Difference between revisions of "Part:BBa K2224002:Experience"
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Here are specific steps of our experiment: | Here are specific steps of our experiment: | ||
| − | + | 1：Preparation of scale insect samples. We caught 6 identical look scale insects from Morning glory. After being disinfected, the shell portions of the scale insect were then cut down, which will be used later in the experiment. And at this time, the scale insects were killed. | |
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2: Prepare Protease. We cultured E. coli that contains Protease gene, then we used Ultrasonication and centrifuge to take out Protease: | 2: Prepare Protease. We cultured E. coli that contains Protease gene, then we used Ultrasonication and centrifuge to take out Protease: | ||
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5: Move these dishes to incubator that held temperature in 37℃. We waited for 72h and then took out the dishes. | 5: Move these dishes to incubator that held temperature in 37℃. We waited for 72h and then took out the dishes. | ||
| − | 6: The student of Shenzhen university helped us to scan the surface of scale insects by using Electron Microscope (S100). | + | 6: The student of Shenzhen university helped us to scan the surface of scale insects by using Electron Microscope (S100). |
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====Pictures and Analysis==== | ====Pictures and Analysis==== | ||
Revision as of 12:17, 31 October 2017
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how you used this part and how it worked out.
Applications of BBa_K2224002
iGEM2017_SMS_Shenzhen conducted two experiments on part BBa_K2224002.
First is enzyme activity essay. Second is to conduct a Scanning Electron Microscopy of test the enzyme on shell (containing high concentration of protein) of dead scale insect. However, due to our misconduct during preserving the enzyme activity essay kit, we failed in getting the accurate enzyme activity factors. Behind is the SEM result.
Scanning Electron Microscopy
Purpose
We want to find how effective this Protease can be on the insects’ shells so that we can adjust our final product in the future.
Method
In this experiment, in order to find if our protease can decompose the protein layer of scale insect and how effective this Protease can be on the insects’ shells，we submerged scale insects (dead and we have resolved its wax layer)in our protease for 72h (37℃）and used Electron Microscopy to scan the surface of shells.
Here are specific steps of our experiment:
1：Preparation of scale insect samples. We caught 6 identical look scale insects from Morning glory. After being disinfected, the shell portions of the scale insect were then cut down, which will be used later in the experiment. And at this time, the scale insects were killed.
2: Prepare Protease. We cultured E. coli that contains Protease gene, then we used Ultrasonication and centrifuge to take out Protease: 1.7ml -50mM-ph8.0-Tris-HCl solution + Precipitation (17ml E. coli broth after centrifuging triple times). After using Ultrasonication, we got Protease solution and fracted cells. Then centrifuged solution for 10 min(25℃，13000rpm)
(The Ultrasonication we used) (The solution after centrifuging, and Protease is the clear liquid)
3：Eliminate the Wax on scale insects’ shells. We used alcohol solution (C=75%) to soak scale insects for 1h and killed them in this step. [The wax can solute in alcohol] (After eliminating the wax on the shell, we got the scale insects that just covered with protein.)
4: Use culture two dishes to take scale insects (Each dish takes three scale insects). Then we dropped the Protease that we got in the first step into the first dish that we called it: No.1 until the scale insects were covered by liquid. For another dish that we called it: No.2, we dropped water into it until the liquid covered the scale insects.
5: Move these dishes to incubator that held temperature in 37℃. We waited for 72h and then took out the dishes.
6: The student of Shenzhen university helped us to scan the surface of scale insects by using Electron Microscope (S100).
Pictures and Analysis
Fig.1 - Experimental group
Fig.2 - Control group：without protease
The insect body that was soaked by protease was very different from that of the control group. In the control group, the insect structure was relatively complete and the characteristics were clear, but the insect body of the experimental group had lost its structural characteristics under the action of protease, and the outer shell was severely eroded.
More Details:
Fig.3 - Details of experiment group
Fig.4 - Details of control group
The insect body of the experimental group (arrow marker) has obvious erosion marks, compared to the control group, which is relatively complete and flat.
Conclusion:
Basing on our experiment result that the experimental group has showed more serious erosion than the control group has done, we are sure that our protease, which is expressed by BBa K2224002 in E.coli system, can dissolve scale insect’s protein on its shell successfully. As a result, it is possible that our protease would degrade the shell of scale insect in real situation that bacteria are spread onto vivo scale insect and release the enzyme.
Applications of BBa_K2224002
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