Difference between revisions of "Part:BBa K3102030:Design"
(→Source) |
(→References) |
||
Line 19: | Line 19: | ||
===References=== | ===References=== | ||
+ | Lin Z, et al., "Metabolic engineering of Escherichia coli for the production of riboflavin". Microb Cell Fact. 2014;13(1):1–12. | ||
+ | |||
+ | Zhenquan Lin et al., “Metabolic engineering of Escherichia coli for the production of riboflavin," Microbial Cell Factories, 2014, 13:104. |
Latest revision as of 17:56, 13 October 2019
T7-RBS-RibF-Ter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 193
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
None
Source
E.coli, sequence found through Biocyc https://biocyc.org/gene?orgid=ECOLI&id=EG11079
Promoter (BBa_I719005) , RBS (BBa_B0034) and Terminator (BBa_B0015) are from the iGEM Registry.
References
Lin Z, et al., "Metabolic engineering of Escherichia coli for the production of riboflavin". Microb Cell Fact. 2014;13(1):1–12.
Zhenquan Lin et al., “Metabolic engineering of Escherichia coli for the production of riboflavin," Microbial Cell Factories, 2014, 13:104.