Difference between revisions of "Part:BBa K2407012"
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The experiment design<br>
 
The experiment design<br>
 
1. Fluorescence microplate reader measurement<br>
 
1. Fluorescence microplate reader measurement<br>
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The red colonies on the medium were cultured alone overnight. Then take 200 μL of bacterial solution, centrifugate it for 2 min at 4000R, pour out the supernatant and then re spin it with 200 μ l of water, place it in the hole, take its culture medium as the control, and measure its equal bacterial amount fluorescence intensity under the emission / excitation of 611 / 588 (literature value).
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The red colonies on the medium were cultured alone overnight. Then take 200 μL of bacterial solution, centrifugate it for 2 min at 4000R, pour out the supernatant and then re spin it with 200 μ l of water, place it in the hole, take its culture medium as the control, and measure its equal bacterial amount fluorescence intensity under the emission / excitation of 611 / 588.
 
[[File:T--Tianjin--70123.png|500px|thumb|none|Fig 3.mRFP fluorescene when the excitation spectrum is 588nm and the emission spectrum is 611nm]]
 
[[File:T--Tianjin--70123.png|500px|thumb|none|Fig 3.mRFP fluorescene when the excitation spectrum is 588nm and the emission spectrum is 611nm]]
 
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Revision as of 03:29, 22 October 2019


a modified yEmRFP for use in Yeast from mCherry mRFP

It is the RFP variant sequence that codon-optimized for the expression in Saccharomyces cerevisiae as yeast-enhanced mRFP (yEmRFP) and can combine fluorescence and a purple visible phenotype.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]



Team: Tianjin 2019 characterization

Team:Tianjin 2019 contributed to the reporter's characterization by connecting it to the combined promoters TEF and testing their fluorescence intensity and detailed fluorescence excitation curves.

Figure 1. Characterization scheme used by Team Tianjin

We transformed the constructed fragment directly into Saccharomyces cerevisiae and cultured it overnight under normal conditions (YES solid medium, 30 ℃). On the next day, the colony was visible to the naked eye, and the appearance was reddish.

Fig 2.Cell morphology on medium


The experiment design
1. Fluorescence microplate reader measurement
The red colonies on the medium were cultured alone overnight. Then take 200 μL of bacterial solution, centrifugate it for 2 min at 4000R, pour out the supernatant and then re spin it with 200 μ l of water, place it in the hole, take its culture medium as the control, and measure its equal bacterial amount fluorescence intensity under the emission / excitation of 611 / 588.

Fig 3.mRFP fluorescene when the excitation spectrum is 588nm and the emission spectrum is 611nm


2. Fluorescence curve determination
We measured the specific fluorescence intensity at 540 ~ 670nm emission wavelength under the condition of fixed excitation wavelength (611nm), and obtained the following results:

Fig 4.Fluorescene curve of mRFP when the excitation spectrum is 500nm

Then we measured the specific fluorescence intensity at 470 ~ 631nm under the condition of fixed emission wavelength (588nm), and obtained the following results:

Fig 5.Fluorescene curve of mRFP when the emission spectrum is 650nm