Team:Victoria Australia/Notebook

From 2009.igem.org

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<div id=" .2F12_May_2009">
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<div id=" .2F13_May_2009">
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<div id=" .2F14_May_2009">
==14 May 2009==
==14 May 2009==
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</div></div>
</div></div>
</div></div>
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- Team meeting in which we discussed ideas of how we are going to get the biological lighting system to work
- Team meeting in which we discussed ideas of how we are going to get the biological lighting system to work
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<div id=" .2F19_May_2009">
<div id=" .2F19_May_2009">
<div id=" .2F20_May_2009">
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<div id=" .2F21_May_2009">
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==21 May 2009==
==21 May 2009==
</div></div>
</div></div>
</div></div>
</div></div>
</div></div>
</div></div>
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</div>
- Team meeting discussed fundraising ideas – a silent auction cocktail was an idea
- Team meeting discussed fundraising ideas – a silent auction cocktail was an idea
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<div id=" .2F26_May_2009">
<div id=" .2F26_May_2009">
<div id=" .2F27_May_2009">
<div id=" .2F27_May_2009">
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<div id=" .2F28_May_2009">
==28 May 2009==
==28 May 2009==
</div></div>
</div></div>
</div></div>
</div></div>
</div></div>
</div></div>
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</div>
- Team meeting brainstormed ideas for the silent auction, made a list of people to invite and things to auction of.
- Team meeting brainstormed ideas for the silent auction, made a list of people to invite and things to auction of.
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- Began working on the Sponsorship template
- Began working on the Sponsorship template
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<div id=" .2F1_June_2009">
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<div id=" .2F2_June_2009">
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<div id=" .2F3_June_2009">
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<div id=" .2F4_June_2009">
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==4 June 2009==
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</div></div>
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</div></div>
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- Team meeting came to a vote to use the cell free systems for our biological lighting system and discussed using E.coli strain from cell free chassis submitted to iGEM parts registry
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- Found GFP parts available through iGEM toolkit
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o BBa_E0030 – Yellow Fluorescent protein (A. Victoria)
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o BBa_E0020 – Cyan Fluorescent protein (A. Victoria)
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o BBa_E0010 – Red Fluorescent protein (D. Striata)
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o BBa_E0040 – Green Fluorescent protein (A. Victoria)
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- Contacted Airline companies in regards to sponsorship
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<div id=" .2F5_June_2009">
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<div id=" .2F6_June_2009">
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<div id=" .2F7_June_2009">
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==5 June 2009==
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</div></div>
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</div>
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- Contacted New England Biolabs in regards to E.coli strains
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<div id=" .2F8_June_2009">
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<div id=" .2F9_June_2009">
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<div id=" .2F10_June_2009">
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<div id=" .2F11_June_2009">
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<div id=" .2F12_June_2009">
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<div id=" .2F13_June_2009">
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<div id=" .2F14_June_2009">
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<div id=" .2F15_June_2009">
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==11 June 2009==
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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- Received an email from New England Biolabs in regards of the E.coli strains- as we decided to use the protein expression strains i.e. PR1031 or ER2508
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<div id=" .2F16_June_2009">
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<div id=" .2F17_June_2009">
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<div id=" .2F18_June_2009">
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<div id=" .2F19_June_2009">
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<div id=" .2F20_June_2009">
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<div id=" .2F21_June_2009">
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<div id=" .2F22_June_2009">
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<div id=" .2F23_June_2009">
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<div id=" .2F24_June_2009">
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<div id=" .2F25_June_2009">
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==25 June 2009==
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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- Two students along side our supervisor went to Japan for an iGEM workshop
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<div id=" .2F26_June_2009">
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<div id=" .2F27_June_2009">
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<div id=" .2F28_June_2009">
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<div id=" .2F29_June_2009">
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==29 June 2009==
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</div></div>
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</div></div>
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- Team meeting – discussed logo, began thinking of t-shirt designs and team names
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<div id=" .2F30_June_2009">
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==30 June 2009==
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</div>
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- Found protocols regarding E.coli and wheat germ cell free systems
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- Continued working and finalizing our sponsorship template
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<div id=" .2F1_July_2009">
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==1 July 2009==
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</div>
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- A list of reagents and products was made from the protocols was items were found from the www.sigmaldrish.com catalogue
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<div id=" .2F2_July_2009">
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<div id=" .2F3_July_2009">
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==3 July 2009==
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</div></div>
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- Had a team meeting Caroline Northwood  to discuss our approach to sponsorship and our sponsorship template
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<div id=" .2F4_July_2009">
