Team:Newcastle/Meetings/6 October 2010
From 2010.igem.org
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Formal Meeting - 6 October 2010
- Apologies: Colin Harwood, Jem and Phil
Presentation
Introduction
- Mention why do we use this bug and that it is able to live in high pH
- Have to menetion that we all biobrick have been modelled by SBML and copasi
Bacilla Filla slide
- The solution words to be smaller than the logo
- Logo have to be the biggest!
- Solution at the top of the page with a small logo below it then zoom into the logo
Technical review slide
- Show the link between the genes
- Some of the summary slide's information to go here, example: swim down the cracks, the tent, spray on, etc.
- A single shot overview then to the biobricks
- SAY: This is a crack, and here is our bug on the surface of the crack, etc
- Label the pictures!
- Animation for the overview, ie, the background to remain the same
Swarming slide
- Change the flagella of the bug
- Zoom into the plates
Subtilin slide
- Show subtilin only when the bug is at the end of the crack
- Fill up the crack with bugs
- Describle the subtilin signalling system
- Change the pveg promoter to the oxygen sensitive promoter
Subtilin immunity slide
- SAY: Subtilin immunity ablready in the registry, that is why we use it
- Mention what the individual CDS do
- Green tick for those that we did and a red cross for those that we did not
Workflow slide
- Change the word interesting to valuable to all synthetic biologist
- Cut down on the script
- Have to make it fit to the presentation
- Integration of lots of data that is why we use e-science
YneA slide
- Put filamentous cells into the pictures
- Metabolic pathway picture and link it
Glue slide
- The iGEM plates to go onto it
Kill switch
- Can bin it
- Move to the ethic page
Ethic slide
- Move it to the front after the introduction and also mention in the summary
- What is the danger and how we make it safe
Others
- Show that the bug is able to grow in concrete
Urease slide
- Have to show that calcium carbonate is filling up the cracks
- Have to say that we are better than the rest
- Highlight the advantage of ours and the disadvantage of others
- Mention SR1
Lab feedback
Filamentous cells
- Redo the microscopic
- Correlate between the expression of GFP and the length
SR1
- We have colonies
Scanning electron microscopy
- The concrete samples are already with the EM unit
Agenda
- To re-edit the agenda
Action points
- Rachel and Phil: Characterisation data for filamentous cells brick needs to be put on the wiki and the parts registry.
- Everyone to do up the presentation slides first.
Next meeting
- 13th, Wed October, 4 p.m.
- Chair: Steven, Computer: Alan, Minutes: Deena