Difference between revisions of "Part:BBa K3815002"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K3815002 short</partinfo> | <partinfo>BBa_K3815002 short</partinfo> | ||
− | + | <h3><font size="4.5">Descriotion of this part</font> </h3> | |
− | This part is | + | <h3><font size="3">Targeted protein</font> </h3> |
+ | This part is for the purfication of antimicrobial peptide, Defensin1. This is derived from <i>Homo Sapiens</i>. This can inhibit the growth of the gram-positive bacteria. In our experiment, we used it to kill the bacteria in the vase water.<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> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 09:41, 20 October 2021
Defensin1-Mxe GryA intein-PTlinker-ELK16
Descriotion of this part
Targeted protein
This part is for the purfication of antimicrobial peptide, Defensin1. This is derived from Homo Sapiens. This can inhibit the growth of the gram-positive bacteria. In our experiment, we used it to kill the bacteria in the vase water.
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.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 249
Illegal SpeI site found at 573 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 249
Illegal SpeI site found at 573 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 249
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 249
Illegal SpeI site found at 573 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 249
Illegal SpeI site found at 573
Illegal NgoMIV site found at 682 - 1000COMPATIBLE WITH RFC[1000]