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<div id=" .2F5_July_2009">
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<div id=" .2F6_July_2009">
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<div id=" .2F7_July_2009">
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<div id=" .2F8_July_2009">
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<div id=" .2F9_July_2009">
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<div id=" .210_July_2009">
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<div id=" .2F11_July_2009">
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<div id=" .2F12_July_2009">
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<div id=" .2F13_July_2009">
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<div id=" .2F14_July_2009">
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<div id=" .2F15_July_2009">
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<div id=" .2F16_July_2009">
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<div id=" .2F17_July_2009">
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<div id=" .2F18_July_2009">
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<div id=" .2F19_July_2009">
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<div id=" .2F20_July_2009">
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<div id=" .2F21_July_2009">
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==6 July 2009==
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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- Reagent list to be ordered was given to Wade to be ordered
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- Sent out sponsorship template to all potential airline sponsors
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<div id=" .2F22_July_2009">
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<div id=" .2F23_July_2009">
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<div id=" .2F24_July_2009">
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<div id=" .2F25_July_2009">
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<div id=" .2F26_July_2009">
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<div id=" .2F27_July_2009">
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<div id=" .228_July_2009">
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<div id=" .2F29_July_2009">
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<div id=" .2F30_July_2009">
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<div id=" .2F31_July_2009">
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<div id=" .2F1_August_2009">
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<div id=" .2F2_August_2009">
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<div id=" .2F3_August_2009">
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<div id=" .2F4_August_2009">
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==24 July 2009==
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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- Team meeting – voted on team name, logo and mascot
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- Discussed our progress in individual research on the project
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<div id=" .2F5_August_2009">
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<div id=" .2F6_August_2009">
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<div id=" .2F7_August_2009">
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<div id=" .2F8_August_2009">
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<div id=" .2F9_August_2009">
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<div id=" .2F10_August_2009">
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<div id=" .2F11_August_2009">
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<div id=" .2F12_August_2009">
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<div id=" .2F13_August_2009">
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<div id=" .2F14_August_2009">
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<div id=" .2F15_August_2009">
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<div id=" .2F16_August_2009">
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==11 August 2009==
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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</div></div>
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- Began working on the Funding proposal to the  RMIT Vice Chancellor
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<div id=" .2F17_August_2009">
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<div id=" .2F18_August_2009">
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<div id=" .2F19_August_2009">
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<div id=" .2F20_August_2009">
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==20 August 2009==
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</div></div>
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</div></div>
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- Meeting with the Vice Chancellor
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<div id=" .2F21_August_2009">
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==21 August 2009==
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</div>
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- Began working in the Lab
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o LB- Media was made and autoclaved which went to make the LB-Agar plates
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o Ampicillin was made
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o SOC media was made and autoclaved
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o Magnesium Chloride solution and Sodium Chloride solution were also made and autoclaved
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<div id=" .2F22_August_2009">
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<div id=" .2F23_August_2009">
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<div id=" .2F24_August_2009">
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<div id=" .2F25_August_2009">
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==25 August 2009==
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</div></div>
 +
</div></div>
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-We did the transformation of the GFP and the BFP; this was completed by Pre-incubating the LB-agar plates while thawing the component cells. Plasmid DNA was added to the tube followed by a heat shock. 800μl of SOC medium is added and incubated for 45 mins. The transformed cells were then spread thoroughly on the LB agar plates and were left to incubate overnight.
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<div id=" .2F26_August_2009">
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<div id=" .2F27_August_2009">
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==26 August 2009==
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</div></div>
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- Went in to the lab to see the colonies that grew on the LB- Agar plate
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<div id=" .2F28_August_2009">
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<div id=" .2F29_August_2009">
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<div id=" .2F30_August_2009">
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<div id=" .2F31_August_2009">
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==31 August 2009==
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</div></div>
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</div></div>
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-We began the protein expression by using previously autoclaved LB media and placing 100ml into two conical flasks we then transferred a single colony from the transformed bacteria of the GFP and BFP into the flasks. We left these to incubate overnight.
