Team:KULeuven/Project/Output
From 2008.igem.org
(→Action) |
(→Components) |
||
Line 11: | Line 11: | ||
===Components=== | ===Components=== | ||
- | A GFP with a C-terminal [https://2008.igem.org/Team:KULeuven/Literature#LVA_tag LVA tag] for rapid degradation of the protein (Anderson et al, 1998) was chosen so that we can follow the output signal quickly in time. The | + | A GFP with a C-terminal [https://2008.igem.org/Team:KULeuven/Literature#LVA_tag LVA tag] for rapid degradation of the protein (Anderson et al, 1998) was chosen so that we can follow the output signal quickly in time. The Tet promoter ([http://partsregistry.org/Part:BBa_R0040 '''BBa_R0040''']) behaves as described in the [https://2008.igem.org/Team:KULeuven/Project/Input input] section. For fine-tuning reasons, the RBS was chosen [http://partsregistry.org/Part:BBa_B0032 '''BBa_B0032'''] with a relative efficiency of 0,3. |
===Action=== | ===Action=== |
Revision as of 10:26, 27 August 2008
Contents |
Output
We have been searching for an easy accessible output system, that could provide us qualitative and quantitative information in a quick and easy way. The choice for GFP was easily made.
BioBricks
Components
A GFP with a C-terminal LVA tag for rapid degradation of the protein (Anderson et al, 1998) was chosen so that we can follow the output signal quickly in time. The Tet promoter ([http://partsregistry.org/Part:BBa_R0040 BBa_R0040]) behaves as described in the input section. For fine-tuning reasons, the RBS was chosen [http://partsregistry.org/Part:BBa_B0032 BBa_B0032] with a relative efficiency of 0,3.
Action
This is a very easy system. As the input results in inactivation of the tetR repressor, there is GFP production, proportional to the input signal.
References
Appl Environ Microbiol. 1998 Jun;64(6):2240-6. New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Andersen JB, Sternberg C, Poulsen LK, Bjorn SP, Givskov M, Molin S. PMID: 9603842