Team:ETH Zurich/Project/Medal Relevant
From 2008.igem.org
(→Demonstrate that at least one new BioBrick Part or Device of your own design and construction works as expected) |
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=====Demonstrate that at least one new BioBrick Part or Device of your own design and construction works as expected===== | =====Demonstrate that at least one new BioBrick Part or Device of your own design and construction works as expected===== | ||
- | Based on atomic structures of LacI and evidence from genetic studies we have constructed a set of eight mutants of LacI, which are unresponsive to IPTG or lactose and are a useful component of genetic circuits or pulse generators. [[Team:ETH_Zurich/Wetlab/Switch_Circuit|Qualitative genetic experiments]] were conducted to estimate the strength of repression exerted by the LacI IS mutants and the mutants were found to repress expression from lac-controlled promoters even at 10mM IPTG. We have provided the LacI IS mutants by themselves (BioBricks [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142000 K142000] through [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142007 K142007]) and with RBS and terminator (BioBricks [] through []) for straigthforward integration into genetic circuits. | + | Based on atomic structures of LacI and evidence from genetic studies we have constructed a set of eight mutants of LacI, which are unresponsive to IPTG or lactose and are a useful component of genetic circuits or pulse generators. [[Team:ETH_Zurich/Wetlab/Switch_Circuit|Qualitative genetic experiments]] were conducted to estimate the strength of repression exerted by the LacI IS mutants and the mutants were found to repress expression from lac-controlled promoters even at 10mM IPTG. We have provided the LacI IS mutants by themselves (BioBricks [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142000 K142000] through [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142007 K142007]) and with RBS and terminator (BioBricks [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142008 K142008] through [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142015 K142015]) for straigthforward integration into genetic circuits. |
=====Characterize the operation of at least one new BioBrick Part or Device and enter this information on the Parts or Device page via the Registry of Parts===== | =====Characterize the operation of at least one new BioBrick Part or Device and enter this information on the Parts or Device page via the Registry of Parts===== |
Revision as of 03:00, 30 October 2008
Medal Relevant IssuesBronze RelevantRegister the team, have a great summer, and have fun attending the JamboreeAll registration task done, as can be seen here and we hope to have fun at Jamboree. Successfully complete and submit a Project Summary formYou can see our submitted Abstract here The general project description can be found on this page of the wiki. Present a Poster and Talk at the iGEM JamboreeEnter information detailing at least one new standard BioBrick Part or Device in the Registry of PartsSubmit DNA for at least one new BioBrick Part or Device to the Registry of PartsSilver RelevantDemonstrate that at least one new BioBrick Part or Device of your own design and construction works as expectedBased on atomic structures of LacI and evidence from genetic studies we have constructed a set of eight mutants of LacI, which are unresponsive to IPTG or lactose and are a useful component of genetic circuits or pulse generators. Qualitative genetic experiments were conducted to estimate the strength of repression exerted by the LacI IS mutants and the mutants were found to repress expression from lac-controlled promoters even at 10mM IPTG. We have provided the LacI IS mutants by themselves (BioBricks [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142000 K142000] through [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142007 K142007]) and with RBS and terminator (BioBricks [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142008 K142008] through [http://partsregistry.org/wiki/index.php?title=Part:BBa_K142015 K142015]) for straigthforward integration into genetic circuits. Characterize the operation of at least one new BioBrick Part or Device and enter this information on the Parts or Device page via the Registry of PartsGold RelevantAnalysis, modeling, and simulation of BioBrick Parts or DevicesWe propose a novel method of random gene deletion and chemostat-based selection of species with a reduced genome. For this we provide an algorithm described here. |