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<div id=" .2F1_September_2009">
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<div id=" .2F2_September_2009">
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==1 September 2009==
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</div></div>
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-We continued with the protein expression by dividing the incubated GFP and BFP into two falcon tubes and centrifuging them. The supernatant was emptied and the pellet was resuspended. We then read the absorbance of the solution at 600nm.
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o GFP=0.93A
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o BFP=0.95A
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-Two conical flasks were set up with SOC solution and Ampicillin with GFP and BFP in them. They were incubated for an hour then the absorbance of the solution was obtained:
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o GFP= 0.7A
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o BFP = 0.64 A
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- The proteins were then induced and centrifuged then stored at -80ºC (Phil Poronnik) .
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<div id=" .2F3_September_2009">
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<div id=" .2F4_September_2009">
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==4 September 2009==
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</div></div>
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- Went into the lab to make reagents
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o Lysis buffer
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o Phosphate buffer
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o Chaps
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o 1M sucrose solution
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o 1M imidazole solution
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o 6M Guanidine hydrochloride solution
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o Tris Buffer solution (pH 7.8)
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|width="50%" |<div id=" .2F3_September_2009">
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<div id=" .2F6_September_2009">
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<div id=" .2F7_September_2009">
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<div id=" .2F8_September_2009">
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==7 September 2009==
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</div></div>
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</div></div>
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-We began the purification of the GFP and BFP by taking the pallets from the  -80ºC (Phil Poronnik) freezing and resuspending them with Lysis buffer. These cells were then sonicated for 3 cycles and then centrifuged. The supernatant was then transferred to eppendorf tubes and resin was added then tubes placed on suspension mixer. Phosphate buffer was then added to the pellet and centrifuged. The resulting pellet was then resuspended with the elution buffer and centrifuged again and the supernatant formed contained the GFP and BFP.
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<div id=" .2F9_September_2009">
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<div id=" .2F10_September_2009">
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<div id=" .2F11_September_2009">
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<div id=" .2F12_September_2009">
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==10 September 2009==
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</div></div>
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</div></div>
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-Team meeting – discussed what part we were going to add to the iGEM Biobrick and decided to modify an existing fluorescing protein to allow it to fluoresce blue.
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<div id=" .2F13_September_2009">
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<div id=" .2F14_September_2009">
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==14 September 2009==
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</div></div>
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-We did the transformation of the Vic GFP, YFP AZ, blueberry cherry and the BFP; this was completed by Pre-incubating the LB-agar plates while thawing the component cells. Plasmid DNA was added to the tube followed by a heat shock. 800μl of SOC medium is added and incubated for 45 mins. The transformed cells were then spread thoroughly on the LB agar plates and were left to incubate overnight.
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<div id=" .2F15_September_2009">
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<div id=" .2F16_September_2009">
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==15 September 2009==
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</div></div>
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-Went into the lab to see which LB agar plates we had colony growth on.
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<div id=" .2F17_September_2009">
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<div id=" .2F18_September_2009">
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<div id=" .2F19_September_2009">
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<div id=" .2F20_September_2009">
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==18 September 2009==
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</div></div>
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</div></div>
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- Team meeting- discussed what had been done on the wiki, and what else needed to be added
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- Discussed with team members what was being done in the lab
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- Discussed which fluorescing protein would be best to modify to made our BFP for the Biobrick
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<div id=" .2F21_September_2009">
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==21 September 2009==
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</div>
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- Celebrated our team members 21st Birthday
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- Began the preparation of the yellow plasmid this was done by placing LB medium in a falcon tube with the E.Coli bacteria allowing it to incubate overnight.
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<div id=" .2F22_September_2009">
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==22 September 2009==
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</div>
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-Continued the preparation of the yellow plasmid. By adding 1ml of incubated bacteria to conical flask containing 2YT solution. This was then incubated and centrifuged and the pellet was frozen at -80ºC (Phil Poronnik)
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<div id=" .2F23_September_2009">
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==23 September 2009==
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</div>
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-Continued the preparation of the yellow plasmid this was done by adding LB media to the falcon with ampicillin and a stab of the yellow fluorescent protein which was then incubated overnight.
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<div id=" .2F24_September_2009">
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<div id=" .2F25_September_2009">
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<div id=" .2F26_September_2009">
