Difference between revisions of "Part:BBa K3859005"

 
 
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<partinfo>BBa_K3859005 short</partinfo>
 
<partinfo>BBa_K3859005 short</partinfo>
  
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BBa_K3859004 is one of our barcodes which contains specific DNA sequences. This barcode has the meaning of TO ERR TO FALL TO TRIUMPH AND TO RECREATE LIFE OUT OF LIFE. 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.
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<b><font size="+1.2"> Barcode design </font></b>
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Firstly, we transferred the sentence TO ERR TO FALL TO TRIUMPH AND TO RECREATE LIFE OUT OF LIFE into DNA sequence using the DNA writer website(fig.6A). The picture below shows the DNA sequence and words translation chart (fig.2). Then we attached a cpf1-PAM sequence(TTTA)to the upstream of the barcode sequences for CRISPR Cas12a detection[3]. Finally, this short segment of DNA was inserted into yeast for spore production(fig.3).
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<div style='text-align: center;'>
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[[File:T--GreatBay_SZ--GBSZ_barcode.png|600px|thumb|center]]
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<b> 【fig.1】The process of transferring words sentence into DNA sequence. </b>
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[[File:T--GreatBay_SZ--DNA_sequence_translation.png|600px|thumb|center]]
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<b> 【fig.2】Character and DNA sequence translation chart  </b>
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</div>
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<b><font size="+1.2"> Spores producing </font></b>
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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.3).
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These yeast will be used to produce spores(fig.4)[1]. We will do a microscope examination to check whether the spores are produced or not. The microscope examination results are shown below(fig.5)(fig.6).
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<div style='text-align: center;'>
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[[File:T--GreatBay_SZ--gene_editing.png|450px|thumb|center]]
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<b> 【fig.3】The process of editing the yeast gene </b>
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[[File:T--GreatBay_SZ--spore_formation.png|600px|thumb|center]]
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<b> 【fig.4】Overview of the stages of spore formation  </b>
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[[File:T--GreatBay_SZ--part_BBa_K3859005_6D.png|400px|thumb|center]]
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<b> 【fig.5】Yeast and spores stained with Methylene blue, we can see the endospores inside the vegetative cell(bule transparent)  </b>
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[[File:T--GreatBay_SZ--part_BBa_K3859005_6E.png|400px|thumb|center]]
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<b> 【fig.6】Spore staining of yeast after sporulation, the red small dot represent yeast and green dot represent yeast spores.  </b>
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</div>
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<b><font size="+1.2"> References </font></b>
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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
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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
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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
  
 
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Latest revision as of 04:47, 16 October 2021


TO ERR TO FALL TO TRIUMPH AND TO RECREATE LIFE OUT OF LIFE barcode

BBa_K3859004 is one of our barcodes which contains specific DNA sequences. This barcode has the meaning of TO ERR TO FALL TO TRIUMPH AND TO RECREATE LIFE OUT OF LIFE. 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.

Barcode design

Firstly, we transferred the sentence TO ERR TO FALL TO TRIUMPH AND TO RECREATE LIFE OUT OF LIFE into DNA sequence using the DNA writer website(fig.6A). The picture below shows the DNA sequence and words translation chart (fig.2). Then we attached a cpf1-PAM sequence(TTTA)to the upstream of the barcode sequences for CRISPR Cas12a detection[3]. Finally, this short segment of DNA was inserted into yeast for spore production(fig.3).


T--GreatBay SZ--GBSZ barcode.png


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

T--GreatBay SZ--DNA sequence translation.png

【fig.2】Character and DNA sequence translation chart

Spores producing

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.3). These yeast will be used to produce spores(fig.4)[1]. We will do a microscope examination to check whether the spores are produced or not. The microscope examination results are shown below(fig.5)(fig.6).

T--GreatBay SZ--gene editing.png

【fig.3】The process of editing the yeast gene


T--GreatBay SZ--spore formation.png

【fig.4】Overview of the stages of spore formation

T--GreatBay SZ--part BBa K3859005 6D.png

【fig.5】Yeast and spores stained with Methylene blue, we can see the endospores inside the vegetative cell(bule transparent)

T--GreatBay SZ--part BBa K3859005 6E.png

【fig.6】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
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 53
    Illegal NheI site found at 157
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]