Team:Davidson-Missouri Western/Experience Gained on New Registry Parts
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!align="center"|[[Team:Davidson-Missouri_Western/Notebook|Notebook]] | !align="center"|[[Team:Davidson-Missouri_Western/Notebook|Notebook]] | ||
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'''Cell-to-cell signaling by XOR gate constructs''' - The ability of two different XOR gate constructs to send a signal via the Lux system was measured by coplating bacterial XOR clones with bacteria containing a Lux receiver construct. | '''Cell-to-cell signaling by XOR gate constructs''' - The ability of two different XOR gate constructs to send a signal via the Lux system was measured by coplating bacterial XOR clones with bacteria containing a Lux receiver construct. | ||
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[http://partsregistry.org/Part:BBa_K091112:Experience '''Improved pLac promoter called pLacI'''<sup>Q1</sup>] | [http://partsregistry.org/Part:BBa_K091112:Experience '''Improved pLac promoter called pLacI'''<sup>Q1</sup>] | ||
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+ | We introduced mutations into the Lac promoter in order to improve its ability to promote transcription. The graph below shows the results of an experiment with GFP reporting that demonstrates that the new Lac promoters function better than the existing Registry promoter. | ||
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[[Image:Trial1.png]] | [[Image:Trial1.png]] |
Latest revision as of 03:39, 30 October 2008
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Cell-to-cell signaling by XOR gate constructs - The ability of two different XOR gate constructs to send a signal via the Lux system was measured by coplating bacterial XOR clones with bacteria containing a Lux receiver construct.
Positive control using a Lux sender and a Lux receiver (K09100) Green fluorescence indicates LuxI expression in the Lux sender and receipt of the intercellular signal by the receiver.
XOR gate construct [http://partsregistry.org/wiki/index.php?title=Part:BBa_K091173 K091173] coplated with the K09100 Lux receiver. Green fluorescence indicates that at least one of the two hybrid promoters in the XOR construct is driving expression of the LuxI gene.
XOR gate construct [http://partsregistry.org/wiki/index.php?title=Part:BBa_K091182 K091182] coplated with the K09100 Lux receiver. Green fluorescence indicates that at least one of the two hybrid promoters in the XOR construct is driving expression of the LuxI gene.
[http://partsregistry.org/Part:BBa_K091112:Experience Improved pLac promoter called pLacIQ1]
We introduced mutations into the Lac promoter in order to improve its ability to promote transcription. The graph below shows the results of an experiment with GFP reporting that demonstrates that the new Lac promoters function better than the existing Registry promoter.
Home | The Team | E. nigma Project | Parts Submitted to the Registry | Notebook |
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