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<div id=" .2F27_September_2009">
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==24 September 2009==
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</div></div>
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</div></div>
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-Began the purification of the yellow fluorescent plasmid, this was done by centrifuging the incubated plasmid from the night before and followed the Aurum plasmid spin format protocol.
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<div id=" .2F28_September_2009">
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<div id=" .2F29_September_2009">
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<div id=" .2F30_September_2009">
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<div id=" .2F1_October_2009">
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==1 October 2009==
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</div></div>
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</div></div>
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-Team meeting- began researching the active site of the YFP in the iGEM Biobrick and looked into designing of the primers that we are going to use.
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<div id=" .2F2_October_2009">
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<div id=" .2F3_October_2009">
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<div id=" .2F4_October_2009">
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<div id=" .2F5_October_2009">
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==5 October 2009==
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</div></div>
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</div></div>
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- Made the S30 buffer(A and B) however did not add the 2 mercaptoethanol
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- Continued to do research on primer design and sequencing of the YFP
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<div id=" .2F6_October_2009">
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==6 October 2009==
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</div>
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-Added 2 mercaptoethanol to S30 A buffer.
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-Began the preparing the E. coli Cell free system. This was done by thawing the bacteria cells on ice and resuspending them with the S30 A buffer. These were then centrifuged and the pellet was resuspended with s30A buffer, this was done a total of 3 times. Then the pellet was resuspended with the S30 B buffer and sonicated.  The samples were then divided and centrifuged and the supernatant was transferred and centrifuged again. The supernatant is removed and serves as the cell lysate in the E. coli cell free system.
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<div id=" .2F7_October_2009">
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==7 October 2009==
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</div>
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-Searching for flights and accommodation for the Jamboree, sending Exam deferral letters and finalising Per Diem’s
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-Made TAE buffer and began protein expression by setting up an overnight culture of GFP and YFP
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<div id=" .2F8_October_2009">
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<div id=" .2F9_October_2009">
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<div id=" .2F10_October_2009">
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<div id=" .2F11_October_2009">
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==8 October 2009==
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</div></div>
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</div></div>
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-We continued with the protein expression by dividing the incubated GFP and YFP into two falcon tubes and centrifuging them. The supernatant was emptied and the pellet was resuspended. Spectrophotometeric analysis of the GFP and YFP was done in the nanodrop 2000.
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-We then read the absorbance of the solution at 600nm.
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oGFP=1.4A
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oYFP=0.8A
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-The proteins were then induced centrifuged and then stored at  -80ºC (Phil Poronnik)
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<div id=" .2F12_October_2009">
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<div id=" .2F13_October_2009">
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<div id=" .2F14_October_2009">
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<div id=" .2F15_October_2009">
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==13 October 2009==
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</div></div>
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</div></div>
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-Began preparing for the Electrophoresis of YFP. This was done by initially preparing the reagents we needed.
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o6 X DNA loading dye
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oAgarose gel
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-Agarose was then poured into the plate and cooled. The samples for the loading gel weer prepared by adding the YFP sample, 6X DNA loading dye, this was then loaded into the gel and electrophoreses for 30mins
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<div id=" .2F16_October_2009">
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<div id=" .2F17_October_2009">
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<div id=" .2F18_October_2009">
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==16 October 2009==
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</div></div>
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</div>
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-We began the mutagenesis of the YFP; this was done by a polymerase chain reaction. To do this the YFP plasmid and both the primers were diluted. 10X reaction buffer, YFP plasmid, primers, dNTP mix, quick solution, DNA polymerase and Milli Q water were all added to make a total volume of 50µL. the reaction was then completed using 18 cycles.
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<div id=" .2F19_October_2009">
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==19 October 2009==
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</div>
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-Completed the Dpn I digest, this was done by adding Dpn I restriction enzyme to the amplification reaction and gently resuspending the solution, the reaction was then centrifuged and incubated for 7 hours
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-In the evening we began the transformation of the ultracompetent cells. This was completed by pre-incubating the LB-agar plates while thawing the cells. Beta Mercaptoethanol and Dpn I treated DNA was added to the ultracompetent cells and mixed gently, and incubated for 30 mins. After incubation the cells were heat shocked. 800μl of SOC medium is added and incubated for 45 mins. The transformed cells were then spread thoroughly on the LB agar plates and were left to incubate overnight.
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<div id=" .2F20_October_2009">
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==20 October 2009==
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</div>
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-Went in to the lab to see if there was any colony growth on the agar plates.
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|}

