Difference between revisions of "Part:BBa K3351017"
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===Summary=== | ===Summary=== | ||
PhaP contains a hydrophobic granule binding domain and a cytosol-facing hydrophilic domain. PhaP-tagged proteins could interact with various types of hydrophobic surfaces. A (Gly4Ser2)2 flexible linker is inserted between PhaP and P6.2 to facilitate attaching of P6.2 on surface and displaying sufficient flexibility of this peptide. | PhaP contains a hydrophobic granule binding domain and a cytosol-facing hydrophilic domain. PhaP-tagged proteins could interact with various types of hydrophobic surfaces. A (Gly4Ser2)2 flexible linker is inserted between PhaP and P6.2 to facilitate attaching of P6.2 on surface and displaying sufficient flexibility of this peptide. | ||
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| + | ===Characterization=== | ||
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| + | <html> | ||
| + | <img style="display: block; | ||
| + | width: 60%;height: 60%;" src="https://static.igem.org/mediawiki/parts/3/32/T--NWU-CHINA-A--od-11.png"><div>Figure.1 growth curve</div></html> | ||
===Reference=== | ===Reference=== | ||
Latest revision as of 10:49, 26 October 2020
HisTag-PhaP-linker-P6.2-HisTag
Summary
PhaP contains a hydrophobic granule binding domain and a cytosol-facing hydrophilic domain. PhaP-tagged proteins could interact with various types of hydrophobic surfaces. A (Gly4Ser2)2 flexible linker is inserted between PhaP and P6.2 to facilitate attaching of P6.2 on surface and displaying sufficient flexibility of this peptide.
Characterization
Reference
[1] Xue Q, Liu XB, Lao YH, Wu LP, Wang D, Zuo ZQ, Chen JY, Hou J, Bei YY, Wu XF, Leong KW, Xiang H, Han J. Anti-infective biomaterials with surface-decorated tachyplesin I. Biomaterials. 2018 Sep;178:351-362. doi: 10.1016/j.biomaterials.2018.05.008. Epub 2018 May 9. PMID: 29778319. 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]
Burden Imposed by this Part:
Burden is the percent reduction in the growth rate of E. coli cells transformed with a plasmid containing this BioBrick (± values are 95% confidence limits). This BioBrick did not exhibit a burden that was significantly greater than zero (i.e., it appears to have little to no impact on growth). Therefore, users can depend on this part to remain stable for many bacterial cell divisions and in large culture volumes. Refer to any one of the BBa_K3174002 - BBa_K3174007 pages for more information on the methods, an explanation of the sources of burden, and other conclusions from a large-scale measurement project conducted by the 2019 Austin_UTexas team.
This functional parameter was added by the 2020 Austin_UTexas team.