Difference between revisions of "Part:BBa K4417015"
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This part is the coding sequence of ureEFG accessory proteins from Sporosarcina pasteurii. It was cloned into the master plasmid (BBa_K4417017). | This part is the coding sequence of ureEFG accessory proteins from Sporosarcina pasteurii. It was cloned into the master plasmid (BBa_K4417017). | ||
+ | |||
+ | This part is not Type IIS compatible as it has BsaI sites. | ||
[[File:Adkjb.png|600px|thumb|center|'''Figure 1:''' Basic part ureEFG TU2B]] | [[File:Adkjb.png|600px|thumb|center|'''Figure 1:''' Basic part ureEFG TU2B]] |
Latest revision as of 13:25, 12 October 2022
CuO-RBS-ureABC-rrnB T1 Terminator TU1B
Description
This part is the coding sequence of ureEFG accessory proteins from Sporosarcina pasteurii. It was cloned into the master plasmid (BBa_K4417017).
This part is not Type IIS compatible as it has BsaI sites.
Usage and Biology
- This basic part can be used to produce urease accessory proteins.
- It can be cloned into the master plasmid (BBa_K4417017) to express the nature urease operon from Sporosarcina pasteurii using Golden Gate assembly.
- The part was synthesized by IDT as a gBlock.
Reference
1. Zerner, B. “Recent advances in the chemistry of an old enzyme, urease.” Bioorg. Chem. 19 (1991):116-131
2. Krajewska, Barbara. "Ureases I. Functional, catalytic and kinetic properties: A review". Journal of Molecular Catalysis B: Enzymatic 59 no.1-3 (2009):9–21. doi:10.1016/j.molcatb.2009.01.003
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 969
Illegal BamHI site found at 1
Illegal XhoI site found at 1723 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 7
Illegal BsaI.rc site found at 2066