Latest revision as of 08:58, 21 October 2009

Finalised fluoroforce header.jpg




Notebook

May
MTWTFSS
        [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F1_May_2009 1] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F2_May_2009 2] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F3_May_2009 3]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F4_May_2009 4] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F5_May_2009 5] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F6_May_2009 6] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F7_May_2009 7] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F8_May_2009 8] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F9_May_2009 9] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F10_May_2009 10]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F11_May_2009 11] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F12_May_2009 12] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F13_May_2009 13] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F14_May_2009 14] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F15_May_2009 15] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F16_May_2009 16] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F17_May_2009 17]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F18_May_2009 18] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F19_May_2009 19] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F20_May_2009 20] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F21_May_2009 21] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F22_May_2009 22] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F23_May_2009 23] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F24_May_2009 24]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F25_May_2009 25] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F26_May_2009 26] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F27_May_2009 27] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F28_May_2009 28] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F29_May_2009 29] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F30_May_2009 30] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F31_May_2009 31]
June
MTWTFSS
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F1_June_2009 1] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F2_June_2009 2] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F3_June_2009 3] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F4_June_2009 4] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F5_June_2009 5] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F6_June_2009 6] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F7_June_2009 7]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F8_June_2009 8] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F9_June_2009 9] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F10_June_2009 10] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F11_June_2009 11] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F12_June_2009 12] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F13_June_2009 13] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F14_June_2009 14]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F15_June_2009 15] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F16_June_2009 16] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F17_June_2009 17] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F18_June_2009 18] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F19_June_2009 19] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F20_June_2009 20] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F21_June_2009 21]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F22_June_2009 22] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F23_June_2009 23] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F24_June_2009 24] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F25_June_2009 25] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F26_June_2009 26] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F27_June_2009 27] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F28_June_2009 28]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F29_June_2009 29] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F30_June_2009 30]
July
MTWTFSS
    [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F1_July_2009 1] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F2_July_2009 2] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F3_July_2009 3] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F4_July_2009 4] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F5_July_2009 5]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F6_July_2009 6] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F7_July_2009 7] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F8_July_2009 8] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F9_July_2009 9] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F10_July_2009 10] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F11_July_2009 11] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F12_July_2009 12]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F13_July_2009 13] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F14_July_2009 14] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F15_July_2009 15] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F16_July_2009 16] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F17_July_2009 17] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F18_July_2009 18] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F19_July_2009 19]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F20_July_2009 20] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F21_July_2009 21] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F22_July_2009 22] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F23_July_2009 23] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F24_July_2009 24] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F25_July_2009 25] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F26_July_2009 26]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F27_July_2009 27] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F28_July_2009 28] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F29_July_2009 29] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F30_July_2009 30] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F31_July_2009 31]
August
MTWTFSS
