Team:Bielefeld-Germany/Labjournal/May

From 2013.igem.org

(Difference between revisions)
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*Initiating lab work on the sub-project endogenous mediator [[Team:Bielefeld-Germany/Project/GldA|Glycerol dehydrogenase]].
*Initiating lab work on the sub-project endogenous mediator [[Team:Bielefeld-Germany/Project/GldA|Glycerol dehydrogenase]].
-
*Starting lab work with the first successful PCR: GldA with Pre- and Suffix overlaps could be amplified from ''Escherichia coli'' genome.
+
*Starting lab work with the first successful PCR: gldA with pre- and suffix overlaps could be amplified from ''Escherichia coli'' genome.
-
*The main work however is still planning of our subprojects, designing experiments and a lot of research.  
+
*The main work however is still planning of our sub-projects, designing experiments and a lot of research.  
*Finding sponsors goes ahead. Many companies like our project and want to support us.
*Finding sponsors goes ahead. Many companies like our project and want to support us.
<br><br><br><br>
<br><br><br><br>
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====Mediators====
====Mediators====
*Glycerol dehydrogenase
*Glycerol dehydrogenase
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**Primerdesign for isolation of GldA gene from ''Escherichia coli'' KRX strain, with overlaps for BioBrick Prefix and Suffix:
+
**Primerdesign for isolation of ''gldA'' gene from ''Escherichia coli'' KRX strain, with overlaps for BioBrick prefix and suffix:
-
**Forward Primer GldA (43 bp): GAATTCGCGGCCGCTTCTAGATGGACCGCATTATTCAATCACC
+
**Forward primer ''gldA'' (43 bp): GAATTCGCGGCCGCTTCTAGATGGACCGCATTATTCAATCACC
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**Reverse Primer GldA (45 bp): CTGCAGCGGCCGCTACTAGTATTATTCCCACTCTTGCAGGAAACG
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**Reverse primer ''gldA'' (45 bp): CTGCAGCGGCCGCTACTAGTATTATTCCCACTCTTGCAGGAAACG
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**Starting first cultivation of ''Escherichia coli'' KRX strain for [[Team:Bielefeld-Germany/Labjournal/Molecular#Whole Genome Isolation |complete genome isolation]].  
**Starting first cultivation of ''Escherichia coli'' KRX strain for [[Team:Bielefeld-Germany/Labjournal/Molecular#Whole Genome Isolation |complete genome isolation]].  
**Successful [[Team:Bielefeld-Germany/Labjournal/Molecular#Whole Genome Isolation| genome isolation]] of ''Escherichia coli'' KRX.  
**Successful [[Team:Bielefeld-Germany/Labjournal/Molecular#Whole Genome Isolation| genome isolation]] of ''Escherichia coli'' KRX.  
-
**Successful PCR on the GldA gene of ''Escherichia coli'' KRX strain.
+
**Successful PCR on the ''gldA'' gene of ''Escherichia coli'' KRX strain.
-
[[Image:IGEM_Bielefeld_Standard_Phusion_PCR_Master_MixLRO.jpg|300px|thumb|left| <p align="justify">'''Table 1: Standard Phusion PCR Master Mix. '''</p>]]
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[[Image:IGEM_Bielefeld_Standard_Phusion_PCR_Master_MixLRO.jpg|300px|thumb|left| <p align="justify">'''Table 1: Standard phusion PCR master mix. '''</p>]]
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[[Image:IGEM_Bielefeld_Standard_Phu_PCR_GldA_OprF.jpg|300px|thumb|center| <p align="justify">'''Table 2: Two step standard Phusion PCR program for GldA amplification. '''</p>]]
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[[Image:IGEM_Bielefeld_Standard_Phu_PCR_GldA_OprF.jpg|300px|thumb|center| <p align="justify">'''Table 2: Two step standard phusion PCR program for ''gldA'' amplification. '''</p>]]
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**GldA PCR product was isolated by agarose gel electrophoresis and [[Team:Bielefeld-Germany/Labjournal/Molecular#Used Kits| purified]].
+
**The ''gldA'' PCR product was isolated by agarose gel electrophoresis and [[Team:Bielefeld-Germany/Labjournal/Molecular#Used Kits| purified]].
**Bands are on at the expected size of 1050 bp.
**Bands are on at the expected size of 1050 bp.
-
[[Image:IGEM_Bielefeld_GldA_PCR_Gel.jpg|200px|thumb|left| <p align="justify">'''Figure 1: Agarose gel from PCR on the GldA gene of ''Escherichia coli'' KRX strain with forward and reverse primer GldA. As a ladder we used [http://www.thermoscientificbio.com/nucleic-acid-electrophoresis/generuler-1-kb-dna-ladder-ready-to-use-250-to-10000-bp GeneRuler™ 1 kb DNA Ladder from Thermo Scientific]. '''</p>]]
+
[[Image:IGEM_Bielefeld_GldA_PCR_Gel.jpg|200px|thumb|left| <p align="justify">'''Figure 1: Agarose gel from PCR on the ''gldA'' gene of ''Escherichia coli'' KRX strain with forward and reverse primer ''gldA''. As a ladder we used [http://www.thermoscientificbio.com/nucleic-acid-electrophoresis/generuler-1-kb-dna-ladder-ready-to-use-250-to-10000-bp GeneRuler™ 1 kb DNA Ladder from Thermo Scientific]. '''</p>]]
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====Organization====
====Organization====
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*We will also take part at the congress "Next generation of biotechnological processes 2020+" in Berlin at June 27th, 2013.
+
*We will also take part at the congress ‘‘Next generation of biotechnological processes 2020+‘‘ in Berlin on June 27th, 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.
*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.

Revision as of 01:57, 5 October 2013



May


Milestones

  • Initiating lab work on the sub-project endogenous mediator Glycerol dehydrogenase.
  • Starting lab work with the first successful PCR: gldA with pre- and suffix overlaps could be amplified from Escherichia coli genome.
  • The main work however is still planning of our sub-projects, designing experiments and a lot of research.
  • Finding sponsors goes ahead. Many companies like our project and want to support us.






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 barbecue to thank the working group 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 October 11th to 13th, 2013.


MFC

Mediators

  • Glycerol dehydrogenase


Table 1: Standard phusion PCR master mix.

Table 2: Two step standard phusion PCR program for gldA amplification.


    • The gldA PCR product was isolated by agarose gel electrophoresis and purified.
    • Bands are on at the expected size of 1050 bp.


Figure 1: Agarose gel from PCR on the gldA gene of Escherichia coli KRX strain with forward and reverse primer gldA. As a ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.










4.Week

Organization

  • We will also take part at the congress ‘‘Next generation of biotechnological processes 2020+‘‘ in Berlin on June 27th, 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


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