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Team:Bielefeld-Germany/Labjournal/week4
From 2012.igem.org
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*'''Team Bacterial Laccases''': | *'''Team Bacterial Laccases''': | ||
| - | ** After there were no colonies on our pSB1C3 + CopA ( | + | ** 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. | ** Purification of the ''T. thermo'' laccase PCR product out of agarose gel. | ||
Revision as of 08:46, 5 September 2012
Contents |
Labjournal
Week1 Week2 Week3 Week4 Week5 Week6 Week7 Week8 Week9 Week10 Week11 Week12 Week13 Week14 Week15 Week16 Week17 Week18 Week19
Week 4 (05/21 - 05/27/12)
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 restrictions to clone our laccase PCR products from Xanthomonas campestris and E. coli in pSB1C3 backbone. Therefore we transformed pSB1C3 with RFP in our competent KRX cells, picked colnies and made plasmidisolations. After that we ligated the cutted products with the cutted plasmid backbone.
Tuesday May 22nd
Team Bacterial Laccases: Transformation of the ligated plasmids in competent E. coli KRX cells.
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.