          [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F1_August_2009 1] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F2_August_2009 2]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F3_August_2009 3] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F4_August_2009 4] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F5_August_2009 5] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F6_August_2009 6] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F7_August_2009 7] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F8_August_2009 8] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F9_August_2009 9]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F10_August_2009 10] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F11_August_2009 11] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F12_August_2009 12] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F13_August_2009 13] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F14_August_2009 14] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F15_August_2009 15] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F16_August_2009 16]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F17_August_2009 17] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F18_August_2009 18] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F19_August_2009 19] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F20_August_2009 20] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F21_August_2009 21] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F22_August_2009 22] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F23_August_2009 23]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F24_August_2009 24] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F25_August_2009 25] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F26_August_2009 26] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F27_August_2009 27] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F28_August_2009 28] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F29_August_2009 29] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F30_August_2009 30]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F31_August_2009 31]
September
MTWTFSS
  [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F1_September_2009 1] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F2_September_2009 2] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F3_September_2009 3] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F4_September_2009 4] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F5_September_2009 5] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F6_September_2009 6]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F7_September_2009 7] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F8_September_2009 8] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F9_September_2009 9] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F10_September_2009 10] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F11_September_2009 11] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F12_September_2009 12] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F13_September_2009 13]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F14_September_2009 14] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F15_September_2009 15] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F16_September_2009 16] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F17_September_2009 17] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F18_September_2009 18] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F19_September_2009 19] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F20_September_2009 20]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F21_September_2009 21] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F22_September_2009 22] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F23_September_2009 23] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F24_September_2009 24] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F25_September_2009 25] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F26_September_2009 26] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F27_September_2009 27]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F28_September_2009 28] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F29_September_2009 29] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F30_September_2009 30]
October
MTWTFSS
      [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F1_October_2009 1] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F2_October_2009 2] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F3_October_2009 3] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F4_October_2009 4]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F5_October_2009 5] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F6_October_2009 6] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F7_October_2009 7] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F8_October_2009 8] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F9_October_2009 9] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F10_October_2009 10] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F11_October_2009 11]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F12_October_2009 12] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F13_October_2009 13] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F14_October_2009 14] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F15_October_2009 15] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F16_October_2009 16] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F17_October_2009 17] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F18_October_2009 18]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F19_October_2009 19] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F20_October_2009 20] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F21_October_2009 21] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F22_October_2009 22] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F23_October_2009 23] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F24_October_2009 24] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F25_October_2009 25]
[http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F26_October_2009 26] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F27_October_2009 27] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F28_October_2009 28] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F29_October_2009 29] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F30_October_2009 30] [http://2009.igem.org/Team:Victoria_Australia/Notebook#.2F31_October_2009 31]


14 May 2009

- Team meeting in which we discussed ideas of how we are going to get the biological lighting system to work

- Discussed potential sponsors and other fundraising ideas


21 May 2009

- Team meeting discussed fundraising ideas – a silent auction cocktail was an idea

- Came up with two systems to light the biological lighting system:

- Cell free systems

- Blue tongue orbivirus system


28 May 2009

- Team meeting brainstormed ideas for the silent auction, made a list of people to invite and things to auction of.

- Discussed the advantages and disadvantages of the two systems


29 May 2009

- Found protocols to put the fluorescent protein into the E.coli system

- Began working on the Sponsorship template


4 June 2009

- Team meeting came to a vote to use the cell free systems for our biological lighting system and discussed using E.coli strain from cell free chassis submitted to iGEM parts registry

- Found GFP parts available through iGEM toolkit

o BBa_E0030 – Yellow Fluorescent protein (A. Victoria)

o BBa_E0020 – Cyan Fluorescent protein (A. Victoria)

o BBa_E0010 – Red Fluorescent protein (D. Striata)

o BBa_E0040 – Green Fluorescent protein (A. Victoria)

