://partsregistry.org/Part:BBa_J04450 BBa_J04450] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_I13522 BBa_I13522] with new competent cells. For setup see here. Got intense red fluorescing colonies but no green fluorescing colonies. Made a backup of [http://partsregistry.org/Part:BBa_J04450 BBa_J04450]. Asking for other plasmids containing GFP at the working groups of our University.
- Team Bacterial Laccases:
- After there were no colonies on our pSB1C3 + CopA (Xanthomonas campestris) plate we did the transformation with the same ligation preparation again. For the other ligation with pSB1C3 + Cueo (E. coli) we started colony PCRSs to find postive colonies. Sadly the colony PCR showed no product.
- Purification of the T. thermo laccase PCR product out of agarose gel.
Thursday May 24th
- Team Student Academy: Made a liquid culture of [http://partsregistry.org/Part:BBa_J04450 BBa_J04450] at 30°C. There was no fluorescence. Furthermore [http://partsregistry.org/Part:BBa_J23100 BBa_J23100] was transformed. Also got intense red fluorescing colonies.
Friday May 25th
Team Bacterial Laccases:
- We had to do the PCR on T. thermo laccase again, because before the amount of purified PCR product was very low.
