Difference between revisions of "Part:BBa K606035"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This part is the concatenation of the promoter pT7 (I719004) with the RBS SpoVG (K143021), that is design for B. subtilis but that also works in E. coli. This part works very efficiently and have been caracterized in E. coli BL21 cells. | + | This part is the concatenation of the promoter pT7 (I719004) with the RBS SpoVG (K143021), that is design for B. subtilis but that also works in E. coli. This part works very efficiently and have been caracterized in E. coli BL21 cells. The part is in pSB1C3. |
See the experiment page of this part or our wiki page[http://2011.igem.org/Team:Paris_Bettencourt/Experiments/T7_diffusion] for additional information | See the experiment page of this part or our wiki page[http://2011.igem.org/Team:Paris_Bettencourt/Experiments/T7_diffusion] for additional information | ||
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− | + | ===Characterization=== | |
+ | |||
+ | Growth of this part in BL21 strain under various concentration of IPTG. | ||
+ | |||
+ | [[Image:GrowthpT7GFPt7ter.png|center|thumb|500px|Fig1: Growth curves for BL21 strain carrying the part, in the presence of cloramphenicol]] | ||
+ | |||
+ | See the experiment page for more details. | ||
+ | |||
===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K606035 parameters</partinfo> | <partinfo>BBa_K606035 parameters</partinfo> | ||
− |
Revision as of 10:27, 21 September 2011
pT7 SpoVG GFP T7terminator.
T7 RNA polymease controlled GFP expression system for B. subtilis and E. coli
Usage and Biology
This part is the concatenation of the promoter pT7 (I719004) with the RBS SpoVG (K143021), that is design for B. subtilis but that also works in E. coli. This part works very efficiently and have been caracterized in E. coli BL21 cells. The part is in pSB1C3.
See the experiment page of this part or our wiki page[http://2011.igem.org/Team:Paris_Bettencourt/Experiments/T7_diffusion] for additional information
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 917
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 693
Characterization
Growth of this part in BL21 strain under various concentration of IPTG.
See the experiment page for more details.