August/6 August 2009
From 2009.igem.org
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*Transformation | *Transformation | ||
**About 16 kinds of parts | **About 16 kinds of parts | ||
- | + | We transform thesefollowing parts today. | |
+ | B0015 Plate 1 23L | ||
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2. Breeding | 2. Breeding | ||
* | * |
Revision as of 22:59, 6 August 2009
Contents |
Morning Meeting
To do in lab
1. Transform & Selection
- 培地作り
- LB
- LB Amp+
- LB Kan+
- Transformation
- About 16 kinds of parts
We transform thesefollowing parts today. B0015 Plate 1 23L
2. Breeding
3. Refinement
To bring
- Timer
- Pen
- Slipper
Design genetic circuits
We take notice of signal molecules. So I put them in order in the chart below.
*Inducer ⇒(synthesize) signal moleculer ⇒(synthesize) Receiver
* LuxI ⇒ 3OC6HSL ⇒ LuxR * LasI ⇒ AI-1(3OC12HSL) ⇒ LasR * CinI ⇒ 3OH,C14:1-HSl ⇒ CinR * RhlI ⇒ AI-1(C4HSL) ⇒ RhlR * (exception)agrD synthesize AIP with agrB.AIp synthesize agrC . AgrA which is synthesized by agrC activate promoter.
From now on,We have to do what I mention below 1.Search other cell-cell comunication system 2.Check systems component completely 3.Create new systems or reinforce cell funcution with additional ideas 4.Search the effect of cross talk written by Tadasi Nakamura