Difference between revisions of "Part:BBa K2317001"
Line 17: | Line 17: | ||
[[File:T--Jilin_China--fg5.png|650px|thumb|center|Figure 4. The result of agarose gel electrophoresis. ]] | [[File:T--Jilin_China--fg5.png|650px|thumb|center|Figure 4. The result of agarose gel electrophoresis. ]] | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
+ | |||
+ | A toxin-antitoxin system is a set of two or more closely linked genes that together encode both a "toxin" protein and a corresponding "antitoxin". Toxin-antitoxin systems are widely distributed in prokaryotes, and organisms often have them in multiple copies.[ ] | ||
+ | In nature, toxins and antitoxins form a stable complex inhibiting the toxin activity under normal growth conditions. In case of cellular damage or stress conditions, antitoxins are degraded, allowing the free toxin to bind its cellular target. | ||
+ | In type IV TA systems, the antitoxin does not inhibit the toxin through direct binding but neutralizes its toxicity by stabilizing the toxin target proteins. CbtA, as a representative toxin, aimed at MreB and FtsZ, two major cytoskeleton proteins in Escherichia coli. | ||
+ | By the way, MreB and FtsZ are the homologues of eukaryotic actin and tubulin respectively | ||
+ | Those two proteins are important for cell growth and division. MreB is responsible for maintaining the cell shape, polarity ,as well as orienting cell wall synthesis. FtsZ forms a ring structure at the mid-cell and functions as a scaffold during the assembly of divisomes, which is a multi-protein complex and essential for cell division. | ||
+ | Therefore, CbtA holds the advantages of controllable toxic and less effects to the growing environment during co-culture. | ||
+ | |||
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 16:20, 26 October 2020
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]