Difference between revisions of "Part:BBa K1632021"

Line 9: Line 9:
 
[[Image:Tokyo_Tech Pcon_rbs_lsaR_TT_Plux_rbs_cmRssrA modeling.png|thumb|center|500px|<b>Fig. 3.</b> The results of modeling]]
 
[[Image:Tokyo_Tech Pcon_rbs_lsaR_TT_Plux_rbs_cmRssrA modeling.png|thumb|center|500px|<b>Fig. 3.</b> The results of modeling]]
 
[[Image:ssrA tag .png|thumb|center|500px|<b>Fig. 4.Adding an ssrA degradation tag</b>]]
 
[[Image:ssrA tag .png|thumb|center|500px|<b>Fig. 4.Adding an ssrA degradation tag</b>]]
[[Image:Tokyo_Tech Pcon_rbs_lsaR_TT_Plux_rbs_cmRssrA.png|thumb|center|440px|<b>Fig. 4.</b> The cells which have BBa_K1632022 growth with Cm]]
+
[[Image:Tokyo_Tech Pcon_rbs_lsaR_TT_Plux_rbs_cmRssrA.png|thumb|center|440px|<b>Fig. 5.</b> The cells which have BBa_K1632022 growth with Cm]]
[[Image:Tokyo_Tech Pcon_rbs_rhlR_TT_Plux_rbs_cmRssrA.png|thumb|center|440px|<b>Fig. 5.</b> The cells which have BBa_K1632023 growth with Cm]]
+
[[Image:Tokyo_Tech Pcon_rbs_rhlR_TT_Plux_rbs_cmRssrA.png|thumb|center|440px|<b>Fig. 6.</b> The cells which have BBa_K1632023 growth with Cm]]
  
<span style="margin-left: 10px;">In the experiment using the Pcon_''lasR''_TT_Plux_''CmRssrA'' (<partinfo>BBa_K1632022</partinfo>) (Fig.4.) and Pcon_''rhlR''_TT_Plux_''CmRssrA'' (<partinfo>BBa_K1632023</partinfo>) (Fig.5.), we could not observe cell growth for cells that owned the ssrA-taged plasmid, in the absence of AHL<br>
+
<span style="margin-left: 10px;">In the experiment using the Pcon_''lasR''_TT_Plux_''CmRssrA'' (<partinfo>BBa_K1632022</partinfo>) (Fig.5.) and Pcon_''rhlR''_TT_Plux_''CmRssrA'' (<partinfo>BBa_K1632023</partinfo>) (Fig.6.), we could not observe cell growth for cells that owned the ssrA-taged plasmid, in the absence of AHL<br>
 
<span style="margin-left: 10px;">From our experiment, ''CmRssrA'' is confirmed work better than ''CmR'' without ssrA tag for our project.
 
<span style="margin-left: 10px;">From our experiment, ''CmRssrA'' is confirmed work better than ''CmR'' without ssrA tag for our project.
  

Revision as of 00:19, 19 September 2015

In our project, we wanted to use the CmR. At the first stage of wet experiment, we used the cells which have the plasmid which is Pcon_rhlR_TT_Plux_rbs_CmR(Fig. 1.) to characterize the function of rbs_CmR(BBa_K395160 by iGEM10_Tokyo_Tech). But the cells showed active growth even in the absence of AHL (Fig. 2.)

Fig. 1.Our initially design of a part containing a previously existing part
Fig. 2. The cells growth with Cm

From the results of this experiment, initially designed circuits showed leaky expression of CmR. We came up with two solutions, either increasing the chloramphenicol (Cm) concentration or inserting an ssrA tag to the CmR gene, to this problem. From modeling allowed us to successfully solve the influence of the leakage by adding an ssrA degradation tag right after the CmR gene(Fig.3. and Fig.4.).

Fig. 3. The results of modeling
Fig. 4.Adding an ssrA degradation tag
Fig. 5. The cells which have BBa_K1632022 growth with Cm
Fig. 6. The cells which have BBa_K1632023 growth with Cm

In the experiment using the Pcon_lasR_TT_Plux_CmRssrA (BBa_K1632022) (Fig.5.) and Pcon_rhlR_TT_Plux_CmRssrA (BBa_K1632023) (Fig.6.), we could not observe cell growth for cells that owned the ssrA-taged plasmid, in the absence of AHL
From our experiment, CmRssrA is confirmed work better than CmR without ssrA tag for our project.

For more information, see [http://2015.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2015 wiki].


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]