Difference between revisions of "Part:BBa K3852002"
(→Introduction) |
|||
| (2 intermediate revisions by the same user not shown) | |||
| Line 5: | Line 5: | ||
===Introduction=== | ===Introduction=== | ||
| − | + | In the human body, the taste receptor protein will be expressed and located on the cell membrane and perform normal functions. In order to verify whether the expressed protein is located on the cell membrane after the gene is transferred into Saccharomyces cerevisiae, we connect the taste receptor through the link sequence. After using fluorescent proteins of different colors, the positioning of the receptors on the cell membrane can be observed through a fluorescence microscope. The following will specifically show the experimental data related to the construction and verification of Pfba1+T2R1+eGFP. | |
[[File:T--BIT-China--Engeering 6.png|550px|thumb|center|Figure1. Receptors are followed by fluorescent proteins]] | [[File:T--BIT-China--Engeering 6.png|550px|thumb|center|Figure1. Receptors are followed by fluorescent proteins]] | ||
| Line 27: | Line 27: | ||
[[File:T--BIT-China--Engeering 9.png|550px|thumb|center|Figure4. The stripe is an eGFP fragment]] | [[File:T--BIT-China--Engeering 9.png|550px|thumb|center|Figure4. The stripe is an eGFP fragment]] | ||
| − | 3. Enzyme-cutting and enzyme-joint method to build Pfba1+T2R1+eGFP | + | ====3. Enzyme-cutting and enzyme-joint method to build Pfba1+T2R1+eGFP==== |
| − | + | We culled the bacteria and then extracted the plasmid. The plasmids were firstly digested by Swa1 single enzyme, then digested by Avr 11 single enzyme, and then linked by enzyme.At last we obtained the pESC-LEU containing Pfba1+T2R1+eGFP. After that, the plasmids were introduced into E. coli through the receptive state transformation experiment, and then cultured in the medium containing ampicillin. Colony growth was observed on the medium. | |
| − | [[File:T--BIT-China--Engeering 10.png|550px|thumb|center|Figure5. | + | [[File:T--BIT-China--Engeering 10.png|550px|thumb|center|Figure5. The colonies grew after transfection with Pfba1+T2R1+eGFP plasmid]] |
| − | + | In order to verify whether the plasmid was successfully introduced into E. coli, we carried out bacterial liquid PCR. After that, correct bands were observed by running the verification gel, which proved the successful construction of the plasmid. | |
| − | [[File:T--BIT-China--Engeering 11.png|550px|thumb|center|Figure6. | + | [[File:T--BIT-China--Engeering 11.png|550px|thumb|center|Figure6. The stripe is a Pfba1-T2R1-eGFP fragment]] |
| − | ====4. | + | ====4. Saccharomyces cerevisiae conversion experiment==== |
| − | + | The plasmid extracted from E. coli was successfully introduced into S. cerevisiae by electric transformation. | |
Latest revision as of 17:39, 21 October 2021
Pfba1+T2R1+eGFP
Introduction
In the human body, the taste receptor protein will be expressed and located on the cell membrane and perform normal functions. In order to verify whether the expressed protein is located on the cell membrane after the gene is transferred into Saccharomyces cerevisiae, we connect the taste receptor through the link sequence. After using fluorescent proteins of different colors, the positioning of the receptors on the cell membrane can be observed through a fluorescence microscope. The following will specifically show the experimental data related to the construction and verification of Pfba1+T2R1+eGFP.
Experimental
1. OE-PCR (connecting Pfba1 with eGFP)
We obtained the Pfba1-eGFP fragment by OE-PCR, and the following is a picture from the agar gel electrophoresis, which verifies the success of the synthesis of the fragment by comparing the length of the fragment.
2. Gibson Assembly and E. coli conversion experiment
After the successful connection between Pfba1 and eGFP, we integrated the fragment into pESC-LEU, then introduced it into E. coli by E. coli receptor transformation experiment, cultured with a medium containing ampicillin, and observed that the colonies on the medium grew.
In order to verify the successful introduction of plasmids into E. coli, we carried out a bacterial liquid PCR, and then by running the verification glue, observed the correct strip, proving the successful construction of plasmids.
3. Enzyme-cutting and enzyme-joint method to build Pfba1+T2R1+eGFP
We culled the bacteria and then extracted the plasmid. The plasmids were firstly digested by Swa1 single enzyme, then digested by Avr 11 single enzyme, and then linked by enzyme.At last we obtained the pESC-LEU containing Pfba1+T2R1+eGFP. After that, the plasmids were introduced into E. coli through the receptive state transformation experiment, and then cultured in the medium containing ampicillin. Colony growth was observed on the medium.
In order to verify whether the plasmid was successfully introduced into E. coli, we carried out bacterial liquid PCR. After that, correct bands were observed by running the verification gel, which proved the successful construction of the plasmid.
4. Saccharomyces cerevisiae conversion experiment
The plasmid extracted from E. coli was successfully introduced into S. cerevisiae by electric transformation.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 638
Illegal XbaI site found at 1345 - 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 638
Illegal XbaI site found at 1345 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 638
Illegal XbaI site found at 1345 - 1000COMPATIBLE WITH RFC[1000]