Team:Bielefeld-Germany/Labjournal/May

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Revision as of 13:40, 2 October 2013



May


Milestones

  • Starting lab work with the first successful PCR: GldA with Pre- and Suffix overlaps could be amplified from Escherichia coli genome.






Week 1

Organization

  • We were already able to find sponsors for our team: IIT BIEKUBA, IIT Biotech, Evonik, PlasmidFactory and FisherScientific will support us.


MFC

Mediators

  • Glycerol dehydrogenase
    • Primerdesign for isolation of GldA gene from Escherichia coli KRX strain, with overlaps for Biobrick Prefix and Suffix:
    • Forward Primer GldA (43 bp): GAATTCGCGGCCGCTTCTAGATGGACCGCATTATTCAATCACC
    • Reverse Primer GldA (45 bp): CTGCAGCGGCCGCTACTAGTATTATTCCCACTCTTGCAGGAAACG










2.Week

Organization

  • Distribution of our team in various subgroups for best work efficiency.
  • We’ve organized a working group barbecue to thank the AG of Dr. Jörn Kalinowski in the CeBiTec for the appropriation of space and support in the laboratory.


MFC









3.Week

Organization

  • Planning the trip to the European jamboree in Lyon from 11.-13. October 2013.


MFC

Mediators

  • Glycerol dehydrogenase


Table 1: Standard Phusion PCR Master Mix.

Table 2: Two step standard Phusion PCR programm for GldA amplification.


    • GldA PCR product was isolated by Agarose gel electrophorese and purificated.
    • Bands are at expected size of 1050 bp.


Figure 1: Agarosegel from PCR on the GldA gene of Escherichia coli KRX strain with forward and reverse primer GldA. For Ladder we used GeneRuler™ 1 kb DNA Ladder fromThermo Scientific.










4.Week

Organization

  • We will also take part at the congress "Next generation of biotechnological processes 2020+" in Berlin at 27. June 2013.
  • Having a second presentation at Merck KGaA head office in Darmstadt for explaining our project in detail. We are happy that Merck will be our next supporter in 2013.


MFC










Contents