Difference between revisions of "Part:BBa K3332082"
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===Usage and Biology===
 
===Usage and Biology===
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[[File:T--XMU-2082.circuit.png|none|500px|caption]]
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＇＇＇Fig 1.＇＇＇pBAD_B0034_eyfp_B0015
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'''Fig 1.''' pBAD_B0034_eyfp_B0015
  
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EYFP was designed in the downstream control of proBAD/araC to be set as a comparison of proBAD/araC-Inverter-EYFP-terminator (BBa_K3332079). By comparing the fluorescence intensity of induced and non-induced to characterize the function of the inverter.
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This composite part is used as a control group to demonstrate the effect of inverter, comparing with proBAD/araC-inverter-EYFP-terminator (BBa_K3332079). EYFP serves as a reporter gene. By comparing the fluorescence intensity/OD600 of induced and non-induced bacteria, we can characterize the function of the inverter.
  
 
===Characterization===
 
===Characterization===

Revision as of 15:58, 27 October 2020


pBAD/araC promoter-RBS-EYFP-terminator

It can express cyan fluorescent protein under certain conditions.It is used to characterize the function of the MazF as a control group


Usage and Biology

Fig 1. pBAD_B0034_eyfp_B0015

This composite part is used as a control group to demonstrate the effect of inverter, comparing with proBAD/araC-inverter-EYFP-terminator (BBa_K3332079). EYFP serves as a reporter gene. By comparing the fluorescence intensity/OD600 of induced and non-induced bacteria, we can characterize the function of the inverter.

Characterization

When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit was built, we sent the plasmid to sequence, and got the correct sequencing. After new molecular cloning experiments, we did Enzyme-Cut identification to certify the plasmid is correct. We used the Spe I and Pst I to cut the plasmid, then we got the target separate fragment.

caption

Fig.2 proBAD/araC-B0034-E0030-B0015_pSB1C3 (BBa_K3332082) digested by Spe I and Pst I (about 4148 bp)

Protocol:

1. Preparation of stock solution

Dissolve arabinose in ddH2O to make 100× stock solution（the work concentration is 0.2%）

2.Culture glycerol bacteria containing the corresponding plasmid in test tube for 12h.

3.Add 4mL of the above bacterial solution into 200 mL LB medium and maintain the culture condition at 37 ℃ and 180 rpm.

4.Add 2 mL arabinose stock solution into the induction group when OD600 increased to 0.6.

5.Induce for 6 hours and the condition is the same as before.

6.Then, sampling culture in 96-well plate reader to measure the fluorescence intensity (EYFP) and corresponding OD600, then calculate the fluorescence / OD value of each group.

Here is the result:

caption

We discovered that the downstream gene of proBAD/araC can be expressed in the presence of arabinose and decrease expression without arabinose. When the inverter is added to the circuit, the effect is reversed.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961