Difference between revisions of "Part:BBa K2292003"

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Figure 2 Agarose gel electrophoresis of PCR product (pSBBS1C)
 
Figure 2 Agarose gel electrophoresis of PCR product (pSBBS1C)
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The DNA size we expect to show up is 2563 bp, hence from the electrophoresis gel photos above, we can say that the plasmid DNA in well number 1, 3, 4, 8, 9, 10, 11, 13, 16, 19, 21, 24, 25, 27, 28 are those we want, and the corresponding patch are those that are successfully transformed.
  
 
https://static.igem.org/mediawiki/parts/b/b4/Agarose_gel_electrophoresis_of_pSBBS4S.jpg
 
https://static.igem.org/mediawiki/parts/b/b4/Agarose_gel_electrophoresis_of_pSBBS4S.jpg
  
 
Figure 3 Agarose gel electrophoresis of PCR product (pSBBS4S)
 
Figure 3 Agarose gel electrophoresis of PCR product (pSBBS4S)
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 +
The DNA size we expect to show up is 1344 bp, hence from the electrophoresis gel photos above, we can say that the plasmid DNA in all wells, except well number 5,17, 18 ,31, are the ones we want, and the corresponding patch are those bacteria that has been successfully transformed.
  
 
For the measurement of the fluorescent plate reader (excitation: 485 nm, emission: 520 nm), we found out that the best amount of bacteria for measuring, the CSP conc. is at the value of OD600 = 0.2 after a series of experiment.
 
For the measurement of the fluorescent plate reader (excitation: 485 nm, emission: 520 nm), we found out that the best amount of bacteria for measuring, the CSP conc. is at the value of OD600 = 0.2 after a series of experiment.

Revision as of 03:40, 2 November 2017


comDE two components signal transduction system

This is a composite used for producing comD, comE, two essential protein for the CSP two components signal transduction system. Originated from Streptococcus mutans. ComD is a kinase and membrane-associated receptor. After comD binded to the quorum sensing molecule CSP, the comD-CSP complex will phosphorylate comE. Then, the phosphorylated comE can turn on the transcription of downstream gene. FLAG-TAG is added after comE and c-Myc is added after comD

TCSTS~23~.jpg

Figure 1 Mechanism of CSP detection

Agarose_gel_electrophoresis_of_pSBBS1C.jpg

Figure 2 Agarose gel electrophoresis of PCR product (pSBBS1C)

The DNA size we expect to show up is 2563 bp, hence from the electrophoresis gel photos above, we can say that the plasmid DNA in well number 1, 3, 4, 8, 9, 10, 11, 13, 16, 19, 21, 24, 25, 27, 28 are those we want, and the corresponding patch are those that are successfully transformed.

Agarose_gel_electrophoresis_of_pSBBS4S.jpg

Figure 3 Agarose gel electrophoresis of PCR product (pSBBS4S)

The DNA size we expect to show up is 1344 bp, hence from the electrophoresis gel photos above, we can say that the plasmid DNA in all wells, except well number 5,17, 18 ,31, are the ones we want, and the corresponding patch are those bacteria that has been successfully transformed.

For the measurement of the fluorescent plate reader (excitation: 485 nm, emission: 520 nm), we found out that the best amount of bacteria for measuring, the CSP conc. is at the value of OD600 = 0.2 after a series of experiment.

664px-Fluorescence-CSP_concentration-Time.jpg

Figure 4 Three-dimension diagram (Fluorescence-CSP concentration-Time)

The intensity of fluorescence slowly drops after a sharp rise in a small amount of time, hence we can tell that the reaction starts right away as soon as CSP is added.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 268
    Illegal XhoI site found at 123
    Illegal XhoI site found at 153
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]