Difference between revisions of "Part:BBa F2620"
Line 1: | Line 1: | ||
− | |||
− | |||
<div style="padding: 40px; width: 720px; border: 1px solid #000000;"> | <div style="padding: 40px; width: 720px; border: 1px solid #000000;"> | ||
{{Template:F2620 page header| | {{Template:F2620 page header| |
Revision as of 19:31, 19 September 2006
|
|
Description
A transcription factor [LuxR] (BBa_C0062) that is active in the presence of cell-cell signaling molecule 3OC6HSL is controlled by a tetR regulatable operator (BBa_R0040. Device input is 3OC6HSL. Device output is PoPS from a LuxR-regulated operator.
Usage
Full PoPS output at high 3OC6HSL levels and high plasmid copy [e.g., pSB1A2] results in a reduced cell growth rate (see Load section). If used in a cell containing TetR then a second input signal such as [http://openwetware.org/wiki/ATc aTc] can be used to produce a logical AND function.
Characteristics
|
Key Subparts
|
Transfer Function |
Specificity |
Latency |
Stability |
Demand
|
Stability
|
Compatibility
Device has been shown to work in BBa_V1002, MG1655 and BBa_V1001
Device has been shown to work on pSB3K3 and pSB3K3
Device has been shown to work with BBa_E0430,BBa_E0434,BBa_E0240
Crosstalk with devices using 3OC6HSL or add in the other molecule names here.
Crosstalk with systems containing TetR (BBa_C0040)
Characterization Conditions
Device output was measured using the composite part BBa_T9002, ([BBa_F2620].[BBa_E0240]). The characterization platform was BioBrick plasmidpSB3K3 with E. coli MG1655 as chassis. Cultures were grown in [http://openwetware.org/wiki/Endy:M9_media/supplemented supplemented M9 media] at 37C. Full characterization protocols can be found here.