Team:Hawaii/Meeting/2008-06- 5
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Normanwang (Talk | contribs) (New page: {{Team:Hawaii/Header}} == Agenda == 9am St. John 515 # Update progress on experiments performed this week ## competent cell creation (taken 2 days), and testing results # Part B proposals...) |
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== Minutes == | == Minutes == | ||
+ | Present: GK, KS, MR, SC, GP, KS, NW, LG | ||
+ | Presentations: | ||
+ | Grace: lux operon night light | ||
+ | : <b>Discussion Points</b> | ||
+ | :*rbc may be too strong a promoter for use in the proposed construct | ||
+ | :*test the strength of RBC and explore if it is leaky by creating a lacZ/GFP fusion protein | ||
+ | ::*use the fusion protein plasmid from SC, use amplifier to get the RBCL promoter, cut out the fusion site and put into pCC1383. -> 'It can be made into a biobrick if it works.' | ||
+ | :*expression of lux as controlled by lac may not be enough without available lactose | ||
+ | ::**question: Is lactose membrane permeable for S. PCC6803? 'yes' | ||
+ | ::**may need to find a membrane permeable substance that can bind to the lac promoter | ||
+ | Krystle: bacterial export system, soluble proteins | ||
+ | : <b>Discussion Points</b> | ||
+ | :*it will be best to focus on pilA and slr2016, signal sequences that have already been experimentally confirmed | ||
- | + | Margaret: synthetic plasmid biobricks | |
- | + | : <b>Discussion Points</b> | |
- | + | ||
== Action Items == | == Action Items == |
Revision as of 02:48, 6 June 2008
Projects | Events | Resources | ||
---|---|---|---|---|
Sponsors | Experiments | Milestones | Protocols | |
Notebook (t) | Meetings (t) |
Contents |
Agenda
9am St. John 515
- Update progress on experiments performed this week
- competent cell creation (taken 2 days), and testing results
- Part B proposals
- Grace
- Krystle
- Margaret (teleconference in from US mainland)
Minutes
Present: GK, KS, MR, SC, GP, KS, NW, LG Presentations: Grace: lux operon night light
- Discussion Points
- rbc may be too strong a promoter for use in the proposed construct
- test the strength of RBC and explore if it is leaky by creating a lacZ/GFP fusion protein
- use the fusion protein plasmid from SC, use amplifier to get the RBCL promoter, cut out the fusion site and put into pCC1383. -> 'It can be made into a biobrick if it works.'
- expression of lux as controlled by lac may not be enough without available lactose
- question: Is lactose membrane permeable for S. PCC6803? 'yes'
- may need to find a membrane permeable substance that can bind to the lac promoter
Krystle: bacterial export system, soluble proteins
- Discussion Points
- it will be best to focus on pilA and slr2016, signal sequences that have already been experimentally confirmed
Margaret: synthetic plasmid biobricks
- Discussion Points
Action Items
- <Person A>: Task
Coming Up
[http://manoa.hawaii.edu/ ][http://manoa.hawaii.edu/ovcrge/ ][http://www.ctahr.hawaii.edu ]