Difference between revisions of "Part:BBa K3859000"

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<b> 【fig.1A】The process of transferring words sentence into DNA sequence. </b>
 
<b> 【fig.1A】The process of transferring words sentence into DNA sequence. </b>
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https://2021.igem.org/wiki/images/d/d0/T--GreatBay_SZ--DNA_sequence_translation.png
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<b> 【fig.1B】Character and DNA sequence translation chart  </b>
  
 
<b><font size="+1.2"> Barcode construction </font></b>
 
<b><font size="+1.2"> Barcode construction </font></b>
  
Firstly, we transferred the words GBSZ ARTAG into DNA sequence using the DNA writer website(fig.1A).  Then we attached a cpf1-PAM sequence(TTTA) to upstream of the barcode sequences for CRISPR Cas12a detection[3]. Finally, this short segment of DNA was inserted into yeast for spore production(fig.1B).  
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Firstly, we transferred the words GBSZ ARTAG into DNA sequence using the DNA writer website(fig.1A).  Then we attached a cpf1-PAM sequence(TTTA) to upstream of the barcode sequences for CRISPR Cas12a detection[3]. Finally, this short segment of DNA was inserted into yeast for spore production(fig.1C).  
  
 
https://2021.igem.org/wiki/images/1/18/T--GreatBay_SZ--gene_editing.png
 
https://2021.igem.org/wiki/images/1/18/T--GreatBay_SZ--gene_editing.png
  
<b> 【fig.1B】The process of editing the yeast gene </b>
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<b> 【fig.1C】The process of editing the yeast gene </b>
  
 
<b><font size="+1.2"> Producing spores with barcode </font></b>
 
<b><font size="+1.2"> Producing spores with barcode </font></b>
  
 
Firstly, we replace the the GFP with barcode using golden gate assembly. Then the plasmid is cut in to linear by notl digestion. At last we transfer the linear DNA into yeast, it will insert into yeast plasmid by homologous recombination(fig.1A).  
 
Firstly, we replace the the GFP with barcode using golden gate assembly. Then the plasmid is cut in to linear by notl digestion. At last we transfer the linear DNA into yeast, it will insert into yeast plasmid by homologous recombination(fig.1A).  
These yeast will be used to produce spores(fig.1C)[1]. We will do a microscope examination to check whether the spores are produced or not. The microscope examination results are shown below(fig.1D)(fig.1E).
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These yeast will be used to produce spores(fig.1D)[1]. We will do a microscope examination to check whether the spores are produced or not. The microscope examination results are shown below(fig.1E)(fig.1F).
  
 
https://2021.igem.org/wiki/images/8/89/T--GreatBay_SZ--spore_formation.png
 
https://2021.igem.org/wiki/images/8/89/T--GreatBay_SZ--spore_formation.png
  
<b> 【fig.1C】Overview of the stages of spore formation  </b>
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<b> 【fig.1D】Overview of the stages of spore formation  </b>
  
 
https://2021.igem.org/wiki/images/4/4d/T--GreatBay_SZ--part_K3859000_1D.png
 
https://2021.igem.org/wiki/images/4/4d/T--GreatBay_SZ--part_K3859000_1D.png
  
<b> 【fig.1D】Yeast and spores stained with Methylene blue, we can see the endospores inside the vegetative cell(bule transparent)  </b>
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<b> 【fig.1E】Yeast and spores stained with Methylene blue, we can see the endospores inside the vegetative cell(bule transparent)  </b>
  
 
https://2021.igem.org/wiki/images/0/01/T--GreatBay_SZ--part_K3859000_1E.png
 
https://2021.igem.org/wiki/images/0/01/T--GreatBay_SZ--part_K3859000_1E.png
  
<b> 【fig.1E】Spore staining of yeast after sporulation, the red small dot represent yeast and green dot represent yeast spores.  </b>
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<b> 【fig.1F】Spore staining of yeast after sporulation, the red small dot represent yeast and green dot represent yeast spores.  </b>
  
 
<b><font size="+1.2"> References </font></b>
 
<b><font size="+1.2"> References </font></b>

Revision as of 10:22, 15 October 2021


GBSZ ARTAG barcode

BBa_K3859000 is one of our barcodes which contains specific DNA sequences. This barcode has the meaning of GBSZ ARTAG. This word includes our team name and the products we made, which are very representative. Barcode is a unique DNA sequence which we inserted into yeast spore in order to achieve an efficient, simple and durable spore detection system.[2] We will use Cas12a to detect the barcode in spore in order to identify the authenticity of items, such as artworks.

T--GreatBay_SZ--GBSZ_barcode.png

【fig.1A】The process of transferring words sentence into DNA sequence.

T--GreatBay_SZ--DNA_sequence_translation.png

【fig.1B】Character and DNA sequence translation chart

Barcode construction

Firstly, we transferred the words GBSZ ARTAG into DNA sequence using the DNA writer website(fig.1A). Then we attached a cpf1-PAM sequence(TTTA) to upstream of the barcode sequences for CRISPR Cas12a detection[3]. Finally, this short segment of DNA was inserted into yeast for spore production(fig.1C).

T--GreatBay_SZ--gene_editing.png

【fig.1C】The process of editing the yeast gene

Producing spores with barcode

Firstly, we replace the the GFP with barcode using golden gate assembly. Then the plasmid is cut in to linear by notl digestion. At last we transfer the linear DNA into yeast, it will insert into yeast plasmid by homologous recombination(fig.1A). These yeast will be used to produce spores(fig.1D)[1]. We will do a microscope examination to check whether the spores are produced or not. The microscope examination results are shown below(fig.1E)(fig.1F).

T--GreatBay_SZ--spore_formation.png

【fig.1D】Overview of the stages of spore formation

T--GreatBay_SZ--part_K3859000_1D.png

【fig.1E】Yeast and spores stained with Methylene blue, we can see the endospores inside the vegetative cell(bule transparent)

T--GreatBay_SZ--part_K3859000_1E.png

【fig.1F】Spore staining of yeast after sporulation, the red small dot represent yeast and green dot represent yeast spores.

References

1. Neiman A. M. (2005). Ascospore formation in the yeast Saccharomyces cerevisiae. Microbiology and molecular biology reviews : MMBR, 69(4), 565–584. https://doi.org/10.1128/MMBR.69.4.565-584.2005

2. Qian, J., Lu, Z. X., Mancuso, C. P., Jhuang, H. Y., Del Carmen Barajas-Ornelas, R., Boswell, S. A., Ramírez-Guadiana, F. H., Jones, V., Sonti, A., Sedlack, K., Artzi, L., Jung, G., Arammash, M., Pettit, M. E., Melfi, M., Lyon, L., Owen, S. V., Baym, M., Khalil, A. S., Silver, P. A., … Springer, M. (2020). Barcoded microbial system for high-resolution object provenance. Science (New York, N.Y.), 368(6495), 1135–1140. https://doi.org/10.1126/science.aba5584

3. Zetsche, B., Gootenberg, J. S., Abudayyeh, O. O., Slaymaker, I. M., Makarova, K. S., Essletzbichler, P., Volz, S. E., Joung, J., van der Oost, J., Regev, A., Koonin, E. V., & Zhang, F. (2015). Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system. Cell, 163(3), 759–771. https://doi.org/10.1016/j.cell.2015.09.038

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]