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Team:Tsinghua-A/Parts
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<P ALIGN=LEFT><FONT FACE="Arial, sans-serif"><FONT SIZE=5 STYLE="font-size: 20pt"><SPAN LANG="en-US">Parts | <P ALIGN=LEFT><FONT FACE="Arial, sans-serif"><FONT SIZE=5 STYLE="font-size: 20pt"><SPAN LANG="en-US">Parts | ||
Data</SPAN></FONT></FONT></P> | Data</SPAN></FONT></FONT></P> | ||
| - | <P ALIGN=LEFT> <FONT FACE="Arial Unicode MS, sans-serif"><SPAN LANG="en-US"> | + | <P ALIGN=LEFT> <FONT FACE="Arial Unicode MS, sans-serif"><SPAN LANG="en-US"> |
| - | + | ||
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| - | + | '''Description:''' we assembled E0840 (''<partinfo>E0840</partinfo>'') under the pLas promoter (''<partinfo>R0079</partinfo>'') that was contained into K574009. We kept pSB1A2 as the scaffold vector. | |
| - | + | <br><br> | |
| - | + | '''Methods:''' <br> | |
| + | 1. ligate E0840 (''<partinfo>E0840</partinfo>'') downstream of K574009, which acts as a reporter. <br> | ||
| + | 2. culture the positive colony at 37°C, 220 rpm for 12 hours, as well as the DH5alpha. <br> | ||
| + | 3. dilute 1:25 the former in 12 falcon tubes (4 ml cultures), each 3 tubes as a group. The later is also diluted in 3 tubes as the negative control. <br> | ||
| + | 4. after culturing for another 2 hours, as their OD600 reach 0.2, induce with 3OC12HSL 0, 10^-6M, 10^-5M and 10^-4M respectively. <br> | ||
| + | 5. take samples after 1 hour, 4 hours, 8 hours and 24 hours, that is, centrifugalizate 0.5 mL of each culture and suspend them by 1 mL of PBS (phosphate-buffered saline). <br> | ||
| + | 6. measure the fluorescence of the samples with the flow cytometer. | ||
| + | <br><br> | ||
| + | [[File:k574009_chart.png]] | ||
| + | <br> | ||
| + | [[File:k574009_img.jpg]] | ||
| + | <br><br> | ||
| + | '''Results:''' From the chart, we can see that cells were hardly induced in the control group, and with the concentration of inducer growing, the intensity of GFP increased by groups. The most efficient concentration of inducer was around 10^-6M, and to most groups, the intensity of GFP reached its maxium after 4 hours. | ||
| + | <br> | ||
| + | |||
| + | |||
| + | </SPAN></FONT></P> | ||
Revision as of 14:48, 5 October 2011
Parts List
|
Name |
Type |
Description |
Length |
|---|---|---|---|
|
Composite |
pLux + TetR |
903 |
|
|
Composite |
TetR regulated by 3OC6HSL |
1890 |
|
|
Composite |
pluxR + CFP |
941 |
|
|
Device |
3OC6HSL -> TetR && reporter |
2839 |
|
|
Composite |
3OC12HSL regulated by TetR |
797 |
|
|
Composite |
3OC12HSL and YFP regulated by pBad |
1712 |
|
|
Device |
3OC12HSL regulated by pTet and pBad |
2517 |
|
|
Composite |
lasR + TT |
918 |
|
|
Composite |
a constitutive LasR producer |
982 |
|
|
Composite |
3OC12HSL -> PoPS Receiver |
1147 |
Parts Data
Parts Data
'''Description:''' we assembled E0840 (''
'''Methods:'''
1. ligate E0840 (''
2. culture the positive colony at 37°C, 220 rpm for 12 hours, as well as the DH5alpha.
3. dilute 1:25 the former in 12 falcon tubes (4 ml cultures), each 3 tubes as a group. The later is also diluted in 3 tubes as the negative control.
4. after culturing for another 2 hours, as their OD600 reach 0.2, induce with 3OC12HSL 0, 10^-6M, 10^-5M and 10^-4M respectively.
5. take samples after 1 hour, 4 hours, 8 hours and 24 hours, that is, centrifugalizate 0.5 mL of each culture and suspend them by 1 mL of PBS (phosphate-buffered saline).
6. measure the fluorescence of the samples with the flow cytometer.
[[File:k574009_chart.png]]
[[File:k574009_img.jpg]]
'''Results:''' From the chart, we can see that cells were hardly induced in the control group, and with the concentration of inducer growing, the intensity of GFP increased by groups. The most efficient concentration of inducer was around 10^-6M, and to most groups, the intensity of GFP reached its maxium after 4 hours.
