Team:TUDelft/Achievements

From 2009.igem.org

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(Conjugation System)
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'''''Verification and Characterization of Wild R751'''''
'''''Verification and Characterization of Wild R751'''''
*Determination of wild R751 conjugation efficiency.
*Determination of wild R751 conjugation efficiency.
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'''''Verification and Characterization of trbK entry exclusion protein'''''
*Design and test of a a method to prevent back propagation of the signal by expressing trbK. This allows having receiver side control over communication.
*Design and test of a a method to prevent back propagation of the signal by expressing trbK. This allows having receiver side control over communication.
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'''''Verification and Characterization of Conjugation Testing Plasmid 1'''''
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*A conjugation test was done using our conjugation protocol to verify that Conjugation Testing Plasmid 1 was transmitted during conjugation.
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'''''R751 Gene Knockouts'''''
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*A third attempt to knockout oriTR and trbK is currently in progress using the Quick & Easy Conditional Knock Out Kit - FRT from Gene Bridges.
[https://2009.igem.org/Team:TUDelft/Conjugation_Results more]
[https://2009.igem.org/Team:TUDelft/Conjugation_Results more]

Revision as of 16:50, 20 October 2009

Achievements

Conjugation System

Verification and Characterization of Wild R751

  • Determination of wild R751 conjugation efficiency.

Verification and Characterization of trbK entry exclusion protein

  • Design and test of a a method to prevent back propagation of the signal by expressing trbK. This allows having receiver side control over communication.

Verification and Characterization of Conjugation Testing Plasmid 1

  • A conjugation test was done using our conjugation protocol to verify that Conjugation Testing Plasmid 1 was transmitted during conjugation.

R751 Gene Knockouts

  • A third attempt to knockout oriTR and trbK is currently in progress using the Quick & Easy Conditional Knock Out Kit - FRT from Gene Bridges.

more

Time-Delay Device

Synthetic Transcriptional Cascade

  • Assembly of plasmid 1 and 2 ([http://partsregistry.org/Part:BBa_K175046 K175046]) and 2 ([http://partsregistry.org/Part:BBa_K175047 K175047]).
  • Partial confirmation of sequence of both plasmids.
  • Transformation in Escherichia coli
  • Confirmation of both biobrick individual functionality. ... more

Biosynthetic AND gate

  • Successful assembly of parts [http://partsregistry.org/wiki/index.php?title=Part:BBa_K175023 K175023] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_K175024 K175024] which correspond to Plasmid 1 and 2 of the Biosynthetic AND gate section respectively.
  • Electroporation of plasmid 1 and 2 into Escherichia coli TOP10 cells... more

Lock and Key Library

  • Construction of an algorithm capable to generate locks (cis regulation) for different ribosome binding sites (RBS’s) and their correspond key (trans).
  • Online lock and key generator derived from the algorithm.
  • Construction of four DNA sequences in biobrick format and [http://partsregistry.org/wiki/index.php?title=Part:BBa_pSB1A3 pSB1A3] plasmid backbone which encode lock for medium RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175031 K175031]), key for the lock of medium RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175032 K175032]), lock for weak RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175029 K175029]) or key for the lock of weak RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175030 K175030]).
  • Assembly of two composed biobricks ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175034 K175034] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_K175035 K175035]), designed to test the functionality of the lock/key pairs constructed.
  • Assembly of two GFP generators under the control of PLacI with weak RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175033 K175033]) or medium RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K175048 K175048])... more

Modeling