Coding
PETaseB3B4
Part:BBa_K2984011
Designed by: Alejandro Gaston Castro Group: iGEM19_Humboldt_Berlin (2019-10-13)
PETase CDS; Enzyme that catalyzes the first degradation step of PET B3-B4
This part is a part of the Chlamy-HUB-Collection. The PETase is an enzyme that was discovered in the bacterium Ideonella sakaiensis and catalyzes the hydrolysis of PET to MHET (Yoshida et al. 2016). This enzyme has caught the attention of many research groups around the world for its potential to be used for biotechnological applications regarding PET degradation. Austin et al. (2018) engineered this enzyme to improve its capacity to degrade PET.
This part was designed to be used with the MoClo standard and has B3-B4 overhangs.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 879
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 418
Illegal PstI site found at 879 - 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 142
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 879
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 879
- 1000COMPATIBLE WITH RFC[1000]
Characterization
References
- Yoshida, S., Hiraga, K., Takehana, T., Taniguchi, I., Yamaji, H., Maeda, Y., ... & Oda, K. (2016). A bacterium that degrades and assimilates poly (ethylene terephthalate). Science, 351(6278), 1196-1199. Austin, H. P., Allen, M. D., Donohoe, B. S., Rorrer, N. A., Kearns, F. L., Silveira, R. L., . . . Beckham, G. T. (2018). Characterization and engineering of a plastic-degrading aromatic polyesterase. Proceedings of the National Academy of Sciences, 115(19), E4350.
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Categories
Parameters
//cds/enzyme
protein |