August/6 August 2009

From 2009.igem.org

(Difference between revisions)
(To do in lab)
(To do in lab)
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*Transformation
*Transformation
**About 16 kinds of parts
**About 16 kinds of parts
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    We transform thesefollowing parts today.
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      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