- Contacted Airline companies in regards to sponsorship


5 June 2009

- Contacted New England Biolabs in regards to E.coli strains


11 June 2009

- Received an email from New England Biolabs in regards of the E.coli strains- as we decided to use the protein expression strains i.e. PR1031 or ER2508



25 June 2009

- Two students along side our supervisor went to Japan for an iGEM workshop


29 June 2009

- Team meeting – discussed logo, began thinking of t-shirt designs and team names


30 June 2009

- Found protocols regarding E.coli and wheat germ cell free systems - Continued working and finalizing our sponsorship template


1 July 2009


- A list of reagents and products was made from the protocols was items were found from the www.sigmaldrish.com catalogue


3 July 2009

- Had a team meeting Caroline Northwood to discuss our approach to sponsorship and our sponsorship template



6 July 2009


- Reagent list to be ordered was given to Wade to be ordered

- Sent out sponsorship template to all potential airline sponsors


24 July 2009

- Team meeting – voted on team name, logo and mascot

- Discussed our progress in individual research on the project



11 August 2009

- Began working on the Funding proposal to the RMIT Vice Chancellor



20 August 2009

- Meeting with the Vice Chancellor

21 August 2009

- Began working in the Lab

o LB- Media was made and autoclaved which went to make the LB-Agar plates

o Ampicillin was made

o SOC media was made and autoclaved

o Magnesium Chloride solution and Sodium Chloride solution were also made and autoclaved


25 August 2009

-We did the transformation of the GFP and the BFP; this was completed by Pre-incubating the LB-agar plates while thawing the component cells. Plasmid DNA was added to the tube followed by a heat shock. 800μl of SOC medium is added and incubated for 45 mins. The transformed cells were then spread thoroughly on the LB agar plates and were left to incubate overnight.


26 August 2009

- Went in to the lab to see the colonies that grew on the LB- Agar plate


31 August 2009

-We began the protein expression by using previously autoclaved LB media and placing 100ml into two conical flasks we then transferred a single colony from the transformed bacteria of the GFP and BFP into the flasks. We left these to incubate overnight.


1 September 2009

-We continued with the protein expression by dividing the incubated GFP and BFP into two falcon tubes and centrifuging them. The supernatant was emptied and the pellet was resuspended. We then read the absorbance of the solution at 600nm.

o GFP=0.93A

o BFP=0.95A

-Two conical flasks were set up with SOC solution and Ampicillin with GFP and BFP in them. They were incubated for an hour then the absorbance of the solution was obtained:

o GFP= 0.7A

o BFP = 0.64 A

- The proteins were then induced and centrifuged then stored at -80ºC (Phil Poronnik) .


4 September 2009

- Went into the lab to make reagents

o Lysis buffer

o Phosphate buffer

o Chaps

o 1M sucrose solution

o 1M imidazole solution

o 6M Guanidine hydrochloride solution

o Tris Buffer solution (pH 7.8)


7 September 2009

-We began the purification of the GFP and BFP by taking the pallets from the -80ºC (Phil Poronnik) freezing and resuspending them with Lysis buffer. These cells were then sonicated for 3 cycles and then centrifuged. The supernatant was then transferred to eppendorf tubes and resin was added then tubes placed on suspension mixer. Phosphate buffer was then added to the pellet and centrifuged. The resulting pellet was then resuspended with the elution buffer and centrifuged again and the supernatant formed contained the GFP and BFP.


10 September 2009

-Team meeting – discussed what part we were going to add to the iGEM Biobrick and decided to modify an existing fluorescing protein to allow it to fluoresce blue.


14 September 2009

-We did the transformation of the Vic GFP, YFP AZ, blueberry cherry and the BFP; this was completed by Pre-incubating the LB-agar plates while thawing the component cells. Plasmid DNA was added to the tube followed by a heat shock. 800μl of SOC medium is added and incubated for 45 mins. The transformed cells were then spread thoroughly on the LB agar plates and were left to incubate overnight.


15 September 2009

-Went into the lab to see which LB agar plates we had colony growth on.


