Difference between revisions of "Part:BBa K112000"

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[[File:T--NYMU-Taipei--TAS-FunctionalTest.png|600px]]
 
[[File:T--NYMU-Taipei--TAS-FunctionalTest.png|600px]]
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===Team 2020 SZ-SHD===
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Application of pBAD, L-arabinose-inducible promoter, to regulate T4 holin and T4 endolysin production as a cell suicide switch. Which has been applied to control the release of cytoplasmic proteins.<br>
 +
Plasmid circuit map:<br>
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[[File:Pbad_T4_map.png|600px|thumb|center|]]
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The experiment of the suicide efficiency was investigated using E. coli (strain DH10B), a gradual decline in OD600 value of recombined DH10B (pSB1C3-pBAD-T4) in response to 1mM arabinose could be observed comparing to non-transformed ones (control).<br>
 +
[[File:T4_test.jpeg|600px|thumb|center|]]
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We have co-transformed this plasmid with a protein expressing circuit, which we have observed a increase in protein concertation after 1mM of arabinose has been added.<br>
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[[File:T4_test2.png|600px|thumb|center|the release of xncht after induction by arabinose (1mM) was measured over 42 hours: the abundance of protein released ≈ the concentration of proteins in supernatant of induced bacterial culture minus uninduced. Where the concentration could be determined by measuring the absorption of light with 280nm wavelength. Results have a PMCC value of 0.48]]

Revision as of 13:55, 25 October 2020

T4 holin, complete CDS, berkeley standard

T4 holin gene, with start and stop codons.


This part is in BBb Format. It is flanked by BamHI and BglII sites instead of XbaI and SpeI. More information about the BBb Format is available at:
[http://openwetware.org/wiki/Template:AndersonLab:BBb_Standard BBb Standard Description Page]


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]



Team NYMU-Taipei 2017: Successfully construct T4 holin into suicide mechanism

Improvement

We successfully combine T4 holin with a lactose-induced promoter (BBa_R0010), a ribosome binding site (BBa_B0034) and a double terminator (BBa_B0010 and BBa_B0012). Therefore, holin can be induced by lactose and regulate the suicide mechanism. Moreover, we construct T4 holin and T4 endolysin together as a functional suicide mechanism. Besides, in NYMU-Taipei 2017 team’s project, we also put the suicide mechanism into practice by constructing them with NrtA.


Result

Figure 1 is the gene map of T4 holin construct, pSB1C3-J04450-K112000.

Figure 1

T--NYMU-Taipei--Holin.png


Figure 2 is electrophoresis result of holin (from BBa_K112000) PCR product. The marker is 100bp. The length is 657bp as expected.

Figure 2

T--NYMU-Taipei--Holin PCR 657bp.png


Figure 3 is electrophoresis result of holin backbone (from BBa_J04450) PCR product. The marker is 1kb. The length is 2458bp as expected.

Figure 3

T--NYMU-Taipei--Holin BB PCR 2458bp.png


Figure 4 and Figure 5 are the results of suicide mechanism functional test. Both figure show that our suicide mechanism can be induced by adding lactose, and the effectiveness of suicide mechanism goes better as the concentration of lactose goes higher.


Figure 4 is the bacterium with holin-endolysin construct. As figure 3 shows, the suicide mechanism is induced immediately when lactose is added into the samples. Besides, we can see that the lactose concentration and the OD value of the bacterium with holin-endolysin construct are positively correlated, which means our suicide mechanism does work.

Figure 4

BBa K2350020 LineGraph.png


Figure 5 is the bacterium with holin-endolysin-NrtA construct. As figure 5 shows, the trend of the relative absorbance is downward as the lactose is added to induce the suicide mechanism. The concentration of lactose is also positively correlated with the declining degree of relative absorbance.

Figure 5

T--NYMU-Taipei--TAS-FunctionalTest.png

Team 2020 SZ-SHD

Application of pBAD, L-arabinose-inducible promoter, to regulate T4 holin and T4 endolysin production as a cell suicide switch. Which has been applied to control the release of cytoplasmic proteins.
Plasmid circuit map:

Pbad T4 map.png

The experiment of the suicide efficiency was investigated using E. coli (strain DH10B), a gradual decline in OD600 value of recombined DH10B (pSB1C3-pBAD-T4) in response to 1mM arabinose could be observed comparing to non-transformed ones (control).

T4 test.jpeg

We have co-transformed this plasmid with a protein expressing circuit, which we have observed a increase in protein concertation after 1mM of arabinose has been added.

the release of xncht after induction by arabinose (1mM) was measured over 42 hours: the abundance of protein released ≈ the concentration of proteins in supernatant of induced bacterial culture minus uninduced. Where the concentration could be determined by measuring the absorption of light with 280nm wavelength. Results have a PMCC value of 0.48