Difference between revisions of "Part:BBa K2317001"
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[[File:T-Jilin_China--fg3.png|700px|thumb|center|Figure 3. (A) and (B) The two figures were taken to compare the turbidities of TA group after 14 hours od culturing, and the difference could be told by eyes. ]] | [[File:T-Jilin_China--fg3.png|700px|thumb|center|Figure 3. (A) and (B) The two figures were taken to compare the turbidities of TA group after 14 hours od culturing, and the difference could be told by eyes. ]] | ||
<h1>'''Characterization:'''</h1> | <h1>'''Characterization:'''</h1> | ||
− | Through agarose gel electrophoresis, the plasmid we constructed was verified.(figure) We chose DL 10000 as the marker and used BBa_K864402 as the control. Eight of the lanes contained pSB1C3-CbtA monoclones and Eight of the lanes contained pSB1C3-CbeA monoclones. After that, we sent them for sequencing and the results showed that the sequences were right. | + | Through agarose gel electrophoresis, the plasmid we constructed was verified.(figure 4.) We chose DL 10000 as the marker and used BBa_K864402 as the control. Eight of the lanes contained pSB1C3-CbtA monoclones and Eight of the lanes contained pSB1C3-CbeA monoclones. After that, we sent them for sequencing and the results showed that the sequences were right. |
− | [[File:T-Jilin_China--fg5.png| | + | [[File:T--Jilin_China--fg5.png|650px|thumb|center|Figure 4. The result of agarose gel electrophoresis. ]] |
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Revision as of 12:05, 1 November 2017
CbtA
CbeA-CbtA is one of the Escherichia coli TA systems, and the Toxin, CbtA, has been reported to inhibit the polymerization of bacterial cytoskeletal proteins, MreB and FtsZ.(Fugure 1.)
Usage and Biology
The population and growth condition can be reflected by Abs600, so through the curve of Abs600-time, the effect of CbeA and CbtA towards bacteria can be displayed. Abs600 values were measured from 0 to 14 hours in two groups and the toxication curves were drawn as shown in Figure 2. The growth rate of vector group bacteria after adding L-Arabinose sped up for a short time and then slowed down. At last, the trend was consistent with that without L-Arabinose. However, TA group, with the addition of L-Arabinose, showed the same OD and Abs600 values from the 4th hour for a while. After that, Abs600 values displayed a little increase.
Besides, after culturing for 14 hrs, difference in turbidities of bacteria in different groups was visible Figure 3.
Characterization:
Through agarose gel electrophoresis, the plasmid we constructed was verified.(figure 4.) We chose DL 10000 as the marker and used BBa_K864402 as the control. Eight of the lanes contained pSB1C3-CbtA monoclones and Eight of the lanes contained pSB1C3-CbeA monoclones. After that, we sent them for sequencing and the results showed that the sequences were right.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]