Team:KAIST Korea/Notebook Labnote/2012 10

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KAIST Korea 2012 iGEM

Notebook : Labnote-October

Labnote

October

October 1st 2012

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October 2nd 2012

 Flip Flop

bFMO template preparation with new primer
Results

0818Fig1

We have found that our bFMO sequence was wrong. So that we have ordered new primers with right sequence.


OE PCR template preparation
Results

0818Fig1


pAutoIntegrase cloning check
Results

0818Fig1


Discussion

We have checked the result of cloning with various ways but we can’t sure about the success of cloning.
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October 3rd 2012

 Flip Flop

Visualization of inversion from GFP to RFP
Procedure


bfmo gene is constructed in the vector(pJ401, Km registance) and transformed into DH5α.
50λ cell from stock is inoculated in 5mL LB


Visualization of inversion from GFP to RFP
Procedure

We sampled the cell every 3hr. We induced one group of samples and un-induced another group of samples as a control. We took the picture of cell with confocal microscope at absorbance 500nm for GFP expression and 600nm for RFP expression.
Results

0818Fig1


Discussion

We obtained proper data. Un-induced sample doesn’t show measurable RFP expression throughout the culture. However, induced sample shows the increase of RFP expression. Increase of GFP level in induced sample is due to the stability of GFP and time delay before inversion.


Insert DNA preparation with OE pcr
Results

0818Fig1


Cloning
Results

0818Fig1
0818Fig1
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October 4th 2012

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October 5th 2012

Regional Jamboree at HKUST!!!!
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October 6th 2012

Regional Jamboree at HKUST!!!!
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October 7th 2012

Regional Jamboree at HKUST!!!!
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October 8th 2012

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October 9th 2012

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October 10th 2012

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October 11th 2012

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October 12th 2012

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October 13th 2012

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October 14th 2012

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October 15th 2012

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October 16th 2012

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October 17th 2012

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October 18th 2012

Flip Flop

Cell culture in 96-well plate for Indigo expression time optimization
Procedure


We set the O.D value to 0.1 and cultured 1.5ml cell in 96 deep well plate. At each time point, we transferred 1ml cell from 96 deep well plate to EP tube and 200λ cell to flat 96 well plate for O.D check.
After cell down in EP tube, we discarded the supernatant and resuspended the pellet in 200λ DMSO. We did sonication to the sample and after another cell down, we took the supernatant for TECAN measurement. Also, we checked absorbance after 3 days incubation and before 3days incubation.
We used TECAN at absorbance 620nm to measure the quantity of indigo production

Results

0818Fig1



We subtracted absorbance value of pure LB from value of samples and we set all samples to have same amount of cell using O.D value
Graph shown below is indigo intensity per cell. After 3 days incubation, indigo seems to be degraded and all the samples seem to have almost same indigo level.

0818Fig1


We excluded 0hr data from the graph to see teh rising tendency clearly.


Discussion


This data shows that the cell successfully produces indigo. We can use this gene as a reporter of our module. However, we only checked the increase of indigo. It may decrease after prolonged culture. We should do additional experiments to get the peak in the graph and optimize the production time of indigo.
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October 19th 2012

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October 20th 2012

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October 21st 2012

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October 22nd 2012

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October 23rd 2012

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October 24th 2012

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October 25th 2012

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October 26th 2012

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October 27th 2012

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October 28th 2012

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October 29th 2012

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October 30th 2012

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October 31st 2012

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