Difference between revisions of "Part:BBa K3815004"
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<partinfo>BBa_K3815004 short</partinfo> | <partinfo>BBa_K3815004 short</partinfo> | ||
+ | <h3><font size="4.5">Descriotion of this part</font> </h3> | ||
+ | <h3><font size="3">Targeted protein</font> </h3> | ||
+ | This part is for the purfication of the small peptide, NOP1. It can prevent the plants from accepting ethylene. In our experiment, we used it to inhibit the acceptance of ethylene that promotes the wilting of a plant and aging of cut flowers.<br><br> | ||
+ | <h3><font size="3">Purification system</font> </h3> | ||
+ | In order to purify the peptide, we adopted ELK16 system that the past iGEM teams had not used. This part is composed of ELK16, Mxe Gyr intein, and PT linker. When this fused protein is produced, ELK16 self-assembles and precipitates. After that, taking this aggregate and adding DTT to it, the N terminal of Mxe GyrA intein is cut. Then, we can get the targeted protein.<br> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 10:03, 20 October 2021
NOP1-Mxe GryA intein-PT-linker-ELK16
Descriotion of this part
Targeted protein
This part is for the purfication of the small peptide, NOP1. It can prevent the plants from accepting ethylene. In our experiment, we used it to inhibit the acceptance of ethylene that promotes the wilting of a plant and aging of cut flowers.
Purification system
In order to purify the peptide, we adopted ELK16 system that the past iGEM teams had not used. This part is composed of ELK16, Mxe Gyr intein, and PT linker. When this fused protein is produced, ELK16 self-assembles and precipitates. After that, taking this aggregate and adding DTT to it, the N terminal of Mxe GyrA intein is cut. Then, we can get the targeted protein.
Usage and Biology
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 117
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 117
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 117
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 117
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 117
Illegal NgoMIV site found at 550 - 1000COMPATIBLE WITH RFC[1000]