Difference between revisions of "Part:BBa K3102035:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | We mutated in the MtrC sequence a Guanine into Cysteine and a Guanine into Adenine at the 1838bp and 1841bp position (G1838C & G1841A), respectively, because of the PstI enzyme. | |
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===Source=== | ===Source=== |
Revision as of 09:02, 16 October 2019
T7-RBS-DLDII Operon-Ter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 4365
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We mutated in the MtrC sequence a Guanine into Cysteine and a Guanine into Adenine at the 1838bp and 1841bp position (G1838C & G1841A), respectively, because of the PstI enzyme.
Source
This sequence comes from Shewanella Oneidensis was found through Biocyc: https://biocyc.org/gene?orgid=SONE211586&id=G1GMP-1405-MONOMER#tab=TU
Promoter (BBa_I719005), RBS (BBa_B0034) and Terminator (BBa_B0015) are from the iGEM Registry.
References
Kouzuma A, Kasai T, Hirose A, Watanabe K. "Catabolic and regulatory systems in shewanella oneidensis MR-1 involved in electricity generation in microbial fuel cells". Front Microbiol. 2015;6(JUN):1–11.