Difference between revisions of "Part:BBa K4275002:Design"
(→Source) |
(→Design Notes) |
||
Line 12: | Line 12: | ||
2. The 79 amino acid long type-I dockerin domain is fused at the terminal of the GS linker, followed by a TEV site and a 8xhis affinity purification tag (HHHHHHHH). | 2. The 79 amino acid long type-I dockerin domain is fused at the terminal of the GS linker, followed by a TEV site and a 8xhis affinity purification tag (HHHHHHHH). | ||
− | 3. DNA sequence is codon-optimized based on the codon-usage table of <i>E.coli</i> Strain K12.MG1655, but the protein was later expressed in <i>K.marxianus</i> due to the lack of post-translational modifications and the formation of inclusion bodies in E. | + | 3. DNA sequence is codon-optimized based on the codon-usage table of <i>E.coli</i> Strain K12.MG1655, but the protein was later expressed in <i>K.marxianus</i> due to the lack of post-translational modifications and the formation of inclusion bodies in <i>E.coli</i> BL21(DE3). |
− | + | ||
===Source=== | ===Source=== |
Latest revision as of 01:06, 14 October 2022
NpaBGS-t
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 502
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1577
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1074
Illegal AgeI site found at 88
Illegal AgeI site found at 106 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
1. The catalytic domain and the dockerin domain is interspaced with a glycine-rich linker.
2. The 79 amino acid long type-I dockerin domain is fused at the terminal of the GS linker, followed by a TEV site and a 8xhis affinity purification tag (HHHHHHHH).
3. DNA sequence is codon-optimized based on the codon-usage table of E.coli Strain K12.MG1655, but the protein was later expressed in K.marxianus due to the lack of post-translational modifications and the formation of inclusion bodies in E.coli BL21(DE3).
Source
Neocallimastix patriciarum W5
Clostridium thermocellum (Dockerin-I domain)
References
1.Chen, Hsin-Liang et al. "A Highly Efficient Β-Glucosidase From The Buffalo Rumen Fungus Neocallimastix Patriciarum W5". Biotechnology For Biofuels, vol 5, no. 1, 2012. Springer Science And Business Media LLC, https://doi.org/10.1186/1754-6834-5-24.