Team:Chiba/lux promoter
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<li><a href="https://2010.igem.org/Team:Chiba/Parts"><span>Parts</span></a></li> | <li><a href="https://2010.igem.org/Team:Chiba/Parts"><span>Parts</span></a></li> | ||
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<li><a href="https://2010.igem.org/Team:Chiba/Result"><span>Result</span></a> | <li><a href="https://2010.igem.org/Team:Chiba/Result"><span>Result</span></a> | ||
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- | <br><br><br> | + | ------------------------------------------------------------------------------- |
- | < | + | ここから下を編集 |
- | [[Image:Plux inv | + | ------------------------------------------------------------------------------- |
+ | ----------------------------------------------------------------------------------- --> | ||
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+ | ==Abstract== | ||
+ | |||
+ | LuxR is an AHL-dependent activator.LuxR-AHL complex bind lux box,a 20-bp sequence and activate transcription. However the lux box is inserted between -35 and -10 and LuxR functions as LuxR-AHL inverter (Plux inv) .The Plux inv was resistered in Biobrick number R0061.We've constructed Plux inv-GFP combinig R0061and E0240 and characterized about it.<br> | ||
+ | |||
+ | ==Experiments== | ||
+ | ===1.Preparing Plux inv-GFP=== | ||
+ | |||
+ | Plasmid:R0061 and E0240<br> | ||
+ | Strain:XL10-G<br> | ||
+ | protocol<br> | ||
+ | Preparing process of Plux inv-GFP is shown in '''Fig. 1'''.We transformed preparing Plux inv-GFP in XL10-G and confirmed the expression GFP Fluorescence.The sequence is also conformed. | ||
+ | |||
+ | [[Image:Plux inv-GFP.png|none|frame|right|'''Fig. 1''' Evaluation of LuxR Inverter]] | ||
+ | |||
+ | ===2.Characterization Plux inv-GFP=== | ||
+ | |||
+ | Plasmid:Plux inv-GFP and Plac-LuxR (LuxR constitutive generator)<br> | ||
+ | strain:DH10B<br> | ||
+ | |||
+ | protocol<br> | ||
+ | We cotransformded Plux inv-GFP and LuxR Plac-LuxR in DH10B. | ||
+ | 1,LBL | ||
+ | incubation for12 h at 37゜C. | ||
+ | |||
+ | ==Results== | ||
+ | |||
+ | We confirmed GFP Fluorescence both AHL+ and -sample.<br> | ||
+ | <br> | ||
+ | [[Image:Plux inv results.png|frame|none|Fig. 3 ]] | ||
+ | |||
+ | ==discussion== | ||
+ | 私たちの系では,LuxRの抑制を確認することができなかった。 | ||
+ | |||
+ | ==Reference== | ||
+ | #Egland.K.A, and Greenberg.E.P, Conversion of the ''Vibrio Fischeri'' Transcriptional Activator,LuxR, to a Repressor, ''J. Bacteriol.'', '''182''', P.805-811 (2000) | ||
+ | #Cox.R.S.3rd, Surette.M.G, Elowitz.M.B, Programming gene expression with combinatorial promoters, ''Mol Syst Biol'', '''3''' ,145 (2007) |
Latest revision as of 13:29, 24 January 2011
Contents |
Abstract
LuxR is an AHL-dependent activator.LuxR-AHL complex bind lux box,a 20-bp sequence and activate transcription. However the lux box is inserted between -35 and -10 and LuxR functions as LuxR-AHL inverter (Plux inv) .The Plux inv was resistered in Biobrick number R0061.We've constructed Plux inv-GFP combinig R0061and E0240 and characterized about it.
Experiments
1.Preparing Plux inv-GFP
Plasmid:R0061 and E0240
Strain:XL10-G
protocol
Preparing process of Plux inv-GFP is shown in Fig. 1.We transformed preparing Plux inv-GFP in XL10-G and confirmed the expression GFP Fluorescence.The sequence is also conformed.
2.Characterization Plux inv-GFP
Plasmid:Plux inv-GFP and Plac-LuxR (LuxR constitutive generator)
strain:DH10B
protocol
We cotransformded Plux inv-GFP and LuxR Plac-LuxR in DH10B.
1,LBL
incubation for12 h at 37゜C.
Results
We confirmed GFP Fluorescence both AHL+ and -sample.
discussion
私たちの系では,LuxRの抑制を確認することができなかった。
Reference
- Egland.K.A, and Greenberg.E.P, Conversion of the Vibrio Fischeri Transcriptional Activator,LuxR, to a Repressor, J. Bacteriol., 182, P.805-811 (2000)
- Cox.R.S.3rd, Surette.M.G, Elowitz.M.B, Programming gene expression with combinatorial promoters, Mol Syst Biol, 3 ,145 (2007)