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	6. measure the fluorescence of the samples with the flow cytometer.		6. measure the fluorescence of the samples with the flow cytometer.
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	[[File:k574009_chart.png]]		[[File:k574009_chart.png]]
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Revision as of 14:49, 5 October 2011

Parts List

Name	Type	Description	Length
BBa_K574000	Composite	pLux + TetR	903
BBa_K574001	Composite	TetR regulated by 3OC6HSL	1890
BBa_K574002	Composite	pluxR + CFP	941
BBa_K574003	Device	3OC6HSL -> TetR && reporter	2839
BBa_K574004	Composite	3OC12HSL regulated by TetR	797
BBa_K574005	Composite	3OC12HSL and YFP regulated by pBad	1712
BBa_K574006	Device	3OC12HSL regulated by pTet and pBad	2517
BBa_K574007	Composite	lasR + TT	918
BBa_K574008	Composite	a constitutive LasR producer	982
BBa_K574009	Composite	3OC12HSL -> PoPS Receiver	1147

Parts Data

Parts Data

'''Description:''' we assembled E0840 (''E0840'') under the pLas promoter (''R0079'') that was contained into K574009. We kept pSB1A2 as the scaffold vector.

'''Methods:'''
1. ligate E0840 (''E0840'') downstream of K574009, which acts as a reporter.
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.