Part:BBa_K165000

MET 25 Promoter

 The is a repressable promoter for use in Saccharomyces cerevisiae.  It is repressed by the presence of methionine.  When unrepresssed, is has a moderate level of activity.

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]

ITRODUCTION

In order to determine the strength of pMET25 promoter, we have conducted the following experiment. First of all, we have constructed 2 plasmids where EGFP is expressed under different constitutive promoters. The empty plasmid was used as a negative control.

MATERIALS AND METHODS

Plasmids used to conduct the experiment are listed in table 1.

Table 1. Plasmids created

		Insert
number	Plasmid name	Promoter	Gene	Terminator	backbone
1	pRS306 pMET25-EGFP-tCYC1	MET25	EGFP	tCYC1	pRS306
2	pRS306	MET25
pRS306

After construction of plasmids was finished, we have transformed S. cerevisiae DOM90 (MATa {leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15 bar1::hisG} [phi+]) strain with plasmids listed above to create the strains (table 2).

Table 2. S. cerevisiae strains created.

	Strain name	Genotype	Plasmid integrated
Negative control	DOM90	MATa {leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15 bar1::hisG} [phi+]	pRS306
Met25 uninduced	DOM90	MATa {leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15 bar1::hisG} [phi+]	pRS306
Met25 induced	DOM90	MATa {leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15 bar1::hisG} [phi+]	pRS306

We have measured the EGFP fluorescence intensity with BioTek Synergy MX microplate reader.

All strains were pregrown overnight at 30°C in liquid CSM/2%Glc media, resuspended in fresh CSM/2%Glc media to OD600 ca. 0.7, divided into 2 parts: half was induced by changing media from CSM to -Met, half was left uninduced. Put to grow for 3 hours. Distributed to 96 well plate (clear flat bottom). 8 replicates from the strain were used. 200 µL of cells were added to each well. As a reference to OD600, fresh CSM/2%Glc media was used. After the 96 well plate was ready, the OD600 and fluorescence (excitation 485 nm, emission 528 nm, bandwidth 20, gain 80) were measured. The layout of the plate is described in table 3.

Table 3. The 96 well plate layout for OD600 and Fluorescence measurements.

	Negative control	Met25 uninduced	MET25 induced
Colony 1 Replicate 1
Colony 1 Replicate 2
Colony 1 Replicate 3
Colony 1 Replicate 4
Colony 1 Replicate 5
Colony 1 Replicate 6
Colony 1 Replicate 7
Colony 1 Replicate 8

As a fluorescence reference, the standard curve of fluorescence for fluorescein concentration was generated according to 2018 iGEM InterLab Study. The only difference from the InterLab protocol was the concentration of the fluorescein used. In the InterLab study, the highest fluorescein concentration used was 10 µM. But due to the higher gain parameter used in our measurement experiment, we have used 0.313 µM to avoid out of range measurements.

CONCLUSIONS

<p> The results are as expected, negative control does not show almost any fluorescence. Uninduced pMET25 shows basic flourescence which can be due to the leaking of promoter. However induced promoter shows high fluorescence.