18 September 2009

- Team meeting- discussed what had been done on the wiki, and what else needed to be added

- Discussed with team members what was being done in the lab

- Discussed which fluorescing protein would be best to modify to made our BFP for the Biobrick


21 September 2009

- Celebrated our team members 21st Birthday

- Began the preparation of the yellow plasmid this was done by placing LB medium in a falcon tube with the E.Coli bacteria allowing it to incubate overnight.


22 September 2009

-Continued the preparation of the yellow plasmid. By adding 1ml of incubated bacteria to conical flask containing 2YT solution. This was then incubated and centrifuged and the pellet was frozen at -80ºC (Phil Poronnik)

23 September 2009

-Continued the preparation of the yellow plasmid this was done by adding LB media to the falcon with ampicillin and a stab of the yellow fluorescent protein which was then incubated overnight.


24 September 2009


-Began the purification of the yellow fluorescent plasmid, this was done by centrifuging the incubated plasmid from the night before and followed the Aurum plasmid spin format protocol.


1 October 2009

-Team meeting- began researching the active site of the YFP in the iGEM Biobrick and looked into designing of the primers that we are going to use.


5 October 2009

- Made the S30 buffer(A and B) however did not add the 2 mercaptoethanol

- Continued to do research on primer design and sequencing of the YFP


6 October 2009


-Added 2 mercaptoethanol to S30 A buffer.

-Began the preparing the E. coli Cell free system. This was done by thawing the bacteria cells on ice and resuspending them with the S30 A buffer. These were then centrifuged and the pellet was resuspended with s30A buffer, this was done a total of 3 times. Then the pellet was resuspended with the S30 B buffer and sonicated. The samples were then divided and centrifuged and the supernatant was transferred and centrifuged again. The supernatant is removed and serves as the cell lysate in the E. coli cell free system.


7 October 2009

-Searching for flights and accommodation for the Jamboree, sending Exam deferral letters and finalising Per Diem’s

-Made TAE buffer and began protein expression by setting up an overnight culture of GFP and YFP



8 October 2009


-We continued with the protein expression by dividing the incubated GFP and YFP into two falcon tubes and centrifuging them. The supernatant was emptied and the pellet was resuspended. Spectrophotometeric analysis of the GFP and YFP was done in the nanodrop 2000.

-We then read the absorbance of the solution at 600nm.

oGFP=1.4A

oYFP=0.8A

-The proteins were then induced centrifuged and then stored at -80ºC (Phil Poronnik)



13 October 2009


-Began preparing for the Electrophoresis of YFP. This was done by initially preparing the reagents we needed.

o6 X DNA loading dye

oAgarose gel

-Agarose was then poured into the plate and cooled. The samples for the loading gel weer prepared by adding the YFP sample, 6X DNA loading dye, this was then loaded into the gel and electrophoreses for 30mins


16 October 2009


-We began the mutagenesis of the YFP; this was done by a polymerase chain reaction. To do this the YFP plasmid and both the primers were diluted. 10X reaction buffer, YFP plasmid, primers, dNTP mix, quick solution, DNA polymerase and Milli Q water were all added to make a total volume of 50µL. the reaction was then completed using 18 cycles.


19 October 2009


-Completed the Dpn I digest, this was done by adding Dpn I restriction enzyme to the amplification reaction and gently resuspending the solution, the reaction was then centrifuged and incubated for 7 hours

-In the evening we began the transformation of the ultracompetent cells. This was completed by pre-incubating the LB-agar plates while thawing the cells. Beta Mercaptoethanol and Dpn I treated DNA was added to the ultracompetent cells and mixed gently, and incubated for 30 mins. After incubation the cells were heat shocked. 800μl of SOC medium is added and incubated for 45 mins. The transformed cells were then spread thoroughly on the LB agar plates and were left to incubate overnight.


20 October 2009

-Went in to the lab to see if there was any colony growth on the agar plates.

Retrieved from "http://2009.igem.org/Team:Victoria_Australia/Notebook"