Difference between revisions of "Team:Newcastle/Results"

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<p> We also decided to add Glyphosate to determine the efficiency of the native C-P Lyase pathway. Everything was repeated the same but instead we added 0 µl, 20 µl, 200 µl and 2 ml of glyphosate at 10mg/L. After 8 hours of testing and left overnight, none of the samples had produced formaldehyde according to the testing strips. The testing strips detect a minimum formaldehyde concentration of 10 mg/L, so it was possible that formaldehyde had been produced but that there was too little of it to detect with the strips.</p>
 
<p> We also decided to add Glyphosate to determine the efficiency of the native C-P Lyase pathway. Everything was repeated the same but instead we added 0 µl, 20 µl, 200 µl and 2 ml of glyphosate at 10mg/L. After 8 hours of testing and left overnight, none of the samples had produced formaldehyde according to the testing strips. The testing strips detect a minimum formaldehyde concentration of 10 mg/L, so it was possible that formaldehyde had been produced but that there was too little of it to detect with the strips.</p>
  
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           <h2 style="font-family: Rubik; text-align: left; margin-top: 1%"> Conclusions and Future Work </h2>
 
           <h2 style="font-family: Rubik; text-align: left; margin-top: 1%"> Conclusions and Future Work </h2>

Revision as of 20:21, 1 November 2017

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Our Experimental Results

Key Achievements

A condensed list of our most notable results


  • - Designed a novel framework for biosensor development
  • - Proved that multicellular biosensors are able to co-ordinate responses to input molecules through a proof-of-concept IPTG responsive biosensor
  • - Successful characterisation of a transpose-based “stand-by switch” capable of producing eforRed in the “OFF” state, and C4 AHL in the “ON” state
  • - Used a Design of Experiments approach to successfully optimise a cell-free system
  • - Improved the BLANK plasmid for promoter screening
  • - Expressed and characterised Sarcosine Oxidase, showing successful degradation of sarcosine to formaldehyde
  • - Designed, and began to construct, a variety of framework compatible systems, including a synthetic promoter library
  • - Determined optimal cell ratios from our multicellular model

Below is a diagram of our Sensynova Framework. Clicking on each part of the framework (e.g. detector modules) links to the relevant results.

Alternatively, at the bottom of this page are tabs which will show you results for every part of the project



Framework

Framework Chassis

Biochemical Adaptor

Target

Detector Modules

Multicellular Framework Testing

C12 HSL: Connector 1

Processor Modules

Framework in Cell Free Protein Synthesis Systems

C4 HSL: Connector 2

Reporter Modules



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