Difference between revisions of "Part:BBa K3805138:Experience"
 
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how you used this part and how it worked out.
 
how you used this part and how it worked out.
  
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===Applications of BBa_K3805138===
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==Experiments of BBa_K3805138==
  
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For the synthesis of AIP by agrB-D, we also carried out the corresponding experiments
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For the synthesis of AIP by agrB-D and the verification of toggle switch functionality using AIP, we also carried out the related experiments
  
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Experiment 1: Measurement of standard experimental data
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===Experiment1：Toggle Switch Verification===
  
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We incubated the guards overnight for 12-16h, and then split the experimental material in the ultra-clean bench: five wells of a 96-well plate were poured with 200ul of bacterial solution, followed by 1mM of AIP, and 1ul each of diluted 107, 108 and 109 AIP into the first four wells, leaving a control of the original bacterial solution without AIP.
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We incubated the guards overnight for 12-16h, and then split the experimental material in the ultra-clean bench: five wells of a 96-well plate were poured with 200ul of bacterial solution, followed by 1mM of AIP, and 1ul each of diluted 10^7, 10^8 and 10^9 AIP into the first four wells, leaving a control of the original bacterial solution without AIP.
  
  
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Then we put the partitioned experimental material into the enzyme marker to detect the fluorescence intensity of mcherry and record the experimental data
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Then we put the partitioned experimental material into the microplate reader to detect the fluorescence intensity of mCherry and record the experimental data
  
  
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Experiment 2: Deceiver data collection
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===Experiment 2: Vertification of AIP generation===
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After collecting the standard experimental data, we filtered the 12h culture of the deceiver and mixed the remaining culture with an equal amount of the guard's bacterial solution. 200ul of the culture was placed in a 96-well plate and the mcherry was measured under the ELISA.
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After collecting the standard experimental data, we filtered the 12h culture of the deceiver and mixed the remaining culture with an equal amount of the guard's bacterial solution. 200ul of the culture was placed in a 96-well plate and the mCherry was measured under the microplate reader.
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==result==
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===experiment1===
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When a certain amount of exogenous AIP was applied to the bacterial fluid, red fluorescence(mCherry) was observed under the microscope. After a period of time, red fluorescence disappeared, and green fluorescence was observed under the microscope.
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[[File:FangruAIP.png|500px|thumb|center|Images under fluorescence microscope.(A)Before putting into AIPs, red fluorescence was observed.(B).After putting into AIP, red fluorescence disappeared,green fluorescence was observed.]]
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We then applied a concentration gradient of synthetic AIP to the bacterial fluid to establish an accurate coordination between AIP concentration and mCherry secretion and plotted the corresponding curve.
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The corresponding curve is as follows:
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[[File:Aip1.png|600px|thumb|center]]
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[[File:Aip2.png|600px|thumb|center]]
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[[File:Aip3.png|600px|thumb|center]]
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===experiment2===
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After a period of testing, we finally got our experimental results
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[[File:Hahaha.png|500px|thumb|center]]
  
  

Latest revision as of 13:08, 21 October 2021


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Experiments of BBa_K3805138

For the synthesis of AIP by agrB-D and the verification of toggle switch functionality using AIP, we also carried out the related experiments

Experiment1：Toggle Switch Verification

We incubated the guards overnight for 12-16h, and then split the experimental material in the ultra-clean bench: five wells of a 96-well plate were poured with 200ul of bacterial solution, followed by 1mM of AIP, and 1ul each of diluted 10^7, 10^8 and 10^9 AIP into the first four wells, leaving a control of the original bacterial solution without AIP.


Then we put the partitioned experimental material into the microplate reader to detect the fluorescence intensity of mCherry and record the experimental data


Experiment 2: Vertification of AIP generation

After collecting the standard experimental data, we filtered the 12h culture of the deceiver and mixed the remaining culture with an equal amount of the guard's bacterial solution. 200ul of the culture was placed in a 96-well plate and the mCherry was measured under the microplate reader.

result

experiment1

When a certain amount of exogenous AIP was applied to the bacterial fluid, red fluorescence(mCherry) was observed under the microscope. After a period of time, red fluorescence disappeared, and green fluorescence was observed under the microscope.

Images under fluorescence microscope.(A)Before putting into AIPs, red fluorescence was observed.(B).After putting into AIP, red fluorescence disappeared,green fluorescence was observed.

We then applied a concentration gradient of synthetic AIP to the bacterial fluid to establish an accurate coordination between AIP concentration and mCherry secretion and plotted the corresponding curve.

The corresponding curve is as follows:

Aip1.png


Aip2.png


Aip3.png


experiment2

After a period of testing, we finally got our experimental results

Hahaha.png


User Reviews

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