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| | ===Applications of BBa_K649001=== | | ===Applications of BBa_K649001=== |
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| − | Fluorescence intensity of BBa_K649001 was increased by 3O-C12-HSL induction.
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| − | [[Image:PlasI-GFP_experience.png|thumb|center|500px|Effect of 3O-C12-HSL induction on fluorescence intensity ]]
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| − | Generally, in the presence of 3O-C12-HSL, lasR activates lasI promoter and the transcription level of downstream gene increases, but in the absence of 3O-C12-HSL, lasR can't activate lasI promoter. To characterize BBa_K649000, we used Ptrc-rbs-lasR-TT on pBR as regulator part. Because lasR is constitutively expressed, the difference of fluorescence intensity by 3O-C12-HSL induction indicates that BBa_K649000 is successfully regulated by 3O-C12-HSL.
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| − | '''[Sample]'''
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| − | Ptrc-rbs-lasR-TT on pBR / PlasI(BBa_I649000)-rbs-gfp-TT on pSB3K3
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| − | '''Method'''
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| − | ①Overnight cultures of sample strain grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:100 in the medium, and then they were incubated at 37 °C as fresh cultures.
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| − | ②After their OD600 reached 0.2, we added 3 µL of 500 µM 3O-C12-HSL (3O-C12-HSL+) or 3µL of DMSO (3O-C12-HSL-) into the fresh cultures.
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| − | ③After 3-hour incubation at 37 °C, 0.25 mL of each culture was harvested by centrifugalization and suspended by adding 1 mL of PBS (phosphate-buffered saline).
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| − | ④We dispensed 500 µL of each suspension into a disposable tube through a cell strainer, and its fluorescence intensity was measured with a flow cytometer of Becton, Dickinson and Company.
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| − | [https://parts.igem.org/Part:BBa_J64010:Experience our assay of BBa_J64010]
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| | ===User Reviews=== | | ===User Reviews=== |
Revision as of 17:19, 1 October 2011
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Applications of BBa_K649001
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UNIQa09abc7b530fb8e2-partinfo-00000000-QINU
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