Difference between revisions of "Part:BBa K1415205"

 
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[[File:FLSL.png|thumb|center|650px|'''Fig.1-3-1'''  The blue light fluorescence expression curve of E.coli containing Pcons + RBS + PBAN(HAH) + RBS + BFP + Ter plasmid (control: competent cells that cannot emit blue light).
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[[File:nFLSL.png|thumb|center|650px|'''Fig.1-3-1'''  The blue light fluorescence expression curve of E.coli containing Pcons + RBS + PBAN(HAH) + RBS + BFP + Ter plasmid (control: competent cells that cannot emit blue light).
 
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[[File:ODSL.png|thumb|center|650px|'''Fig.1-3-2''' The growth curves of PBAN(SL)]]
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[[File:nODSL.png|thumb|center|650px|'''Fig.1-3-2''' The growth curves of PBAN(SL)]]
  
  

Latest revision as of 10:37, 24 October 2014

Pcons+B0034+PBAN(Spodoptera litura)+B0034+BFP+J61048

Fig.1-1 Biobrick of Pcons + RBS + PBAN(Spodoptera litura ) + RBS + BFP + Ter.

To predict the PBAN expression in E.coli by computer modeling, we next tested PBAN BFP biobricks. We obtained the average expressive value of the blue fluorescence in the biobrick part (above) and also the control part of Pcons + RBS + BFP + Ter. Therefore, we can use the average value to generate predictions of the PBAN expression in E.coli. Below is the blue fluorescence expression curve and bacterial growth curve (OD 600) in a long period of time. We used these data to predict the PBAN expression in E.coli.

Fig 1-2 Blue Fluorescence of Pcons + RBS + PBAN(Spodoptera litura) +RBS + BFP + Ter.


Fig.1-3-1 The blue light fluorescence expression curve of E.coli containing Pcons + RBS + PBAN(HAH) + RBS + BFP + Ter plasmid (control: competent cells that cannot emit blue light).




Fig.1-3-2 The growth curves of PBAN(SL)


Modeling

Fig.1-5 Modeling result of Pcons + RBS + PBAN(Spodoptera litura) + BFP + Ter. The blue line is the expression profile of the theoretical biobrick. And the green line is the expression data of Pcons + RBS + PBAN(Spodoptera litura) + BFP + Ter. And the red line is the adjusting line from the green and blue one. This line represent the correcting line of theoretical data and real condition data which can make our model not only fit the theoretical condition but also stay away from experimental bias.


The device we design and working mechanism

Fig.1-6 Our Project Overview.

In our project, we will biologically synthesize PBAN with our E.coli. We store the PBAN inside a trapping device. In the device, there will be appropriate lighting and nutrient sources that will attract insects.

Once an insect is attracted into our device and ingests the nutrient sources we provide, it will also inevitably come in contact with our PBAN. As the PBAN works and activates the pheromone synthesis of the attracted insect, more of this species of insect’s counterparts will be attracted and later captured.

Owing to the first feature mentioned above, PBAN are species-specific, which means that it doesn't matter if other kind of insect fly into our device and eat PBAN, because the insects we don't want to catch will not be stimulated by PBANs to produce pheromone; our PBAN are only for what we want to catch, and we are sure that our method won't affect other kinds of insects.


          

          

Fig.1-7 Shows the entering times of moths(Spodoptera litura) in different conditions. Entering times is defined as the times that moths get into the device. In this experiment, the moth might get out of our device due to it was just a model without trap, such as nets for keeping the moths. However, we can still clearly see the magic power of our pyramidal device by using blue light with PBAN treatment, which attracted more moths to get into the device than the other experiment (only blue light treatment). In addition, we can even observe a unique periodicity of attracting moths only in blue light with PBAN treatment. We consider this phenomenon is related to the physiology of the female moths' rut situation.

Fig.1-7 The entering number (into our pyramidal device) per hour shows that the combination of blue light, PBAN, and our device is indeed magically powerful in insect attraction.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 79
    Illegal NgoMIV site found at 909
  • 1000
    COMPATIBLE WITH RFC[1000]