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Team:Newcastle/Meetings/6 October 2010
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| - | =6 October 2010 | + | ==Formal Meeting - 6 October 2010== |
| - | + | * Apologies: Colin Harwood, Jem and Phil | |
| + | * [[Team:Newcastle/Agendas/6_October_2010#Agenda_for_the_formal_meeting:_Wednesday__6th_October_2010 | Agenda]] | ||
| - | + | ===Presentation=== | |
| - | == | + | =====Introduction===== |
| - | ===Bacilla Filla slide=== | + | * 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 | * The solution words to be smaller than the logo | ||
* Logo have to be the biggest! | * Logo have to be the biggest! | ||
* Solution at the top of the page with a small logo below it then zoom into the logo | * Solution at the top of the page with a small logo below it then zoom into the logo | ||
| - | ===Technical review slide=== | + | =====Technical review slide===== |
* Show the link between the genes | * 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. | * 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 | * 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! | * Label the pictures! | ||
* Animation for the overview, ie, the background to remain the same | * Animation for the overview, ie, the background to remain the same | ||
| - | ===Swarming slide=== | + | =====Swarming slide===== |
* Change the flagella of the bug | * Change the flagella of the bug | ||
* Zoom into the plates | * Zoom into the plates | ||
| - | ===Subtilin slide=== | + | =====Subtilin slide===== |
* Show subtilin only when the bug is at the end of the crack | * Show subtilin only when the bug is at the end of the crack | ||
* Fill up the crack with bugs | * Fill up the crack with bugs | ||
| Line 31: | Line 35: | ||
* Change the pveg promoter to the oxygen sensitive promoter | * Change the pveg promoter to the oxygen sensitive promoter | ||
| - | ==Lab feedback== | + | =====Subtilin immunity slide===== |
| - | ===Filamentous cells=== | + | * SAY: Subtilin immunity already 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 | * Redo the microscopic | ||
* Correlate between the expression of GFP and the length | * Correlate between the expression of GFP and the length | ||
| - | ===SR1=== | + | =====SR1===== |
* We have colonies | * We have colonies | ||
| - | ===Scanning electron microscopy=== | + | =====Scanning electron microscopy===== |
* The concrete samples are already with the EM unit | * The concrete samples are already with the EM unit | ||
| - | ==Agenda== | + | ===Agenda=== |
| - | * To | + | * To re-edit the agenda |
| - | ==Action points== | + | ===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. | * Everyone to do up the presentation slides first. | ||
| - | ==Next meeting== | + | ===Next meeting=== |
| - | Wed | + | *13th, Wed October, 4 p.m. |
| - | + | *Chair: Steven, Computer: Alan, Minutes: Deena | |
| - | * | + | |
| - | + | ||
| - | + | ||
Latest revision as of 01:10, 26 October 2010
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Contents |
Formal Meeting - 6 October 2010
- Apologies: Colin Harwood, Jem and Phil
- Agenda
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 already 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
