Difference between revisions of "Part:BBa K4156101:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | |||
+ | In the Llprd operon, we were the first to use a combination of the promoter hyper-spnak with RBS spoVG to initiate downstream sequences. After the lldR regulatory protein with the LldPRD promoter, we also introduced the RiboJ and RBS B0034 sequences to enhance transcriptional efficiency. | ||
===Source=== | ===Source=== | ||
− | + | Experimental constructed. | |
===References=== | ===References=== | ||
+ | |||
+ | <i> | ||
+ | Dual role of lldR in regulation of the lldPRD operon, involved in L-lactate metabolism in E. coli. Aguilera et al. J. Bacteriol. 2008, 190(8):2997 | ||
+ | </i> |
Latest revision as of 06:21, 9 October 2022
pLldR
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 688
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
In the Llprd operon, we were the first to use a combination of the promoter hyper-spnak with RBS spoVG to initiate downstream sequences. After the lldR regulatory protein with the LldPRD promoter, we also introduced the RiboJ and RBS B0034 sequences to enhance transcriptional efficiency.
Source
Experimental constructed.
References
Dual role of lldR in regulation of the lldPRD operon, involved in L-lactate metabolism in E. coli. Aguilera et al. J. Bacteriol. 2008, 190(8):2997